Surgery Flashcards

(4281 cards)

1
Q

Pathophysiology of acute pancreatitis

A

Pancreatic enzymes released and activated-> multi stage process

Oedema + fluid shift + vomiting —> hypovolaemic shock

Enzymes—-> autodigestion

Vessel autodigestion—> retroperitoneal haemorrhage

Inflammation—–> pancreatic necrosis

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2
Q

Implications of pancreatic necrosis

A

Super-added infection in 50% of patients with necrosis

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3
Q

Epidemiology of acute pancreatitis

A

1% of surgical admissions

4th and 5th decades

10% mortality

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4
Q

Aetiology of pancreatitis

A

Idiopathic (?microstones)

Gallstones

Ethanol

Trauma

Steroids

Mumps (+ other infections e.g. Coxsackie B)

Autoimmune: PAN

Scorpion (Trinidadian)

Hyperlipidaemia, Hypercalcaemia, Hypothermia

ERCP

Drugs: thiazides, azathioprine

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5
Q

Severe epigastric pain radiating to the back

May be relieved by sitting forward

Vomiting

A

?Acute pancreatitis

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6
Q

Raised HR, Raised RR

Fever

Hypovolaemia—> shock

Epigastric tenderness

Jaundice

Ileus (absent bowel sounds)

Ecchymoses

A

?Acute pancreatitis

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7
Q

Grey turner’s

A

Flank ecchymoses

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8
Q

Cullen’s

A

Periumbilical ecchymosis (tracks up falciform)

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9
Q
A

Grey Turner’s sign

Flank ecchymosis

Acute pancreatitis

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10
Q
A

Cullens sign

Peri-umbilical ecchymosis

Acute pancreatitis

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11
Q

Ddx for acute pancreatitis

A

Perforated duodenal ulcer

Mesenteric infarction

MI

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12
Q

Difference between Glasgow and Ranson criteria

A

Glasgow criteria valid for EtOH and gallstones
whereas Ranson only applicable to Etoh and can only be fully applied after 48 hours

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13
Q

Components of modified glasgow score

PANCREAS

A

PaO2 <8kPA

Age >55

Neutrophils >15 x 10^9

Ca <2mM

Renal function, U >16mM

Enzymes: LDH >600iu/L, AST >200 iu/L

Albumin <32 g/L

Sugar >10mM

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14
Q

Modified Glasgow criteria cut offs

A

1= mild

2= moderate

3= severe

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15
Q

Ix in acute pancreatitis and what would be seen

Bloods

A

Bloods:

FBC- raised WCC

Raised amylase (>1000/3x ULN) and raised lipase

U+Es: dehydration and renal failure

LFTs: cholestatic picture, raised AST, raised LDH

Ca: reduced

Glucose: raised

CRP: monitor progress, >150 after 48 hours= severe

ABG: reduecd O2 suggests ARDS

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16
Q

Ix in acute pancreatitis and what would be seen

Urine

A

Glucose

Raised conjugated bilirubin

Reduced urobiliongen

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17
Q

Ix in acute pancreatitis and what would be seen

Imaging

A

CXR: ARDS, exclude perforated DU

AXR: sentinel loop, pancreatic calcification

USS: gallstones and dilated ducts, inflammation

Contrast CT: Balthazar severity score

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18
Q

Cut offs for amylase in acute pancreatitis

A

>1000/ 3xULN

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19
Q

Difference between lipase and amylase

A

Lipase is more sensitive and speciic

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20
Q

CRP >150 after 48hrs in acute pancreatitis

A

Severe

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21
Q

What is used to grade severity of pancreatitis on CT?

A

Balthazar severity score

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22
Q

Complications of acute pancreatitis

Early: systemic

A

Respiratory: ARDS, pleural effusion

Shock: hypovolaemic or septic

Renal failure

DIC

Metabolic: hypocalcaemia, raised glucose, metabolic acidosis

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23
Q

Complications of acute pancreatitis

Late (>1w)

A

Pancreatic necrosis

Pancreatic infection

Pancreatic abscess: may form in pseudocyst or in pancreas, may require open or percutaenous drainage

Bleeding: e.g. from splenic artery, may require embolisation

Thrombosis: splenic artery, GDA or colic branches of SMA, may subsequently lead to bowel necrosis. Portal vein, may subsequently lead to portal HTN

Fistula formation: pancreato-cutaneous due to skin breakdown

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24
Q

Def: pancreatic pseudocyst

A

Collection of pancreatic fluid in the lesser sac, surrounded by granulation tissue

Occurs in 20% especially in EtOHic pancreatitis

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25
4-w after acute attack Persisting abdominal pain Epigastric mass-\> early satiety
?Pancreatic pseudocyst
26
Complications of pancreatic pseudocyst
Infection-\> abscess Obstruction of duodenum or common bile duct
27
Ix in pancreatic pseudocyst
Persistently raised amylase +/- deranged LFTs USS/CT
28
Management of pancreatic pseudocyst
\<6cm: spontaneous resolution \>6cm: Endoscopic cyst-gastrostomy Percutaenous drainage under US/CT
29
Causes of chronic pancreatitis AGITS
Alcohol: 70% Genetic: CF, HH Immune: lymphoplasmacytic sclerosing pancreatitis (raised IgG4) TGs raised Structural: obstruction by tumour, pancreas divisum
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Sentinal loop Focal dilated proximal jejunal loop in the LUQ Acute pancreatitis
31
Pancreatic calcification
32
Epigastric pain: bores through to back Relieved by sitting back or hot water bottle: erythema ab igne Exacerbated by fatty food or EtOH Steatorrhoea and weight loss (Polyuria and polydipsia) (Epigastric mass)
Chronic pancreatitis (DM) (pancreatic pseudocyst)
33
Complications of chronic pancreatitis
Pseudocyst DM Pancreatic cancer Pancreatic swelling-\> biliary obstruction Splenic vein thrombosis
34
Ix in chronic pancreatitis
Raised glucose Reduced faecal elastase= indicative of reduced exocrine function LFTs USS: pseudocyst AXR: speckled pancreatic clacifications CT: pancreatic calcifications
35
Serum amylase in chronic pancreatitis
serum amylase level is not routinely raised, is not diagnostic in chronic pancreatitis, and testing should therefore not be performed.
36
Px of chronic pancreatitis
1/3rd die within 10y
37
Conservative management of chronic pancreatitis
No EToH or smoking Reduced fat and increased carb diet
38
Medical management of chronic pancreatitis
Analgesia: NSAIDS/paracetamol first line. ?weak opiate (codeine phospohate) if not effective. May need additional pain relief in primary care e.g. coeliac plexus block. Enzyme supplementation e.g. Creon Cobalamin/thiamine supplementation ADEK vitamins DM Rx (Octreotide: somatostatin analgoe that inhibits pancreatic enzyme secretions)
39
Screening in chronic pancreatitis
DM Osteoporosis
40
Indications for Surgical Mx of chronic pancreatitis
Unremitting pain Weight loss Duct blockage
41
Surgical options of management of chronic pancreatitis
Distal pancreatectomy: Whipple's Pancreaticojejunostomy: drainage Endoscopic stenting
42
Monitoring in management of acute pancreatitis
Manage at appropriate level e.g. ITU if severe Constant reassessment: Hourly TPR, UO Daily FBC, U+Es, Ca, glucose, amylase
43
Medical management of acute pancreatitis
ABC approach Aggressive fluid resus: keep UO \>30ml/h Catheter+/- CVP Pancreatic rest: NBM NGT if vomiting TPN may be required Analagesia: pethidine or buprenorphine ± intravenous (IV) benzodiazepines. Morphine is relatively contra-indicated because of possible spastic effect on the sphincter of Oddi. Antibiotics: Not routinely given, use if suspected infection or before ERCP Penems often used, but use to treat specific infections Mx complications
44
Mx of the complications of acute pancreatitis
ARDS: O2 therapy or ventilation Raied glucose: insulin sliding scale Ca EToH withdrawal: chlordiazepoxide
45
ERCP use in acute pancreatitis
Diagnostic Can be used if pancreatitis with dilated ducts secondary to gallstones. ERCP and sphincterectomy -\> reduces complications
46
Indications for surgical management of acute pancreatitis
Infected pancreatic necrosis Pseudocyst or abscess Unsure re dx
47
Operations used in treatment of acute pancreatitis
Laparotomy + necrosectomy (pancreatic debridement) Laparotomy + peritoneal lavage Laparostomy: abdomen left open with sterile packs in ITU
48
Epidemiology of gallstones
~8% of the population \>40 years Incidence increasing Slight increased incidence in females 90% of gallstones remain asymptomatic
49
5Fs of gallstones
Fair Fat Female Forty Fertile
50
What is the general composition of gallstones
Phopsholipids: lecithin Bile pigments (broken down Hb) Cholesterol
51
What are the relative proportions of the different types of gall stones?
Mixed stones: 75% Cholesterol stones: 20% Pigment stones: 5%
52
What is the aetiology of gallstones
Lithogenic bile: Admirand's triangle Biliary sepsis GB hypomotility-\> stasis: pregnancy, OCP, TPN, fasting
53
What is admirand's triangle
A delicate balacnce exists between the levels of bile acids, phospholipids and cholesterol When this balance is disrupted, especially when there is supersaturation with cholesterol, there is predisoposition to the formation of lithogenic bile and the conseuqent development of cholesterol-type gallstones. This is because when cholesterol supersaturates it tends to crystallise and in the presence of enucleating factors can be a nidus for stone formation
54
Large often solitary gallbladder stone
Cholsterol
55
Formation of cholesterol gallstones
According to Admirand's triangle: decreased bile salts decreased lecithin increased cholesterol
56
What are the risk factors for the development of cholesterol stones?
Female OCP/pregnancy Increasing age High fat diet + obesity Racial e.g. American Indian tribes Loss of terminal ileum (reduction in bile salt reabsorption)
57
What is the composition of pigment stones in the gall bladder
Calcium bilirubinate
58
With what are pigment GB stones associated?
Haemolysis
59
Small, black gritty, fragile GB stones
Pigment stones
60
Often multiple GB stones with cholesterol as the major component
Mixed stones
61
What are the complications of gallstones
In the gallbladder: Biliary colic Acute cholecystitis +/- empyema Chronic cholecystitis Mucocele Carcinoma Mirizzi's syndrome In the CBD: Obstructive jaundice Pancreatitis Cholangitis In the gut: Gallstone ileus
62
Mirizzi's syndrome
Mirizzi's syndrome is a rare complication in which a gallstone becomes impacted in the cystic duct or neck of the gallbladder causing compression of the common bile duct (CBD) or common hepatic duct, resulting in obstruction and jaundice. The obstructive jaundice can be caused by direct extrinsic compression by the stone or from fibrosis caused by chronic cholecystitis (inflammation). A cholecystocholedochal fistula can occur
63
Pathogenesis of biliary colic
Gallbladder spasm against a stone impacted in the neck of the gallbladder: Hartmann's pouch Less commonly, the stone may be in the CBD
64
What is Hartmann's pouch?
a spheroid or conical pouch at the junction of the neck of the gallbladder and the cystic duct.
65
RUQ pain radiating to back (scapular region) Associated with sweating, pallor, N+V Attacks may be precipitated by fatty food and last \<6h O/E tenderness in right hypochondrium (jaundice)
?Biliary colic | (if stone is in the CBD)
66
DDx for biliary colic
Cholecystitis/other gallstone disease Pancreatitis Bowel perforation
67
Ix in biliary colic Urine
Same work up as cholecystitis Urine: Bilirubin, urobilinogen, Hb
68
Ix in biliary colic Bloods
Bloods: FBC, U+E, amylase, LFTs, G+S, clotting CRP
69
Ix in biliary colic Imaging
AXR: 10% of gallstones are radio-opaque Erect CXR: ?perforation USS: stones: acoustic shadow dilated ducts \>6mm Inflamed GB: wall oedema
70
Indications for MRCP in biliary colic
bile duct dilated and or liver function tests abnormal and USS has not detected CBD stones
71
What is the indication for endoscopic USS in biliary colic
If MRCP does not allow diagnosis to be made
72
Mx of biliary colic
Conservative: Rehydrate and NBM Opioid analgesia: morphine 5-10mg/2h max High recurrence rate therefore surgical management is favoured NB asymptomatic gallbladder stones do not need treatment Surgical: Laparoscopic cholecystectomy: Urgent (within 1w of diagnosis in those with acute cholecystitis) Elective at 6-12w Percutaenous choleystotomy
73
Indications for percutaenous cholecystotomy
Management of gallbladder empyema when: surgery is contraindicated at presentation and conservative management is unsuccessful. Reconsider lap chole for people whho have had percutaenous cholecystotomy once they are well enough for surgery
74
Mx of CBD stones
Offer bile duct clearance and lap chole to people with symptomatic or asymptomatic CBD stones Clear the bile duct: surgically at the time of lap chole or with ERCP before or at time of surgery If the bile duct cannot be cleared with ERCP, use bilirary stenting to achieve drainage as a definitive measure until definitive clearance
75
Pathogenesis of acute cholecystitis
Stone or sludge impaction in Hartmann's pouch leading to chemical and or bacterial inflammation 5% are acalculous: sepsis, burns, DM
76
Sequelae of acute cholecystitis
Resolution +/- recurrence Gangrene and rarely perf Chronic cholecystitis Empyema
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Servere RUQ pain Continuous radiating to right scapula and epigastrium Fever Vomiting
?Acute cholecystitis
78
Local peritonism in RUQ, tachycardia with shallow breathing +/- jaundice Murphy's sign Phlegmon Boas's sign
?Acute cholecystitis
79
What is Murphy's sign
2 fingers over the GB and ask patient to breath in Pain and breath catch, must be -ve on the left
80
What is phlegmon
May be palpable in acute cholecystitis Mass of adherent omentum and bowel
81
What is Boas' sign
Hyperaesthesia below the right scapula
82
Ix in acute cholecystitis Urine
Bilirubin, urobilinogen
83
Ix in acute cholecystitis Bloods
FBC: raised WCC U+E: dehydration from vomiting Amylase, LFTs, G+S, clotting, CRP
84
Ix in acute cholecystitis Imaging
AXR: gallstone, porcelain GB Erect CXR: perforation USS: stones, acoustic shadow Dilated ducts \>6mm Inflamed GB: wall oedema MRCP if dilated ducts seen on USS
85
Porcelain gallbladder is an uncommon manifestation of chronic cholecystitis, characterized by intramural calcification of the gallbladder wall [1]. The term "porcelain gallbladder" is used to describe the bluish discoloration and brittle consistency of the gallbladder wall seen in this condition [
86
Mx of acute cholecystitis
Admit Conservative: NBM Fluid resuscitation Analgesia: paracetamol, diclofenac, codeine, naproxen, IM pethidine Abx: cef and met 80-90% settle over 24-48h Deterioration may be suggestive of perforation/empyema Surgical: May be elective surgery at 6-12w (once inflammation has reduced) Or if \<72h can perform lap chole in acute phase
87
High fever RUQ mass
Think ?GB empyema Percutaenous drainage via cholecystotomy may be indicated
88
Vague upper abdominal discomfort Distension, bloating Nausea Flatulence, burping Symptoms exacerbated by fatty foods
Flatulent dyspepsia ?Chronic cholecystitis
89
Ddx in chronic cholecystitis
PUD IBS Hiatus hernia Chronic pancreatitis
90
Ix in chronic cholecystitis
AXR: porcelain GB US: stones, fibrotic, shrunken GB MRCP
91
Mx of chronic cholecystitis
Medical: bile salts (not very effective) Surgical: Elective cholecystectomy ERCP first if USS shows dilated ducts and stones
92
What are the features of gallstone mucocele
Neck of the GB blocked by stone but contents remain sterile Can be very large-\> palpable mass May become infected--\> empyema
93
Features of GB carcinoma
Rare Associated with gallstones and gallbladder polyps May see porcelain GB Incidental Ca found in 0.5-1% of lap choles
94
Features of Gallstone ileus
Large stone \>2.5cm erodes from GB into duodenum through a cholecysto-duodenal fistula 2o to inflammation May impact in the distal ileum leading to obstruction Rigler's triad
95
What is Rigler's triad
Pneumobilia SBO Gallstone in RLQ
96
Rigler triad consists of three findings seen in gallstone ileus: pneumobilia small bowel obstruction gallstone, usually in the right iliac fossa Rigler triad should not be confused with Rigler sign or the Hoffman-Rigler sign.
97
What is Bouveret's syndrome?
Gastric outlet obstruction due to gallstone
98
Causes of obstructive jaundice Rule of 30%s...
30% stones 30% Ca head of the pancreas 30% other
99
What are other causes of obstructive jaundice
LNs @ porta hepatis: TB, Ca Inflammatory: PBC, PSC Drugs: OCP, sulfonylureas, fluclox Neoplastic: cholangiocarcinoma Mirizzi's syndrome
100
Jaundice Dark urine, pale stools Itch
Obstructive jaundice Itch due to bile salts
101
At what [serum] is obstructive jaundice noticeable and where is it seen first
Noticable at ~50mM Seen at tongue frenulum first
102
Ix in obstructive jaundice Urine
Dark Raised bilirubin Reduced urobilinogen
103
Ix in obstructive jaundice Bloods
FBC: raised WCC in cholangitis U+Es: hepatorenal syndrome LFTs: raised conjugated bilirubin, ++ ALP, +AST/ALT Clotting: reduced VitK--\> Raised INR G+S: may need ERCP Immune: AMA, ANCA, ANA
104
Ix in obstructive jaundice Imaging
AXR: may visualise stone Pneumobilia suggests gas forming infection USS: DIlated ducts \>6mm Stones (95% accurtate) Tumour MRCP or ERCP PTC: percutaneous transhepatic colangiography
105
What is PCT
Percutaneous transhepatic cholangiography (PTHC or PTC) or percutaneous hepatic cholangiogram is a radiologic technique used to visualize the anatomy of the biliary tract. A contrast medium is injected into a bile duct in the liver, after which X-rays are taken.
106
Pneumobilia May be suggestive of a gas forming infection
107
Mx of stone causing obstructive jaundice
Conservative: Monitor LFTs, stone passage may lead to resolution Vits ADEK Analgesia Cholestyramine Interventional: If no resolution, worsening LFTs or cholangitis ERCP with sphincterectomy and stone extraction Surgical: Open/lap stone removal with T tube placement T tube cholangiogram 8d later to confirm stone removal Delayed cholecystectomy to prevent recurrence
108
MOA cholestyramine
Cholestyramine is a bile acid sequestrant. It works by helping the body remove bile acids, which can lower cholesterol levels in the blood. The medicine is also used to relieve itching that's caused by a bile duct blockage
109
Features of ascending cholangitis
Charcot's triad Reynolds pentad
110
What is Charcot's triad
Fever/rigors RUQ pain Jaundice
111
What is Reynolds pentad
Charcot's tirad Shock Confusion
112
Mx of ascending cholangitis
Cef and met 1st ERCP 2nd: open or lap stone removal with T tube drain
113
Risk factors for pancreatic carcinoma SINED
Smoking Inflammation: chronic pancreatitis Nutrition: high fat diet EtOH DM
114
Pathology of pancreatic carcinoma
90% are ductal adenocarcinomas Present late, metastasise early Direct extension to local structures, lymphatics, haematogenously to liver and lungs
115
Location of pancreatic adenocarcinoma
60% in head 25% in body 15% in tail
116
(Male) \>60y Painless obstructive jaundice picture or epigastric pain radiating to back and relieved by sitting forward Anorexia, weight loss and malabsorption Acute pancreatitis Sudden onset DM
?Pancreatic carcinoma
117
Palpable gallbladder Jaundice Epigastric mass (Trousseau's sign) Splenomegaly Ascites
Pancreatic adenocarcinoma (Thrombophlebitis migrans) Splenomegaly due to PV thrombosis leading to portal HTN
118
What is Courvossier's law
In the presence of painless obstructive jaundice, a palpable gall bladder is unlikely to be due to stones
119
Why does Coruvossier's sign occur
Cause unlikely to be gallstones, gallstones form over an extended period of time resulting in a shrunken, fibrotic gall bladder that does not easily distend, this is less likely to be palpable on examination In contrast, the gallbladder is more enlarged in pathologies that cause obstruction of the biliary tree over longer periods of time e.g. pancreatic malgiancny leading to passive distension from back pressure
120
Ix in pancreatic carcinoma Bloods
Cholestatic LFTs Ca 19-9 Raised Ca
121
Ix in pancreatic carcinoma Imaging
USS: pancreatic mass, dilated ducts, hepatic mets, guide biopsy EUS: better than CT/MRI for staging CXR: mets Laparoscopy: mets, staging
122
ERCP in pancreatic caricnoma
Shows anatomy Allows stenting Biopsy of peri-ampullary lesions
123
5y survival of pancreatic carcinoma
\<2% Mean survival \<6m
124
Mx of pancreatic carcinoma
Sx: fit, nomets, tumour \<3cm (\<10% patients) Whipple's pancreaticoduodenectomy Distal pancreatectomy Post-op chemo delays progression Palliation: Endoscopic/percutaneous stenting of CBD Paliative bypass surgery: cholecystojejunosostomy, gastrojejunostomy Pain relief: may need coeliac plexus block
125
Epidemiology of pancreatic endocrine neoplasia
30-60 y/o 15% associated with MEN1
126
With which MEN are pancreatic endocrine neoplasias associated?
MEN1
127
Fasting/exercise induced hypoglycaemia Confusion, stuipor\< LOC Raised insulin, raised c-peptide, reduced glucose
Insulinoma
128
Hypergastrinaaemia--\> hyperchlorhydia---\> PUD and chronic diarrhoea due to inactivation of pancreatic enzymes
Gastrinoma (Zollinger-Ellison)
129
Raised glucagon Necrolytic migratory erythema
Glucagonoma
130
Necrolytic migratory erythema Characteristic rash of glucagonoma
131
Watery diarrhoea Hypokalaemia Achlorrhydia Acidosis
VIPoma/ Verner-Morrison/ WDHA syndrome
132
MOA somatostatin
Inhibits glucagon and insulin release Inhibits pancreatic enzyme secretion
133
DM Steatorrhoea Gallstones Usually very malignant tumour with poor prognosis
Somatostatinoma
134
Favoured sites are stomach and duodenum followed by jejunum and ileum Usually located in submucosa Maybe visualised as a sessile mass May cause pain from localised inflammation or more rarely, mucosal bleeding 2% of tumours arise in this tissue
Ectopic pancreas
135
Failuire of fusion of dorsal and ventral buds---\> bulk of pancreas drains through smaller accessory duct. Usually asymptomatic May present with chronic pancreatitis
Pancreas divisum
136
Fusion of dorsal and ventral buds around duodenum May present with infantile duodenal obstruction
Annular pancreas
137
Pancreas divisum
138
Annular pancreas
139
What is a Klatskin tumour
Typically occuring cholangiocarcinoma at confluence of right and left hepatic ducts
140
Features of cholangiocarcinoma
Rare bile duct tumour Adenocarcinoma [Klatskin tumour[
141
Klatskin tumour
142
Risk factors for cholangiocarcinoma
PSC UC Choledocholithiasis Hep B/C Choledochal cysts Lynch 2 Flukes
143
Progressive painless obstructive jaundice GB not palpable Steatorrhoea Weight loss
?Cholangiocarcinoma
144
Ix in cholangiocarcinoma
Cholestatic LFTs CA19-9
145
Mx of cholangiocarcinoma
Poor Px Palliative stenting
146
Pathophysiology of Hydatid cyst
Zoonotic infection by Echinococcus granulosus Occurs in sheep-rearing communities Parasite penetrates the portal system and infects the liver---\> calcified cyst
147
Mostly asymptomatic Pressure effects: non-specific pain, abdominal fullness, obstructive jaundice Rupture: biliary colic, jaundice, urticaria, anaphylaxis, 2o infection
?Hydatid cyst
148
Ix in hydatid cyst
Eosinophilia CT
149
Rx in hydatid cyst
Rx: albendazole Sx: cystectomy for large cysts
150
What are the aims of pre-operative assessment and planning
Informed consent Assess risk vs benefits Optimise fitness of patient Check anaesthesia/analgesia type with anaesthetist
151
OP CHECS
Operative fitness: cardiorespiratory comorbidities Pills Consent History: MI, asthma, HTN, jaundice, complications of anaesthesia, DVT Ease of intubation: neck arthritis, dentures, loose teeth Clexane: DVT prophylaxis Site: correct and marked
152
Anticoagulants pre-op
Balance risk of haemorrhage with risk of thrombosis Avoid epidural, spinal and regional blocks
153
AED pre-op
Continue as usual Post-op give IV or via NGT if unable to tolerate orally
154
OCP/HRT pre-op
Stop 4w before major/leg sx Restart 2w post-op if mobile
155
Beta-blockers pre-op
Continue as normal
156
What are the routine pre-op bloods?
FBC U+Es G+S Clotting Glucose
157
What specific bloods are used pre-op
LFTs: liver disease, EtOH, jaundice TFT: thyroid disease Electrophoresis if from risk background
158
Cross-match for gastrectomy
4u
159
X-match for AAA
6u
160
How is cardiorespiratory function assessed pre-operatively
CXR: cardiorespiratory disease/symptoms, \>65 y/o Echo: poor LV function,?murmurs ECG: HTN, Hx of cardiac disease, \>55y Cardiopulmonary exercise testing PFT: known pulmonary disease or obesity
161
Why may you do an C spine XR pre-operatively
Flexion and extension views, in RA/AS
162
What are the different ASA grades
1: Normally healthy 2: Mild systemic disease 3: Severe systemic disease that limits activity 4: Systemic disease which is a constant threat to life 5: Moribund, not expected to survive 24h even with operation
163
NBM pre-op
\>2h for clear fluids \>6h for solids
164
Bowel prep indications
May be needed in left-sided operations Not usually needed in right-sided procedures Necessity is controversial
165
What are the risks of bowel prep
Liquid bowel contents spilling during Sx Electrolyte disturbance Dehydration Increased rate of post-op anastamotic leak
166
Indications for prophylactic Abx
Gi Sx Joint replacement
167
Elective GI Sx post-op infection rate
20%
168
When are prophylactic Abx given preoperatively
15-60 mins before Sx
169
What are some bowel prep options
Picloax: picosulfate and Mg citrate Klean-prep: macrogol
170
Abx prophlyaxis for Biliary sx
Cef 1.5g and met 500mg IV
171
Abx prophlyaxis for CR or appendicetomy
Cef and Met TDS
172
Abx prophlyaxis for Vascular Sx
Co-amoxiclav 1.2g IV TDS
173
DVT prophylaxis in surgery
Low risk: early mobilisation Medium risk: early mobilisation + TEDs + 20mg enoxaparin High: early mobilisation + TEDS + 40mg enoxaparin and intermittent compression boots perioperatievely
174
Risk of DM in surgery
Increased risk of post-operative complications
175
How does DM increase the risk of post-operative complications?
Sx leads to the release of stress hormones which antagonise insulin Patients are NBM Increased risk of infection Coexistant IHD and PVD
176
What should be done in DM patients pre-operatively?
Urine dipstick: proteinuria Venous glucose U+Es: K
177
What is the practical management of patients with IDDM when having surgery
Put patient first on list and inform surgeon and anaesthetist Some centres prefer to use GKI infusions (mixture of glucose, insulin and potassium) Sliding scale is not always necessary for minor ops, if in doubt, liase with diabetes specialist nurse
178
Management of insuilin pre and peri-operatively
Stop long acting insulin the night before Omit AM insulin if sx if in the morning Start sliding scale
179
Outline sliding scale
5% Dextroes with 20mmol KCl 125ml/hr Infusion pump with c50u actrapid Check CPG hourly and adjust insulin rate
180
What is target glucose when on a sliding scale
7-11mM
181
Post-op Mx of sliding scale
Continue sliding scale until tolerating food Switch to SC regimen around meal
182
Mx of NIDDM and surgery
If glucose control poor (fasting glucose \>10mM) treat as IDDM Omit oral hypoglycaemics on the AM of Sx Eating post-op: resume oral hypoglycaemics with meal Not eating post-op: check fasting glucose on AM of surgery, start insulin sliding scale. Consult specialist team about restrting PO Rx
183
Mx of diet controlled DM in surgery
Usually no problem Patient may be briefly insulin-dependant post-op Monitor CPGs
184
Risks of steroids and surgery
Poor wound healing Infection Adrenal crisis
185
Mx of LT steroids and surgery
Need to increase steroids to cope with stress Consider cover if high-dose steroids have been received within the past year
186
Steroid Rx in major surgery
Hydrocortisone 50-100mg IV with pre-med then 6-8 hourly for 3d Usual pre-operative steroids +25 mg hydrocortisone @ induction +100 mg day-1 for 48 – 72h
187
Steroid Rx in minor surgery
As for major but only for 24h
188
Jaundice and surgery
Best to avoid operating Use ERCP instead
189
Risks of jaundice and surgery
Patients with obstructive jaundice have increased risk of post-op renal failure, need to maintain a good UO Coagulopathy Increased infection risk---\> cholangitis
190
Pre-Op Mx of jaundice
Avoid morphine in pre-med due to possible spastic effect on the sphincter of Oddi Check clotting and consider pre-op vit K Give 1L NS pre-op unless CCF-\> moderate diuresis Catheterise to monitor UO Abx prophlyaxis
191
Intra-op Mx of jaundice
Hourly UO monitoring NS titrated to output
192
Post-op mx of jaundice
Intensive monitoring of fluid status Consider CVP and frusemide if poor output despite NS
193
Anticoagulated patients and surgery
Risk of haemorrhage vs risk of thrombosis Consultant surgeon, anaesthetist and haemotologist Very minor surgery can be undertaken without stopping warfarin if INR \<3.5 Avoid spinal, epidural and regional blocks In general continue aspirin/clopidogrel unless risk of bleeding is high, in which case stop 7d before surgery
194
Mx of anticoagulated with low-thromboembolic risk e.g. AF
Stop warfarin 5d pre-op, need INR \<1.5 Restart next day
195
Mx of anticoagulated with high thromboembolic risk e.g. valves, recurrent VTE
Need bridging with LMWH Stop warfaring 5d pre-op and start LMWH Stop LMWH 12-18h pre-op Restart LMWH 6h post-op Restart warfarin next day Stop LMWH when INR \>2
196
Mx of anticoagulated patients requiring emergency surgery
Discontinue warfarin Vit K 5mg slow IV Request FFP or PCC (prothrombin complext concentrate) to cover surgery
197
Risks of COPD and surgery
Basal atelectasis Aspiration Chest infection
198
Pre-op Mx of smoking/COPD
CXR PFTs Physio Quit smoking at least 4w prior to surgery
199
What are the aims of anaesthesia
Hypnosis, analgesia, muscle relaxation
200
Principles of anaesthesia
Induction Muscle relaxation Airway control Maintenance End of anaesthesia
201
Induction agent for anaesthesia
IV propofol
202
Muscle relaxation for anaesthesia
Depolarising: suxamethonium Non-depolarising: vecuronium , atracurium
203
Airway control for anaesthesia
ET tube LMA
204
Maintenance for anaesthesia
Usually volatile agent added to NO2/O2 mix e.g. halothan, enflurane
205
End of anaesthesia
Change inspired gas to 100% O2 Reverse paralysis: neostigmine and atropine (prevents muscarinic side effects)
206
Pre-medications for anaesthesia 7As
Anxiolytics and Amnesia: temazepam Analgesics: opioids, NSAIDs, paracetamol Anti-emetics: ondansteron 4mg/ metoclopramide 10mg Antacids: lansoprazole Anti-sialogue: glycopyrolate (reduces secretion) Antibiotics
207
Features of regional anaesthesia
May be used for minor procedures or if unsuitable for GA Nerve or spinal blocks Use long-acting agents e.g. bupivacaine
208
What are the contraindications to nerve/spinal blocks
Local infection Clotting abnormality
209
Complications of Propofol induction
Cardiorespiratory depression
210
Complications of Intubation
Oro-pharyngeal injury with laryngoscope Oesophageal intubation
211
Complications of Loss of pain sensation
Urinary retention Pressure necrosis Nerve palsies
212
Complications of Loss of muscle power in anaesthesia
Corneal abrasion No cough---\> atelectasis + pneumonia
213
Complications of Malignant hyperpyrexia
Rare complication precipitated by halothane or suxamethonium AD inheritance Rapid rise in temperature and masseter spasm Rx: dantrolene and cooling
214
Complications of Anaphylaxis in anaesthetics
Rare Possible triggers: antibiotics colloid NM blockers
215
What is the necessity of analgesia in surgery
Pain-\> autonomic acitvation--\> arteriolar constriction-\> reduced wound perfusion--\> impaired wound healing Pain-\> decreased mobilisation-\> increased VTE and decreased function Pain-\> decreased respiratory excursion and decreased cough--\> atelectasis and pneumonia Humanitarian considerations
216
General guidance for anaesthesia
Give regular doses at fixed intervals Consider best route: PO if possible PCA (patient-controlled) should be considered: morphine, fentanyl Follow stepwise approach Liaise with acute pain service
217
Pre-op analgesia
Epidural e.g. bupivacaine
218
End-op analgesia
Infiltrate wound edge with LA Infiltrate major regional nerves with LA
219
Features of spinal/epidural anaesthesia
Decreased SE as drugs more localised First line for major bowel resection Caution: respiratory depression, neurogenic shock (reduced BP)
220
What is the WHO pain ladder
Non-opiod +/- adjuvants Weak opiod + non-opioid +/- adjuvants Strong opiod + non-opioid +/- adjuvants
221
Non-opioid pain medications
Paracetamol NSAIDs: ibuprofen, diclofenac
222
Weak opioid pain medications
Codeine Dihydrocodeine Tramadol
223
Strong opioid analgesia
Morphine Oxycodone Fentanyl
224
What is ERAS
Enhanced recovery after surgery Commonly employed in colorectal and orthopaedic surgery
225
Aims of EPAR
Optimisie pre-op preparation for surgery Avoid iatrogenic problems e.g. ileus Minimise adverse physiological/immunological responses to surgery: (raised cortisol, reduced insulin) (hypercoagulbility) (immunosuppression) Increase speed of recover and return to function Recognise abnormal recovery and allow early intervention
226
Pre-op approach EPAR
Optimisation: Aggressive physiological optimisation e.g. Hydration, BP, anaemia, DM, co-morbidities Smoking cessation \>4w before surgery Admission on day of surgery, avoidance of prolonged fast Carb loading prior to surgery Fully informed patient encouraged to participate in recovery
227
Intra-op approach EPAR
Short-acting anaesthetic agents Epidural use Minimally invasive technqiues Avoid drains and NGTs where possible
228
Post-op approach to EPAR
Aggressive Rx of pain and nausea Early mobilisation and PT Early resumption of oral intake Early discontinuation of IV fluids Remove drains and urinary catheters ASAP
229
How can surgical complications be characterised
Immediate (\<24h) Early (1d-1m) Late (\>1m)
230
What are the immediate surgical complications
\<24h Intubation leading to oropharyngeal trauma Surgical trauma to local structures Primary or reactive haemorrhage
231
What are the early surgical complications
1d-1m Secondary haemorrhage VTE Urinary retention Atelectasis and pneumonia Wound infection and dehiscence Antibitoic associated colitis
232
What are the late surgical complications
\>1m Scarring Neuropathy Failure or recurrence
233
How can post-op haemorrhage be classified?
Primary Reactive Secondary
234
What is primary haemorrhage
Continuous bleeding starting during surgery
235
What is reactive bleeding
Bleeding at the end of surgery or early post-op 2o to increased CO and BP
236
What is secondary bleeding
Bleeding \>24h post op Usually due to infection
237
What are the causes of post-op urinary retention?
Drugs: opioids, epidural/spinal, anti-AChM Pain: sympathetic activation leading to sphincter contraction Psychogenic: hospital environment
238
What are the risk factors for post-op urinary retention?
Male Increasing age Neuropathy e.g. DM, EtOH BPH Surgery type: hernia and anorectal
239
Mx of post-op urinary retention
Conservative: Privacy, ambulation, void to running taps or in hot bath, analgesia Catheterise +/- gent 2.5mg/kg IV stat TWOC: if failed may be sent home with silicone catheter and urology output f/up
240
Features of pulmonary atelectasis
Occurs after nearly every GA Mucus plugging + absorption of distal air---\> collapse
241
What are the causes of pulmonary atelectasis
Pre-op smoking Anaesthetic: increases mucus production, reduced mucociliary clearance Pain inhibitng respiratory excursion and cough
242
First 48 hours post-sx Mild pyrexia Dyspnoea Dull bases with reduced air entry
?Pulmonary atelectasis
243
Mx of pulmonary atelectasis
Analgesia to aid coughing Chest PT
244
Features of wound infection
5-7d post-op S. aureus and coliforms
245
How can operations be classified
Clean Clean/cont Contaminated Dirty
246
What is a clean operation
Incision of uninfected skin without opening viscus
247
What is a clean/cont operation
Intraoperative beach of viscus (not colon)
248
What is a contaminated operation?
Breach of viscus and spillage or opening of colon
249
What is a dirty operation
Site already contaminated- faeces, urine, trauma
250
How can the risk factors for post-op wound infection be classified?
Pre-operative Operative Post-operative
251
What are the pre-op risk factors for wound infection
Increasing age Comorbidities e.g. DM Pre-existing infection e.g. appendix perf Patient colonisation e.g. MRSA
252
What are the operative risk factors for wound infection?
Op classification and wound infection risk Duration Technical: pre-op Abx, asepsis
253
What are the post-operative risk factors for wound infection
Contamination to wound from staff
254
Mx of wound infection
Regular wound dressing Abx Abscess drainage
255
Occurs 10d post-op Preceded by serosanguinous discharge from wound
Wound dehiscence
256
How can the risk factors for wound dehiscence be classified?
Pre-op Op Post-op
257
What are the pre-op risk factors for wound dehiscence?
Increasing age Smoking Obesity, malnutrition, cachexia Comorbidities e.g. DM, uraemia, chronic cough, Cancer Drugs: steroids, chemo, RTx
258
What are the operative risk factors for wound dehiscence?
Length and orientation of incision Closure technique: follow Jenkin's rule Suture material
259
What is Jenkin's rule?
It is a rule for closure of the abdominal wound. It states that for a continuous suture, the length of suture used should be at least four times the length of the wound with sutures 1cm apart and with 1cm bites of the wound edge (More recent research has shown that the optimal ratio may in fact be 6:1)
260
What are the post-operative risk factors for wound dehiscence?
Increased IAP e.g. prolonged ileus leading to distension Infection Haematoma/seroma formation
261
Mx of wound dehiscence
Replace abdo contents and cover with sterile soaked gauze IV Abx: cef and met Opioid analgesia Call senior and arrange theatre Repair: wash bowel, debride wound edge, close with deep non-absorbable sutures e.g. nylon May require VAC dressing or grafting
262
What are the Cxs of cholecystectomy
Conversion to open: 5% CBD injury: 0.3% Bile leak Retained stones needing ERCP Fat intolerance/ loose stools
263
What are the early complications of inguinal hernia repair?
Haematoma/seroma formation: 10% Intra-abdominal injury (laparoscopic) Infection Urinary retention
264
What are the late complications of inguinal hernia repair?
Recurrence (\<2%) Ischaemic orchitis (0.5%) Chronic groin pain/paraesthesia (5%)
265
What are the complications of appendicectomy
Abscess formation Fallopian tube trauma Right hemicolectomy e.g. for carcinoid, caecal necrosis
266
What are the early complications of colonic surgery?
Ileus AAC (acute acalculous cholecystitis) Anastomotic leak Enterocutaneous fistulae Abdominal or pelvic abscess
267
What are the late complications of colonic surgery?
Adhesions leading to obstruction Incisional hernia
268
What are the causes of post-op ileus?
Bowel handling Anaesthesia Electrolyte imbalance
269
Post surgery: Distension Constipation +/- vomiting Absent bowel sounds
?post-op ileus
270
Mx of post-op ileus
IV fluids and NGT TPN if prolonged
271
What are the complications of anorectal surgery?
Anal incontinence Stenosis Anal fissure
272
What are the complications of small bowel surgery?
Short gut syndrome (\<250cm)
273
Def: short gut syndrome
Malabsorption disorder caused by the surgical removal of a large portion of the small intestine
274
Abdominal pain Diarrhea and steatorrhea (oily or sticky stool, which can be malodorous) Fluid depletion Weight loss and malnutrition Fatigue
?Small gut syndrome May also have complications caused by malabsorption in vitamin absoprtion e.g. anaemia, hyperkeratosis, easy brusing, muscle spasms, poor blood clotting and bone pain
275
What are the complications of splenectomy
Gastric dilatation 2o to gastric ileus: prevent with NGT Thrombocytosis-\> VTE Infection: encapsulated organisms
276
What are the complications of arterial surgery
Thrombosis and embolisation Anastomotic leak Graft infection
277
What are the complications of aortic surgery?
Gut ischaemia Renal failure Aorto-enteric fistula Anterior spinal syndrome Emboli: distal ischaemia--\> trash foot
278
Complications of breast surgery
Arm lymphoedema Skin necrosis Seroma
279
What are the complications of urological surgery?
Sepsis Uroma: extravasation or urine
280
What are the complications of prostatectomy?
Urinary incontinence Erectile dysfunction Retrograde ejaculation Prostatitis
281
What are the complications of thyroidectomy?
Wound haematoma--\> tracheal obstruction Recurrent laryngeal nerve trauma-\> hoarse voice - transient in 1.5% - permanent in 0.5% Damage to R nerve more common due to it being more medial Hypoparathyroidism---\> hypocalcaemia Thyroid storm Hypothyroidism
282
What are the complications of tracheostomy?
Stenosis Mediastinitis Surgical emphysema
283
What are the complications of # repair?
Mal/non-union Osteomyelitis AVN Compartment syndrome
284
What are the complications of hip replacement?
Deep infection VTE Dislocation Nerve injury: sciatic, SGN Leg length discrepancy
285
What are the complications of cardiothoracic surgery
Pneumo/haemothorax Infection: mediastinitis, empyema
286
How can post-op pyrexia be classified?
Early 0-5d Delayed \>5d
287
What are the early causes of post-op pyrexia
0-5d post-op Blood transfusion Physiological: SIRS from trauma, 0-1d Pulmonary atelectasis: 24-48hr Infection: UTI, superficial thrombophlebitis, cellulitis Drug reaction
288
What are the delayed causes of post-op pyreixa
\>5d post-op Pneumonia VTE: 5-10d Wound infection: 5-7d Anastomotic leak: 7d Collection: 5-20d
289
Examination work up in post-op pyrexia
Obs, notes and drug chart Wound Abdo + DRE Legs Chest Lines Urine Stool
290
What are the Ix in post-op pyrexia?
Urine: dip, MC+S Bloods: FBC, CRP, cultures +/- LFTs Cultures: wound swabs, CVP tip for culture CXR
291
Cause of post-op pneumonia
Anaesthesia-\> atelectasis Pain-\> reduced cough Sx-\> immunosuppression
292
Rx of post-op pneumonia
Chest physio: encourage coughing Good analgesia Abx
293
Malaise Swinging fever, rigors Localised peritonitis Shoulder tip pain (if subphrenic) Post-op
?Collection
294
What are the locations of collections?
Pelvic: 4-10d post-op Subphrenic: present 7-21d post-op Paracolic gutters Lesser sac Hepatorenal recess (Morrison's space) Small bowel (interloop spaces)
295
What is Morrison's space
Hepatorenal recess
296
Ix in collection
FBC, CRP, cultures USS, CT Diagnostic lap
297
Rx of post-op collection
Abx Drainage/washout
298
Def: cellulitis
Acute infection of subcutaneous connective tissue
299
Cause of cellulitis:
Beta haemolytic strep and staph aureus
300
Pain, swelling, erythema and warmth Systemic upset +/- lymphadenopathy
Cellulitis
301
Rx of cellulitis
Benpen IV Pen V and fluclox PO
302
Def: diverticulum
Out-pouching of tubular structure
303
True diverticulum
Composed of complete wall e.g. Meckel's
304
Def: false diverticulum
Composed of mucosa only (pharyngeal, colonic)
305
Diverticular disease
Symptomatic diverticulosis
306
Def: diverticulitis
Inflammation of diverticula
307
Epidemiology of diverticular disease
30% have diverticulosis by 60 years F\>M
308
Pathophysiology of diverticular disease
Associated with increased intraluminal pressure: low fibre diet has no osmotic effect to keep stool wet Mucosa herniates through muscularis propria at points of weakness i.e. where perforating arteries enter Most commonly located in the sigmoid colon
309
What is Saint's triad Unifying factor?
Hiatus hernia Cholelithiasis Diverticular disease ?Obesity
310
Symptoms of diverticular disease
Altered bowel habit +/- left sided colic, relieved by defecation Nausea Flatulance
311
Altered bowel habit +/- left sided colic, relieved by defecation Nausea Flatulance
?Diverticular disease
312
Rx for diverticular disease
High fibre diet Mebeverine may help Elective resection for chronic pain
313
Pathophysiology of diverticulitis
Inspissated faeces-\> obstruction of diverticulum Think in elderly patient with previous history of constipation
314
Presentation of diverticulitis
Abdominal pain and tenderness Typically LIF Localised peritonitis Pyrexia
315
Abdominal pain and tenderness Typically LIF Localised peritonitis Pyrexia
Diverticulitis
316
Ix in diverticulitis: bloods
FBC Raised WCC Raised CRP/ESR Amylase G+S/x-match
317
Ix in diverticulitis: imaging
Erect CXR: ?perforation AXR: fluid level/air in bowel wall Contrast CT Gastrograffin enema
318
Ix in diverticulitis: endoscopy
Flexi sig Colonscopy (not used in acute attack)
319
What can be used to grade diverticulitis perforation
Hinchey grading
320
Hinchey 1
Localised para-colonic abscess- surgery rarely needed
321
Hinchey 2
Large abscess extending into pelvis May resolve without surgery
322
Hinchey 3
Generalised purulent peritonitis Surgery needed
323
Hinchey 4
Generalised faecal peritonitis Surgery needed
324
Mx of mild acute diverticulitis
Can be treated at home with bowel rest (fluids only) and abx- some conflicting evidence about use of abx in uncomplicated diverticular disease.. (augmentin +/- met)
325
Indications for admission acute diverticulitis
Unwell Fluids can't be tolerated Pain can't be controlled
326
Medical Mx of acute diverticulitis
NBM IV fluids Analgesia: paracetamol Antibiotics: cef and met Most cases settle
327
NSAIDs and opioid analgesics in diverticulitis
Have been identified as risk factors for perforation
328
Indications for surgical management of diverticulitis
Perforation Large haemorrhage Stricture leading to obstruction
329
Surgical procedure used in diverticulitis
Harmann's to resect diseased bowel
330
Complications of diverticulitis
Perforation Haemorrhage Abscess Fistulae Strictures
331
Sudden onset pain Generalised peritonitis and shock +/- preceding diverticulitis
?Perforation
332
Mx of perforation in diverticulitis
CXR: free air under the diaphragm Rx: Hartmann's
333
Suddeen painless, bright red PR bleed Following diverticulitis
?Haemorrhage
334
Ix in ?haemorrhage in diverticulitis
Mesenteric angiography or colonoscopy
335
Mx of haemorrhage in diverticulitis
Usually stops spontaneously May need transfusion Colonoscopy +/- diathermy/adrenaline Embolisation Resection
336
Walled off perforation Swinging fever Localising signs e.g. boggy rectal mass Leukocytosis Hx of diverticulitis
?Abscess
337
Mx of diverticulitis abscess
Abx + CT/US guided drainage
338
Types of of fistulae following diverticulitis
Enterocolic Colovaginal Colovesicular
339
Pneumaturia + intractable UTIs
?Colovesciular fistula
340
What may occur after diverticulitis
Colon may heal with fibrous strictures
341
Mx of strictures post diverticulitis
Resection (usually with primary anastomosis) Stenting
342
How can bowel obstruction be classified
Simple Closed loop Strangulated
343
Simple bowel obstruction
1 obstructing point + no vascular compromise May be partial or complete
344
Closed-loop bowel obstruction
Bowel obstructed at two points Left CRC with competent ileocaecal valve. Volvulus Gross distension can lead to perforation
345
Strangulated bowel obstruction
Compromised blood supply Localised, constant pain + peritonism Fever and raised WCC
346
What are the commonest causes of SBO
Adhesions: 60% Hernia
347
What are the commonest causes of LBO
Colorectal neoplasia (60%) Diverticular stricture (20%) Volvulus 5%
348
How can bowel obstruction be classified
Non-mechanical Mechanical
349
What is non-mechanical bowel obstruction?
Paralytic ileus
350
Causes of paralytic ileus
Post-op Peritonitis Pancreatitis or any localised inflammation Posions/drugs: anti-AChM Pseudo-obstruction Metabolic: hypokalaemia, hyponatraemia, hypomagnesia, uraemia Mesenteric ischaemia
351
Intestinal pseudo-obstruction
Intestinal pseudo-obstruction is a clinical syndrome caused by severe impairment in the ability of the intestines to push food through. It is characterized by the signs and symptoms of intestinal obstruction without any lesion in the intestinal lumen.[1] Clinical features can include abdominal pain, nausea, severe distension, vomiting, dysphagia, diarrhea and constipation, depending upon the part of the gastrointestinal tract involved.[2] The condition can begin at any age and it can be a primary condition (idiopathic or inherited) or caused by another disease (secondary).[3] It can be chronic[4] or acute.[5]
352
How can mechanical bowel obstruction be classified?
Intraluminal Intramural Extramural
353
What are the intraluminal causes of bowel obstruction
Impacted matter: faeces, worms, bezoars Intussuception Gallstones
354
What are the intramural causes of mechanical obstruction?
Benign stricutre: IBD, Sx, ischaemic colitis, diverticulitis, RTx Neoplasia Congenital atresia
355
What are the extramural causes of bowel obstruction
Hernia Adhesions Volvulus (sigmoid, caecal, gastric) Extrinsic compression: pseudocyst, abscess, haematoma, tumour e.g. ovarian, congenital bands e.g. Ladds
356
Ladd's bands
Ladd's bands, sometimes called bands of Ladd, are fibrous stalks of peritoneal tissue that attach the cecum to the abdominal wall and create an obstruction of the duodenum. This condition is found in malrotation of the intestine.
357
Presentation of bowel obstruction
Abdominal pain: Colicky, central but level depends on gut region, constant/localised pain suggest strangulation or impending perforation Distension: with lower bowel involvement Vomiting: early in high, late or absent in low Absolute constipation
358
Abdominal pain: Colicky, central but level depends on gut region, constant/localised pain suggest strangulation or impending perforation Distension: with lower bowel involvement Vomiting: early in high, late or absent in low Absolute constipation
?Bowel obstruction
359
Absolute constipation
Of flatus and faeces
360
Examination findings in bowel obstruction
Tachycardia: hypovolaemia, strangulation Dehydration, hypovolaemia Fever: suggests inflammatory disease or strangulation Surgical scars Hernias Mass: neoplastic or inflammatory Bowel sounds: increased in mechanical obstruction, reduced in ileus PR: empty rectum, rectal mass, hard impacted stool, blood from higher pathology
361
Bowel obstruction, increased bowel sounds
Mechanical obstruction
362
Bowel obstruction, reduced bowel sounds
Ileus
363
Ix in bowel obstruction: bloods
FBC: raised WCC U+Es: dehydration, electrolyte abnormalities Amylase: ++ in strangulation/perforation VBG: raised lactate in strangulation G+S, clotting: may need Sx
364
Ix in bowel obstruction: imaging
Erect CXR AXR +/- erect film for fluid levels CT: can show transition point
365
Ix in bowel obstruction: gastrograffin studies
Look for mechanical obstruction: no free flow Follow through or enema Follow through may relive mild mechanical obstruction, usually adhesional
366
Ix in bowel obstruction: colonoscopy
Can be used in some cases Risk of perforation May be used to therapeutically stent
367
AXR findings in ileus
Both small and large bowel may be visible No clear transition point
368
SBO AXR findings
Diameter \>3 Central Valvulae coniventes: completely across LB gas absent Many loops Many, short fluid levels
369
370
LBO AXR findings
\>6cm (caecum \>9cm) Peripheral loccation Haustra- partially across LB gas present in rectum Few loops Few, long fluid levels
371
372
373
Def: Meckel's diverticulum
Ileal remnant of vitellointestinal duct Joins yoke sac to midgut lumen
374
Features of Meckel's diverticulum
A true diverticulum 2 inches long 2ft from ileocaecal vavle on antimesenteric border 2% of population 2% symptomatic Contain ectopic gastric or pancreatic tissue
375
Symptomatic Meckel's presentation
Rectal bleeding from gastric mucosa Diverticulitis mimicking appendicitis Intussuception Volvulus Malignant change: adenocarcinoma Raspberry tumour: musoca protruding at umbilicius: vitello-intestinal fistula Littre's hernia
376
Rectal bleeding from gastric mucosa Diverticulitis mimicking appendicitis Intussuception Volvulus Malignant change: adenocarcinoma Raspberry tumour: musoca protruding at umbilicius: vitello-intestinal fistula Littre's hernia
Meckels diverticulum
377
Littre hernia
Littre hernia is a hernia containing a Meckel's diverticulum. Also known as a persistent omphalomesenteric duct hernia. It is most frequently encountered in the inguinal region.
378
Dx of Meckel's
Tc pertechnecate scan +ve in 70% (detects gastric mucosa)
379
Rx Meckels
Surgical resection
380
Def: intussuception
Portion of the intestine (the intussuception) is invaginated into its own lumen (the intussuscipiens)
381
Causes of intussuception
Hypertrophied Peyer's patch Meckel's HSP Petuz-Jeghers Lymphoma
382
Presentation of intussuception
6-12mo Colicky abdo pain: episodic incosolable crying, drawing up legs +/- bilious vomiting Redcurrent jelly stools Sausage shaped abdominal mass
383
6-12mo Colicky abdo pain: episodic incosolable crying, drawing up legs +/- bilious vomiting Redcurrent jelly stools Sausage shaped abdominal mass
Intussuception
384
NB intussuception in adults
Rarely occurs If it does, consider neoplasm as a lead point
385
Mx of intussusception
Resuscitate and X-match, NGT US + reduction by air enema Sx if irreducible
386
Def: mesenteric adenitits
URTI/viral infeciotn-\> enlargement of mesenteric LNs= pain tenderness and fever
387
Differentiating features of mesenteric adenitis
Post URTI Headache + photophobia Higher temperature Tenderness is more generalised Lymphocytosis
388
Gross anatomy: External ear
Auricle External auditory meatus
389
Gross antomy: middle ear
Tympanic: malleus, incus and stapes
390
Gross anatomy: inner ear
Semicircular canals, vestibule, cochlea
391
392
Purpose of audiometry
Quantify loss and determine its nature
393
Features of pure tone audiometry
Headphones deliver tones at different frequencies and strengths Patient indicates when sound appears and disappears Mastoid vibrator- bone conduction threshold Threshold at different frequences are plotted to give an audiogram
394
Purpose of tympanometry
Measures stiffness of the ear drum Evaluates middle ear function
395
Flat tympanogram=
Mid ear fluid or perforation
396
Shifted tympanogram=
+/- mid ear pressure
397
Features of evoked response audiometry
Auditory stimulus with measurement of elicited brain response by surface electrode Used for neonatal screening if otoacoustic emission test negative
398
Presentation of otitis externa
Watery discharge Itch Pain and tragal tenderness
399
Watery discharge Itch Pain and tragal tenderness
?Otitis externa
400
Causes of otitis externa
Moisture e.g. swimming Trauma e.g. fingernails Absence of wax Hearing aid
401
Organisms causing otitis externa
Pseudomonas Staph aureus
402
OE
403
OE
404
Mx of otitis externa
Conservative: remove precipitating factors Medical: Analgesia e.g. paracetamol or ibuprofen Treat inflammation: Topical acetic acid For more severe cases consider topical antibitoic +/- corticosteroid Surgical: ?Cleaning of ear if required
405
Rx in non-infected eczematous OE
Betamethasone
406
Combination therapies for OE
Betamethasone with neomycin Hydrocortisone with gentamicin
407
Rx for fungal OE
Consider clotrimazole
408
Consideration for amingoglycoside treatment of OE
If perf can lead to ototoxicity
409
Severe otalgia which is worse at night Copious otorrhoea Granulation tissue in the canal (90% in DM)
Malignant otitis externa
410
Implications of malignant OE
Life-threatening infection which can lead to skull osteomyletitis Look for tenderness of mastoid process
411
Rx of malignant OE
Admit for IV abx +/- surgical debridement
412
Malignant OE
413
Def: bullous myringitis
Painful haemorrhagic blisters on deep meatal skin and tympanic membrane Associated with influenza infection
414
With what is bullous myringitis associated
Influenza infection
415
Bullous myringitis
416
What are the symptoms of TMJ dysfunction
Earache (referred pain from auriculo temporal nerve) Facial pain Joint-clicking/popping Teeth-grinding (bruxism) Stress (associated with depression)
417
Joint tenderness exacerbated by lateral movements of open jaw
?TMJ dysfunction
418
Ix of TMJ dysfunction
MRI
419
Mx of TMJ dysfunction
NSAIDs stabilising orthodontic occlusal prostheses
420
How can OM be classified?
Acute OME Chronic Chronic suppurative OM
421
Acute OM=
Acute phase OM
422
OME=
Effusion after symptom regression
423
Chronic OM=
Effusion \>3mo if bilateral or \>6mo if unilateral
424
Def: chronic suppurative OM
Ear discharge with hearing loss and evidence of central drum perforation
425
Presentation of acute OM
Usually children post viral UTI Rapid onset ear pain, tugging Irrritability, anorexia, vomiting Purulent discharge if perforation
426
Usually children post viral UTI Rapid onset ear pain, tugging Irrritability, anorexia, vomiting Purulent discharge if perforation
Acute OM
427
Bulging red TM Fever
Acute OM
428
Rx in acute OM
Paracetamol Amoxicillin: may used delayed presecription
429
How can the cx of OM be classified
Intratemporal Intracranial Systemic
430
Intratemporal complications of OM
OME Perforation of TM Mastoidis Facial N. palsy
431
Intracranial Cxs of OM
Meningitis/encephalitis Brain abscess Sub/epidural abscess
432
Systemic cxs of OM
Bacteraemia Septic arthritis IE
433
Acute OM
434
Features of delayed antibiotic prescribing strategies
Should be started if symptoms not improving within 4d of onset of symptoms or signficiant worsening of symptoms Safety net
435
Inattention at school Poor speech development Hearing impairment
?OME
436
OME Retracted, dull TM Fluid level
437
Audiometry in OME
Flat tympanogram
438
Mx of OME
Usually resolves spontaenously Consider grommets if persistent hearing loss SE: infections and tympanosclerosis
439
Painless discharge with hearing loss
Chronic suppurative OM
440
Chronic suppurative OM
441
Rx chronic suppurative OM
Aural toilet Abx/steroid ear drops
442
Complications of chronic suppurative OM
Cholesteatoma
443
Def: mastoiditis
Middle-ear inflammation-\> destruction of mastoid air cells and abscess formation
444
Fever Mastoid tenderness Protruding auricle
?Mastoiditis
445
Ix in mastoiditis
CT
446
Mx in mastoiditis
IV Abx Myringotomy and mastoidectomy
447
Def: cholesteatoma
Locally destructive expansion of stratified squamous epithelium within the middle ear
448
How can cholesteatoma be classified?
Congenital Acquired: secondary to attic perforation in chronic suppurative OM
449
Foul smelling white discharge Headache/pain CN involvement: vertigo, deafness, facial paralysis
?Cholesteatoma
450
Cholesteatoma Pearly white with surrounding inflammation
451
Cx of cholesteatoma
Deafness (ossicle destruction) Meningitis Cerebral abscess
452
Mx of cholesteatoma
Sx
453
Def: tinnitus
Sensation of sound without external sound stimulation
454
How can causes of tinnitus be classified?
Specific General Drugs
455
Specific causes of tinnitus
Meniere's Acoustic neuroma Otosclerosis Noise-induced Head injury Hearing loss e.g. presbyacusis
456
Presbyacusis
Loss of hearing that gradually occurs in most individuals as they grow older
457
General causes of tinnitus
Raised BP Anaemia
458
Drugs causing tinnitus
Aspirin Aminoglycosides Loop diuretics ETOH
459
Components of tinnitus history
Character: constant or pulsatile Unilateral (acoustic neuroma) FHx: otoscleoris Alleviating/exacerbating factors e.g. worse at night Associations: Vertigo: Meniere's, acoustic neuroma Deafness: Meniere's, acoustic neuroma Causes e.g. head injury, noise, drugs, Fhx
460
Def: otosclerosis
Hereditary disorder causing progressive deagness due to bone overgrowth in the inner ear
461
Examination in tinnitus
Otoscopy Tuning fork tests Pulse and BP
462
Ix in tinnitus
Audiometry and tympanogram MRI if unilateral to exclude acoustic neuroma
463
Mx of tinnitus
Treat underlying causes Psych support: tinnitus retraining therapy Hypnotics at night may help
464
Def: vertigo
The illusion of movement
465
How can the causes of vertigo be classified
Peripheral/vestibular Central Drugs
466
Peripheral causes of vertigo
Meniere's BPPV Labyrinthitis
467
Central causes of vertigo
Acoustic neuroma MS Vertebrobasilar insufficiency Stroke Head injury Inner ear syphillis
468
Drugs causing vertigo
Gentamicin Loop diuretics Metronidazole Co-trimoxazole
469
Components of vertigo history
Is it true vertigo or light-headedness: which way are things moving: spinning/whirling when not moving (vertigo), sense of imbalance or staggering when walking (disequilibirium), light headedness (presyncope), dizziness caused by hyperventilation Timespan Associated symptoms: n/v, hearing loss, tinnitus, nystagmus
470
Nystagmus
Condition of involuntary eye movement can be physiological or pathological
471
Examinations and tests in vertigo
Hearing Cranial nerve Cerebellar and gait Rombergs +ve= vestibular or proprioception Hallpike manouvre Audiometry, calorimetry, LP, MRI
472
Meniere's triad
Vertigo Tinnitus Hearing loss
473
Pathology of Meniere's disease
Dilatation of endolymph spaces of membranous labyrinth (endolymphatic oedema)
474
Attacks occuring in clusters lasting up to 12h Progressive SNHL Vertigo and n+v Tinnitus Aural fullness (pressure in the ears)
?Meniere's
475
Audiometry showing low frequency SNHL which fluctuates
Meniere's
476
Mx: Meniere's disease
Medical: Symptomatic reliefe: prochlorperazine (if severe) or betahistine or cyclizine Surgical: Gentamicin instillation via grommets Saccus decompression
477
Follows febrile illness (e.g. URTI) Sudden vomiting Severe vertigo exacerbated by head movemenet
Vestibular neuronitis/viral labyrinthistis
478
Mx of viral labyrinthitis
Cyclizine Improvement in days
479
Pathology of BPV
Displacement of otoliths in semicircular canals Common after head injury
480
Sudden rotational vertigo for \<30s Provoked by head turning Nystagmus
BPV
481
Features of classic BPPV
Geotropic nystagmus with the problem ear down Predominantly rotatory fast phase toward undermost ear Latency (a few seconds) Limited duration (\< 20 s) Reversal upon return to upright position Response decline upon repetitive provocation
482
How can nystagmus be classified
Begins as a slow pursuit movement followed by a fast rapid, resetting phase Named by direction of the fast phase Right or left beating (horizontal nystagmus) Up-beating or down-beating (vertical) Or direction changing If the movements are not horizontal or vertical then the nystagmus is rotational (clockwise or counter-clockwsie) Can also have visual evoked nystagamus (VER)- implies central lesion
483
Causes of BPV
Idiopathic Head injury Otosclerosis Post-viral
484
Dx of BPV
Hallpike manoeuvre-\> upbeat torsional nystagmus
485
Rx of BPV
Self-limiting Epley manoeuvre Betahistine
486
Difference between primary and secondary otalgia
Primary there is usually abnormality on examination Secondary is normal looking ear
487
Causes of primary otalgia
OE/OM FB Barotrauma Rarely: OME Ramsay hunt Perichorditis Cellulitis Relapsing polychondritis etc.
488
Causes of secondary otalgia
Can be classified on basis of nerve territory e.g. Trrigeminal TMJ problems Facial: CPA lesions etc Glossopharyngeal: tumours in PNS/pharynx Vagus: tumours in pharynx/larynx, GORD Spinal nerves: arthritis/tumours
489
Borders of the anterior triangle of the neck
Mandible Midline Sternocleidomastoid
490
Borders of the posterior triangle of the neck
Sternocleidomastoid Trapezius Clavicle
491
Quinsy=
Peritonsillar abscess
492
Definition of a definitive airway
In the trachea Cuffed below the vocal cords Attached to oxygen Secured
493
What are the indications for intubation
A: protection and patency B: respiratory failure, increase FRC, decreased WOB, secretion management, to facilitate bronchoscopy C: minimise oxygen consumption and optimise O2 delivery D: unresponsive to pain, prevent brain injury E: temperature control
494
Causes of stridor
Children: croup, inhaled FB, tracheitis, abscess (retropharyngeal, peritonsillar), anaphylaxis, epiglottits, laryngomalacia, VC dysfunction, subglottic stenosis, laryngeal web, laryngeal tumours, tracheomalacia, choanal atresia, tracheal stenosis Adults: anaphylaxis, laryngitis, epiglottits/supraglottitis, FB, abscess, laryngospasm, tumour
495
Sound of stridor
Insipiratory NB: stridor can be biphasic if obstruction is at the level of the glottis
496
Causative organisms in epiglottits
Strep Staph HiB Pseudomonas Moraxella catarrhalis TB
497
Rapid onset Unwell Odynophagia Drooling Fever Anterior tenderness over hyoid bone Lymphadenopathy Tripod sign Progressing rapibldy to SOB, resp distress, airway obstruction, stridor
?Epiglottis/supraglottits
498
Ix in epiglottits
Airway prep Lateral neck XR Bloods +/- cultures
499
Mx of epiglottits
IV antibiotics: usually 3rd gen cephalosporin Steroids Intubation +/- cricothyroidotomy c trachy if airway obstructed
500
Mx of stridor
ABCDE Appropriate area e.g. A&E resus Adrenaline (1:1000) nebulised Steroids: budenoside nebs + IV dex O2 Intubation if needed Cricothyroidotomy either needle or surgical
501
Site of location of cricothyroidotomy?
Through cricothyroid membrane inbetween thyroid cartilage and cricoid Can be done with large bore cannulae or surgically
502
Mx of epistaxis
1. External compresion: 90% anterior, 10% posterior, lean forward and distal part of nose, spit anything that enters mouth 2. Packing: Anterior: merocel (nasal tampon)/ Rapid rhino 48hrs After removal cauterise and give naseptin cream (NB contain peanut oil) Posterior packing: urinary catheter, insert until tip seen at back of mouth, inflate balloon slowly, don't let go of catheter 3. Cautery using silver nitrate 4. Theatre Surgical ligation of the sphenopalantine artery
503
What is Little's area?
AKA Kiesselbach's plexus Kiesselbach's plexus, which lies in Kiesselbach's area, Kiesselbach's triangle, or Little's area, is a region in the anteroinferior part of the nasal septum where four arteries anastomose to form a vascular plexus. The arteries are:[1] Anterior ethmoidal artery and posterior ethmoidal artery (both from the ophthalmic artery) Sphenopalatine artery (terminal branch of the maxillary artery) Greater palatine artery (from the maxillary artery) Septal branch of the superior labial artery (from the facial artery) 90% of nosebleeds occur here due to the drying effect of air
504
What are the red flags in epistaxis?
Age \>50y Nasal obstruction Facial pain Hearing loss Proptosis/double vision Lymphadenopathy, weight loss
505
Middle-aged Chinese people with epistaxis think
?Nasopharyngeal carcinoma as high incidence
506
Occupational exposure to dust/chemicals with epistaxis
Think nasopharyngeal carcinoma as RF
507
Epistaxis in child \<2
Shouldn't happen ?NAI
508
Risk factors for mastoiditis
Young children Immunocompromised Cholesteatoma
509
Organisms causing mastoiditis
Strep pneumonia, pyogenes, staph, pseudomonas, HiB
510
Unwell Fever Painful over mastoid process Swollen and boggy Young children: irritable, pinna protrusion +/- discharge TM perforation Hx of otitis media Chronic: recurrent otalgia, headache, fever, OME/suppurative OM
?Mastoiditis
511
Mastoiditis
512
O/E 6th or 7th nerve palsy Conductive deafness Boggy swelling behind ear
?Mastoiditis
513
Ix in mastoiditis
FBC, CRP, blood cultures Ear swab CT/MRI Audiogram
514
Mx of mastoiditis
High dose broad specrutm IV Abx Analgesia Emergency mastoidectomy for cholesteatoma and mastoid oteitits or intracranial spread or not improving
515
Dizziness what other questions should you ask?
N+V Tinnitus Hearing loss Feeling of aural fullness Headaches Visual changes Weakness Numbness
516
Usually preceded by paranasal sinusitits Medical emergency Also caused by local trauma, insect or animal bites, FB, URTI
Periorbital cellulitis
517
Ocular pain Eyelid swelling Erythema
?Periorbital cellulitis
518
What differentiates between periorbital cellulitis and orbital cellulitis
Orbital also presents with painful eye movements, proptosis, opthalmoplegia, visual impairment, chemosis
519
Aetiology of SNHL
Usually idiopathic
520
Mx of idiopathic SNHL
Short-course high dose steroids (+/- PPI cover) With repeat audiogram F/U
521
Def: acoustic neuroma
Benign slow-growing tumour of the vestibular nerve (vestibular schwanomma)
522
Sudden onset or progressive SNHL, tinnitus, balance issues, vertigo
?Acoustic neuroma
523
Local effects of acoustic neuroma
5th trigeminal causing facial numbness and tingling Facial nerve can also be affected If very large can compress the brainstem or cuse raised ICP
524
Most common site of acoustic neuroma growth
Cerebellopontine angle
525
Mx of acoustic neuroma
Watchful waiting with MRI/audiogram Stereotactic radiotherapy
526
Cx of acoustic neuroma sx?
Loss of hearing Damage to other cranial nerves esepcially the 7th
527
Bell's palsy
528
Sudden onset unilateral facial droop +/- hyperacusis Loss of sensation in anterior 2/3rds of tongue
Bell's palsy
529
What differentiates between LMN and UMN Bell's palsy
UMN lesions have forehead sparing as frontalis receives innervation from both hemispheres) For it to be true Bell's it must not have forehead sparing
530
Why should Lyme disease serology be done in Bell's palsy in endemic areas
As LD can lead to facial nerve palsy
531
Mx of Bell's palsy
Short term high dose (60-80mg) steroids + eye care (drops with taping at night)
532
Bell's palsy px
Incomplete lesions have better prognosis
533
What is Ludwig's angina
Submandibular space infection Aggressive and rapidly spreading cellulits from which patients can become quickly septic with compromised airway
534
Unwell Fever Mouth pain Drooling Dysphagia
Ludwig's angina
535
Mx of Ludwig's angina
IV Abx with anaerobe cover Close monitoring Airway +++
536
Def: conductive hearing loss
Impaired conduciton anywhere between auricle and round window
537
How can the causes of conductive hearing loss be classified?
External canal obstruciton TM perforation Ossicle defects Inadequate eustachian tube ventilation of midddle air
538
Causes of external canal obstruction Leading to conductive hearing loss
Wax Pus FB
539
Causes of TM perforation Leading to conductive hearing loss
Trauma Infection
540
Causes of ossicle defects leading to conductive hearing loss?
Otosclerosis Infection Trauma
541
Def: sensorineural hearing loss
Defects of cochlea, cochlear nerve or brain
542
Which drugs can cause sensorineural hearing loss?
Aminoglycosides Vancomycin
543
Which post-infective syndromes are associated with sensorineural hearing loss?
Meningitis Measles Mumps Herpes
544
What are some miscellaneous causes of sensorineural hearing loss?
Meniere's Trauma MS CPA lesions e.g. acoustic neuroma Low B12
545
Acoustic neuroma=
Benign slow-growing tumour of superior vestibular nerve
546
􀁸 Slow onset, unilat SNHL, tinnitus ± vertigo 􀁸 Headache (↑ICP) 􀁸 CN palsies: 5,7 and 8 􀁸 Cerebellar signs
?Acoustic neuroma
547
All patients with unilateral tinnitus/deafness should receive an?
MRI
548
What syndrome associated with acoustic neuromas?
NF2
549
What accounts for 80% of CPA tumours?
Acoustic neuromas
550
Common cause of CPA syndrome?
Acoustic neuromas
551
Bruns nystagmus
Dancing eyes Seen in large tumours due to compression of the flocculi in CPA syndrome
552
Features of CPA syndrome
Tumours within nerve cannaliculi: unilateral SNHL, tinnitus or disequilibirium Tumours extending into the CPA may present with disequilibrium and ataxia With brainstem extension, midfacial and corneal hypesthesia, hydrocephalies and other CN palsies become more prevalent | (speech discrimination out of proportion to hearing loss and difficulty talking on the telephone are frequent accompaniements)
553
DDx slow onset unilateral SNHL
Meningioma Cerebellar astrocytoma Mets
554
Otosclerosis
AD condition characterised by fixation of the stapes at the oval window F\>M 2:1
555
Begins early in adult life Bilateral conductive deafness + tinnitus HL improved in noisy places (Willis' paracousis) Worsened by pregnancy/menstruation
Otosclerosis
556
\>65y Bilateral slow onset hearing loss +/- tinnitus
Age-related hearing loss i.e. presbyacussis
557
Congenital causes of conductive hearing loss in children
Anomalies of pinna, external auditory canal, TM or ossicles Congenital cholesteatoma Pierre-Robin
558
Congenital causes of SNHL in children
AD: Waardenburgs: SNHL, heterochromia + telecanthus AR: Alports (SNHL + haematuria), Jewell-Lange-Nielson X-Linked: Alports Infections: CMV, rubella, HSV, toxo, GBS Ototoxic drugs
559
Perinatal causes of paediatric hearing loss
Anoxia CP Kernicterus Infeciton: meningitis
560
Acquired causes of paediatric hearing loss
OM/OME Infection: meningitis, measles Head injury
561
What are some congenital anomalies seen in the ear
1st and 2nd branchial arches form auricle while 1st branchial groove forms external auditory canal Malfusion leads to accessory tags/auricles and preauricular pits, fistulae or sinuses Sinuses may get infected
562
Features of pinna heamatoma
Blunt trauma leading to subperichondrial haematoma Can lead to ischaemic necrosis of cartilage and subsequent fibrosis to cauliflower ears
563
Mx of pinna haematoma
Aspiration and firm packing to auricle contour
564
Def: exostoses
Smooth, symmetrical bony narrowing of external canals
565
Pathology of exostoses
Bony hypertrophy due to cold exposure e.g. from swimming/surfing Asymptomatic unless narrowing occludes the canal leading to conductive deafness
566
Causes of TM perforation
OM Trauma Barotrauma FB
567
What are the classifications of allergic rhinosinusitis?
Seasonal Perennial
568
Pathology of allergic rhunosinusitis?
T1HS Ig-E mediated inflammation from allergen exposure leading to mediator relesase from mast cells Allergens include pollen, house dust mites
569
Sneezing Pruritus Rinorrhoea
?Allergic rhinosinusitis
570
Swollen, pale and boggy nasal turbinates Nasal polyps
?Allergic rhinosinusitis
571
External nose parameters
Extends from the nasal bones and surrounding parts of the maxilla and frontal bone Supported by the central septal cartilage and its lateral processes At the apex there are two major alar cartilages Near the maxilla there are smaller minor alar cartilages
572
573
Internal nose parameters
Comprises two paired nasal cavities which extend and expand supero-posteriorly from the anterior nares Nasal septum separates left and right Hard palate makes up the floor of the cavities and separates them from the oral cavity Posterior nares open posteriorly into the nasopharynx
574
What are the three regions of the internal nose?
Vestibular: just inside nostrils Respiratory: ciliated epithelium making up the bulk of the cavity walls Olfactory: specialised olfactory epithelium on the roofs of the cavities
575
What are found on the lateral walls of each nasal cavities?
Superior middle and inferior conchae
576
Which bone do the superior and middle conchae arise from?
Ethmoid
577
Which bone do the inferior conchae extend from?
The maxilla
578
What do the conchae form?
Narrow air passages known as the superior, middle and inferior meatus
579
What is the major route for nerve entry into the nasal cavity?
Sphenopalatine formaen and is found on the postero-lateral wall of the superior meatus
580
What is the space above the superior concha called?
The spheno-ethmoidal recess
581
What are the 4 paranasal sinuses?
Ethmoidal Sphenoidal Maxillary Frontal
582
583
584
Features of the ethmoidal sinus
Collection of specialised ethmoidal air cells in the respiratory region of the nose Openings in the bulla ethmoidalis on the lateral wall of the middle meatus Cells between medial and lateral plates of the ethmoid labyrinths
585
Features of the sphenoidal sinuses?
Posterior to the nasal cavity within the sphenoid bone Openings in the posterior wall of the spheno-ethmoidal recess Immediately antero-inferior to the pituitary fossa
586
What is the largest of the nasal sinuses?
Maxillary
587
Features of the maxillary sinus
Beyond the lateral walls of the nasal cavity within the maxillae Openings in the hiatus semilunaris floor on the lateral wall of the middle meatus Drain at the apex- prone to filling with fluids that are hard to drain
588
Features of the frontal sinus
Superior to the nasal cavities within the frontal bone Openings in the hiatus semilunaris roof on the lateral wall of the middle meatus Drains through the frontonasal duct to the ethmoidal infundibulum
589
What is the course of the nasolacrimal duct?
Carries tears from the corner of the eye opening in the inferior meatus, inerfo-anterior to the hiatus semilunaris
590
Whence does the blood supply of the nose come?
Internal and external carotid arteries
591
What are the significant arteries supplying the nose?
Sphenopalantine artery Greater palantine artery Anterior and posterior ethmoidal arteries
592
593
Features of the sphenopalatine artery?
Terminal branch of the maxillary artery- branch of external carotid Enters the cavity through the sphenopalatine formaen Gives lateral branches supplying most of the lateral wall and medial branches to medial wall
594
Features of the greater palatine artery
Branch of maxillary artery: branch of external carotid Enters the anterior floor of the nasal cavity through the incisive canal and supplies the anterior septum and floor Anastomoses with septal branches of the sphenopalatine artery
595
From which artery do the ethmoidal arteries branch and what carotid does it originate from?
Ophthalmic artery Internal carotid
596
How do the ethmoidal arteries enter the nasal cavity?
Through the cribiform plate
597
Course of the anterior and posterior ethmoidal arteries
Anterior: anastomoses with branches of the sphenopalatine artery and terminates as the external nasal artery Posterior division supplies the upper lateral and medial walls
598
Whence comes the general sensory innervation of the nose?
Ophthalmic and maxillary division of V
599
What innervates the mucous glands in the nose?
Parasympathetic fibres of the facial nerve: arise form the pterygopalatine ganglion and run with V2 fibres
600
Branches of the facial nerve To Zanzibar By Motor Car
Temporal Zygomatic Buccal Mandibular Cervical
601
Branches of the trigeminal nerve
Ophthalmic Maxillary Mandibular
602
Cranial exits of trigeminal nerve branches Standing Room Only
Superior orbital fissure Foramen rotundum Foramen ovale
603
Features of ophthalmic nervous supply of the nose
Two key branches: ethmoidal nerves Anterior branch: travels with anterior ethmoidal artery and supplies the anterior medial and lateral walls before terminating as the external nasal nerve Posterior branch supplies the ethmoidal air cells and does not enter the nasal cavity
604
Features of maxillary nerve supply of nasal cavity
Lateral branches supply the lateral wall Nasopalantine nerve supplies the medial wall before terminating in the oral muscoa
605
606
Ix in allergic rhinosinusitis
Skin-prick testing to find allergnes RAST
607
Mx of allergic rhinitis
Allergen avoidance: regulalry washing bedding, avoid pollen Rx: 1st Line: PRN: Oral antihistamine e.g. cetirazine, desloratidine or intranasal e.g. azelastine Preventative: intranasal corticosteroid e.g. beclometasone (if nasal blockage or polyps) or oral antihistamine 2nd line: Intranasal steroid + antihistamine (oral) 3rd line: Zafirlukast (leukotriene antag) 4th line: Immunotherapy: to induce desensitisation to allergen Oral corticosteroids can be considered for severe symptoms
608
What are some adjuvant nasal decongestants?
Pseudoephedrine, otrivine
609
Pathophysiology of sinusitis
Viruses-\> mucosal oedema and decreased mucosal ciliary actions leading to mucus retention and secondary bacterial infection
610
Causative organisms acute bacterial sinusitis?
Pneumococcus, Haemophilus, Moraxella
611
Causative organisms chronic bacterial sinusitis
S. aureus, anaerobes
612
Causes of sinusitis
Majority are bacterial infection 2o to viral 5% due to dental root infections Diving/swimming in infected water Anatomical variation may leave individuals susceptile e.g. deviated septum, nasal polyps Systmic disease e.g. PCD/Kartagener's
613
Pain increasing on bending/straining Discharge from nose-\> foul taste Nasal obstruciton/congestion Anosmia or cacosmia (bad smell without external source) Systemic symptoms
?Bacterial sinusitis
614
Which sinus liklely to be invovled if cheek/teeth pain in sinusitis
Maxillary
615
Which sinus liklely to be invovled if pain between eyes in sinusitis
Ethomidal
616
Ix in sinusitis
Nasendoscopy +/- CT
617
Mx of acute single episode of sinusitis
Bed-rest, decongestants, analgesia Nasal douching and topical steroids Abx of uncertain benefit
618
Mx of chronic/recurrent sinusitis?
Usually a structural or drainage problem Stop smoking and fluticasone nasal spray Functional endoscopic sinus sx if medical therapy fails
619
Complications of sinusits (rare)
Mucoceles-\> pyoceles Orbital cellulitis/abscess Ostemoyelitis e.g. staph in frontal bone Intracranial infection e.g. meningitis, encephalitis, abscess, CVST
620
What are the sites of nasal polyps
Middle turbinates Middle meatus Ethmoids
621
Water, anterior rhinorrhoea Purulent post-nasal drip Nasal obstruciton Sinusitis Headaches Snoring
?Nasal polyps
622
Mobile pale insensitive growths in nasal cavity
?Nasal polyps
623
What are the associations of nasal polyps?
Allergic/non-allergic rhinitis CF Aspirin hypersensitvity Asthma
624
Single unilateral nasal polyp
May be a sign of rare but sinister pathology e.g. Nasopharyngela Ca Glioma Lymphoma Neuroblastoma Sarcoma CT + histology
625
Nasal polyps in children
Rare in \<10, must consider neoplastic disease or CF
626
Mx of nasal polyps
Drugs: Betamethasone for 2/7 Short course of oral steroids Endoscopic polypectomy
627
No direct response but intact conseunsual response to light Cannot initiate consensual response in contralteral eye Dilatation on moving light from normal to abnormal eye What is the defect?
Afferent defect
628
Cause of afferent pupillary defect?
Total CNII lesion
629
Marcus-Gunn pupil=
RAPD
630
Minor constriction to direct light Dilatation on moving light from normal to abnormal eye
RAPD- Marcus Gunn pupil
631
Causes of RAPD
Optic neuritis Optic atrophy Retinal disease
632
Dilated pupil does not react to light Initiates consensual response in contralateral pupil Ophthalmoplegia and ptosis
Efferent defect
633
Cause of efferent pupillary defect
3rd nerve palsy
634
Medical 3rd nerve palsy
Pupil sparing as the visceral constrictive fibres run on the outisde of the nerve so are spared in vascular aetiologies
635
Complete 3rd nerve palsy=
"surgical third"
636
Ptosis Down and out pupil Dilated pupil
?3rd nerve palsy
637
Causes of third nerve palsy
DM (75% pupil sparing) Temporal arteritis SLE MS Cavernous sinus thrombosis Amyloid PCA aneurysm Tumour
638
Ipsilateral third nerve palsy with contralateral hemiplegia
Weber syndrome= midbrain stroke
639
Whence does the CNIII arise?
Rostral midbrain
640
What are the nuclei of CNIII?
Oculomotor nucleus (somatic fibres)- eye movements Edinger-Westphal nucleus (visceral fibres)- pupillary constriciton
641
Course of the oculomotor nerve?
Passes between the posterior cerebral and superior cerebellar arteries and then through the cavernous sinus and out through the superior orbital fissure
642
Branches of CNIII
Superior branch- levator palpebrae Inferior branch- MR, IR and IO muscles and carries the visceral fibres
643
3rd nerve palsy ptosis 'down and out' pupil dilated pupil
644
DDx of a fixed, dilated pupil
Mydriatics e.g. tropicamide Iris trauma Acute glaucoma CN3 compression: tumour, coning
645
646
RAPD
647
Young woman with sudden blurring of near vision Initially unilateral and then bilateral pupil dilatation Dilated pupil has no response to light and sluggish response to accomodation = a tonic pupil
Holmes-Adie pupil
648
Iris shows spontaneous wormy movmenets on slit-lamp examination Iris streaming
Holmes-Adie pupil
649
Aetiology of Holmes-Adie pupil
Damage to postganglionic parasympathetic fibres Idiopathic: may have viral aetiology
650
Homes-Adie pupil
651
Tonic pupil + absent knee/ankle jerks + reduced BP=
Holmes-Adie syndrome
652
Johann Horner
Swiss opthalmologist
653
Features of Horner's syndrome PEAS
Ptosis: partial (superior tarsal muscle) Enophthalmos Anhydrosis Small pupil
654
Horner's syndrome
655
How can the causes of Horner's syndrome be classified?
Central Pre-ganglionic Post-ganglionic
656
What are the central causes of Horner's
MS Wallenberg's Lateral Medullary Syndrome
657
Small, irregular pupils Accomodate but don't react to light Atrophied and depigmented Iris
Argyll-Robertson
658
Argyll-Robertson pupil "prostitutes pupil"
Accomodates but doens't react
659
Causes of Argyll Robertson
DM Quaternary syphillis
660
Reduced acuity Reduced colour vision (especially red) Central scotoma Pale optic disc RAPD
?Optic atrophy/opticneuropathy
661
What are the most common causes of optic atrophy?
MS and glaucoma
662
How can the causes of optic neuropathy be classified? CAC VISION
Congenital Alcohol and other toxins Compression Vascular Inflammatory Sarcoid Infection Oedema Neoplastic infiltration
663
What are the congenital causes of optic atrophy?
Leber's hereditary optic neuropathy Hereditary motor and sensory neuropathy/ Charcot Marie Tooth Friedrich's ataxia Wolfram (DIDMOAD) Retinitis pigmentosa
664
Attacks of acute visual loss, sequential in each eye +/- ataxia and cardiac defects FHx Onset in 20-30s
Leber's hereditary optic neuropathy Mitochondrial disease
665
What are the toxins causing optic neuropathy?
Ethambutol Pb B12 deficiency
666
What are the compressive causes of optic neuropathy
Neoplasia: optic glioma, pituitary adenoma Glaucoma Paget's
667
What are the vascular causes of optic atrophy
DM, GCA, thromboembolic
668
What are the inflammatory causes of optic atrophy
MS, Devic's, DM
669
Devic's disease
Neuromyelitis optica (NMO), also known as Devic's disease or Devic's syndrome, is a heterogeneous condition consisting of the simultaneous inflammation and demyelination of the optic nerve (optic neuritis) and the spinal cord (myelitis). It can be monophasic or recurrent.
670
What are the infective causes of optic atrophy?
Herpes zoster, TB, syphillis
671
oedematous causes of optic atrophy
Papilloedema
672
Anteroposterior anatomy of the eyeball
Cornea Anterior chamber (aqueous humours) Uvea (Iris, ciliary body, choroid plexus) Posterior chamber Lens Vitreous humour
673
What are the two muscles responsible for eyelid movement
Obicularis oculi- closes the eyelids, innervated by CN7 (Bell's palsy) Levator palpebrae- opens the eyelid, innervated by CN3 (Horner's)
674
What is the conjunctiva
Mucus membrane covering the eyeball Semi-transparent hence the white colouring Starts at the edge of the cornea (imbus) and loops forward to form the inner surface of the eyelid.
675
Where are the majority of tears produced?
Accessory tear glands located within the eyelid and the conjunctiva Lacrimal gland itself is primarily responsible for reflexive tearing.
676
What is a consideration for lid laceration in the nasal quadrant of the lid?
Compromising the canalicular tear-drainage pathway.
677
What is a consideration re drug administration and nasolacrimal duct
Nasal absorption of drugs can have profound effects. hence why squeezing the medial canthus during administration of eye drops can help mitigate htis
678
Features of the sclera
White fibrous outer layer of the eyeball, continuous with the cornea anteriorly and the optic nerve sheath posteriorly
679
Anterior chamber of the eye=
Between cornea and the iris
680
Posterior chamber of the eye
Between the iris and the lens
681
Viterous chamber of the eye
Extends from the lens to the retina
682
What is PVD in the context of ophthalmology?
Posterior viterous detachment usually benign but can cause retinal tears
683
Where in the eye is the aqueous humor produced?
Posterior chamber, flowing through the pupil into the anterior chamber where it drains into the venous circulation via the Canal of schlemm
684
Features of the cornea
Avascular receiving its nutrition from tears on the outside and aqueous fluid internally with peripheral blood vessels
685
What are the layers of the cornea
Epithelium Bowman's layer (belfry) Stroma Descemet's membrane (deep) Endothelium
686
Damage to which layer of the cornea can lead to scar formation?
Corneal stroma
687
What forms the anterior chamber angle
Angle formed by the inner cornea and the root of the iris Location of the Schlemms canal
688
Def: uvea
Iris Ciliary body (secretes aqueous fluid and controls the shape of the lens) Choroid plexus
689
Components of the lens
Capsule Nucleus Cortex
690
How are cataracts described?
Described by where they occur I.e. nucleur, cortical, subcapsular
691
What does contraction of the ciliary muscle lead to?
Causes the zonule ligaments holding the lens in place to relax Allowing the lens to become rounder
692
Presbyopia
Difficulty focusing on nearby objects
693
What is the macula
Pigmented area of the retina responsible for central vision Within the macula lies the fovea (susceptible to injury during retinal detachments)
694
What are the bones making up the orbital walls?
Frontal Sphenoid (greater wing) Ethmoid Lacrimal Palatine Maxillary Zygomatic
695
What is the entry point for the nerves and vessels supplying the orbit
Orbital apex
696
Nerves passing through the orbital fissure Live Frankly To See Absolutley No Insult
Lacrimal and Frontal divisions of V1 Trochlear nerve Superior division fo the oculomotor nerve Abducens Nasociliary branch of V1 Inferior division of III
697
What is the thinnest bone in the orbit?
Ethmoid Mose likely to perforate from an eroiding sinus infection in children
698
699
Funciton of LR
Abduction
700
Function of MR
Adduction
701
Extraocular muscle lesion, patients report
Diplopia when looking in the affected direction
702
Featuers of Horner's syndrome PAMEL
Ptosis Anhydrosis Miosis Enophthalmos Loss of ciliospinal reflex
703
Ciliospinal reflex
The ciliospinal reflex (pupillary-skin reflex) consists of dilation of the ipsilateral pupil in response to pain applied to the neck, face, and upper trunk. If the right side of the neck is subjected to a painful stimulus, the right pupil dilates (increases in size 1-2mm from baseline). This reflex is absent in Horner's syndrome and lesions involving the cervical sympathetic fibers. The enhanced ciliospinal reflex in asymptomatic patients with cluster headache is due to preganglionic sympathetic mechanisms.
704
Mydriasis
Excessive dilataion of the pupil
705
Crossed eye Nerve palsy
6th nerve palsy
706
Causes of 6th nerve palsy
Vasculopathic Tumour False localising sign i.e. raised ICP
707
Action of Trochlear nerve
SO Causes eye depression and intorsion Looking towards nose: more up down Looking laterally: more rotational
708
4th nerve palsy
Nasal upshoot
709
Nasal upshoot nerve palsy causing?
4th nerve palsy
710
Causes of 4th nerve palsy
Vasculopathic Tumour Congenital Trauma
711
Why do pupils blow first in 3rd nerve compression
As the fibres controlling pupillary constriction run on the external surface of the nerve
712
Pseudotumour cerebri
=Idiopathic intracranial HTN
713
What are the components of visual history?
Vision Sensation Appearance Discharge
714
What are some significant symptoms in a red eye history Vision
Blurred Distorted Diplopia Field defect/scotoma Floaters/flashes
715
What are some significant symptoms in a red eye history: Sensation
Irritation Pain Itching Photophobia FB
716
What are some significant symptoms in a red eye history Appearance
Red: ?distribution Lump Puffy lids
717
What are some significant symptoms in a red eye history Discharge
Watering Sticking Stringy
718
What are the key questions in the examination of a red eye?
Inspect A-P Is acuity affected Is the globe painful Pupils equal and reactive? Corena: intact, cloudy? Use fluorescein
719
What are the signs of serious disease in a red eye history?
Photophobia Poor vision Corneal fluorescein staining Abnromal pupil
720
Red eye ++++ pain No photoboia Reduced acuity Hazy/cloudy cornea Large pupil Raised IOP
?Acute glaucoma
721
?Acute glaucoma
722
Eclipse sign
The eclipse sign using an oblique flashlight has been well described as a tool to detect shallow anterior chamber. A beam of light shone from the temporal aspect of the cornea towards the root of nose produces a semicircular shadow of the iris in the nasal area. The width of the semicircular shadow gives an indication of the depth of the anterior chamber. A shallow anterior chamber produces a broader shadow compared to an anterior chamber of normal depth as it is the eclipse of the light.
723
Red eye ++ pain ++ photophobia Reduced acuity Pain on accomodation Normal cornea Small pupil Normal IOP
?Anterior uveitis
724
Red eye Abdominal pain
?Acute closed angle glauocma
725
Red eye +/- pain + photobia Normal acuity Normal cornea Normal pupil Normal IOP
?Conjunctivitis
726
How can the ddx of red eye be classified?
Site: Lids Conjunctiva Sclera Cornea Anterior chamber
727
What are the mechanical causes of red eye
Lids: Ectropion, entropion, FB, trichiasis Conjunctiva: Sub cojunctival haemorrhage Sclera: Perforation Cornea: Foreign body Abrasion Anterior chamber; Acute glaucoma
728
What are the inflammatory causes of red eye?
Lids: Blepharitis, Chalazion Conjunctiva: Allergic conjunct Sclera: Chemical burn, episcleritis, scleritis Anterior chamber: Iritis/uveitis
729
What are the infective causes of red eye?
Lids: Perioribital cellulitis, orbital cellulitis Conjunctiva: Conjunctivitis Cornea: Keratitis Ant chamber: Endophthalmitis
730
Anterior uveitis
731
Scleritis
732
Aetiology of acute closed angle glaucoma?
Blocked drainage of aqueous from anterior chamber vis the canal of Schlemm Pupilar dilatation worsens the blockage IOP rises from 15-20--\> 60mmHg
733
RFs for acute closed angle glaucoma
Hypermetropia Shallow anterior chamber Female FHx Increased age Drugs: anticholinergics sympathomimetics TCAs Anti-histmaines
734
Prodrome: rainbow haloes around lights at night time Severe pain with n+v Reduced acuity and blurred vision
Acute closed angle glaucoma
735
Cloudy cornea with circumcorneal injection Fixed dilated, irregular pupil Raised IOP makes eye feel hard
Acute cloesd angle glaucoma
736
Ix in acute closed angle glaucoma
Tonometry: raised IOP, usually \>40mmHg
737
Mx of acute closed angle glaucoma
Refer to ophthalmology Lie the person flat Pilocarpine eye drops (2% blue, 4% brown) (miosis opens blockage) Acetazolamide 500mg IV stat: reduces aqueous formation Analgesia +/- antiemetic
738
What are the aims of the treatment of angle closure glauocma
Reduce intraocular pressure Ease symptoms Prevent development/further progression of glaucoma
739
Definitive treatment for angle closure glaucoma
Laser iridotomy to allow aqueous humour to freely flow into posterior chamber.
740
Pathophysiology of uveitis
Inflammation of uvea (iris, ciliary body and choroid) If just iris and ciliary body= anterior uveitis
741
Acute pain and photophobia Pain on accomodation Blurred vision
?Acute uveitis
742
Small pupil initially, irregular later Circumcorneal injection Hypopyon (pus in anterior chamber) Keratic precipitates on back of cornea Talbots test: pain on convergence
Anterior uveitis
743
What are the systemic associations of anterior uveitis
Seronegative arthritits: AS, psoriatic, Reiter's Stills'/JIA IBD Sarcoidosis Behcet's Infections: TB, leprosy, syphilis, HSV, CMV, toxo
744
Mx of anterior uveitis
Refer to ophthalmology Prednisolone Cyclopentolate drops: dilates pupil and prevents adhesions between the iris and lens
745
Def: episcleritis
Inflammation below conjunctiva in the episclera
746
Localised reddening that can be moved over sclera Painless/mild discomfort Acuity preserved
Episcleritis
747
Causes of episcleritis
Usually idiopathic May complicate RA or SLE
748
Rx in episcleritis
Topical or systemic NSAIDs
749
What is the most common cause of red eye?
Conjunctivitis
750
Def: scleritis
Vasculitis of the sclera
751
Severe pain worse on eye movement Vessels won't move over sclera Conjunctival oedema (chemosis)
Scleritis
752
Causes of scleritis
Wegener's RA SLE Vasculitis
753
Scleritis, what should you do?
RFTs as may be first presentation of Wegner's
754
Cx of scleritis
Scleromalacia leading to globe perforation
755
Mx of scleritis?
Refer to specialist Most need corticosteroids or immunosuppressants
756
Often bilateral with purulent discharge Bacterial: sticky (staph, strep, haemophilus) viral: watery Discomfort Vessels may be moved over slcera Acuity unaffected
Conjunctivitis
757
What are the classes of conjunctivitis?
Viral Bacterial Allergic
758
Rx bacterial conjunctivitis
Chloramphenicol 0.5% ointment
759
Rx allergic conjunctivitis
Anti-histamine drops e.g. emedastine
760
What are the divisions of the pharynx
Nasopharynx Oropharynx Laryngopharynx
761
Extent of the nasopharynx
From the posterior nares to the soft palate
762
Extent of the oropharynx
From the soft palate to the superior margin of the epiglottis
763
Extent of the laryngopharynx
From the superior margin of the epiglottis to the oesophagus
764
765
How are the layers of the neck arranged
In various fascial layers: superficial fascia which surrounds the anterior neck and is innervated by CNVII Deep fascia: surrounds rest of the neck, several different layers
766
What are the layers of the deep fascia in the neck?
Investing layer: surrounds all structures within the neck Carotid sheaths: laterally surrounds the neurovascular components Pre-treacheal layer: ventrally, surrounds the viscera Pre-vertebral layer: dorsally: surrounds the vertebrae and associated muscles
767
768
What are the four longitudinal compartments in the neck
2 vascular compartments: bilaterally, covered by the carotid sheath Visceral compartment: ventrally: covered by the pre-tracheal fascia Vertebral compartment: dorsally: covered by the pre-vertebral fascia
769
What are the contents of the vascular compartment of the neck?
Internal jugular vein Common carotid Vagus nerve
770
What are the contents of the visceral compartment of the neck?
Contains the pharynx, larynx, trachea, oesophagus and thyroid gland
771
What are the contents of the vertebral compartment of the neck?
Contains the vertebral column and associated deep muscles
772
What are the branches of the external carotid artery? Some Anatomists Like Fucking, Others prefer S and M
Superior thyroid: supplies thyroid gland Ascending pharygneal: small posterior branch supplying around the pharynx Lingual: anterior branch to the tongue Facial: supplies the front of the face, soft palate and submandibular glands Occipital: supplies the posterior scalp Posterior auricular: ssupplies the ear Terminates at the parotid gland, bifurcating into two terminal branches: Superficial temporal: supplies the parotid gland, lateral face and temple region Maxillary: supplies numerous structures around the maxilla and mandible
773
Where does the common carotid bifurcate?
At the superior margin of the thyroid cartilage
774
How can the muscles of the neck be divided?
Supra and infrahyoid (strap)
775
What are the suprahyoid muscles?
Digastric: both insert on the medial hyoid: anterior belly (innervated by nerve to mylohyoid (of V3), posterior belly (arises from mastoid process and innervated by CNVII Stylohyoid: arses from the base of the sytloid process and inserts on the lateral hyoid (CNVII)
776
What is the innervation of the infra-hyoid strap muscles?
C1-C3
777
What are the infra-hyoid muscles?
Omohyoid Sternohyoid Thyrohyoid Sternothyroid
778
Action of the suprahyoid muscles
Depress the mandible or raise the hyoid
779
Actions of the infrahyoid
Depress the hyoid or fix the hyoid so that the suprahyoid muscles can act
780
What are the constricter muscles of the pharynx?
Superior: from the pterygomandibular raphe to the pharyngeal tubercle Middle: from the hyoid bone Inferior: from the thyroid cartilage All overlap to make up the pharyngeal walls
781
What innervates the constrictor muscles of the pharynxx?
Vagus nerve
782
What are the three longitudinal muscles of the pharynx?
Stylopharyngeus Salpingopharyngeus Palatopharyngeus All innervated by vagus except stylopharyngeus which is innervated by the glossopharyngeal
783
Which muscle of the pharynx is innervated by glossopharyngeal nerve rather than vagus?
Stylopharyngeus
784
785
def: corneal abrasion
Epithelial breach w/o keratitis Cause: trauma
786
Pain Photophobia Blurred vision Following trauma
?Corneal abrasion
787
Ix in corneal abrasion
Slit lamp: fluorescein stains defect green
788
Rx in corneal abrasion
Chloramphenicol ointment for infection prohpylaxis
789
Causes of corneal ulcer + keratitis
Bacterial, herpetic, fungal, protozoa, vasculitic (RA)
790
Corneal ulcer
791
Dendritic ulcer=
Herpes simplex keratitis
792
Dendritic ulcer Herpes simplex keratitis
793
Acanthomoeba
Protozoal infection affecting contact lens wearers in swimming pools
794
Acanthomoeba
795
Pain, photophobia Conjuncitval hyperaemia Reduced acuity White corneal opacity
?Corneal ulcer
796
RF for corneal ulcer?
Contact lens wearers
797
Ix in corneal ulcer
Fluorescein on slit lamp
798
Rx in corneal ulcer
Refer to specialist who will Take smears and cultures Abx drops, oral/topical aciclovir Cyclopegics/mydriatics to ease photophobia NB steroids may worsen symptoms
799
Complications of corneal ulcer
Scarring and visual loss
800
Def: ophthalmic shingles
VZV of CNV1 20% of all shingles
801
Pain in CNV1 dermatome preceding blistering rash keratitis, iritis Hutchinson's sign Ophthalmic involvement: keratitis + corneal ulceration
?Opthalmic shingles
802
Hutchinson's sign
Nose-tip zoster due to involvement of nasociliary branch Increased risk of globe involvement as nasociliary involvement also supplies globe
803
Ophthalmic shingles
804
Hutchinson's sign Nose tip zoster due to involvement of nasociliary branch Increased risk of globe involvement as nasociliary branch also supplies globe
805
Key questions in sudden loss of vision HELLP
Headache associated? GCA Eye movements hurt? Optic neuritis Lights/flashes preceding visual loss? Retinal detachment Like curtain descending? TIA/GCA Poorly controlled DM? Vitreous bleed from new vessels
806
Anterior ischaemic optic neuropathy
Optic nerve damage due to occlusion of posterior ciliary arteries, etiher by inflammation or atheroma Pale/swollen optic disc
807
Causes of anterior ischaemic optic neuropathy?
Arteritic: GCA Non-arteritic: HTN, DM, raised lipids, smoking
808
809
Unilateral loss of acuity over hours-days Reduced colour discrimination (dyschromatopsia) Eye movements may hurt Reduced acuity Reduced colour vision Enlarged scotoma Optic disc may be: swollen, normal, blurred Afferent defect
?Optic neuritis
810
Causes of optic neuritis?
MS (45-80% \>15y) DM Drugs: ethambutol, chloramphenicol Vitamin deficiency Infection: Zoster, Lyme disease
811
Rx Optic neuritis
High dose IV methyl predniosolone for 72h Then oral pred for 11/7
812
What are the sources of vitreous haemorrhage
New vessles: DM Retinal tears/detachment/trauma
813
Optic neuritis
814
Small black dots/ring floaters Obscured vision
?Viterous haemrorrhage
815
Viterous haemorrhage
816
What can happen in large vitreous bleeds
Can obscure vision-\> no red reflex Difficulty visualising retina
817
Mx of vitreous haemorrhage
Vitrectomy may be performed in dense VH Usually undergoes spontaneous absorption
818
Dramatic unilateral visual loss in seconds Afferent pupil defect may precede retinal changes Pale retina with cherry-red macula
Central retinal artery occlusion
819
Causes of central retinal artery occlusion
GCA Thromboembolism: clot, infective, tumour
820
Rx in retinal artery occlusion
If seen \<6h aim is to increas retinal blood flow by reducing IOP: Ocular massage, surgical removal of aqueous, local and systemic antihypertensives
821
What is more common retinal vein or artery occlusion
Retinal vein occlusion
822
Retinal artery occlusion Pale retina with cherry red macula
823
Causes of central retinal vein occlusion?
Arteriosclerosis, raised BP, DM, polycythaemia
824
Sudden unilateral visual loss with RAPD
?Central Retinal vein occlusion
825
Fundus: Stormy sunset apperaance Torutous dilated vessels Haemorrhages Cotton wool spots
?Central Retinal vein occlusion
826
Stormy sunset apperaance Torutous dilated vessels Haemorrhages Cotton wool spots Central retinal vein occlusion
827
Cx of central retinal vein occlusion?
Glaucoma Neovascularisation
828
Px for central retinal vein occlusion
Possibel improvement for 6mo-1 year
829
Unilateral visual loss Segemental fundal changes
?Retinal vein branch occlusion
830
Blood supply of the retina
Central retinal artery branches off the ophthalmic artery
831
What supplies blood to the fovea?
The choroid
832
Of which cartoid is the ophhthalmic artery a branch?
Internal
833
What is the aetiology of cherry red sport in central retinal artery occlusion
Retina supplied by retinal artery Fovea supplied by the vascular choroid that surrounds the eye Thus in retinal artery occlusion the retinal blood supply is compromised and becomes pale and swollen, while the central fovea appears reddish as the choroid colour shows throguh
834
Complications of branch artery occlusion?
Retinal ischaemia-\> VEGF release and neovascularisation Treated with anti-VEGFR monoclonal
835
Def: retinal detachment
Holes/tears in retina which allow fluid to separate sensory retina from retinal pigmented epithelium. May be secondary to cataract surgery, trauma, DM
836
4Fs Floaters: numerous, acute onset, spiders web Flashes Field loss Fall in acuity Painless
?Retinal detachment
837
Grey, opalescent retina ballooning forwards ?Retinal detachment
838
Rx in retinal detachment
Urgent surgery Vitrectomy and gas tamponade with laser coagulation to secure the retina
839
What are the causes of transient visual loss?
Vascular: TIA, migraine MS Subacute glaucoma Papilloedema
840
What are common causes of gradual visual loss?
Diabetic retinopathy ARMD Cataracts Open-angle glaucoma
841
What are rarer causes of gradual visual loss?
Genetic retinal disease: retinitis pigmentosa HTN Optic atrophy
842
What is the commonest cause of blindness \>60y?
ARMD
843
What are the risk factors for ARMD?
Smoking Increasing age Genetic factors
844
Elderly patient Central visual loss
ARMD
845
What are the two types of ARMD
Dry: geographic atrophy and Wet: subretinal neovascularisation
846
Drusen: fluffy white spots around macula Macula degeneration Slow visual decline over 1-2y
Dry ARMD
847
Aberrant vessels growing into retina from choroid with haemorrhage Rapid visual decline (sudden/days/weeks) with distortion Fundoscopy shows macular haemorrhage + scarring
Wet ARMD
848
What can be used to detect wet ARMD
Amsler grid
849
What is OCT?
Optic coherence tomography Used to give high resolution images of the retina
850
Rx for Wet AMRD
Intravitreal inhibitors e.g. Bevacizumab Ranibizumab Antioxidant vitamines (C,E) and zinc may help ARMD
851
What are Bevacizumab and ranibizumab?
Intravitreal VEGF inhibitors
852
Optic atrophy Loss of red/green discrimination Scotoma Due to toxic effects of cyanide radicals when combined with thiamine deficiency
Tobacco-alcohol amyblopia
853
Rx in tobacco-aclohol ambylopia
Vitamins may help
854
Pathogenesis of chronic simple (open-angle) glaucoma
Depends on susceptibility of patients retina and optic nerve to raised IOP damage IOP \>21mmHg: reduced blood flow and damage to optic nerve leading to optic disc atrophy + cupping
855
Optic disc atrophy and cupping
Chronic simple glaucoma
856
857
Peripheral visual field defect: superior nasal first Central field is intact with acuity maintained until late Presentation is thus delayed until optic nerve damage is irreversible
Chronic Simple Glaucoma
858
Def: glaucoma
Optic neuropathy +/- pressure (pressure is not part of definition)
859
What population are at high risk of glaucoma?
\>35y Afro-carribean FHx Drugs: steroids Comorbidities: DM, HTN, migraines Myopia Screening
860
Tonometry: IOP \>21mmHg Cupping of optic disc Visual field loss: peripheral in arcuate pattern
Chronic simple glaucoma
861
What are the commonest causes of blindness worldwide?
Trachoma Cataracts Glaucoma Keratomalacia: vitamin A deficiency Onchoceriasis Diabetic retinopathy
862
Mx of open angle glaucoma
Life long F/U Set target pressure related to degree of damage Medical therapy first line 1st line: Prostaglandin analogue Latanoprost, travoprost 2nd line: Beta blockers: timolol, betaxalol muscarinic alpha agonsts e.g. brominidine, apraclonidine Carbonic anyhdrase inhibitors: dorzolamide, drops, acetazolmide PO Miotics Non-medical options include laser trabeculoplasty, generally if drugs fail
863
Action in treatment of chronic glaucoma: Prostaglandin analogues
Increase aqueous outflow via the uveoscleral route
864
Action in treatment of chronic glaucoma: Beta blockers
Reduce aqueous secretion by inhibiting beta=adrenoreceptors on the ciliary body
865
Action in treatment of chronic glaucoma: Carbonic anhydrase inhibitors
Reduce aqueous secretion by ciliary body
866
Action in treatment of chronic glaucoma: Sympathomimetics
Reduce aqueous secretion and increase outflow through trabecular meshwork
867
Action in treatment of chronic glaucoma: Miotics
Open up the drainage channels in the trabecular meshwork by ciliary muscle contraction
868
Issue with beta blockers in treating glaucoma
Caution in asthma/heart failure
869
Side-effects of prostaglandin analogues in chronic glaucoma
Change in eye colour and lash lengthening
870
Issue with DM and the eye
Leading cause of blindness up to 60y 30% have ocular probelms at presentation Good BP and sugar control reduces diabetic retinopathy
871
Pathophysiology of diabetic eye disease
Cataract: DM accelerates cataract formation, lens absorbs glucose which is converted to sorbitol by aldose reducatse Retinopathy: Microangiopathy-\> occlusion Occlusion-\> ischaemia and new vessel formation in retina: bleed-\> viterous haemorrhage, carry fibrous tissue with them-\> retinal detachment Occlusion also leads to cotton wool spots (ischaemia Vascular leakage-\> oedema and lipid exudates Rupture of micro-aneurysms-\> blot haemorrhage
872
Screening of DM in context of eye disease
All diabetics should be screened annually Fundus photogrophay Refer those with maculopathy, NPDR and pDR to opathlmologist
873
Conversion rate of NPDR to DPR?
30% in 1y
874
Ix in DM eye disease
Fluorescein angiography
875
Mx of diabetic eye disease
Good BP and glycaemic control Rx concurrent disease: HTN, dyslipidaemia, renal disease, smoking, anaemia Laser photocoagulation: maculopathy: focal or grid, proliferative disease: pan-retinal
876
What EOM palsies occur in DM?
CNII and VI In diabetic CNIII the pupil may be spared as its nerve fibres run peripherally and receive blood from plial vessels
877
DM eye grading
Background retinopathy: leakage Pre-proliferative retinopathy: ischaemia Proliferative retinoapthy Maculopathy
878
Dots and blots with hard exudates
Background DM retinopathy
879
Dots in DM retinopathy
Microaneurysms
880
Blots in DM retinopathy
Haemorrhages
881
Hard exudates in DM retinopathy
Yellow lipid patches
882
Cotton wool spots Venous beading Dark haemorrhages Intra-retinal microvascular abnormalities
Pre-proliferative retinopathy (ischaemia)
883
New vessels Pre-retinal or vitreous haemorrhage Retinal detachment
Proliferative Retinopathy
884
Macular oedema Reduced acuity Hard exudates within one disc width of macula
Maculopathy
885
886
Diabetic maculopathy
887
Anatomy relevant to nose #
Upper 3rd of nose has bony support Lower 2/3rd and septum are cartilaginous
888
Aspects of #nose hx
Time of injury LOC CSF rhinorrhoea Epistaxis Previous nose injury Obstruction Consider facial# check for teech malocclusion, diplopia (orbital floor#)
889
Ix in nose #
Cartilaginous injury won't show and radiographs don't alter management
890
Mx of nose #
Exclude septal haematoma Re-examine after 1w once swelling reduced Reduction under GA with post-op splinting best within 2w
891
Features of septal haematoma
Septal necrosis and nasal collapse if untreated as cartilage blood supply comes from the mucosa Boggy swelling and nasal obstruction Needs evacuation under GA with packing and suturing
892
Septal haematoma
893
Causes of epistaxis
80% unknown Trauma: nose picking/fractures Local infection: URTI Pyogenic granuloma: overgrowth of tissues on Little's area due to irritation or hormonal factors Osler-Weber-Rendu/HHT Coagulopathy: Warfarin, NSAIDs, haemophilia, thrombocytopenia, vWD, EToH Neoplasm
894
Initial mx of epistaxis
Wear PPE Assess for shock and manage accordingly If bleeding not controlled, remove clots with suction or by blowing and try to visualise bleeding through rhinoscopy
895
Post epistaxis advice
Don't pick nose Sit upright, out of sun Avoid bending, lifting or straining Sneeze through mouth No hot food or drink Avoid EtOH and tobacco
896
Inheritance of OWR/HHT
Autosomal dominant with 5 genetic subtypes
897
Telangectasias in mucosae: recurrent spontaneous epistaxis, painless GI bleeds Internal telangectasias and AVMs in lungs, liver, brain Pulmonary HTN Colonic polyps-\> CRC
Osler-Weber-Rendu/HHT
898
Osler-Weber-Rendu/HHT
899
Sore throat, fever, malaise Lymphadenopathy esp. jugulodigastric node Inflamed tonsils and oropharynx Exudates
Tonsillitis
900
Most common cause of tonsilitis
Viruses (consider EBV)
901
Organisms causing tonsillitis
Viruses (EBV) GAS: pyogenes Staph Moraxella
902
Mx of tonsiltis
Swabbing superficial bacteria is irrelevant and can lead to overdiagnosis Analgesia: ibuprofen/paracetamol +/- diffiam gargle Consider Abx only if ill, use Centor criteria: Pen V 250mg QDS (125mg TDS in children) or erythromycin for 5/7
903
Why is amoxicillin not used in tonsilitis
EBV-\> maculopapular rash
904
Centor criteria
Fever \>38 by history Tender anterior cervical adenopathy Tonsilar exudates Absence of cough
905
Cut offs for Centor criteria
0-1: no Abx (risk of strep infection \<10%) 2: consider rapid Ag test + Rx if +ve 3: Abx
906
Indications for tonsillectomy
Recurrent tonsilitis if all of the below criteria are met: Caused by tonsilitis 5+ epsidoes/y Symptoms \>1y Episodes are disabling and prevent normal functioning Quinsy Suspicion of carcinoma: unilateral enlargement or ulceration
907
Methods of tonsillectomy
Cold steel Cautery
908
Cx of tonsillectomy
Reactive haemorrhage Tonsillar gag may damage teeth, TMJ or posterior pharyngeal wall Mortality is 1/30000
909
EBV tonsillitis
910
Strep tonsillitis
911
Trismus, odonophagia, halitosis Tonsillitis, unilateral tonsilar enlargement, contralateral uvula displacement, cervical lymphadenopathy Typically occuring in adults
?Quinsy
912
Quinsy
913
Mx of Quinsy abscess
Admit IV Abx I&D under LA or tonsillectomy under GA
914
Unwell child with stiff extended neck who refuses to eat and drink Fails to improve with IV Abx Unilateral swelling of tonsil and neck
?Retropharyngeal absceess
915
Ix in retropharyngeal abscess
Lateral neck XR show soft tissue swelling CT skull and thorax
916
Rx in Retropharyngeal abscess
IV Abx I&D
917
Throbophlebitis of the internal jugular vein occuring as a complication of bacterial sore throat infection Most commonly affect lungs
Lemierre's syndrome
918
Which bacteria is associated with Lemierre's syndrome?
Fusobacterium necrophorum
919
Rx in Lemierre's syndrome
IV Abx: pen G, clindamycin, metronidazole
920
Sandpaper like rash on chest, axillae or behind ears 12-48h after pharyngotonsillits Circumoral pallor Strawberry tongue
Scarlet fever
921
Rx in Scarlet fever
Start Pen V/G and notify HPA
922
Rheumatic fever CASES
Carditis Arthritis Subcutaenous nodules Erythema marginatum Sydenham's chorea
923
Malaise and smoky urine occuring 1-2w after pharyngitis
?Post-streptococcal GN
924
What are the functions of the larynx?
Phonation Positive thoracic pressure including auto-PEEP Respiration Prevention of aspiriation
925
Features of Laryngitis
Usually viral and self-limiting 2o bacterial infection may develop
926
Pain, hoarseness and fever Redness and swelling of the vocal cords
?Laryngitis
927
Rx in laryngitis
Supportive, Pen V if necessary
928
Pedunculated vocal cord swellings caused by HPV Present with hoarsness Usually occur in children Rx laser removal
Laryngeal papilloma
929
Hoarseness Breathy voice with bovine cough Repeated coughing from aspiration due to reduced supraglottic sensation Exertional dyspnoea due to narrow glottis
Recurrent laryngeal nerve palsy
930
Action of the recurrent laryngeal nerve
Supplies all of the intrinsic muscles of the larynx except cricothyroideus Exterior branch of superior laryngeal nerve Responsible for ab and adduction of the vocal folds
931
Causes of laryngeal nerve palsy
30% are cancers: larynx, thyroid, oesophagus, hypopharynx, bronchus 25% iatrogenic: para-/thyroidectomy, carotid endarterectomy Other: aortic aneurysm, bulbar/pseudobulbar palsy
932
933
Associations of laryngeal SCC
Smoking, EtoH
934
Male smoker Progressive hoarseness-\> stridor Dys/odono-phagia Weight loss
?Laryngeal SCC
935
Trismus
spasm of the jaw muscles, causing the mouth to remain tightly closed, typically as a symptom of tetanus. Origin
936
Ix in laryngeal SCC
Laryngoscopy + biopsy MRI staging
937
Mx of laryngeal SCC
Based on stage RTx Laryngectomy
938
Post total laryngectomy
Patients have a permanent tracheostomy - speech valve - electrolarynx - oesophageal speech Regular f/u for recurrence
939
Immature and floppy aryepiglottic folds and glottis leading to laryngeal collapse on inspiration Stridor Seen in neonates
Laryngomalacia
940
What is the commonest cause of stridor in children?
Laryngomalacia
941
Stridor Presenting within first weeks of life Noticeable at certain times: lying on back, feeding, excited/ upset Problems can occur with concurrent laryngeal infections Conservative management
Laryngomalacia
942
Sudden onset Continuous stridor Drooling Toxic
?Epiglottits
943
Pathogens causing epiglottitis
Haemophilus GAS
944
Rx in epiglottitis
Don't examine Consult anaesthetist and ENT O2 + nebulised adrenaline IV dexamethasone Cefotaxime Take to theatre for airway securing
945
Sudden onset stridor in a previously normal child
?FB
946
Mx of foreign body in throat
Encourage cough Back slaps Needle cricothyrotomy if necessary FB in bronchus can only be excluded through bronchoscopy
947
Stridor FTT
?Subglottic stenosis
948
Causes of subglottic stenosis
Prolonged intubation Congential abnormalities
949
Def: Bell's palsy
Inflammatory oedema from entrapment of CNVII in narrow facial canal Probably of viral origin 75% of facial palsy
950
Sudden onset (e.g. overnight) Complete, unilateral facial weakness Failure of eye closure-\> dryness and conjunctivitis Drooling/speech difficulty Numbness or pain around the ear Reduced taste Hyperacusis
Bell's palsy
951
Ix in Bell's palsy
Serology: borrelia or VZV Abs MRI: SOL, stroke, MS LP
952
Mx of Bell's palsy
Protect eye: dark glasses, artifical tears, tape closed at night Give high dose prednisolone within 72h: 60mg/d PO for 5/7 followed by tapering Valaciclovir if ?zoster, otherwise antivirals don't help Plastic surgery if no recovery
953
Complications of Bell's palsy
Aberrant neural connections: Synkinesis e.g. blinking causes up-turning of mouth Crocodile tears: eating stimulates unilateral lacrimation rather than salivation
954
Px of Bell's palsy
Incomplete paralysis usually recovers completely within weeks With complete lesions, 80% get full recovery but the remainder may have delayed or permanent neurological/cosmetic abnormalities
955
Hx of Ramsay Hunt syndrome
American neurologist James Ramsay Hunt in 1907
956
Def: Ramsay Hunt Syndrome
Reactivation of VZV in geniculate ganglion of CNVII
957
Preceding ear pain or stiff neck Vesciular rash in auditory canal +/- TM, pinna, tongue, hard palate Ipsilateral facial weakness May also affect CNVIII-\> vertigo, tinnitus, deafness
Ramsay Hunt Syndrome
958
What is Ramsay Hunt syndrome without the rash known as?
Zoster sine herpete
959
Mx of Ramsay Hunt Syndrome
Valaciclovir and prednisolone within first 72h
960
Px of Ramsay Hunt?
Rxed within 72h: 75% recovery Otherwise: 1/3 full, 1/3 partial, 1/3 poor
961
What features may suggest an alternative cause of facial palsy?
Bilateral symptoms (Lyme, GBS, leukaemia, sarcoid) UMN signs: sparing of frontalis and obicularis oculi Other CN palsies (also seen in 8% of Bell's) Limb weakness Rahses
962
Ramsay Hunt Snydrome
963
How can the causes of facial nerve palsy be classified?
Intracranial Intratemporal Infratemporal Systemic
964
What are the intracranial lesions causing facial nerve palsy?
Vascular, MS, SOL: motor cortex= UMN signs. Brainstem nuclei= LMN signs Cerebellopontine angle lesion: may be accompanied by 5th, 6th and 8th CN palsy
965
What are the intratemporal lesions causing facial nerve palsy?
Otitis media Cholesteatoma Ramsay Hunt
966
What are the infratemporal lesions causing Facial nerve palsy
Parotid tumours Trauma
967
What are the potential systemic causes of facial nerve palsy?
Peripheral neuropathy e.g. GBS (demyelinating) or DM, Lyme, HIB, Sarcoid (axonal) Pseudopalsy e.g. MG, botulism
968
What are the components of CNVII function
Motor: innervates the muscles of facial expression, the posterior belly of digastric, the stylohyoid and stapedius muscles Sensory: nil Special sensory: taste sensation to anterior 2/3rds of the tongue PNS: supplies the submandibular, sublingual, nasal, palatine, lacrimal and pharyngeal glands
969
What provides taste sensation to anterior 2/3rds of tongue?
Facial nerve
970
Intracranial course of the facial nerve
Arises in the pons, begins as two roots a large motor and small sensory root (intermediate nerve is the part of the facial nerve that arises from the sensory root) The two roots travel through the internal acoustic meatus, a 1cm opening in the petrous part of the temporal bone Leaves the internal acoustic meatus and enters the facial canal where: The two roots fuse to form the facial nerve. The nerve forms the geniculate ganglion The nerve gives rise to the greater petrosal nerve, the nerve to staepdius and the chorda tympani Exits via the facial canal, posterior to the styloid process of the temporal bone
971
Greater petrosal nerve
Branch of facial nerve, PNS fibres to glands
972
Nerve to stapedius
Facial nerve branch Motor fibres to stapedius muscle
973
Chorda tympani
Branch of the facial nerve, special sensory fibres to the anterior 2/3rds of the tongue
974
What innervates the parotid gland
Sensory and autonomic innervation Sensory innervation is supplied by the auriculotemporal nerve (V3) Parasympathetic innervation begins with CNIX which then synapses with the otic ganglion. The auriculotemporal nerve then carries fibres from the otic ganglion to the parotid Sympathetic innervation originates from the superior cervical ganglion.
975
976
Extracranial course of the facial nerve
First branch is the posterior aruicular nerve- provides motor innervation to some of the muscles around the ear, immediately dital to this it sends branches to the posterior belly of digastric and the stylohyoid muscle Main trunk, now termed the motor root continuse anteriorly and inferiorly to the parotid (which it does not innervate) Within the parotid gland, the nerve splits into its 5 terminal branches TZBMC
977
Posterior auricular nerve
Branch of the facial nerve Ascends in front of the mastoid process and innervates the intrinsic and extrinsic muscles of the outer ear
978
What is innervated by (of facial nerve) Temporal
Innervates the frontalis, obicularis oculi and corrugator supercili
979
What is innervated by (of facial nerve) Zygomatic
Innervates obicularis ori
980
What is innervated by (of facial nerve) Buccal
Innervates the obicularis oris, buccinator and zygomaticus
981
What is innervated by (of facial nerve) Marignal mandibular branch
Innervates the mentalis muscle
982
What is innervated by (of facial nerve) Cervical branch
Innervates the platysma
983
Increasing myopia Blurred vision-\> gradual visual loss Dazzling in sunshine/bright lights Monocular diplopia
?Cataracts
984
Causes of cataracts?
Age: \>75% of \>65 DM Steroids Congenital: Idiopathic Infeciton: rubella Metabolic: Wilson's, galactosaemia Myotonic dystrohpy
985
Ix in cataracts
Visual acuity DIlated fundoscopy Tonometry Blood glucose to exclude DM
986
Mx of cataracts
Conservative: glasses Medical: mydriatic drops and sunglasses may give some relief Sx: Consider if symptoms affect lifestyle or driving Day case surgery Pacoemulsion and lens implant
987
Cx of cataracts sx
1% risk of serious complication Anterior uveitis/iritis VH Retinal detachment Secondary glaucoma Endophthalmitis (blindness in 0.1%) Post op capsule thickening is common and treated with laser capsulotomy Post-op eye irritation is common and requires drops
988
Def: The retina
Outer pigmented layer in contact with the choroid Inner sensory layer in contact with vitreous At the centre is the fovea
989
Colour of the optic disc
Pale pink
990
Pale optic disc
?Optic atrophy
991
Blurred margins of optic disk
?Papilloedema and optic neuritis
992
What are the features of the optic disk
Colour Contour Cup: physiological- 1/3rd. Cup widening and deepening seen in glaucoma
993
Normal retina
994
Optic atrophy
995
996
What is the most prevalent inherited degeneration of the macula?
Retinitis pigmentosa Various modes of inheritance Mostly AR, AD has best prognosis X-linked has worst prognosis Affects 1/2000
997
Night blindness Reduced visual fields-\> tunnel vision Most registered blind by mid 30s
?Retinitis pigmentosa
998
Pale optic disc Peripheral retinal pigmentation
?Retinitis pigmentosa
999
Classic Retinitis pigmentosa, with mid-peripheral bony spicules, baring of RPE, vessel attenuation, and sparing of central macula
1000
DM retinopathy post laser treatment
1001
What conditions are associated with retinitis pigmentosa?
Friedrich's ataxia Refsum's disease Kearns-Sayre syndrome Usher's syndrome
1002
Inheritance of retinoblastoma
Herediatry type differs from non-hereditary type AD mutations of RB gene Patients typically have on mutant allele in every retinal cell, if the other alleles mutates-\> retinoblastoma 2 HIT hypothesis
1003
With what conditions are retinoblastomas associated?
5% occur with pineal or other tumour Increased risk of osteosarcoma and rhabdomyosarcoma
1004
Strabismus Leukocoria
?Retinoblastoma
1005
Leucokoria ?Retinoblastoma
1006
An abscess/infection in a lash follicle which points outwards Rx with local Abx e.g. fusidic acid
Stye or horeolum externum
1007
Hordeolum externum (stye)
1008
Abscess of the Melbomian glands which point inwards onto the conjunctiva
Chalazion or hoedolum internum
1009
Hordeolum internum/ Chalazion
1010
Def: Blepharitis
Chronic inflammation of the eyelid
1011
Red eyes Gritty/itchy sensation Scales on lashes Rosacea
?Blepharitis
1012
Causes of Blepharitis
Seborrhoic dermatitis Staphs
1013
Rx in Blepharitis
Clean crusts of lashes with warm soaks May need fusidic acid drops
1014
Blepharitis
1015
Entropion
Lid inversion-\> corneal irritation Degeneration of the lower lid fascia
1016
Ectropion
Low lid eversion-\> watering and exposure keratitis Associated with ageing and facial N. palsy
1017
Def: true ptosis
Intrinisc LPS weakness
1018
Causes of bilateral ptosis
Congenital Senile MG Myotonic dystrophy
1019
Causes of unilateral ptosis
3rd Nerve palsy Horner's (partial) Mechanical: xanthelasma, trauma
1020
Def: lagophthalmos
Difficulty in lid closure over the globe which may lead to exposure keratitis
1021
Causes of lagophthalmos
Exophthalmos Facial palsy Injury
1022
Rx of lagophthalmos
Lubricate eyes Temporary tarsorrhaphy may be needed if corneal ulcers develop
1023
Pinguecula
Yellow vascular nodules either side of the cornea
1024
Pinguecula
1025
Pterygium
Similar to pinguecula but grows over the cornea-\> reduced vision Benign growth of conjunctiva Associated with dusty, wind-blown life styles, sun exposure
1026
Pterygium
1027
Pathophysiology of orbital cellulitis
Infection spreading locally e.g from paranasal sinuses, eyelid or external eye Staphs, pneumococcus, GAS
1028
Inflammation of the orbit and lid swelling Pain and reduced range of eye movement Exopthalmos Systemic signs e.g. fever Tenderness over the sinuses
Orbital cellulitis
1029
Orbital cellulitis
1030
Rx in orbital cellulitis
IV Abx: Cefuroxime (20mg/kg/8h IV)
1031
Cx of orbital cellulitis
Local extension-\> meningitis and cavernous sinus thrombosis Blindness due to optic nerve pressure
1032
Features of carotico-cavernous fistula
May fallow carotid aneurysm rupture with reflex of blood into cavernous sinus Spontaneous/trauma
1033
Engorgement of eye vessels Lid and conjunctival oedema Pulsatile exophthalmos Eye bruit
Carotico-cavernous fistula
1034
Carotid-cavernous fistula
1035
Exophthalmos/proptosis
Protrusion of one or both eyes
1036
Common causes of proptosis
Graves: 25-50%, increased in smoker's, anti-TSH Abs-\> retro-orbital inflammation and lymphocyte infiltration leading to swelling Orbital cellulitis Trauma
1037
Other causes of proptosis
Idiopathic orbital inflammatory disease Vasculitis- Wegener's Neoplasm: lymhpoma, optic glioma, capillary haemangioma, metastatic Carotico-cavernous fistula
1038
What is used to classify hypertensive retinopathy?
Keith-Wagener Classification
1039
Keith-Wagener classification of hypertensive retinopathy
1. Tortuosity and silver wiring 2. AV nipping 3. Flame haemorrhages and soft/cotton wool spots 4. Papilloedema Grades 3 and 4= malignant HTN
1040
A. Earliest sign of hypertension showing only generalized narrowing of the arterioles with no change in the vessel wall thickness or reflex. B. Grade II hypertension showing generalized narrowing plus focal constriction and grade I arteriolar sclerosis with widening of the reflex stripe. C. Grade III hypertension showing generalized narrowing, focal constriction, hemorrhages, and exudate, and grade I arteriolar sclerosis with widening of the light reflex. D. Grade IV hypertension showing generalized narrowing, focal constriction, hemorrhages, and exudates and edema of the disc with grade I arteriolar sclerosis
1041
What are the granulomatous disorders causing uveitis and choroidoretinitis
TB, sarcoid, toxoplasmosis, leprosy, brucella
1042
What inflammatory diseases are associated with: Conjunctivitis
SLE, reactive arthritis, IBD
1043
What inflammatory diseases are associated with: Scleritis/episcleritis
RA, vasculitis, SLE, IBD
1044
What inflammatory diseases are associated with: Iritis
Ank spond IBD Sarcoid
1045
What inflammatory diseases are associated with: Retinopathy
Dermatomyositis
1046
Reduced tear production Dry eyes and ry mouth 1o or 2o: SLE\< RA, sarcoid
Keratoconjuncitivities SIcca/ Sjogren's
1047
Roth spots associated with?
Infective endocarditis As a consequence of microemboli
1048
Boat shaped haemorrhage with pale centre Roth spot Infective endocarditis
1049
Kayser-Fleischer Rings Wilson's
1050
Exophthalmos Grave's disease
1051
Corneal calcification Hyperparathyroidism
1052
CMV retinitis Pizza-pie fundus + flames
1053
HIV retinopathy Cotton wool spots
1054
What are the mydriatics?
Anti-muscarinics Sympathomimetics
1055
Indications for mydriatics
Eye examination Prevention of snechiae in anterior uveitis/iritis
1056
Caution with mydriatics?
May lead to acute glaucoma if shallow anterior chamber
1057
Class of drug: Tropicamide, cyclopentolate
Anti-muscarinic Tropicamide -3h Cyclopentolate- 24h
1058
Effects of anit-muscarinics on eye
Pupil dilatation and loss of light reflex Cyclopegia-\> blurred vision
1059
What class of drug is pilocarpine?
Muscarinic agonist
1060
Use of pilocarpine
Acute closed-angle galucoma
1061
What is tetracaine
Anaesthetic used to permit examination of a painful eye
1062
What are emedastine and antazoline
Topical anti-histamines used in ophthalmology
1063
What is hypomellose and carbomer
Eye lubricants
1064
Whence do refractive errors arise?
Disorders of the size and shape of the eye
1065
Myopia=
Short-sightedness
1066
Problem in myopia
Eye is too long, distant objects are focussed too far forward Genetic or excessive close work in early decades
1067
Solution to myopia
Concave lenses
1068
Problem in astigmatism
Cornea or lens doesn't have the same degree of curvature in horizontal and vertical planes Image of object is distorted longitudinally or vertically
1069
Hypermetropia=
Long-sightedness
1070
Problem in hypermetropia
Eye is too short When the eye is relaxed and not accomodating, objects are focussed behind the retina Contraction of ciliary muscles to focus image-\> tiredness of gage and psosible a convergent squint in children
1071
Solution to hypermetropia
Convex lenses
1072
Presbyopia
With age, the lens becomes stiff and less easy to deform Start at about 40y and are complete by 60y Use convex lenses to correct
1073
Esotropia=
Convergent squint May be idiopathic or due to hypermetropia
1074
Esotropia
1075
Exotropia
Divergent squint common in older children, often divergent
1076
Exotropia
1077
Diagnosis of non-paralytic squint
Corneal reflection: should fall centrally and symmetrically on each cornea Cover test: movement of uncovered eye to take up fixation demonstrates manifest squint
1078
Mx of non-paralytic squint 3Os
Optical: correct refractive errors Orthoptic: patching good eye encourages use of squinting eye Operation: e.g. resection and recession of rectus muscles
1079
Diplopia most on looking in direction of pull of paralysed muscle Eye won't fixate on covering
Paralytic squint
1080
How to determine which eye is malfunctioning in paralytic squint
Cover each eye in turn, whichever eye sees the outer image is malfunctioning
1081
In paralytic squint, how can you determine which muscle is affect
Diplopia most on looking in direction of pull of paralysed muscle
1082
Ptosis Fixed dilated pupil Down and out
CNIII lesion
1083
Causes of CNIII palsy
Medical: DM, MS, infarction Surgical: raised ICP, cavernous sinus thrombosis, posterior communicating artery aneurysm
1084
Diplopia, espsecially on going down stairs Head tilt
?CNVI palsy
1085
Causes of CNIV palsy
Peripheral: DM (30%), trauma (30%)- nerve exits posterior of brainstem, compression Central: MS, vascular, SOL
1086
Eye is medially deviated and cannot abduct Diplopia in the horizontal plane
?CNVI palsy
1087
Causes of CNVI palsy
Peripheral: DM, compression, trauma Central: MS, vascular, SOL
1088
Mx of eye trauma
Record acuity of both eyes Take detailed Hx of event If unable to open injured eye, instill LA e.g. tetracaine
1089
Ix in ?FB in orbit
XR orbit if metal suspected Fluorescein may show corneal abrasions
1090
Mx of eye trauma
Chloramphenicol drops 0.5% to prevent infection, usually with coag negative staph Eye patch Cycloplegic drops may reduce pain e.g. tropicamide, cyclopentolate
1091
Features of intra-ocular haemorrhage
Blood in anterior chamber- hyphaema Small amounts clear spontaneously but some may need evacuation Complicated by corneal staining and glaucoma Keep IOP down and monitor
1092
Features of orbital blowout #
Blunt injury-\> sudden increase in orbital pressure with herniation of orbital contents into maxillary sinus
1093
Opthalmoplegia and diplopia (tethering of IR and IO) Loss of sensation to lower lid skin (infraorbital nerve injury) Ipsilateral epistaxis (damage to anterior ethmoidal artery) Reduced acuity Irregular pupil that reacts slowly to light
?Orbital blowout fracture
1094
Mx of chemical injury to the eye
Alkaline solutions are particulary damaging due to saponification Mx with copious irrigation and specialist referral
1095
Small dark spots in the visual field
Floaters
1096
Sudden showers of floaters in one eye may be due to?
Blood or retinal detachment
1097
Causes of floaters
Retinal detachment VH Diabetic retinopathy/ HTN Old retinal branch vein occlusion Syneresis (degenerative opacities in the vitreous)
1098
Flashes in vision=
Photopsia
1099
Causes of flashes
Either from intraocular or intracerebral pathology Headached, NV: migraine Flashes and floater= retinal detachment
1100
What can cause haloes
May be caused by hazy ocular media- cataract, corneal oedema, acute glaucoma
1101
Haloes + eye pain=
Acute glaucoma
1102
Jagged haloes which change shape are usually
Migrainous
1103
Rx in seasonal allergical conjuncitivitis
Antazoline: antihistamine drops Cromoglycate: inhibits mast cell degranulation
1104
Small papillae on tarsal conjuncitvae
?Seasonal allergic/ perenial allergic conjuncitivites
1105
1106
Rx of perennial conjuncitivis
Olopatadine (anti-histamine and mast cell stabiliser)
1107
Causes of giant papillary conjuncitvitis Mx
Iatrogenic FBs: contact lenses, prostheses, sutures Removal of FB, mast cell stabilisers
1108
Giant papillary conjunctivitis
1109
Mx of allergic eye disorders
Remove the allergen responsible where possible General measures: cold compress, artificial tears, oral antihistamine (loratadine 10mg/pd PO) Eye drops: Antihistamines: antazoline, azelastine Mast cell stabilisers: cromoglycate, lodoxamide Steroids: dexamethasone (NB of inducing glaucoma) NSAIDs: Diclofenac
1110
Pathophysiology of trachoma
Caused by Chlamydia trachomatis (A, B, C) Spread by flies Inflammatory reaction under the lids-\> scarring-\> entropion-\> eyelashes scratching cornea-\> ulceration-\> blindness
1111
Rx Trachoma
Tetracycline 1% +/- PO
1112
Pathophysiology of onchoceriasis
Caused by microfilariae or nematode Onchocerca volvulus Spread by flies Fly bites-\> microfilariae infeciton-\> invade the eye-\> inflammation-\> fibrosis-\> corneal opacities and synechiae
1113
Rx in onchoceriasis
Ivermectin
1114
Xerophthalmia and keratomalacia are manifestations of?
Vitamin A deficiency
1115
Night blindness and dry conjunctivae Corneal ulceration and perforation
?Vitamin A deficiency
1116
Rx in Vitamin A related Xerophthalmia?
Vitamin A/palmitate reverses early corneal changes
1117
Which two cranial nerves originate from the cerebrum?
Olfactory and optic
1118
What is the origin of the trochlear nerve?
The midbrain, comes from the posterior side of the midbrain and has the longest intracranial length
1119
What is the origin of the oculomotor nerve?
Midbrain-pontine junction
1120
What is the origin of the trigeminal?
Pons
1121
What is the origin of the abducens, facial and vestibulocochlear nerves?
Pontine medulla junction
1122
What is the origin of glossopharyngeal, vagus, accessory nerve?
Posterior to the olive in the medulla oblongata
1123
What is the origin of the hypoglossal?
Anterior to the olive in the medulla oblongata
1124
1125
What cranial nerve exits through the cribiform plate?
Olfactory
1126
What cranial nerve exits through the optic canal?
III
1127
What CNs exit through the superior orbital fissure?
III IV V1 VI
1128
What cranial nerve exits through the foramen rotundum
V2
1129
What CN exits through the formaen ovale?
V3
1130
What cranial nerve exits through the internal acoustic meatus?
VII VIII
1131
What cranial nerves exit through the jugular foramen?
IX X XI
1132
What CN exits through the hypoglossal canal?
XII
1133
What modality is carried by: CNI
Special visceral sensory: smell
1134
What modality is carried by: CNII
Special somatic sensory (Vision)
1135
What modality is carried by: III
General somatic motor: skeletal muscles General visceral motor: pupillary sphincter (autonomic)
1136
What modality is carried by: IV
General sensory motor: SO
1137
What modality is carried by: V1
General somatic sensory: scalp, forehead and nose
1138
What modality is carried by: V2
General somatic sensory: cheeks, lower eye lid, nasal mucosa, upper lip, upper teeth, palate
1139
What modality is carried by: V3
General somatic sensory: anterior 2/3rd tongue, skin over mandible and lower teeth Special visceral motor: Muscles of mastication
1140
What modality is carried by: VI
General somatic motor: LR
1141
What modality is carried by: VII
General somatic sensory: sensation to part of external ear Special visceral sensory: taste from anterior 2/3rds of tongue and soft palate General somatic motor: muscles of facial expression General visceral motor: lacrimal, submandibular, sublingual glands and mucous glands of mouth and nose
1142
What modality is carried by: VIII
Special somatic sensory: hearing and balance
1143
What modality is carried by: IX
General somatic sensory: posterior 1/3rd of the tongue, external ear and middle ear cavity General visceral sensory: carotid body and sinus Special visceral sensory: taste from posterior 1/3rd of tonuge General visceral motor: parotid gland Special visceral motor: stylopharyngeus
1144
What modality is carried by: X
General somatic sensory: external ear, larynx, pharynx General visceral motor: larynx, pharynx and thoracic and abdominal viscera Special visceral sensory: taste from epiglottis region of tongue General visceral motor: smooth muscles of the pharynx larynx and most of the GIT Special visceral motor: most muscles of the pharynx and larynx
1145
What modality is carried by: Accessory nerve?
General somatic motor: trapezius and sternocleidomastoid Special visceral motor: few fibres run with CNX to visceral
1146
What modality is carried by: XII
Intrinsic and extrinsic tongue muscles (except palatoglossus)
1147
What innervates palatoglossus?
CNX Only muscle of the tongue not innervated by XII
1148
What is the composition of the olfactory nerve?
Peripheral olfactory processes (in the olfactory mucosa) Central processes that return the information to the brain
1149
Course of the olfactory nerve
Enters the cranial cavity through the cribiform plate of the ethmoid bone Once in the cranial cavity the fibres enter the olfacory bulb which lies in the olfactory groove in the anterior cranial fossa. Pass posteriorly to the olfactory tract As the tract reaches the anterior perforated substance it divides into lateral and medial stria Lateral stria carries axons to the primary olfactory cortex Medial stria carry axons to the olfactory bulb on the other side
1150
How does the optic nerve enter the cranial cavity
Through the optic canal, a passage in the sphenoid bone running along the middle cranial fossa in close proximity to the pituitary gland
1151
Intracranial course of the optic nerve
Within the middle cranial fossa the optic nerves from each eye unite to form the optic chiasm At the optic chiasm the nerves cross over and form the optic tracts Each tract travels to its corresponding cerebral hemisphere to reach the lateral geniculate nucleus, a relay system in the thalamus where the fibres synpase Axons from the LGN carry information via optic radiation The upper optic radiation carries fibres from the superior retinal quadrants (corresponding to the inferior visual field quadrants), travelling through the parietal lobe to reach the visual cortex The lower optic radiation carries fibres from the inferior retinal quadrants (superior visual field quadrants) and travels through the temporal lobe via Meyer's loop.
1152
Course of the oculomotor nerve
Originates from the anterior branch of the midbrain, moving anteriorly Passes below the posterior cerebral artery and above the superior cerebellar artery Pierces the dura mater and enters the cavernous sinus Within the cavernous sinus it receives sympathetic branches from the internal carotid plexus, that travel within its sheath Leaves the cranial cavity via the superior orbital fissure, where it divides into the superior and inferior branches
1153
What does the superior branch of oculomotor innervate?
SR and LPS Sympathetic fibres run with the superior branch to innervate the superior tarsal muscle
1154
What does the inferior branch of III innervate?
IR, MR IO PNS fibres run to the ciliary ganglion which ultimately innervates the sphincter pupillae and ciliary muscles
1155
Which SO do the IV neurones innervate?
. As the fibres from the trochlear nucleus cross in the midbrain before they exit, the trochlear neurones innervate the contralateral superior oblique.
1156
What is unique about the trochlear nerve?
The trochlear nucleus is unique in that its axons run dorsally and cross the midline before emerging from the brainstem posteriorly. Thus a lesion of the trochlear nucleus affects the contralateral eye. Lesions of all other cranial nuclei affect the ipsilateral side. Also the only CN to emerge from the posterior of the brainstem
1157
Action of SO
Depress and intort the eyeball- down and in
1158
What is innervated by the motor component of trigeminal
Only the mandibular branch of CN V has motor fibres. It innervates the muscles of mastication: medial pterygoid, lateral pterygoid, masseter and temporalis. The mandibular nerve also supplies other 1st pharyngeal arch derivatives: anterior belly of digastric, tensor veli palatini and tensor tympani.
1159
Parasympathetic supply and the trigeminal
The post-ganglionic neruones of the PNS ganglia travel with branches of the trigeminal but the trigeminal nerve is not part of the cranial outflow of PNS supply
1160
Anatomical course of V
Originates from three sensory nuclei (mesencephalic, principal sensory, spinal nuceli) and one motor nucleus extending from the midbrain to the medulla At the level of the pons, the sensory nuclei merge to form a sensory root The motor nucleus continues to form a motor root In the middle cranial fossa the sensory root expands into the trigeminal ganglion which is located lateral to the cavernous sinus. In a depression of the temporal bone- the trigeminal cave Trigeminal gives rise to V1, V2, V3. Motor root passes inferiorly to the sensory root and its fibres are only carried in V3
1161
Function of the ophthalmic nerve
Gives rise to 3 terminal branches, frontal, lacrimal and nasociliary which innervate the skin and mucous membrane of derivatives of the frontonasal prominence Also provides PNS supply to the lacrimal gland from the pterygopalatine ganglion (facial nerve derivative) travel with V2 then join the lacrimal branch of V1 providing PNS innervation to the lacrimal gland
1162
Corneal reflex arms
Afferent: V1 Efferent: facial nerve
1163
V2 function
Sensory PNS: initially carries post ganglionic fibres from the pterygopalatine ganglion (VII derivative) and travel with the zygomatic branch of V2 then join the lacrimal branch of V1 Nasal glands: PNS fibres are also carried to the mucous glands of the nasal mucosa travelling with branches of V2
1164
What is the motor funciton of V
Carried by V3 Muscles of mastication: medial and lateral pterygoids, massester, temporalis Anterior belly of digastric and mylohyoid muscles Tensor veli palatini Tensory tympani PNS: post ganglionic fibres from the submandibular ganglion travel with the lingual nerve to innervate submandibular and sublingual glands Parotid gland: post ganglionic fibres from the otic ganglion (derived from CN IX) travel with the auriculotemporal branch of V3 to innervate the parotid gland
1165
Anatomical course of the VIII
Vestibular and cochlear portions of the VIII are functionally discrete so orignate from different nuclei in the brain Vestibular: vesitublar nuclei complex in the pon and medulla Cochlear: from the ventral and dorsal cochlear nuclei in the inferior cerebellar peduncle. Combine in the pons, nerve emerges from the brain at the CPA and exits the cranium via the internal acoustic meatus of the temporal bone. Splits distal to the internal acoustic meatus.
1166
Clinical relevance of basilar skull # to VIII
Basilar skull fracture can cause damage to VIII in the internal acoustic meatus producing symptoms of vestibular and cochlear nerve damage.
1167
Course of CN IX
Arises from the medulla oblongata Leaves the cranium via the jugular foramen at which point the tympanic nerve arises. Immediately outside the jugular foramen lie two ganglia known as the superior and inferior (or petrous) ganglia that contain the cell bodies of the sensory fibres in the glossopharyngeal nerve. Descends to give innervation to stylopharyngeus and the carotid sinus nerve which provides sensation to the carotid sinus and body.
1168
1169
What are the components of the gag reflex?
Afferent= CNIX Efferent= CNX
1170
Course of the vagus nerve in the head
Originates from the medulla and exits via the jugular foramen Within the cranium the auricular branch arises which supplies sensation to the posterior part of the external auditory canal and external ear
1171
Anatomical course of the vagus nerve in the neck
Passes into carotid sheath, travelling inferiorly with the internal jugular vein and common carotid. Right vagus passes anterior to the subclavian artery and posterior to the sternoclavicular joint, entering the thorax Left vagus passes inferiorly between the left common carotid and the left subclavian arteries, posterior to the sternoclavicular joint.
1172
Branches of the vagus nerve in the neck?
Pharyngeal branches: motor innervation to the muscles of the pharynx and soft palate Superior laryngelal nerve: internal and external branches, external innervate the cricothyroid muscle, the internal providing sensory innervation to the laryngopharynx and superior part of the larynx Recurrent laryngeal nerve (on the right only) hooks underneath the subclavian artery and ascends to the larynx, innervating the majority of the intrinsic muscles of the larynx
1173
Course of the vagus nerve in the thorax
Right vagus forms the posterior vagal trunk The left forms the anterior vagal trunk Branches from these trunks contribute to the oesophageal plexus Two other branches arise: the left recurrent laryngeal nerve (hooks under the arch of the aorta) Cardiac branches Vagal trunks enter the abdomen via the oesophageal hiatus
1174
Lesion to one recurrent laryngeal nerve causes? Both?
Dysphonia Aphonia
1175
Anatomical course of the accessory nerve (spinal)
Spinal portion arises from neurones of the upper SC (C1-C5/C6) of the spinal nerve roots. Coalesce to form the spinal part of the accessory nerve which then runs superiorly to enter the cranium via the foramen magnum It travels to the posterior cranial fossa to reach the jugular foramen where it meets the cranial portion of the accessory nerve before exiting the skull. Descends along the internal carotid to reach sternocleidomastoid which it innervates. Extracranial course is relatively superficial leaving it vulnerable to damage.
1176
Cranial course of the accessory nerve
Much smaller and arises from the lateral aspect of the medulla. Leaves the cranium via the jugular foramen where it briefly contacts the spinal part of the accessory nerve. Immediately after leaving the skull, the cranial portion combines with the vagus at the inferior ganglion of the vagus. The fibres are then distributed through the vagus nerve.
1177
What is the most common cause of accessory nerve damage?
Iatrogenic e.g. cervical LN biopsy or cannulation of the IJV. Clinical features include muscle wasting and partial paralysis of the sternocleidomastoid, resulting in the inability to rotate the head or weakness in shrugging the shoulders. Damage to the muscles may also result in an asymmetrical neckline.
1178
Accessory nerve palsy Asymmetrical neck line
1179
What muscles are innervated by the hypoglossal nerve?
All muscles of the tongue except palatoglossus (innervated by the vagus nerve)
1180
What are the extrinsic muscles of the tongue?
Genioglossus Hypoglossus Styloglossus [Palatoglossus- vagus nerve]
1181
What are the intrinsic muscles of the tongue?
Superior longitudinal Inferior longitudinal Transverse Vertical
1182
Classification of hypoglossal nerve palsy
Can be supranuclear (UMN), nuclear, or infranuclear (LMN) UMN: tongue will deviate away from injured side. Only seen during the initial days after the injury, after which it will not deviate. Infranuclear lesions lead to parlaysis of the hpyoglossal nerve leading to atrophy of muscles of the tonuge, tongue will be deviated **TOWARDS** lesion. Due to weaker geniglossal muscle.
1183
What may be seen in supranuclear damage to the left and right tracts of CNXII
Damage to facial and trigemnial nerve dysfunction as a consequence of damage to the brainstem following arteriosclerosis of the vertebrobasilar artery
1184
CN palsy + pain
?Cartoid dissection
1185
What is the only muscle of the tongue not innervated by hypoglossal?
Extrinsic, palatoglossus (Vagus)
1186
Right subclavian arises from the brachiocephalic trunk Left subclavian directly from the arota
1187
When do the subclavian arteries become the axillary arteries?
When they cross the lateral edge of the first 1 rib and enter the axilla
1188
Course of the axillary artery
Passes through the axilla underneath pectoralis minor enclosed in the axillary sheath At the humeral surgical neck the posterior and anterior circumflex humeral arteries arise Circle posteriorly around the humerus to supply the shoulder region The subscapsular artery also arises here (largest brach of the axillary artery) At the level of the teres major the axillary artery becomes the brachial artery
1189
Where does the axillary artery become the brachial
At the lower margin of teres major
1190
1191
What in the axilla can compress the brachial plexus producing neurological symptoms and can be treated surgically
Axillary artery aneurysm
1192
Course of the brachial artery
Immediately distal to teres major gives the profunda brachii- deep artery of the arm which travels along the posterior surface of the humerus in the radial groove, supplying the posterior aspect of the arm Brachial artery descends down the arm immediately posterior to the median nerve, as it crosses the cubital fossa underneath brachialis it terminates by bifurcating into the radial and ulnar arteries
1193
1194
Course of the arteries in the forearm
Radial- posterior aspect of the forearm Ulnar- anterior Areteries anastomose by forming the superficial palmar arch and the deep palmar arch
1195
What are the major superifical veins of the upper limb
The cephalic and basilic veins
1196
Course of the superficial veins of the upper limb
Basilic vein originates from the dorsal venous network of the hand ascending the medial aspect of the upper limb. At the border of teres major the vein moves deep into the arm where it combines with brachial veins to form the axillary vein The cephalic vein arises from the dorsal venous network of the ascending ascending on the anterolateral aspect of the upper limb, passing anteriorly at the elbow. At the shoulder the cephalic vein travels between the delotid and pec major muscles in the deltopectoral groove and enters the axilla via the clavipectoral triangle. It terminates here by joining the axillray vein. At the elbow the cephalic and basilic veins are connected by the median cubital vein
1197
1198
What is the course of the deep veins of the upper limb
Paired veins that accompany and lie either side of an artery Brachial veins are the largest in size and are situated either side of the brachial artery These are vena comitantes Perforating veins run between the deep and superficail veins of the upper limb, connecting the two systems
1199
What are at risk of damage in axillary LN dissection?
Long thoracic nerve (winged scapula) Or the thoracodorsal nerve
1200
Describe the course of the femoral artery
Continuation of the EIA which becomes the femoral artery when it crosses under the inguinal ligament and enters the femoral triangle In the femoral triangle the profunda femoris artery arises from the posterolateral aspect. It travels posteriorly giving off three main branches: Lateral femoral circumflex: wraps around the anterior, lateral side of the femur supplying muscles in the lateral side of the thigh Medial circumflex artery: wraps around the posterior side of the femur supplying the head and neck (avascular necorsis in intracapsular #) Perforating branches: 3/4 arteries that perforate the adductor magnus After exiting the femoral triangle the femoral artery continues down the anterior surface of the thigh via the adductor canal. The adductor canal ends at the adductor hiatus at which point the femoral artery enters the posterior compartment of the thigh proximal to the knee
1201
Borders of the femoral triangle
Superior border: inguinal ligament Lateral border: sartorius Medial border: medial border of adductor longus Anteriorly the roof of the femoral triangle is the fascia lata Posteriorly the base is formed by pectineus, ilopsoas and adductor longus muscles.
1202
Contents of the femoral triangle NAVEL
Femoral nerve: innervates the anterior compartment of the thigh Femoral artery Femoral vein Empty space Lymph canal Contained in the femoral sheath
1203
1204
Location of the femoral pulse
Midway between the pubic symphysis and ASIS
1205
1206
Describe the course of the other arteries supplying the thigh
Obturator artery arises from the IIA in the pelvic region, descends via the obturator canal to enter the medial thigh bifurcating into the canal. Gluteal region is largely supplied by the superior and inferior gluteal arteries which exit the pelvis via the GSF. The IGA also contirbutes to the vasculature of the posterior thigh
1207
What differentiates between the SGA and the IGA
Both exit the GSF SGA superior to piriformis IGA inferior to piriformis
1208
Describe the arterial supply of the leg
Popliteal artery descends down the posterior thigh giving off genicular branches that supply the knee joint. Moves through the popliteal fossa between gastrocnemius and popliteus. At the lower border of popliteus it terminates by dividing into anterior and posterior tibial artery. Posterior tibial continues inferiorly along the surface of the deep muscles accompanying the tibial nerve entering the sole of the foot via the tarsal tunnel. During the descent of the posterior tibial the fibular artery arises which moves laterally penetrating the lateral compartment of the leg. The anterior tibial artery passes anteriorly between the tibia and fibular through a gap in the interoesseous membrane. Moving inferiorly down the leg and into the foot where it becomes dorsalis pedis.
1209
1210
What is the clinical revelance of the fact that the popliteal fascia is tough and non-extensable
Aneurysm of the popliteal artery has consequences for other contents of the popliteal fossa. The tibial nerve is particularly susceptible to compression from the popliteal artery Major features are absent/weakened plantar fleixion, paraesthesia of the foot and posterolateral leg. Can be detected through obvious expansile pulsatile mass and an arterial bruit
1211
Describe the arterial supply of the foot
Dorsalis pedis- continuation of the anterior tibial artery Posterior tibial enters through the sole of the foot through the tarsal tunnel and supplies the lateral and medial plantar surfaces
1212
Where can the femoral pulse be palpated?
be palpated as it enters the femoral triangle, midway between the anterior superior iliac spine of the pelvis, and the pubis synthesis (the mid-inguinal point).
1213
Where can the dorsalis pedis be palpated?
Dorsum of the foot in the fist intermetatarsal space, lateral to the tendon of the great toe
1214
Where can the posterior tibial pulse be palpated
Behind and below the medial malleolus
1215
Where can the popliteal pulse be palpated
In the midline in the popliteal fossa with gentle knee flexion
1216
Describe the course of the deep venous drainage of the lower limb
Dorsal arch drains mainly into the superficial veins, some penetrate deep into the leg forming the anterior tibial vein. On the plantar aspect of the foot the medial and lateral plantar veins arise and combine to form the posterior tibial and fibular vein. The posterior tibial vein accompanies the posterior tibial artery, entering the leg posteriorly to the medial malleolus. On the posterior surface of the knee the anterior tibial, posterior tibial and fibular veins unite to form the popliteal vein which enters the thigh through the adductor canal
1217
Course of the deep venous drainage of the thigh
The popliteal vein becomes the femoral vein once it enters the thigh and is situated anteriorly. The profunda femoris vein is the other main venous structure. Empties into the distal section of the femoral vein. The femoral vein leaves the thigh to become the EIV
1218
Outline the superficial venous drainage of the leg
Two major veins, the great and small saphenous Great saphenous is formed by the dorsal venous arch of the foot. Ascends on the medial side of the leg, passing anteriorly to the medial malleolus and posterior to the medial condyle at the knee. As the vein moves up the leg it receives tributaries from other small superficial veins, and terminates by draining into the femoral vein immediately inferior to the inguinal ligament. The small saphenous vein moves up the posterior side of the leg, passing posterior to the lateral malleolus along the border of the calcaneal tendon. It moves between the two heads of gastrocnemius and empties into the popliteal vein in the popliteal fossa
1219
What is the location of the saphenofemoral junction
2.5cm below and 2.5cm lateral to the pubic tubercle
1220
1221
Incidence of chronic limb ischaemia
5% of males \>50 years have intermittent claudication
1222
Def: chronic limb ischaemia
Ankle artery pressure \<50mmHg (toe \<30) And either: persistent rest pain requiring analgesia for \>2w or Ulceration or gangrene
1223
Cause of chronic limb ischaemia
Atherosclerosis: typically asymptomatic until 50% stenosis Vasculitis and fibromuscular dysplasia are v rare causes
1224
Summary of atherosclerosis
Endothelial injury: haemodynamic, HTN, raised lipids Chronic inflammation: lipid-laden foam cells produce GFs, cytokines, ROS and MMPs-\> lymphocyte and SMC recruitment SM proliferation: conversion of fatty streak to atherosclerotic plaque
1225
Difference betweeen arteriosclerosis and atherosclerosis
Arteriosclerosis= general arterial hardening Atherosclerosis= arterial hardening specifically due to atheroma
1226
Atheroma pathology
Fibrous cap: SM cells, lymphocytes, collagen Necrotic centre: cell debris, cholesterol, Ca, foam cells
1227
Modifiable risk factors for chronic limb ischaemia
Smoking BP DM Hyperlipiademia Reduced exercise
1228
Non modifiable RFs for chronic limb ischaemia
FH and PMHx Male Increased age Genetic
1229
What is the association of vascular disease with chronic limb ischaemia
IHD: 90% Carotid stenosis; 15% AAA Renovascular disease DM microvascular disease
1230
cramping pain after walking a fixed distance Pain rapidly relieved by rest Either calf or buttock
Intermittent claudication
1231
Calf pain in intermittent claudication
Superifical femoral disease (commonest)
1232
Buttock pain in context of intermittent claudication
Iliac disease (internal or common)
1233
Def: critical limb ischaemia
Fontaine 3 or 4 Rest pain Especially at night, usually felt in the foot Patient hangs foot out of bad Due to reduced CO and loss of gravity Ulceration Gangrene
1234
Rest pain Especially at night, usually felt in the foot Patient hangs foot out of bad Due to reduced CO and loss of gravity Ulceration Gangrene
?Critical limb ischaemia
1235
Leriche's syndrome
Aortoiliac occlusive disease Atherosclerotic occlusion of abdominal aorta and iliacs
1236
Triad in Leriche's syndrome
Buttock claudication and wasting Erectile dysfunction Absent femoral pulses
1237
Buerger's disease=
Thromboangitis obliterans
1238
Young, male, heavy smoker Acute inflammation and thrombosis of arteries and veins in hands and feet-\> ulceration and gangrene
Buerger's disease
1239
Buerger's Disease Thrombangitis obliterans
1240
Weak pulses and CRT \>2 Ulcers: painful, punched out on pressure points Nail dystrophy/ onchylosis Skin: cold, white, atrophy, absent hair Venous guttering Muscle atrophy
?Chornic limb ischaemia
1241
What is Buerger's test?
The vascular angle, which is also called Buerger's angle, is the angle to which the leg has to be raised before it becomes pale, whilst in supine decubitus. In a limb with a normal circulation the toes and sole of the foot, stay pink, even when the limb is raised by 90 degrees.
1242
Reduced Buerger's angle seen in?
Chronic limb iscahemia
1243
Buerger's angle cut offs?
\>90= normal 20-30= ischaemia \<20= severe ischaemia
1244
What is positive Buerger's sign?
Pale-\> reactive hyperaemia due to accumulation of deoxygenated blood in dilated capillaries
1245
How can chronic limb ischaemia be classified?
Fontaine or Rutherford
1246
Fontaine classification of chronic limb ischaemia
1. Asymptomatic 2. Intermittent claudication a \>200m b \<200m 3. Iscahemic rest pain 4. Ulceration/ gangrene
1247
Rutherford classification of chronic limb iscahemia
1. Mild claudication 2. Moderate claudication 3. Severe claudication 4. Ischaemic rest pain 5. Minor tissue loss 6. Major tissue loss
1248
Ix in Chronic limb iscahemia
ABPI Doppler Walk test Bloods Imaging Other: ECG
1249
Doppler waveforms in Chronic limb ischaemia
Normal: triphasic Mild stenosis: biphasic Severe stenosis: monophasic
1250
ABPI \>1.4
Calcification: CRF, DM
1251
ABPI \>1
Normal
1252
ABNPI 0.8-0.9
Asymptomatic Fontaine 1
1253
ABPI 0.6-08
Fontaine 2 Claudication
1254
ABPI 0.3-0.6
Fontaine 3 Rest pain
1255
ABPI \<0.3
Ulceration and gangrene Fontaine 4
1256
Why might false ABPI results be obtained in DM/CRF?
Due to calcification of vessels: mediasclerosis Use toe pressure with small cuff, \<30mmHg is the cut off
1257
What is the walk test in chronic limb ischaemia Ix
Walk on treadmill @ certain speed and incline to establish maximum claudication distance ABPI measured before and after, 20% reduction is signifcant
1258
Role of bloods in chronic limb ischaemia Ix
FBC + U+Es: anaemia, renovascular disease Lipids and glucose ESR: arteritis G+S: possible procedure
1259
Role of imaging in chronic limb iscahemia Ix
Assess site, extent and distal run-off Colour duplex US CT/MR angiogram with gadolinium contrast Digital subtraction angiography: invasive, not commonly used for Dx only but used when performing therapeutic angioplasty or stenting
1260
Why perform an ECG in chronic limb ischaemia?
Look for evidence of coronary artery pathology
1261
Mx of chronic limb ischaemia: Conservative
Most patients with claudication can be managed conservatively Increase exercise and employ exercise programs Stop smoking Weight loss Foot care
1262
Prognosis with conservative management of chronic limb iscahemia
1/3 improve 1/3 stay the same 1/3 deteriorate
1263
Mx of chronic limb iscahemia: Medical
Modification of cardiovascular risk fators: BP, lipis, DM Beta blockers don't worsen intermittent caludication but use with caution Parenteral prostanoids reduces pain in patients unfit for surgery Antiplatelet drugs: clopidogrel/aspirin Peripheral vasodilators: naftidrofuryl oxalate
1264
NB re: ACEI intermittent claudication
BP medication may initially worsen pain of claudication but improve LT CV risk However, 25% of patients with PAD also have RAS so ACEI should be used with caution
1265
Management of chronic limb ischaemia: endovascular
Percutaneous transluminal angioplasty Good for short stenosis in big vessels e.g. iliacs, SFA Lower risk for patient as performed under LA Improved inflow can reduce pain but restoration of foot pulses is required for Rx of ulceration/gangrene
1266
Indications for surgical reconstruction in chronic limb ischaemia
V. short claudication distance e.g. \<100m Symptoms greatly affecting patients QoL Development of rest pain NB pre-op assessment as patient likely to have cardiorespiratory co-morbidities
1267
Practicalities of surgery for chronic limb ischaemia
Need good proximal supply and distal run-off Saphenous vein grafts are preferred below the IL More distal grafts have increased rates of thrombosis
1268
Classification of surgeries for chronic limb iscahemia
Anatomical: fem-pop, fem-distal, aortobifemoral Extra-anatomical: axillo-femoral, bifemoral, fem-fem crossover
1269
Other surgical options for chronic limb ischaemia
Endarterectomy Sympathectomy: chemical or surgical Amputation
1270
Px 1yr after critical limb ischaemia
50% alive w/o amputation 25% will have had major amputation 25% dead (usually MI or stroke)
1271
Px following amputation in CLI
1/3 complete autonomy 1/3 partial autonomy 1/3 dead
1272
Def: acute limb iscahemia
Ischaemia \<14d
1273
Def: acute on chronic limb iscahemia
Worsening symptoms and signs \<14d
1274
Def: chronic limb iscahemia
Ischaemia stable for \>14d
1275
Incomplete acute limb iscahemia
Limb not threatened
1276
Complete acute limb ischaemia
Limb threatened, loss of limb unless intervention within 6hrs
1277
Irreversible acute limb ischaemia
Requires amputation
1278
Causes of acute limb ischaemia
Thrombosis in situ: 60% Embolism: 30% Graft/stent occlusion Trauma Aortic dissection
1279
Thrombosis in situ, acute limb iscahemia
A previously stenosed vessel with plaque rupture, usually incomplete iscahemia
1280
Embolism in acute limb ischaemia
80% from LA in AF Valvular disease Can be iatrogenic/surgery Cholesterol in long bone # Paradoxical via PFO Typically lodge at femoral bifurcation causing complete limb ischaemia
1281
6Ps of acute limb ischaemia
Pale Pulseless Perishingly cold Painful Paraesthesia Paralysis
1282
Acute limb ischaemia: Onset in hours to days Less severe collaterals Claudication history present Contralateral pulses absent Diagnosed with angiography Rx with thrombolysis/bypass surgery
Thrombotic cause
1283
Acute limb ischaemia: Sudden onset Profound ischaemia AF Absent claudication history Present contralateral pulses Clinical diangosis Rx with embolectomy + warfarin
Embolic acute limb iscahemia
1284
Ix in acute limb ischaemia
Bloods: FBC, U+E, INR, G+S, CK ECG Imaging: CXR, Duplex doppler
1285
General management of acute limb ischaemia
SENIOR NBM Rehydration: IV fluids Analgesia: morphine + metoclopramide Abx if signs of infection Unfractionated heparin IV: prevent extension If occlusion is complete: urgent surgery If incomplete: angiogram + observe for deterioriation
1286
Angiography in acute limb iscahemia
Not performed if there is complete occlusion as it introduces delay If occlusion is incomplete, pre-op angio will guide any distal bypass
1287
Mx of embolic acute limb iscahemia
1. Embolectomy 2. Thrombolysis 3. Other options
1288
Embolectomy in acute limb ischaemia
Under LA or GA Wire fed through embolus Fogarty catheter fed over the top Balloon inflated and catheter withdrawn removing the embolism Send embolism for histology to exclude atrial myxoma Adequacy can be confirmed by on-table angiography
1289
Thrombolysis in acute limb ischaemia
Consider if embolectomy unsuccessful E.g. local injection of TPA
1290
Other options in acute management of embolic acute limb ischaemia
Emergency reconstruction Amputation
1291
Mx of acute limb post embolectomy
Anticoagulate: IV heparin-\> warfarin ID embolic source: ECG, echo, US aorta, femoral and pop Complications
1292
Complications post embolectomy in acute limb ischaemia
Reperfusion injury: Local swelling-\> compartment syndrome Acidosis and arrhythmia 2o to raised K ARDS GI oedema-\> endotoxic shock Chronic pain syndromes
1293
Mx of thrombotic acute limb ischaemia
Emergency reconstruction if complete occlusion Angiography and angioplasty Thrombolysis Amputation
1294
Pathogenesis of carotid artery diesease
Turbulent flow-\> reduced shear stress at carotid bifurcation promoting atherosclerosis and plaque formation Plaque rupture-\> complete occlusion or distal emboli Causes 15-25% of CVA/TIA
1295
CVA/TIA Bruit
?Carotid artery disease
1296
Ix in carotid artery disease?
Duplex carotid Doppler MRA
1297
Mx of carotid artery disease
Aspirin or clopidogrel Control RFs Surgical: endarterectomy Symptomatic \>70% benefit (5% stroke risk per year) \>50% benefit if low risk Performed within 2w of presentation Asymptomatic: \>60% benefit if low risk
1298
What studies have been used to look at the impact of endarterectomy in symptomatic caroit dartery disease?
ECST vs optimal medical therapy NASCET
1299
Cx of endarterectomy
Stroke or death: 3% HTN: 60% Haematoma MI Nerve injury
1300
What nerves can be damaged in carotid endarterectomy
Hypoglossal: ipsilateral tongue deviation Great auricular: numb ear lobe Recurrent larygneal: hoarse voice, bovine cough
1301
Stenting vs carotid endarterectomy
Less invasive: reduced hospital stay, reduced infection, reduced CN injury Concern over increased stroke risk, esp. in pts \>70y Meta-analysis shows no sig difference in mortality vs CEA
1302
Def: Aneurysm
Abnormal dilatation of a blood vessel \>50% of its normal diameter
1303
Def: true aneurysm
Dilatation of a blood vessel involving all layers of the wall and that is \>50% of its normal diameter Two different morphologies: Fusiform e.g. AAA Saccular: e.g. Berry aneurysm
1304
Difference between fusiform and saccular aneurysm
The shape of an aneurysm is described as being fusiform or saccular, which helps to identify a true aneurysm. The more common fusiform-shaped aneurysm bulges or balloons out on all sides of the blood vessel. A saccular-shaped aneurysm bulges or balloons out only on one side.
1305
Def: false aneurysm
Collection of blood around a vessel wall that communicates with the vessel lumen Usually iatrogenic e.g. puncture, cannulation
1306
Def: dissection
Vessel dilatation caused by blood splaying apart the media to form a channel within the vessel wallt
1307
Layers of a blood vessel
Lumen Intima Media Advenititia
1308
Congenital causes of aneurysms
ADPKD-\> Berry aneurysms Marfan's, Ehlers Danlos
1309
Acquired causes of aneurysms
Atherosclerosis Trauma e.g. penetrating trauma Inflammatory: Takayasu's, HSP, Kawasaki Infection: Mycotic- SBE Tertiary syphillis (esp. thoracic)
1310
Complications of aneurysms
Rupture Thrombosis Distal embolisation Pressure: DVT, oesophagus, nutcracker syndrome Fistula (IVC, intestine)
1311
Nutcracker syndrome
Nutcracker syndrome is a vascular compression disorder, and refers to the compression of the left renal vein between the superior mesenteric artery (SMA) and aorta. This can lead to renal venous hypertension, resulting in rupture of thin-walled veins into the collecting system with resultant haematuria.
1312
Relationship between popliteal aneurysms and AAA
50% of patients with popliteal aneurysm also have AAA AAA is more common than popliteal aneurysm
1313
Very easily palpable popliteal pulse 50% bilateral Expansile and pulsatile mass
Popliteal aneurysm
1314
Main complication of popliteal aneurysm
Thrombosis and distal embolism-\> acute limb ischaemia
1315
Acute Mx of popliteal aneurysm
Embolectomy or fem-distal bypass
1316
Mx of stable popliteal aneurysm
Elective grafting + tie off vessel
1317
Epidemiology of AAA
Prevalence: 5% \>50y Mortality: 10,000 deaths/yr M\>F 3:1
1318
Def: AAA
Dilatation of abdominal aorta \>3cm 90% infrarenal 30% involving iliac arteries
1319
Usually asymptomatic: discovered incidentally May-\> back pain or umbilical pain radiating to groin Acute limb ischaemia Blue toe syndrome: distal embolisation Acute rupture
?AAA
1320
Expansile mass just above the umbilicus Bruits heard Tenderness and shock suggests?
AAA Rupture
1321
Ix in AAA
Bloods: FBC, clotting screen, renal function and liver function Cross match if sx ESR and or CRP if an inflammatory cause suspected AXR: calcification may be seen Abdo US: screening and monitoring CT/MRI: gold standard Angiography: won't show true extent of aneurysm due to endoluminal thrombus but useful to delineate relationship of renal arteries
1322
AAA Calcified
1323
Conservative Mx of AAA
Manage CV RFs esp BP UK small aneurysm trial suggested that AAA \<5.5cm in maximum diameter can be monitored by US \<4cm: yearly monitoring 4.5-5cm: 6 monthly monitoring
1324
Surgical Mx of nonacute AAA
Aim to treat aneurysm before it ruptures Elective mortality: 5%, emergency mortality: 50%
1325
Indications for surgical intervention in AAA
Symptomatic: back pain= imminent rupture Diameter \>5.5cm Expanding \>1cm per year Causing complications e.g. emboli
1326
Open vs EVAR in AAA repair
EVAR has reduced perioperative mortality No reduction in mortality by 5 years due to fatal endograft failures EVAR not better than medical Rx in unfit patients EVAR requires that the aneurysm should have an adequate 1.2cm neck below the renal arteries for stent fixation, currently 65% with AAA are suitable for endovascular repair.
1327
AAA screening in UK
MASS trial revealed 50% reduction in aneurysm-related mortality in males aged 65-74 screened with US. UK- one time screen at 65y
1328
Rupture rates of AAA: \<5.5cm
1%/year
1329
Rupture rates of AAA: \>6cm
25%/year
1330
Increased risk of AAA rupture if?
Raised BP Smoker Female Strong FHx
1331
Sudden onset severe abdominal pain Intermittent or continuous, radiating to back or flanks Collapse-\> shock Expansile abdominal mass
?AAA rupture
1332
Mx of AAA rupture
ABC High flow O2 2x large bore cannulae: Give fluid if shocked but keep SBP\<100mHg (permissive hypotension) Instigate major haemorrhage protocol Call vascular surgeon, anaesthetist and warn theatre Abx prophylaxis: cef+met Analgesia Urinary catheter + CVP line If stable + Dx uncertain: US or CT may be feasible Take to theatre, clamp neck, insert dacron graft
1333
Mortality in AAA rupture
100% without surgery 50% with surgery
1334
Def: thoracic aortic dissection
Blood splays apart the laminar planes of the media to form a channel within the aortic wall
1335
Aetiology of thoracic aortic dissection
Atherosclerosis and HTN cause 90% Minority caused by underlying CTD e.g. Marfan's, Ehlers Danlos Vit CD
1336
Sudden onset, tearing chest pain Radiating through to back Tachycardia and hypertension (1o and sympathetic)
?Aortic dissection
1337
Propagation in thoracic aortic dissection
Distal: sequential occlusion of branches Left hemiplegia Unequal arm pulses and BP Paraplegia Anuria Proximal propagation: AR, tamponade Rupture into pericardial, pleural or peritoneal cavities commonest cause of death
1338
What is the classification system for aortic dissection
Stanford
1339
Outline Stanford classification
Type A: proximal 70% involves ascending aorta +/- descending Higher mortality due to probable cardiac involvement Usually require Sx Type B: distal 30% Involves descending only, distal to left subclavian artery Usually managed conservatively
1340
Ix in thoracic aortic dissection
ECG: exclude MI TTE/TOE can be used in haemodynamically unstable pts CT/MRI not suitable for unstable paitents
1341
Mx of thoracic aortic dissection
ABC Bloods: X-match 10u, FBC, U+E, clotting, amylase ECG: 20% show ischaemia due to involvement of the coronary ostia Ix: CXR, CT/MRI, TOE if haemodynamically unstable Treat: Analgesia Reduce SBP (labetalol or esmolol) 100-110mmHg Type A: open repair, acute mortality \<25% Type B: conservative, sx if persistent pain or complications, consider TEVAR if uncomplicated
1342
Def: gangrene
Death of tissue from poor vascular supply
1343
Classification of gangrene
Wet: tissue death + infection Dry: tissue death only Pregangrene: tissue on brink of gangrene
1344
Black tissues +/- slough May be suppuration +/- sepsis
?Gangrene
1345
Wet gangrene
1346
Dry gangrene
1347
Pregangrene
1348
Cause of gas gangrene
Clostridium perfringes myositis
1349
RFs for gas gangrene
DM Trauma Malignancy
1350
Toxaemia Haemolytic jaundice Oedema Creptius from surgical emphysema Bubbly brown pus
Gas gangrene
1351
Rx of gas gangrene
Debridement: may need amputation Benzylpenicllin and metronidazole Hyperbaric O2
1352
What is synergistic gangrene?
Involves aerobes and anaerobes Can progress rapidly to nec fasc and myositis
1353
Meleney Gangrene
Synergistic gangrene Chronic undermining burrowing ulcer (also known as Meleney gangrene, or Meleney's ulcer) is a cutaneous condition that is a postoperative, progressive bacterial gangrene.[1]:269 It is seen in immunocompromised individuals, mostly after post abdominal surgery and rapidly spreads to involve a large area.[citation needed]
1354
Fournier's gangrene
Synergistic gangrene Fournier gangrene is a type of necrotizing fasciitis or gangreneaffecting the perineum.
1355
Mx of gangrene
Take cultures Debridement Benzlpenicllin +/- clindamycin
1356
Def: varicose veins
Tortuous dilated veins of the superficial venous system
1357
Pathophysiology of varicose veins
One-way flow from superifical-\> deep venous system maintained by valves Valve failure-\> increased pressure in superficial veins-\> varicosity
1358
What are the 3 main sites of valve incompetence in varicose veins
SFJ: 3cm below and 3cm lateral to pubic tubercle SPJ: popliteal fossa Perforators: draining GSV
1359
What are the 3 medial calf perforators?
Cockett's
1360
What is the 1 medial thigh perforator called?
Hunter's
1361
1362
Primary causes of varicose veins
Idiopathic: congenitally weak valves Prolonged standing, pregnancy, obesity, OCP, FHx Congenital valve absence (v. rare)
1363
Secondary causes of varicose veins
Valve destruction-\> reflux: DVT, thrombophlebitis Obstruction: DVT, foetus, pelvic mass Constipation AVM Overactive pumps e.g. cyclists Klippel-Trenaunay: PWS, varicose veins, limb hypertrophy
1364
Trendelenberg test
Torniquet Start 3cm below and 3cm lateral to pubic tubercle Lift patient's leg as high as comfortable and milk leg to empty veins. Once varicosities are empty place thumb or torniquet over SFJ Ask patient to stand while pressure is maintained If varicosities rapidly fill, suggests the incompetent perforator veins lie below the SFJ Now repeat moving down 3cm each time, when varicosities do not refill, the incompetent perforator is above the torniquet but below the previous one.
1365
Cosmetic defect Pain, cramping, heaviness in the legs Tingling Bleeding; may be severe Swelling
Varicose veins
1366
Venous stars Haemosiderin deposition Venous eczma Lipodermatosclerosis Atrophie blanche Ulcer in medial malleolus/gaiter area Oedema Thrombophlebitis
Varicose veins
1367
Venous stars
1368
Haemosiderin deposition Varicose veins
1369
Venous eczema Varicose veins
1370
Lipodermatosclerosis Varicose veins
1371
Atrophie blanche Venous eczema
1372
Venous ulcer
1373
Ix in varicose veins
Duplex ultrasonography: anatomy, presence of incompetence, caused by obstruction or reflux Sx: FBC, U&E, clotting, G+S, CXR, ECG
1374
Referral criteria for varicose veins
Bleeding Pain Ulceration Superficial thrombophlebitis Severe impact on QoL
1375
Classification of varicose veins is with?
CEAP classification
1376
CEAP classification
Chronic venous disease can be classified according to Clinical signs (1-6 + Symptomatic or Asymptomatic) i.e. 1S or 4A Etiology Anatomy Pathophysiology
1377
Conservative Mx of varicose veins
Treat any contributing factors: lose weight, relieve constipation Education: avoid prolonged standing, regular walks Class II Graduated compression stockings: symptomatic relief and slows progression Skin care: maintain hydration with emollients and treat ulcers rapidly
1378
Indications for minimally invasive therapies in varicose veins treatment
Small below knee varicosities not involving GSV or SSV
1379
Techniques of minimally invasive varicose vein therapy
Local or GA Injection scleropathy: 1% Na tetradecyl sulphate Endovenous laser or radiofrequency ablation Post-operatively: Compression bandage for 24h Compression stockings for 1m
1380
Indications for sx management of varicose veins
SFJ incompetence Major perforator incompetence Symptomatic: ulceration, skin changes, pain
1381
Procedures for varicose veins
Trendelenberg: SFJ ligation SSV ligation: popliteal fossa LSV stripping: no longer performed due to risk of saphenous nerve damage Multiple avulsions Perforator ligation: Cockett's operation Subfascial endoscopic perforator surgery
1382
Post-op care for varicose vein patients
Bandage tightly Elevate for 24h Discharge with compression stockings and instruct to walk daily
1383
Cx of varicose vein surgery
Haematoma (esp. groin) Wound sepsis Damage to cutaneous nerve e.g. long saphenous Superficial thrombophlebitis DVT Recurrence: may approach 50%
1384
Def: ulcer
Interruption in the continuity of an epithelial surface
1385
What is the commonest cause of leg ulcer?
Venous
1386
What are the different forms of leg ulcers?
Venous Arterial Neuropathic Traumatic Systemic disease Neoplastic
1387
Painless, sloping, shallow ulcer Usually on gaiter area Associated with lipodermatosclerosis RFs: venous insufficiency, varicosities, DVT, obesity
?Venous ulcer
1388
Proportion of leg ulcers that are venous
75%
1389
Proportion of leg ulcers that are arterial
2%
1390
Hx of vasculopathy and risk factors Painful, deep, punched-out lesions Occur at pressure points: heel, tips of and between toes, metatarsal heads (esp. 5th) Other signs of chronic leg ischaemia
Arterial ulcer
1391
Arterial ulcer
1392
Painless ulcer with insensate surrounding skin Warm foot with good pulses
Neuropathic ulcer
1393
Neuropathic ulcer
1394
Cx of ulcers
Osteomyelitis Development of SCC in ulcer (Marjolin's)
1395
Marjolin's ulcer=
Development of SCC in ulcer
1396
Ix in venous ulcers?
ABPI if possible Duplex ultrasonography Biopsy may be necessary to look for malignant change
1397
Mx of venous ulcers
Refer to leg ulcer community clinic Focus on prevention: graduated compression stockings, venous uclers Optimise risk factors: nutrition, smoking
1398
Specific Rx for venous ulcers
Analgesia Bed Rest and Elevate leg 4 layer graded compression bandage if ABPI \>0.8 Pentoxyfylline PO: increases microcirculatory blood flow, improves healing rates
1399
DDx fo bilateral leg swelling
Increased venous pressure: RHF Venous insufficiency Drugs e.g. nifedipine Reduced oncotic pressure: Nephrotic syndrome Hepatic failure Protein losing enteropathy Lymphoedema Myxoedema: hyper/hypothyroidism
1400
DDx of unilateral leg swelling
Venous insufficiency DVT Infection or inflammation Lymphoedema
1401
Def: Lymphoedema
Collection of interstitial fluid due to blockage or absence of lymphatics
1402
Primary lymphoedema
Congenital absence of lymphatics May or may not be familial
1403
Different types of lymphoedema and presentations
Congenital: evident from birth Praecox: after birth but \<35 Tarda: \>35
1404
Milroy's syndrome
Familial AD subtype of congenital lymphoedema: F\>M
1405
Secondary causes of lymphoedema FIIT
Fibrosis; e.g. post RTx Infiltration: Ca: prostate, lymphoma Filariasis Infection: TB Trauma: block dissection of lymphatics
1406
Ix in lymphoedema
Doppler US Lymphoscintigraphy CT/MRI
1407
Mx of lymphoedema
Conservative: Skin care, compression stockings, physio, treat or prevent comorbid infections Surgical: debulking
1408
Epidemiology of DVT post surgically
DVTs occur in 25-50% of surgical patients
1409
Risk factors for DVT post-Sx
Virchow's triad Blood: Surgery-\> increased plt and fibrinogen Dehydration Malignancy Increased age Blood flow: Sx Immobility Obesity Vessel wall: damage to veins: esp. pelvic veins Previous VTE
1410
Peak incidence @5-10d 65% below knee are asymptomatic Calf warmth, tenderness, erythema, swelling Low grade pyrexia Pitting oedema
?DVT
1411
DVT
1412
DDx for DVT
Cellulitis Ruptured Baker's cyst
1413
Ix in DVT
D-dimers: sensitive but not specific Compression US: clot will be incompressible Thrombophilia screen if no precipitating factors, recurrent DVT or family Hx
1414
Dx of DVT
Assess probability using Well's Score Low probability: perform D-dimers -ve= excludes DVT +ve= compression US Medium/high probability: compression USS
1415
What score is used to assess likelihood of DVT?
Well's score
1416
Well's criteria
Active cancer Paralysis, paresis or recent plaster immobilisation of legs Recently bedridden for \>3d or major sx within last 12w Localised tenderness along the distribution of the deep venous system Entire leg is swollen Calf swelling by more than 3cm compared with asymptomatic leg (10cm below the tibial tuberosity) Piiting oedema (greater than on the asymptomatic leg) Pitting oedema Collateral superficial veins Perviously documented DVT Subtract two points if an alternative cause is considered more likely than DVT \>2= likely, \<2 unlikely
1417
Rx of DVT
Antiocagulate: Therapeutic LMWH: enoxaparin 1.5mg/kg/24h SC Start warfrain Stop LMWH when INR 2.5 Duration depends on cause
1418
Below knee DVT duration of anticoag
6-12w
1419
Above knee DVT duration of anticoag
3-6m
1420
Initiation of warfarin treatment (rapid anticoagulation)
5mg OD for 2 days, measure INR on day 3 subsequent doses depend on INR
1421
What is important about timing of Warfarin dose
Should be taken at the same time each day
1422
What should be considered for patients post-DVT?
Graduated compression stockings to prevent post-phlebitic syndrome
1423
Pre-op prevention of DVT
Pre-op VTE risk assessment TED stockings Aggressive optimisation esp. hydration Stop OCP 4w pre-op
1424
Intra-operative prevention of DVT
Minimise length of sx Use minimal access surgery where possible Intermittent pneumatic compression boots
1425
Post-op prevention of DVT
LMWH Early mobilisation Good analgesia Physio Adequate hydration
1426
Causes of post-operative dyspnoea
Previous lung disease Atelectasis, aspiration, pneumonia LVF PE Pneumothorax (e.g. due to CVP line insertion) Pain-\> hypoventilation
1427
Ix in post-op dyspnoea
FBC, ABG CXR ECG
1428
Rx in post-op dyspnoea
Sit up, give O2, monitor SpO2 Rx cause
1429
Causes of reduced UO post-op
Post renal: Most common cause- blocked/malsited catheter, acute urinary retention Pre-renal: Hypovolaemia Renal: NSAIDs, gentamicin
1430
Anuria post-op usually
Blocked or malsited catheter
1431
Oliguria post op usually
Inadequate fluid replacement
1432
Mx of reduced UO post-operatively
Information: Operation history, obs chart: UO Drugs chart: nephrotoxins Examination: Assess fluid status Examine for palpable bladder Inspect drips, drains, stomas, CVP Action Flush with 50ml NS and aspirate back Fluid challenge
1433
Causes of post-op N+V
Obstruction Ileus Emetic drugs e.g. opioids
1434
Mx of post-op N+V
Consider NGT, AXR and ondansetron 4mg IV TDS
1435
Post op hyponatraemia
What was the pre-op level Common causes: SIADH: pain, nausea, opioids, stress Overadministration of IV fluids
1436
Immediate mx of hypotension post-sx
Tilt bed head down give O2 Assess fluid status
1437
Causes of post-operative hypotension CHOD
Cardiogenic: MI, fluid overload Hypovolaemia: inadequate replacement of fluids losses, haemorrhage Obstructive: PE Distributive: sepsis, neurogenic shock
1438
Mx of hypovolaemic hypotension
Fluid challenge 250-500ml fluid challenge STAT
1439
Mx of haemorrhagic hypotension post-op
Return to theatre
1440
Mx of septic hypotension post-op
Fluid challenge, start Abx
1441
Mx of neurogenic hypotension post-op
Nadr infusion
1442
HTN and sx
Continue anti-hypertensives during peri-operative period
1443
Causes of post-operative HTN
Pain Urinary retention Previous HTN
1444
Rx of post-operative HTN
Rx cause May use labetalol 50mg IV every 5 mins (200mg max)
1445
Def: dermatome
An area of skin that is mainly supplied by a single spinal nerve
1446
1447
Which dermatome is the thumb?
C6
1448
1449
What dermatome at level of the nipples?
T4 T4 at teat pore
1450
What dermatome at level of xihpoid process?
T7 at bottom of sternum
1451
What dermatome at level of umbilicus?
T10 at belly butTEN
1452
What dermatome at level of the inguinal ligament?
L1 for IL
1453
What dermatome at patella/medial malleolus?
L4 to the floor
1454
1455
What are the KLM sounds?
Series of sounds used to examine cranial nerve function Each tests a specific muscle and nerve pair
1456
Kuh-kuh-kuh Muscle tested Nerve tested
Levator palatini: responsible for palatal elevation Nerve required: CNX
1457
La-La-La Muscle required Nerve required
Glossus muscles CNXII
1458
Mi-mi-mi Muscle required Nerve required
Perioral muscles CNVII
1459
What are the most common causes of sudden painless loss of vision?
ischaemic optic neuropathy (e.g. temporal arteritis or atherosclerosis) occlusion of central retinal vein occlusion of central retinal artery vitreous haemorrhage retinal detachment
1460
Flashes of light (photopsia) - in the peripheral field of vision Floaters, often on the temporal side of the central vision
Posterior vitreous detachment
1461
Dense shadow that starts peripherally progresses towards the central vision A veil or curtain over the field of vision Straight lines appear curved Central visual loss
Retinal detachment
1462
Large bleeds cause sudden visual loss Moderate bleeds may be described as numerous dark spots Small bleeds may cause floaters
Vitreous haemorrhage
1463
Red eye Severe pain (ocular or headache) Reduced acuity + haloes Semi-dilated pupil Hazy cornea
Acute angle closure glaucoma
1464
Red eye Acute onset Pain Blurred vision and photophobia Small, fixed, oval pupil, ciliary flush
Anterior uveitis
1465
Red eye Severe pain and tenderness May be underlying autoimmune disease e.g. RA
Scleritis
1466
Red eye Purulent discharge (bacterial) Clear discharge (viral)
Conjunctivitis
1467
Red eye History of trauma of coughing bouts
Subconjunctival haemorrhage
1468
Mx of herpes zoster ophthalmicus
Oral antiviral treatment for 7-0 days, ideally started within 72h Oral corticosteroids may reduce duration of pain Ophthalmology review
1469
Red eye Serous discharge Recent URTI Preauricular lymph nodes
Viral conjunctivitis
1470
Red eye Bilateral symptoms Itch is prominent May be history of atopy May be seasonal (due to pollen) or perennial (due to dust mite, washing powder or other allergens)
Allergic conjunctivitis
1471
Drusen=
Dry macular degeneration
1472
Characterised by choroidal neovascularisation. Leakage of serous fluid and blood can subsequently result in a rapid loss of vision. Carries worst prognosis
Wet macular degeneration
1473
characterised by drusen - yellow round spots in Bruch's membrane
Dry macular degneration
1474
intravitreal ranibizumab
Used to treat wet macular degeneration Anti-VEGF
1475
What are the ocular manifestations of RA?
keratoconjunctivitis sicca (most common) episcleritis (erythema) scleritis (erythema and pain) corneal ulceration keratitis Iatrogenic steroid-induced cataracts chloroquine retinopathy
1476
Which one of the following is not a risk factor for primary open-angle glaucoma? Diabetes mellitus Family history Hypertension Afro-Caribbean ethnicity Hypermetropia
Acute angle closure glaucoma is associated with hypermetropia, where as primary open-angle glaucoma is associated with myopia
1477
What differentiates between central, preganglionic and post-ganglionic lesions in Horners?
Anhydrosis of the face, arm and trunk= central Anhydrosis of the face= preganglionic No anhydrosis= post-ganglionic
1478
Central causes of horner's S
Stroke Syringomelia MS Tumour Encephalitis
1479
Pre-ganglionic causes of Horner's
Pancoast Thyroidectomy Trauma Cervical rib
1480
Post-ganglionic causes of horners
Carotid artery dissection Carotid aneurysm CVST Cluster headache
1481
What is the most likely diagnosis? Ciliary body rupture with lens dislocation Vitreous haemorrhage Ischaemic optic neuropathy Central retinal artery Retinal detachment
Retinal detachment
1482
Causes of papilloedema
Causes of papilloedema space-occupying lesion: neoplastic, vascular malignant hypertension idiopathic intracranial hypertension hydrocephalus hypercapnia Rare causes include hypoparathyroidism and hypocalcaemia vitamin A toxicity
1483
venous engorgement: usually the first sign loss of venous pulsation: although many normal patients do not have normal pulsation blurring of the optic disc margin elevation of optic disc loss of the optic cup Paton's lines: concentric/radial retinal lines cascading from the optic disc
Papilloedema
1484
Theme: Visual field defects A.Left homonymous hemianopia B.Unilateral peripheral visual field loss C.Bitemporal hemianopia, upper quadrant defect D.Unilateral central visual field loss E.Left homonymous hemianopia with macula sparing F.Right homonymous hemianopia G.Bitemporal hemianopia, lower quadrant defect For each one of the following please select the associated visual field defect: Pituitary gland tumour Primary open angle glaucoma in right eye Patient who has had an extensive stroke with right-sided hemiplegia
Pit- upper, cranipharyngioma- lower Bitemporal hemianopia, upper quadrant defect Unilateral peripheral visual field loss Right homonymous hemianopia Remember: the homonymous hemianopia is always on the same side as the paresis.
1485
Upper quadrant vs lower quadrant bitemporal hemianopia
upper quadrant defect \> lower quadrant defect = inferior chiasmal compression, commonly a pituitary tumour lower quadrant defect \> upper quadrant defect = superior chiasmal compression, commonly a craniopharyngioma
1486
A 35-year-old man presents with visual problems. He has had very poor vision in the dark for a long time but is now worried as he is developing 'tunnel vision'. He states his grandfather had a similar problem and was registered blind in his 50's. What is the most likely diagnosis? Leber's congenital amaurosis Vitelliform macular dystrophy Central serous retinopathy Primary open angle glaucoma Retinitis pigmentosa
Retinitis pigmentosa primarily affects the peripheral retina resulting in tunnel vision Features night blindness is often the initial sign tunnel vision due to loss of the peripheral retina (occasionally referred to as funnel vision) fundoscopy: black bone spicule-shaped pigmentation in the peripheral retina, mottling of the retinal pigment epithelium Associated diseases Refsum disease: cerebellar ataxia, peripheral neuropathy, deafness, ichthyosis Usher syndrome abetalipoproteinemia Lawrence-Moon-Biedl syndrome Kearns-Sayre syndrome Alport's syndrome
1487
A 35-year-old female who has recently being diagnosed with Grave's disease presents for review 3 months after starting a 'block and replace' regime with carbimazole and thyroxine. She is concerned about developing thyroid eye disease. What is the best way that her risk of developing thyroid eye disease can be reduced? Reduce alcohol intake A diet rich in omega-3 fatty acids Regular exercise Stop smoking Lose weight
Smoking is the most important modifiable risk factor for the development of thyroid eye disease
1488
What are the indications for urgent opthalmology r/v in thyroid eye disease?
unexplained deterioration in vision awareness of change in intensity or quality of colour vision in one or both eyes history of eye suddenly 'popping out' (globe subluxation) obvious corneal opacity cornea still visible when the eyelids are closed disc swelling
1489
A 34-year-old man with a history of ankylosing spondylitis presents with a painful right eye associated with mild photophobia: Cycloplegic drops have recently been given. What is the most likely diagnosis? Scleritis Acute angle closure glaucoma Anterior uveitis Conjunctivitis Episcleritis
Ankylosing spondylitis is associated with anterior uveitis. The history of pain and photophobia combined with the examination findings of a red eye confirm the diagnosis Note that the pupil in this image is dilated - this is not a typical finding at diagnosis but may reflect the fact that cycloplegic drops are commonly given to patients for pain relief
1490
What is the normal range for intraocular pressure?
10-21 mmHg
1491
A 64-year-old woman presents with bilateral sore eyelids. She also complains of her eyes being dry all the time. On examination her eyelid margins are erythematous at the margins but are not swollen. Of the given options, what is the most appropriate initial management? ## Footnote Topical chloramphenicol + mechanical removal of lid debris Hot compresses + topical steroids Topical chloramphenicol + topical steroids Hot compresses + mechanical removal of lid debris Topical chloramphenicol + hot compresses
Hot compresses + mechanical removal of lid debris
1492
symptoms are usually bilateral grittiness and discomfort, particularly around the eyelid margins eyes may be sticky in the morning eyelid margins may be red. Swollen eyelids may be seen in staphylococcal blepharitis styes and chalazions are more common in patients with blepharitis secondary conjunctivitis may occur
Blepharitis
1493
What eye condition is more common in patients with rosacea?
Blepharitis
1494
Mx of blepharitis
softening of the lid margin using hot compresses twice a day mechanical removal of the debris from lid margins - cotton wool buds dipped in a mixture of cooled boiled water and baby shampoo is often used\* artificial tears may be given for symptom relief in people with dry eyes or an abnormal tear film
1495
A 67-year-old man presents as he has developed a painful blistering rash around his right eye. On examination a vesicular rash covering the right trigeminal nerve dermatome is seen. Currently he has no eye symptoms or signs. Which one of the following is most likely to predict future eye involvement? Presence of the rash on the tip of his nose Smoking history Increasing age Previous courses of corticosteroids Presence of the rash in the ear canal
This is Hutchinson's sign which is strongly predictive for ocular involvement.
1496
A 60-year-old woman who has recently started treatment for polymyalgia rheumatica presents with a five day history of headaches and reduced vision on the right side since this morning There is no eye pain but the there is a 'large, dark shadow' covering the superior visual field on the right side. On examination she has a tender, palpable right temporal artery. What is the most likely explanation for the reduced vision? Anterior ischemic optic neuropathy Central retinal vein occlusion Optic neuritis Acute angle closure glaucoma Central retinal artery occlusion
Anterior ischemic optic neuropathy
1497
What causes the visual disturbances in temporal arteritis?
Anterior ischaemic optic neuropathy
1498
A 54-year-old woman presents with a persistent watery left eye for the past 4 days. On examination there is erythema and swelling of the inner canthus of the left eye. What is the most likely diagnosis? Blepharitis Acute angle closure glaucoma Meibomian cyst Dacryocystitis Pinguecula
Dacryocystitis is infection of the lacrimal sac Features watering eye (epiphora) swelling and erythema at the inner canthus of the eye Management is with systemic antibiotics. Intravenous antibiotics are indicated if there is associated periorbital cellulitis
1499
At what age would the average child be expected to have visual acuity similar to that of an adult? 3 months 6 months 9 months 12 months 2 years
2 years A newborn's visual acuity is only about 6/200. This improves to 6/60 at 3 months but does no reach adult levels until about 2 years of age. The table below summarises the vision tests which may be performed when assessing children: AgeTest BirthRed reflex 6 weeksFix and follow to 90 degrees (e.g. Red ball 90cm away) 3 monthsFix and follow to 180 degrees No squint 12 monthsCan pick up 'hundreds and thousands' with pincer grip \> 3 yearsLetter matching test \> 4 yearsSnellen charts Ishihara plates for colour vision
1500
A 24-year-old man presents to the emergency department complaining of left eye pain. He has not been able to wear his contact lenses for the past 24 hours due to the pain. He describes the pain as severe and wonders whether he has 'got something stuck in his eye'. On examination there is diffuse hyperaemia of the left eye. The left cornea appears hazy and pupillary reaction is normal. Visual acuity is reduced on the left side and a degree of photophobia is noted. A hypopyon is also seen. What is the most likely diagnosis? Acute angle closure glaucoma Viral conjunctivitis Keratitis Episcleritis Anterior uveitis
Whilst a hypopyon can of course be seen in anterior uveitis the combination of a normal pupillary reaction and contact lens use make a diagnosis of keratitis more likely.
1501
A 70-year-old man presented with a watering and sore left eye: What is the diagnosis? Left-sided ectropion Left-sided pinguecula Stroke Bell's palsy Left-sided entropion
Left sided ectropion
1502
What is the most common cause of blindness in adults 35-65 years old?
Diabetic retinopathy
1503
A 54-year-old man is noted to have papilloedema on examination. Which one of the following may be responsible? Vitamin D toxicity Hypercapnia Hyperkalaemia Hypercalcaemia Hypoglycaemia
Hyperventilation to induce hypocapnia may be used in the emergency setting to reduce intracranial pressure
1504
A 23-year-old female presents with recurrent headaches. Examination of her cranial nerves reveals the right pupil is 3 mm whilst the left pupil is 5 mm. The right pupil constricts to light but the left pupil is sluggish. Peripheral neurological examination is unremarkable apart from difficult to elicit knee and ankle reflexes. What is the most likely diagnosis? Acute angle closure glaucoma Migraine Multiple sclerosis Holmes-Adie syndrome Argyll-Roberson syndrome
olmes-Adie pupil is a benign condition most commonly seen in women. It is one of the differentials of a dilated pupil. Overview unilateral in 80% of cases dilated pupil once the pupil has constricted it remains small for an abnormally long time slowly reactive to accommodation but very poorly (if at all) to light Holmes-Adie syndrome association of Holmes-Adie pupil with absent ankle/knee reflexes
1505
A 65-year-old man with a history of primary open-angle glaucoma presents with sudden painless loss of vision in his right eye. On examination of the right eye the optic disc is swollen with multiple flame-shaped and blot haemorrhages. What is the most likely diagnosis? Diabetic retinopathy Vitreous haemorrhage Ischaemic optic neuropathy Occlusion of the central retinal vein Occlusion of the central retinal artery
Central retinal vein occlusion - sudden painless loss of vision, severe retinal haemorrhages on fundoscopy
1506
heme: Primary open-angle glaucoma: management A.Timolol B.Pilocarpine C.Brimonidine D.Dorzolamide E.Acetylcysteine F.Ranibizumab G.Atropine H.Latanoprost I.Cyclopentolate J.Tropicamide For each one of the following questions please select the correct answer: Adverse effects include brown pigmentation of the iris Should be avoided in patients taking MAOI drugs Causes pupillary constriction, blurred vision and headaches
Latanoprost Brimonidine Pilocarpine
1507
A man is recovering after having an operation to remove a meningioma in his left temporal lobe. What sort of visual field defect is he at risk of having following the procedure? Right inferior homonymous quadrantanopia Right superior homonymous quadrantanopia Left inferior homonymous quadrantanopia Right homonymous hemianopia with macula sparing Left superior homonymous quadrantanopia
homonymous quadrantanopias: PITS (Parietal-Inferior, Temporal-Superior)
1508
A 70-year-old man is investigated for blurred vision. Fundoscopy reveals drusen, retinal epithelial and macular neovascularisation. A diagnosis of age related macular degeneration is suspected. What is the most appopriate next investigation? Vitreous fluid sampling MRI orbits Ocular tonometry Fluorescein angiography Kinetic perimetry
optical coherence tomography: provide cross-sectional views of the macula if neovascularisation is present fluorescein angiography is performed
1509
73-year-old man complains of a sore right eye: What is the diagnosis? Dacryocystitis Chalazion Entropion Blepharitis Ectropion
If left untreated this patient may develop a corneal ulcer. The definitive management of entropion is surgical although eye lubricants and tape (to pull the eyelid outwards) may be used whilst awaiting surgery.
1510
Theme: Visual defects A.Right homonymous hemianopia B.Left homonymous hemianopia C.Right superior quadranopia D.Left superior quadranopia E.Right inferior quadranopia F.Left inferior quadranopia G.Upper bitemporal hemianopia H.Lower bitemporal hemianopia A 42-year-old woman is admitted to the vascular ward for an endarterectomy. Her CT report confirms a left temporal lobe infarct. A 22-year-old man is referred to urology with possible urinary retention. He is passing huge amounts of urine. Post void bladder ultrasound is normal. A 53-year-old man is admitted to the vascular ward for a carotid endarterectomy. His CT head report confirms a left parietal lobe infarct.
Right superior quadranopia Lower bitemporal hemianopia Right inferior quadranopia
1511
Conditions associated with anterior uveitits?
ankylosing spondylitis reactive arthritis ulcerative colitis, Crohn's disease Behcet's disease
1512
Each one of the following is a cause of a mydriatic pupil, except: Third nerve palsy Atropine Holmes-Adie pupil Argyll-Robertson pupil Traumatic iridoplegia
Argyll-Robertson pupil is one of the classic pupillary syndrome. It is sometimes seen in neurosyphilis and is often said to be the prostitute's pupil - accommodates but doesn't react. Another mnemonic used for the Argyll-Robertson Pupil (ARP) is Accommodation Reflex Present (ARP) but Pupillary Reflex Absent (PRA) Features small, irregular pupils no response to light but there is a response to accommodate Causes diabetes mellitus syphilis
1513
This man presents with unilateral visual loss. On examination he has a relative afferent pupillary defect. Fundoscopy shows the following: What is the most likely diagnosis? Central retinal vein occlusion Subhyaloid haemorrhage Solar retinopathy Central retinal artery occlusion Optic neuritis
Central retinal artery occlusion The pale retina is the most obvious sign in this slide.
1514
Which one of the following best describes the action of latanoprost in the management of primary open-angle glaucoma? Carbonic anhydrase inhibitor Reduces aqueous production + increases outflow Opens up drainage pores Increases uveoscleral outflow Reduces aqueous production
Increases uveoscleral outflow
1515
What are the acquired causes of optic atrophy?
MS Longstanding papilloedema Raised IOP Retinal damage e.g. choroiditis, retinitis pigmentosa Ischaemia Toxins: tobacco ambylopia, quinine, methanol, arsenic, lead Nutritional: vitamin B1, B2, B6 and B12 deficiency
1516
What are the congenital causes of optic atrophy?
Friedrich's ataxia Mitochondrial disorders DIDMOAD (cranial DI, DM, OA, deafness- Wolfram's)
1517
Which one of the following statements regarding the Holmes-Adie pupil is incorrect? May be associated with absent ankle/knee reflexes Bilateral in 80% of cases It is a benign condition Slowly reactive to accommodation but very poorly (if at all) to light Causes a dilated pupil
The Holmes-Adie pupil is unilateral, rather than bilateral, in 80% of patients
1518
Theme: Primary open-angle glaucoma: management A.Timolol B.Pilocarpine C.Brimonidine D.Dorzolamide E.Acetylcysteine F.Ranibizumab G.Atropine H.Latanoprost I.Cyclopentolate J.Tropicamide Both reduces aqueous production and increases outflow First-line treatment in a patient with a history of heart block Systemic absorption may cause sulphonamide-like reactions
Brimonidine Latanoprost Dorzolamide
1519
Causes of tunnel vision
papilloedema glaucoma retinitis pigmentosa choroidoretinitis optic atrophy secondary to tabes dorsalis hysteria
1520
A 71-year-old man who has recently been diagnosed with macular degeneration asks for advice regarding antioxidant dietary supplements. Which one of the following may contraindicate the prescription of such supplements? Current smoker Pernicious anaemia Treated hypertension History of depression Previous episodes of tendonitis
Beta-carotene has been found to increase the risk of lung cancer and hence antioxidant dietary supplements are not recommended for smokers.
1521
Theme: Visual field defects A.Optic nerve B.Optic chiasm C.Retina D.Occipital cortex E.Optic tract For each one of the following please select where the lesion is likely to be: A 72-year-old man develops visual problems. He is noted to have a left homonymous hemianopia with some macula sparing. A 54-year-old man complains of sweating, headaches and 'tunnel vision'. A 30-year-old man with a family history of early blindness is concerned that he is developing 'tunnel vision'.
Occipital cortex The macula sparing suggests the lesion is most likely to be in the occipital cortex rather than the optic tract. Optic chiasm This patient has a pituitary tumour causing compression of the optic chiasm and bitemporal hemianopia. The sweating and headaches are consistent with acromegaly. Retina This is a common presentation of retinitis pigmentosa. Extensive pigmentation would normally be noted on fundoscopy.
1522
Each one of the following predisposes to cataract formation, except: Down's syndrome Hypercalcaemia Diabetes mellitus Long-term steroid use Congenital rubella infection
Hypocalcaemia, rather than hypercalcaemia, predisposes to cataract formation.
1523
Causes of cataracts Majority Systemic Ocular
Majority age related UV light Systemic diabetes mellitus steroids infection (congenital rubella) metabolic (hypocalcaemia, galactosaemia) myotonic dystrophy, Down's syndrome Ocular trauma uveitis high myopia topical steroids
1524
Causes of lens dislocation?
Marfan's: upwards Homocystinuria: downwards Ehlers-Danlos Trauma Uveal tumours Autosomal recessive ectopia lentis
1525
A 47-year-old female with a history of rheumatoid arthritis presents with a painful and red left eye. Visual acuity is normal. What is the most likely diagnosis? Scleritis Episcleritis Glaucoma Anterior uveitis Keratoconjunctivitis sicca
A key way to discriminate between scleritis and episcleritis is the presence of pain. Keratoconjunctivitis sicca is usually bilateral and associated more with dryness, burning and itch
1526
A 62-year-old woman presents with sudden loss of vision in her left eye. Fundoscopy reveals the following: What is the diagnosis? ## Footnote Retinal detachment Ischaemic optic neuropathy Vitreous haemorrhage Central retinal vein occlusion Central retinal artery occlusion
Central retinal vein occlusion - sudden painless loss of vision, severe retinal haemorrhages on fundoscopy This appearance is sometimes compared to a cheese and tomato pizza.
1527
Composition of bone matrix?
Organic= osteoid (40%) Collagent Type 1 Resists tension, twisting and bending Inroganice (60%) Calcium hydroxapatite Resits compressive forces
1528
How can bone be classified?
Woven bone: disorganised bone that forms the embryonic skeleton and fracture callus Lamellar bone: mature bone that can be of two types: Cortical/compact= dense outer layer Cancellous/trabecular: porous central layer
1529
Process of intramembranous ossification
Direct ossification of mesenchymal bone models formed during embryonic development Skull bones, mandible and clavicle
1530
Process of endochondral ossification
Mesenchyme-\> cartilage-\> bone Most bones ossify this way
1531
What are the phases of fracture healing?
Reactive phase Reparative phase Remodelling phase
1532
Features of reactive phase of bone healing
Injury-48h Bleeding into #site-\> haematoma Inflammation-\> cytokine, GF and vasoactive mediator release-\> recruitment of leukocytes and fibroblasts-\> granulation tissue
1533
Features of the reparative phase of bone healing
2d-2w Proliferation of osteoblasts and fibroblasts-\> cartilage and woven bone production-\> callus formation Consolidation-\> endochondral ossificaiton of woven bone-\> lamellar bone
1534
Features of the remodelling phase of bone healing
1w-7y Remodelling of lamellar bone to cope with mechanical forces applied to it Follows Wolff's law
1535
What is Wolff's Law
Form follows function Wolff's law, developed by the German anatomist and surgeon Julius Wolff (1836–1902) in the 19th century, states that bone in a healthy person or animal will adapt to the loads under which it is placed.[1] If loading on a particular bone increases, the bone will remodel itself over time to become stronger to resist that sort of loading.[2][3] The internal architecture of the trabeculae undergoes adaptive changes, followed by secondary changes to the external cortical portion of the bone,[4] perhaps becoming thicker as a result. The inverse is true as well: if the loading on a bone decreases, the bone will become less dense and weaker due to the lack of the stimulus required for continued remodeling.[5] This reduction in bone density (osteopenia) is known as stress shielding and can occur as a result of a hip replacement (or other prosthesis).[6] The normal stress on a bone is shielded from that bone by being placed on a prosthetic implant.
1536
Healing time for a closed, paediatric, metaphyseal, upper limb #
3w
1537
What are the complicating factors for #s and what do they do?
Double healing time Adult LL Diaphyseal Open
1538
Anatomy of a long bone proximal to distal
Diaphysis= shaft Metaphysis: growth plate region (physis- growth plate) Epiphysis Atrciular cartilage over joint surfaces
1539
Anatomy of a long bone Deep to superficial
Medullary cavity Endosteum Cortical bone Periosteum
1540
How can fractures be classified?
Traumatic Stress Pathological
1541
E.g. of traumatic #
Direct e.g. assualt with metal bar Indirect e.g. FOOSH-\> #clavicle Avulsion
1542
Features of stress#
Bone fatigue due to repetitive strain E.g. foot #s in marathon runners
1543
E.g. of pathological #s
Normal forces but disease bone Local- tumours General: osteoporosis, Cushing's Pagets
1544
XR of #s
Radiographs must be orthogonal request AP and lat films Need images of joint above and below #
1545
Structure for describing fracture PAID
Demographics Pattern Anatomical Intra/extra-articular Deformity Soft tissues Specific #classification/type
1546
Components of pattern when describing #
Transverse Oblique Spiral Multifragmentary Crush Greenstick Avulsion
1547
Deformity when describing XR #
Translation Angulation or tilt Rotation Impaction (shortening) Describe distal relative to proximal
1548
Features of soft tissue when describing XR#
Open or closed Neurovascular status Compartment syndrome
1549
What are the 4Rs of fracture management
Resuscitation Reduction Restriction Rehabilitation
1550
What are the principles of resuscitation in # management
Follow ATLS guidelines Trauma series in 1o survey: C-spine, chest and pelvis usually assessed in 2o survey Assess neurovascular status and look for dislocations Consider reduction and splinting before imaging when: reduced pain, reduced bleeding, risk of neurovascular imaging XR once stable
1551
When should #reduction be considered before imaging?
To reduce pain To reduce bleeding To reduce risk of neurovascular injury
1552
What are the 6As of open #
Analgesia Assess: NV status, soft tissues, photograph Antisepsis: wound swab, copious irrigation, cover with betadine-soaked dressign Alignment: align # and splint Anti-tetanus: check status Abx: fluxclox 500mg IV/IM and benpen 600mg IV/IM Or augmentin 1.2g IV
1553
Mx of open #
Debridement and fixation in theatre
1554
What is the most dangerous complication of open# and why?
Clostridium perfrigens Wound infections and gas gangrene +/- shock and renal failure
1555
Rx in c. perfringens infection of open#?
Debride, benpen, clindamycin
1556
What can be used to classify open #s?
Gustillo
1557
Components of Gustillo classification of open #s
1. Wound \<1cm in length 2. Wound \>1cm with minimal soft tissue damage 3. Extensive soft tissue damage
1558
What are the principles for redcution of #s?
Displaced #s should be reduced unless no effect on outcome e.g. ribs Aim for anatomical reduction, especially if articular surfaces involved Alignment is more important than opposition
1559
What are the methods of # reduction?
Manipulation/closed reduction Traction Open reduction and internal fixation
1560
Features of manipulation/closed reduction
Under local, regional or general anaesthetic Traction to disimpact Manipulation to align
1561
Features of traction for # reduction
Not typically used now Employed to overcome contraction of large muscles e.g. femoral #s Skeletal traction vs skin traction
1562
Features of open reduction and internal fixation
Accurate reduction weighed up vs risks of surgery Intra-articular #s Open #s 2 #s on 1 limb Failure in conservative mx Bilateral identical fractures
1563
What are the principles of restriction in # management
Interfragmentary strain hypothesis dictates that tissue is formed at site dependent on strain it experiences Fixation reduces strain -\> bone formation Fixation also reduces pain, increases stability and ability to function
1564
What are the methods of restriction in # mx
Non-rigid Plaster Functional bracing Continuous traction Ex-fix Internal fixation
1565
What are some examples of non-rigid fixation?
Slings Elastic supports
1566
What are some methods for plaster restriction of #s What is an important consideration?
POP In first 24-48h use back-slab or split cast due to risk of compartment syndrome
1567
What is functional bracing of #
Joints free to move but bone shafts supported in cast segments
1568
What is an example of continuous traction
Collar and cuff sling
1569
Features of external fixation
Fragments held in position by pins/wires which are then connected to an external frame Intervention is away from field of injury Useful in open #s, burns, tissue loss to allow wound access and reduce infection risk However there is a risk of pin-site infections
1570
Features of internal fixation
Pins, plates, screws, IM nails Usually perfect anatomical alignement Increased stability Aid early mobilisation
1571
What are the principles in # rehabilitation
Immobility-\> reduced muscle and bone mass, joint stiffness Need to maximise return to function to reduce later morbidity
1572
What are some methods of # rehabilitation
PT: exercises to improve mobility OT: splints, mobility aids, home modification Social services: meals on wheels, home help
1573
What are the general complications of fractures?
Tissue damage: Haemorrhage and shock Infection Muscle damage-\> rhabdomyolysis Anaesthesia: Anaphylaxis Damage to teeth Aspiration Prolonged bed rest: Chest infection, UTI Pressure sores and muscle wasing DVT, PE Decreased bone mineral density
1574
What are the immediate complications of fractures?
Neurovascular damage Visceral damage
1575
What are the early complications of fractures?
Compartment syndrome Infection (worse if associated with metalwork) Fat embolism-\> ARDS
1576
What are the late complications of fractures?
Problems with union AVN Growth disturbance Post-traumatic osteoarthritis Complex regional pain syndromes Myositis ossificans
1577
What is myositis ossificans
far most common type, nonhereditary myositis ossificans (commonly referred to simply as "myositis ossificans", as in the remainder of this article), calcifications occur at the site of injured muscle, most commonly in the arms or in the quadriceps of the thighs. ## Footnote The term myositis ossificans traumatica is sometimes used when the condition is due to trauma.[1][2] Also Myositis ossificans circumscripta is another synonym of myositis ossificans traumatica refers to the new extraosseous bone that appears after traum
1578
What is the second, rarer type of myositis ossificans?
The second condition, myositis ossificans progressiva (also referred to as fibrodysplasia ossificans progressiva) is an inherited affliction, autosomal dominant pattern, in which the ossification can occur without injury, and typically grows in a predictable pattern. Although this disorder can be passed to offspring by those afflicted with FOP, it is also classified as nonhereditary, as it is most often attributed to a spontaneous genetic mutation upon conception.
1579
Myositis ossificans
1580
What are the features of neurological complications following #
Severance is rare, stretching over bone edge commoner Seddon classification describes three types of injury
1581
What are the components of the Seddon Classification
Descrbie neurological damage post # Neuropraxia Axonotmesis Neurotmesis
1582
What is Neuropraxia
Temprorary interruption of conduction without loss of axonal continuity
1583
What is axonotmesis?
Disruption of nerve axon-\> distal Wallerian degeneration Connective tissue framework of nerve is preserved Regeneration occurs and recovery is possible
1584
Wallerian degeneration
Wallerian degeneration is a process that results when a nerve fiber is cut or crushed, in which the part of the axon separated from the neuron's cell body degenerates distal to the injury. This is also known as anterograde or orthograde degeneration.
1585
What is neurotmesis?
Disruption of the entire nerve fibre Surgery is required and recovery is not usually complete
1586
Ant. shoulder dislocation Humeral surgical neck Nerve damage Result?
Axillary nerve Numb chevron Weak abduction
1587
humeral shaft Nerve affected Clinical manifestation
Radial nerve Waiter's tip
1588
Elbow dislocation Nerve affected Clinical manifestation
Ulnar nerve Claw hand
1589
Hip dislocation Nerve affected Clinical manifestation
Sciatic nerve Foot drop
1590
neck of fibula Knee dislocation Nerve affected Clinical manifestation
Fibular nerve Foot drop
1591
Features of compartment syndrome
Osteofascial membranes divide limbs into separate comparments of muscles Oedema following # can lead to an increase in compartment pressure, this reduces venous drainage increasing compartment pressure further If compartment pressure \> capillary pressure-\> ischaemia Muscle infarction-\> Rhabdomyolsis and ATN Fibrosis-\> Volkman's ischaemic contractrue
1592
Pain \> clinical findings Pain on passive muscle stretching Warm erythematous, swollen limb Prolonged CRT and weak/absent peripheral pulses
?Compartment syndrome
1593
Rx of compartment syndrome
Elevate limb Remove all bandages and split/remove cast Fasciotomy
1594
Def: delayed union
Union takes longer than expected
1595
Non-union of fracture is when
fails to unite
1596
What are the causative factors for problems with bone union? 5Is
Ischaemia: poor blood supply or AVN Infection Increased interfragmentary strain Interposition of tissue between fragments Intercurrent disease: e.g. malignancy or malnutrition
1597
How can non-union be classified?
Hypertrophic: bone end is rounded, dense and sclerotic Atrophic: bone looks osteopenic
1598
Management of non-union
Optimise biology: infection, blood supply, bone graft, BMPs Optimise mechanics: ORIF
1599
Def: malunion
#healed in an imperfect position poor position and or function e.g. gunstock deformity
1600
Gunstock deformity
Cubitus varus (varus means a deformity of a limb in which part of it is deviated towards the midline of the body) is a common deformity in which the extended forearm is deviated towards midline of the body. Cubitus varus is often referred to as "Gunstock deformity", due to the crooked nature of the healing. A common cause is the supracondylar fracture of humerus.
1601
What is Pelllegrini-Stieda disease
Form of myositis ossificans Calcification of the superior attachment of MCL at the knee following traumatic injury
1602
Pellegrini-Stieda disease 􀁸 form of MO 􀁸 Calcification of the superior attachment of MCL @ the knee following traumatic injury.
1603
Def: Complex Regional Pain Syndrome Type 1
=Reflex Sympathetic Dystrophy, Sudek's atrophy Complex disorder of pain, sensory abnormalities, abnormal blood flow, sweating and trophic changes in superficial or deep tissues No evidence of nerve injury
1604
Causes of Complex Regional Pain Syndrome Type 1
Injury: #s, carpal tunnel release, ops for Dupuytren's Zoster, MI, Idiopathic
1605
Weeks-Months after injury Not traumatised area that is affected, affects a neighbouring area Lancing pain, hyperalgesia or allodynia Vasomotor: hot and sweaty or cold and cyanosed Skin: swollen or atrophic and shiny NM: weakness, hyper-reflexia, dystonia, contractures
Complex Regional Pain Syndrome Type 1 (Reflex Sympathetic Dystrophy, Sudek''s atrophy)
1606
Allodynia
Pain caused by something that wouldn't normally cause pain
1607
Rx of CRPS Type I
Usually self-limiting Refer to pain team Amitryptilline, gabapentin Sympathetic nerve blocks can be tried
1608
What is CRPS type II?
Persistent pain following an injury caused by nerve lesions
1609
What can happen in children with fractures
Damage to the physis can result in abnormal bone growth Salter-Harris classification categorises growth plate injuries
1610
What is the Salter-Harris Classification SALT C
Used to classify growth plate injuries 1. Straight across 2. Above 3. Lower 4. Through 5. Crush
1611
Px of SH1
e.g. SUFE Normal growth with good reduction
1612
Px of SH4
Union across physis may interfere with bone growth
1613
Px of SH5
Crush-\> physis injury-\> growth arrest
1614
1615
What is the most common point of # clavicle And mechanism?
Junction of the medial 2/3 and lateral 1/3 After the # the lateral end of the clavicle is displaced inferiorly be the weight of the arm and medially by pectoralis major Medial end is pulled superiorly by sternocleidomastoid FOOSH
1616
Winging of the scapula caused by?
Serratus anterior muscle originates from ribs 2-8 and attaches to the costal face of the scapula pulling it against the ribcage This is innervated by the LTN If the LTN becomes damaged the scapula protrudes out of the back when pushing with the arm.
1617
What rotator cuff muscles attach to the greater tubercle?
Greater tubercle is located laterally on the humerus Serves as attachment site for 3 of the rotator cuff muscles, supraspinatus, infraspinatus, teres minor.
1618
What rotator cuff muscle is attached to the lesser tubercle of the humerus
Subscapularis
1619
Action of supraspinatus
Initiator of abduction up to first 25
1620
What is the action of infraspinatus and teres minor
External rotators of the shoulder Infraspinatus acting when the arm is in neutral and teres minor when the arm is in 90% of abduction
1621
What is the action of subscapularis
Main internal rotator of the shoulder Largest and strongest cuff muslce
1622
Actions of rotator cuff muscles
SITS Supraspinatus: abduction Infraspinatus: external rotation Teres minor: external rotation (when arm is abducted to 90 deg) Subscapularis: internal rotation
1623
Articulation of the distal humerus with ulna and radius
Trochlea articulates with ulnar: located medially and extends onto the posterior of the bone Capitulum articulates with the radius
1624
Monteggia's fracture
Usually caused by a force from behind the ulna Proximal shaft of the ulna is fractured and the head of the radius dislocates anteriorly at the elbow
1625
Monteggia fracture The Monteggia fracture is a fracture of the proximal third of the ulna with dislocation of the head of the radius. It is named after Giovanni Battista Monteggia.[1][2] Fall on an outstretched hand with the forearm in excessive pronation (hyper-pronation injury). The Ulna fractures in the proximal one-third of the shaft due to extreme dislocation. Depending on the impact and forces applied in each direction, degree of energy absorption determines pattern, involvement of the radial head and whether or not open soft tissue occurs. Direct blow on back of upper forearm would be a very uncommon cause. In this context, isolated ulnar shaft fractures are most commonly seen in defence against blunt trauma (e.g. nightstick injury). Such an isolated ulnar shaft fracture is not a Monteggia fracture.[citation needed] It is called a 'nightstick fracture'.
1626
Galeazzi’s Fracture – A fracture to the distal radius, with the ulna head dislocating at the distal radio-ulnar joint.
1627
Colle's fracture
Most common types of radial fracture Fall onto an outstretched hand causing a fracture of the distal radius. Structures distal to the fracture (wrist and hand are displaced posteriorly to produce the dinner fork deformity)
1628
Most common type of radial fracture FOOSH causing a fracture of the distal radius. Structures distal to the fracture (wrist and hand are displaced posteriorly to produce the dinner fork deformity)
1629
Smith's fracture
Smith’s Fracture – A fracture caused by falling onto the back of the hand. It is the opposite of a Colles’ fracture, as the distal fragment is now placed anteriorly.
1630
Smith’s Fracture – A fracture caused by falling onto the back of the hand. It is the opposite of a Colles’ fracture, as the distal fragment is now placed anteriorly.
1631
1632
What are the carpal bones SLTP TTCH
Scaphoid Lunate Triquetrum Pisiform Trapezium Trapezoid Capitate Hamate
1633
Which carpal bones are most commonly fractured?
Scaphoid and lunate FOOSH
1634
Features of scaphoid fracture
Classical clinical features is pain and tenderness in the anatomical snuffbox Fracture needs to be reduced quickly as the blood supply to the proximal part of the bone can be cut off leading to an avascular necrosis
1635
Features of a lunate fracture
Occurs when there is hyperextension at the wrist Associated with damage to the median nerve
1636
What is Boxer's fracture
A fracture of the 5th metacarpal neck Usually caused by a clenched fist striking a hard object The distal part of the fracture is displaced posteriorly producing shortening of the affected finger
1637
Boxer's fracture
1638
Bennet's fracture
Fracture of the 1st metacarpal base extending into the carpometacarpal joint It is caused by hyperabduction of the thumb
1639
Bennet's fracture
1640
Innervation of the rotator cuff muscles
Supraspinatus and infraspinatus both innervated by suprascapular Teres minor innervated by axillary nerve Subscapularis upper and lower subscapular nerve
1641
1642
Abduction of the upper limb
Abduction (upper limb away from midline in coronal plane) The first 0-15 degrees of abduction is produced by the supraspinatus. The middle fibres of the deltoid are responsible for the next 15-90 degrees. Past 90 degrees, the scapula needs to be rotated to achieve abduction – that is carried out by the trapezius and serratus anterior.
1643
Acromioclavicular joint dislocation
1644
What is the difference between tennis elbow and golfer's elbow?
Most of the flexor and extensor muscles in the forearm have a common tendinous origin. The flexor muscles originate from the medial epicondyle, and the extensor muscles from the lateral. Sportspersons can develop an overuse strain of the common tendon – which results in pain and inflammation around the area of the affected epicondyle. Typically, tennis players experience pain in the lateral epicondyle from the common extensor origin. Golfers experience pain in the medial epicondyle from the common flexor origin.
1645
Which carpal bones articulate with the radius and ulna?
Scaphoid, lunate, triqeutrum
1646
1647
1648
1649
1650
Epidemiology of hip fracture
80/100,000 50% \>80 y F\>M 3:1
1651
Pathophysiology of hip #
Old= osteoporosis with minor trauma e.g. fall Young= major trauma
1652
What are the risk factors for osteoporosis? Age + Shattered
Age Steroids Hyper para/thyroidism Alcohol and cigarettes Thin (BMI \<22) Testosterone low Early menopause Renal/ liver failure Ersoive/inflammatory bone disease e.g. RA, myeloma Dietary Ca low/malabsorption DM
1653
Key questions in hip#?
Mechanism RFs for osteoporosis/pathological # Premorbid mobility Premorbid independence Comorbidities MMSE
1654
Hip # O/E
Shortened and externally rotated
1655
Initial management of hip #
Resuscitate: dehydration, hypothermia Analgesia: M + M Assess neurovascular status of limb Imaging: AP and lateral films Prep for theatre
1656
Orthopaedic prep for theatre ABCDEFG
Anaesthetist and book theatre Bloods: FBC, U+Es, clotting, X-match (2u) CXR DVT prophylaxis: TEDS, LMWH ECG Films: orthogonal XR Get consent
1657
Imaging in hip XR
Ask for AP and lateral film Look at Shenton's lines Intra or extracapsular Displaced or non-displaced Osteopenic?
1658
What is Shenton's line?
Shenton's line is formed by the medial edge of the femoral neck and the inferior edge of the superior pubic ramus Loss of contour of Shenton's line is a sign of a fractured neck of femur IMPORTANT NOTE: Fractures of the femoral neck do not always cause loss of Shenton's line
1659
What is the extent of the joint capsule of the hip?
Capsule envelopes the femoral head and neck Subcapital, transcervical and basicervical fractures are intracapsular hip fractures Intertrochanteric and subtrochanteric fractures do not involve the neck of the femur
1660
1661
1662
What is the blood supply of the femoral head
Most of the bloody suppply to the femoral head ariseses from the lateral femoral circumflex artery which gives rise to the retinacular vessels. These run posteriorly until they reach the cartilaginous border of the femoral head. The obturator artery gives rise to the vessels within the ligemantum teres (artery of ligamentum teres) An ascending branch of the medial femoral circumflex artery supplies the greater trochanter and anastomoses with the lateral femoral circumflex artery
1663
Key anatomy of the hip joint
Capsular attaches proximally to the acetabular margin and distally to the intertrochanteric line If retinacular vessels are damaged theres is a risk of AVN of the femoral head -\> pain, stiffness and OA
1664
How can hip fractures be classified
Intracapsular: Subcapital, transcervical, basicervical Extracapsular: Intertrochanteric, subtrochanteric
1665
What can be used to classify intracapsular hip #s?
Garden Classification
1666
Components of the Garden Classification of Intracapsular fractures?
1. Incomplete # undisplaced 2. Complete fracture, undisplaced 3. Complete fracture, partially dispalced 4. Complete fracture, completely dispalced
1667
Surgical management of intracapsular hip #
Depends on Garden classification 1,2. ORIF with cancellous screws 3,4. \<55: ORIF with screws, FU in OPD and do arthroplasty if AVN develops (30%) 55-75: THR \>75: hemiarthroplasty Mobilises: cemented Thompson's Non-mobiliser: uncemented Austin Moore
1668
Surgical management of extracapsular hip fracture
ORIF with DHS
1669
Discharge of patients with hip #
Involve OT and physios Discharge when mobilisation and social circumstances permit
1670
What are the specific complications of hip #
AVN of femoral head in displaced #s (30%) Non/malunion Infection OA
1671
Px of hip #
30% mortality at 1y 50% never regain pre-morbid functioning \>10% unable to return to premorbid residence Majority will have some residual pain or disability
1672
Features of Colles fracture
FOOSH Most common elderly females with osteoporosis Dinner fork deformity
1673
Extra-articular # of distal radius within 1.5" of joint Dorsal displacement of distal fragment Dorsal angulation of distal fragment (normally 11 degrees volar tilt) Reduced radial height (norm= 11m) Reduced radial inclination (norm= 22 deg) +/- avulsion of ulna styloid. +/- impaction
Colles fracture
1674
Management of Colles
Examine for neurovascular injury as median nerve and radial artery lie close If there is much displacement: reduction Under haematoma block, IV regional anaesthesia or GA Disimpact and correct angulation Position: ulnar deviation + some wrist flexion Apply dorsal backslab: provide 3- point pressure Re-XR: satisfactory position No: ortho review and consider MUA +/- K wires Yes: home with clinic follow up witihin 48h for completion of POP 6w in POP + physio If comminuted: intra-articular or redisplaces: surgical fixation with ex-fix, Kirschner-wries or ORIF and plates
1675
What are the specific complications of Colles fractures?
Median nerve injury Frozen shoulder/adhesive capsulitis Tendon rupture especially EPL Carpal tunnel syndrome Mal/nonunion Sudek's atrophy/CRPS
1676
Fall onto back of flexed wrist Fracture of distal radius with volar (palmar) displacement and angulation of distal fragment Reduce to restore anatomy and POP for 6w
Smith's/Reverse Colle's
1677
Oblique intra-articular fracture involving the dorsal aspect of the distal radius and dislocation of the radiocarpal joint
Barton's fracture
1678
Barton fractures are fractures of the distal radius. It is also sometimes termed the dorsal type Barton fracture to distinguish it from the volar type or reverse Barton fracture. Barton fractures extend through the dorsal aspect to the articular surface but not to the volar aspect. Therefore, it is similar to a Colles fracture. There is usually associated dorsal subluxation/dislocation of the radiocarpal joint.
1679
FOOSH Pain in anatomical snuffbox Pain on telescoping the thumb
Scaphoid fracture
1680
Specific management of scaphoid fracture
Request scaphoid XR view If clinical hx and exam suggest a scaphoid fracture it should be initially treated even if the XR is normal as # may take 10d to become apparent Place wrist in scaphoid blaster (beer glass position) If initial XR is negative F/U in clinic in 10d for repeat XR Fracture visible-\> plaster for 6 w No visible fracture but clinically tender-\> 2w No visible fracture not tender, no plaster
1681
Fracture of proximal 3rd of ulna shaft Anterior dislocation of radial head at the capitulum May lead to palsy of deep branch of radial nerve- weak finger extension but no senosry loss
Monteggia
1682
Fractutre of radial shaft between mid and distal 3rds Dislocation of distal radio-ulna joint
Galleazi fracture
1683
Management of radial and ulna shaft fractures
Unstable: adults: ORIF, children: MUA and above elbow plaster Fractures of forearm should be plastered in most stable position Proximal: supination Distal: pronation Mid-shaft: neutral
1684
How can shoulder dislocation be classified?
Anterior Posterior
1685
Features of anterior shoulder dislocation
95% of shoulder dislocations Direct trauma or falling on hand Humeral head dislocates antero-inferiorly
1686
Features of posterior shoulder dislocation
Caused by direct trauma or muscle contraction (electrocution, epileptics)
1687
Anterior shoulder dislocation
1688
Posterior dislocation Lightbulb sign: internally rotated humeral head takes on a rounded appearance
1689
What are the lesions associated with shoulder dislocation?
Bankart lesion Hill-Sachs lesion
1690
What is a Bankart lesion
Damage to anteroinferior glenoid labrum
1691
What is Hill-Sachs lesion
Cortical depression in the posteriolateral part of the humeral head following impaction against the glenoid rim during anterior dislocaiton Occurs in 35-40% of anterior dislocaiton
1692
Hill Sachs
1693
Bankart Lesion
1694
Shoulder contour loss: appears square Bulge in infraclavicular fossa Arm spported in opposite hand Severe pain
?Shoulder dislocation
1695
Specific management of shoulder dislocation
Assess for neurovascular deficit: especially axillary nerve- sensation over chevron area before and after reduction Occurs in 5% XR: AP and transcapular view Reduction under sedation Rest arm in a sling for 3-4w Physio
1696
What are the methods for reduciton of shoulder dislocation?
Hippocratic Kocher's
1697
Features of hippocratic shoulder reduction
Longitudinal traction with arm in 30 degree abduction and counter traction at the axilla
1698
Features of Kocher's reduction of dislocation
External rotation of adducted arm, anterior movement, internal rotation
1699
Complications of shoulder dislocation
Recurrent dislocation 90% of patietns \<20y with traumatic dislocation Axillary nerve injury
1700
TUBS Recurrent shoulder instability
Traumatic Unilateral dislocations with a Bankart lesion often require Surgery Mostly young patients: 15-30y Surgery involves a Bankart repair
1701
AMBRI Recurrent shoulder instability
Atraumatic Multidirectional Bilateral shoulder dislocation is treated with Rehabilitation but may require Inferior capsular shift
1702
Pathology of impingement syndrome/painful arc
Entrapment of supraspinatus tendon and subacromial bursa between acromion and greater tuberosity of humerus -\> subacromial bursitis and or supraspinatus tendonitis
1703
Painful arc: 60-120 degrees Weakness and reduced ROM +ve Hawkins test
Impingement syndrome/ painful arc
1704
Hawkins test
The patient is examined while sitting with their shoulder flexed to 90° and their elbow flexed to 90°. The examiner grasps and supports proximal to the wrist and elbow to ensure maximal relaxation, the examiner and the patient then quickly rotate the arm internally.[4][5] Pain located below the acromioclavicular joint with internal rotation is considered a positive test result
1705
Ix in impingement sydnrome
Plain radiographs may see bony spurs US MRI arthrogram
1706
Rx of impingement syndrome
Conservative: rest, PT Medical: NSAIDs, subacromial bursa steroid +/- LA injeciton Surgical: arthoroscopic acromioplasty
1707
DDx of painful arc
Impingement Supraspinatus tear or partial tear AC joint OA
1708
Progressive reduction in active and passive ROM EXTERNAL ROTATION\<30 deg Abduction \<90 Shoulder pain especially at night (can't lie on affected side)
Frozen shoulder: adhesive capsulitis
1709
Stages of frozen shoulder
Freezing Frozen Unfreezing
1710
With what is frozen shoulder associated?
DM
1711
Mx of frozen shoulder
Conservative: rest, PT Medical: NSAIDs, subacromial bursa steroid +/- LA injection
1712
Features of partial rotator cuff tear
Painful arc
1713
What is rotator cuff tear secondary to?
Degeneration, a sudden jolt or fall
1714
Features of a complete rotator cuff tear
Shoulder tip pain Full range of passive movement Inability to abduct the arm Active abduction possible following passive abduction to 90 degrees Lowering the arm beneath this -\> sudden drop: drop-arm sign
1715
Drop arm test
A positive test is determined by the patient’s inability to smoothly control the lowering of their arm or the inability to hold the arm in 90 degrees of abduction. In a positive test that starts above 90 degrees of abduction, the patient will tend to have difficulty controlling the movement around 90 degrees of abduction. There may or may not be pain reported. Pain alone is not a positive test.
1716
Mx of rotator cuff tear
Open or arthroscopic repair
1717
Common in children after FOOSH Elbow very swollen and held semi-flexed Sharp edge of proximal humerus may injury brachial artery which lies anteriorly to it
Supracondylar fracture of the humerus
1718
How can supracondylar fractures of the humerus be classified?
Extension: commonest type Flexion
1719
How can extension type supracondylar fractures of the humerus be further classified?
Gartland Type 1: non-displaced Type 2: angulated with intact posterior cortex Type 3: displaced with no cortical contact
1720
Supracondylar fracture (extension type)
1721
Supracondylar fracture flexion type
1722
1723
Specific management of supracondylar fractures of the humerus
Ensure there is no neurovascular damage: if radial pulse absent or damage to brachial artery suspected, take urgently to theatre for reduciton +/- on table angiogram. Median nerve is also vulnerable Restore the anatomy: no displacement-\> flex the arm as fully as possible and apply a collar and cuff for 3w. Triceps acts as sling to stabilise fragments. Displacement: MUA + fixation with K wires + collar and cuff with arm flexed for 3w
1724
What are the specific complications to supracondylar fractures of the humerus?
Neurovascular injury Compartment syndrome Gunstock deformity
1725
Features of neurovascular injury following supracondylar humeral fracture
Brachial artery Radial nerve Median nerve All vulnerable to injury: esp anterior ossesus branch of the median nerve which supplies the deep forearm flexors (FPL, lateral half of FDP and pronator quadratus)
1726
Features of compartment syndrome in Supracondylar fractures of humerus
Monitor closely during the first 24h Pain on passive extension of the fingers (stretches flexor compartment) is early sign Mx: try extension of the elbow though surgical Rx may be needed Volkmann's ischaemic contracture can result-\> fibrosis of flexors-\> claw hand
1727
Features of Gunstock deformity following supracondylar humeral fracture
Valgus, varus and rotational deformities in the coronal plane do not remodel and can lead to cubitus varus deformity aka Gunstock deformity
1728
A 19-year-old presents to his general practitioner (GP) with an asymptomatic right sided neck lump that he noticed 4 weeks previously. On examination the lump is soft and mobile, is within the dermal layer of the skin and on transillumination the area is equal to the surrounding tissue. There is no central punctum. What is the most likely diagnosis? Branchial cleft cyst Epidermoid cyst Lipoma Cystic hygroma Deep cervical abscess
The correct answer is a lipoma. Epidermoid cysts are common cutaneous cysts that result from the proliferation of epidermal cells within a circumscribed space of the dermis. They can occur at any age and are typically asymptomatic. On physical examination they are typically firm, round nodules of various sizes and a central punctum may be present. Cystic hygromas are congenital lymphatic lesions that are typically found in the neck and axilla region with a predilection for the left side. The majority present by 2 years of age. On physical examination, cystic hygromas are often soft, painless and transilluminate brightly. Branchial cleft cysts are congenital epithelial cysts that develop due to failure of obliteration of the second branchial cleft in embryonic development. They typically present by early adulthood. On physical examination, they are typically smooth, painless, and do not transilluminate. Deep cervical abscesses typically occur following a source of infection such as recent dental work, upper respiratory tract infections, neck or oral cavity trauma. They can occur at any age. On physical examination, the patient typically presents with a painful and tender swelling that may be hot to touch. The patient may also have other signs of infection such as fever, chills, aches, and pains.
1729
By far the most common cause of neck swellings. There may be a history of local infection or a generalised viral illness
Reactive lymphadenopathy
1730
Rubbery, painless lymphadenopathy The phenomenon of pain whilst drinking alcohol is very uncommon There may be associated night sweats and splenomegaly
Lymphoma
1731
May be hypo-, eu- or hyperthyroid symptomatically Moves upwards on swallowing
Thyroid swelling
1732
More common in patients \< 20 years old Usually midline, between the isthmus of the thyroid and the hyoid bone Moves upwards with protrusion of the tongue May be painful if infected
Thyroglossal cyst
1733
More common in older men Represents a posteromedial herniation between thyropharyngeus and cricopharyngeus muscles Usually not seen but if large then a midline lump in the neck that gurgles on palpation Typical symptoms are dysphagia, regurgitation, aspiration and chronic cough
Pharyngeal pouch
1734
A congenital lymphatic lesion (lymphangioma) typically found in the neck, classically on the left side Most are evident at birth, around 90% present before 2 years of age
Cystic hygroma
1735
An oval, mobile cystic mass that develops between the sternocleidomastoid muscle and the pharynx Develop due to failure of obliteration of the second branchial cleft in embryonic development Usually present in early adulthood
Branchial cyst
1736
More common in adult females Around 10% develop thoracic outlet syndrome
Cervical rib
1737
Pulsatile lateral neck mass which doesn't move on swallowing
Carotid aneurysm
1738
An 18 year old student presents to your GP practice after presenting to you a week ago with a supraclavicular neck lump. The last consultation reads that she had also been feeling unwell with night sweats and loss of appetite. On examination the neck lump was rubbery and non-tender. A biopsy has been taken and she has come for the results. The report shows cells with a 'mirror image nuceli' . What is the most likely diagnosis? Non-Hodgkin's lymphoma Hodgkin's lymphoma Epstein- Barr virus Thyroid adenoma Tuberculosis
Mirror image nuclei = Reed-Sternberg cells Reed-Sternberg cells are diagnostic of Hodgkin's lymphoma. Patient's present with large, non-tender, rubbery lymph nodes. 25% will have constitutional upset with fever, night sweats, weight loss, lethargy and pruritus. An exam favourite, but lesser seen symptom is alcohol induced lymph node pain.
1739
lymphadenopathy (75%) - painless, non-tender, asymmetrical systemic (25%): weight loss, pruritus, night sweats, fever (Pel-Ebstein) alcohol pain in HL normocytic anaemia, eosinophilia LDH raised
Hodgkin's lymphoma is a malignant proliferation of lymphocytes characterised by the presence of the Reed-Sternberg cell. It has a bimodal age distributions being most common in the third and seventh decades
1740
A 23-year-old man is diagnosed as having nasal polyps. Sensitivity to which medication is associated with this condition? Sulfa drugs ACE inhibitors Penicillins Paracetamol Aspirin
Around in 1% of adults in the UK have nasal polyps. They are around 2-4 times more common in men and are not commonly seen in children or the elderly. Associations asthma\* (particularly late-onset asthma) aspirin sensitivity\* infective sinusitis cystic fibrosis Kartagener's syndrome Churg-Strauss syndrome Features nasal obstruction rhinorrhoea, sneezing poor sense of taste and smell Unusual features which always require further investigation include unilateral symptoms or bleeding. Management all patients with suspected nasal polyps should be referred to ENT for a full examination topical corticosteroids shrink polyp size in around 80% of patients
1741
What is Samter's triad?
The association of asthma, aspirin sensitivity and nasal polyposis
1742
A 27-year-old woman complains of recurrent ear discharge. Otoscopy is as follows: What is the most likely diagnosis? ## Footnote Otitis externa Chronic suppurative otitis media Mastoiditis Cholesteatoma Acute otitis media
A cholesteatoma consists of squamous epithelium that is 'trapped' within the skull base causing local destruction. It is most common in patients aged 10-20 years. Main features ## Footnote foul smelling discharge hearing loss Other features are determined by local invasion: vertigo facial nerve palsy cerebellopontine angle syndrome Otoscopy 'attic crust' - seen in the uppermost part of the ear drum Management patients are referred to ENT for consideration of surgical removal
1743
Anaphylaxis doses In adult and child \>12 years
Adrenaline 500 mcg 0.5ml 1 in 1000 200mg Hydrocortisone 10mg Chlorphenamine
1744
A 25 year-old lady with no significant past medical history presents with 2 days of right ear discomfort, discharge and reduced hearing. She is systemically well and has not had a recent cold. On examination the auditory canal appears inflamed and there is a small amount of debris, but you can still see the tympanic membrane. What is the best management from the options below? ## Footnote Start topical acetic acid 2% spray Start oral amoxicillin Refer to ENT Take an ear swab and start a topical antibiotic Start a combination topical antibiotic and steroid
This lady likely has acute otitis externa. The NICE Clinical Knowledge summary suggests that inflammation is more likely to be severe if there is: a red, oedematous ear canal which is narrowed and obscured by debris conductive hearing loss discharge regional lymphadenopathy cellulitis spreading beyond the ear fever This lady has some features of inflammation with a red swollen ear canal and reduced hearing. NICE recommend that for mild cases (mild discomfort and/or pruritus; no deafness or discharge), consider prescribing topical acetic acid 2% spray. When features of more severe inflammation are present, such as in this case, they advise 7 days of a topical antibiotic with or without a topical steroid. Taking swabs from the ear is not useful routinely as virtually all bacteria detected are sensitive to the high concentrations of antibiotic in topical medications. However, this should be done if there is no response to an initial course of treatment or infections are recurrent. All patients should be advised to use simple analgesia if needed and to avoid getting water into the ear until the infection has resolved.
1745
A 35-year-old man presents to his GP surgery as he is having some difficulties with his hearing. He now struggles to follow conversation and often has the TV volume turned up high. Otoscopy is normal. An audiogram is requested: What does the audiogram show? ## Footnote Bilateral mixed hearing loss Right conductive hearing loss Normal hearing Bilateral conductive hearing loss Bilateral sensorineural hearing loss
Audiograms are usually the first-line investigation that is performed when a patient complains of hearing difficulties. They are relatively easy to interpret as long as some simple rules are followed: ## Footnote anything above the 20dB line is essentially normal (marked in red on the blank audiogram below) in sensorineural hearing loss both air and bone conduction are impaired in conductive hearing loss only air conduction is impaired in mixed hearing loss both air and bone conduction are impaired, with air conduction often being 'worse' than bone
1746
Indications for antibiotics in Sore throat
features of marked systemic upset secondary to the acute sore throat unilateral peritonsillitis a history of rheumatic fever an increased risk from acute infection (such as a child with diabetes mellitus or immunodeficiency) patients with acute sore throat/acute pharyngitis/acute tonsillitis when 3 or more Centor criteria are present
1747
Elderly patient Dizziness on extension of neck
Vertebrobasilar ischaemia
1748
A 37-year-old man presents with nasal obstruction and loud snoring. He has noticed these symptoms get gradually worse for the past two months. His left nostril feels blocked whilst his right feels clear and normal. There is no history of epistaxis and he is systemically well. On examination a large nasal polyp can be seen in the left nostril. What is the most appropriate action? Reassure + provide patient information leaflet on nasal polyps Enquire about cocaine use Refer to ENT Trial of intranasal steroids Nasal cautery
Given that his symptoms are unilateral it is important he is referred to ENT for a full examination.
1749
A patient presents due to a 'brown coating' on his tongue. He is 34-years-old and has no significant medical history. The coating has been present for the past few weeks. He is asymptomatic other than a slight 'tickling' sensation on his tongue. What is the most likely diagnosis? ## Footnote Lichen Planus Oral Candida Iron-deficiency anaemia Hairy leukoplakia Black hairy tongue
Black hairy tongue is relatively common condition which results from defective desquamation of the filiform papillae. Despite the name the tongue may be brown, green, pink or another colour. Predisposing factors poor oral hygiene antibiotics head and neck radiation HIV intravenous drug use The tongue should be swabbed to exclude Candida Management tongue scraping topical antifungals if Candida
1750
NICE urgent 2 week referral for lung cancer if
Have CXR findings that suggest lung cancer Are aged 40 and over with unexplained haemoptysis
1751
NICE urgent CX indications
People over 40 with 2 or more of: cough fatigue shortness of breath chest pain weight loss appetite loss
1752
NICE consideration of urgent chest xr for
People aged 40 and over with any of persistent or recurrent chest infection finger clubbing supraclavicular lymphadenopathy or persistent cervical lymphadenopathy chest signs consistent with lung cancer thrombocytosis
1753
A 48-year-old female presents to the GP with a lump in throat. She can swallow foods and liquids normally if she tries, although she has noticed the discomfort is worse on swallowing saliva. She does not have any pain on swallowing, chest pain or heart burn. Her appetite is normal. What is the most likely diagnosis? Achalasia Oesophageal spasm Oesophageal carcinoma Benign oesophageal stricture Globus pharyngis
Globus pharyngis (also known as globus hystericus) is the persistent sensation of having a 'lump in the throat', when there is none. Symptoms are often intermittent and relieved by swallowing food or drink. Swallowing of saliva is often more difficult.
1754
May be history of heartburn Odynophagia but no weight loss and systemically well
Oesophagitis
1755
Dysphagia may be associated with weight loss, anorexia or vomiting during eating Past history may include Barrett's oesophagus, GORD, excessive smoking or alcohol use
Oesophageal cancer
1756
Dysphagia of both liquids and solids from the start Heartburn Regurgitation of food - may lead to cough, aspiration pneumonia etc
Achalasia
1757
Other features of CREST syndrome may be present, namely Calcinosis, Raynaud's phenomenon, oEsophageal dysmotility, Sclerodactyly, Telangiectasia As well as oesophageal dysmotility the lower oesophageal sphincter (LES) pressure is decreased. This contrasts to achalasia where the LES pressure is increased
Systemic sclerosis
1758
Other symptoms may include extraocular muscle weakness or ptosis Dysphagia with liquids as well as solids
Myasthenia gravis
1759
May be history of anxiety Symptoms are often intermittent and relieved by swallowing Usually painless - the presence of pain should warrant further investigation for organic causes
Globus hystericus
1760
A 20-year-old girl presents with a thyroid cancer, she is otherwise well with no significant family history. On examination she has a nodule in the left lobe of the thyroid with a small discrete mass separate from the gland itself. Which of the following is the most likely cause? Follicular carcinoma Anaplastic carcinoma Medullary carcinoma Papillary carcinoma B Cell Lymphoma
Papillary carcinoma is the most common subtype and may cause lymph node metastasis (mass separate from the gland itself) that is rare with follicular tumours. Anaplastic carcinoma would cause more local symptoms and would be rare in this age group
1761
Thyroid malignancy: ## Footnote Commonest sub-type Accurately diagnosed on fine needle aspiration cytology Histologically they may demonstrate psammoma bodies (areas of calcification) and so called 'orphan Annie' nuclei They typically metastasise via the lymphatics and thus laterally located apparently ectopic thyroid tissue is usually a metastasis from a well differentiated papillary carcinoma.
Papillary carcinoma
1762
Are less common than papillary lesions Like papillary tumours they may present as a discrete nodule. Although they appear to be well encapsulated macroscopically there invasion on microscopic evaluation. Lymph node metastases are uncommon and these tumours tend to spread haematogenously. This translates into a higher mortality rate. Follicular lesions cannot be accurately diagnosed on fine needle aspiration cytology and thus all follicular FNA's will require at least a hemi thyroidectomy.
Follicular carcinoma of thyroid
1763
Thyroid malignancy ## Footnote Less common and tend to occur in elderly females Disease is usually advanced at presentation and often only palliative decompression and radiotherapy can be offered.
Anaplastic carcinoma
1764
These are tumours of the parafollicular cells ( C Cells) and are of neural crest origin. The serum calcitonin may be elevated which is of use when monitoring for recurrence. They may be familial and occur as part of the MEN -2A disease spectrum. Spread may be either lymphatic or haematogenous and as these tumours are not derived primarily from thyroid cells they are not responsive to radioiodine.
Medullary carcinoma
1765
A 21-year-old man presents with halitosis and mouth pain. Examination reveals very poor dental hygiene with bleeding gums and widespread gingival ulceration. He has a temperature of 38.0ºC. You advise him to see a dentist. What other treatment options should be offered? Paracetamol + oral phenoxymethylpenicillin Paracetamol + oral phenoxymethylpenicillin + chlorhexidine mouthwash Paracetamol + chlorhexidine mouthwash Paracetamol + oral metronidazole + chlorhexidine mouthwash Paracetamol + oral metronidazole
This man has acute necrotizing ulcerative gingivitis with systemic upset. Treatment should be commenced whilst he is awaiting to see a dentist. Paracetamol + oral metronidazole + chlorhexidine mouthwash
1766
A 53-year-old comes to the GP complaining of an ulcer in his mouth which has been present for 6 weeks. He believes it first started when he went out with his colleagues for some Indian food, which was quite spicy. He reports that the area is painful at times. He reports feeling otherwise well. On examination a 1cm by 1cm lesion is seen with irregular edging. Which one of the following is the most suitable course of action? Bonjela to be applied as needed, up to 4 times a day Routine referral to dental hygienist Urgent referral to dentist Routine referral to maxillo-facial surgery 2 week wait referral to oral surgery
All mouth ulcers persisting for greater than 3 weeks should be sent to oral surgery as a 2 week wait referral. 2 week wait referrals to oral surgery should be done in all of the following cases: Unexplained oral ulceration or mass persisting for greater than 3 weeks Unexplained red, or red and white patches that are painful, swollen or bleeding Unexplained one-sided pain in the head and neck area for greater than 4 weeks, which is associated with ear ache, but does not result in any abnormal findings on otoscopy Unexplained recent neck lump, or a previously undiagnosed lump that has changed over a period of 3 to 6 weeks Unexplained persistent sore or painful throat Signs and symptoms in the oral cavity persisting for more than 6 weeks, that cannot be definitively diagnosed as a benign lesion The level of suspicion should be higher in patients who are over 40, smokers, heavy drinkers and those who chew tobacco or betel nut (areca nut).
1767
A 62 year old man presents 2 days after receiving a punch to his head on the right side. Since the injury he feels his hearing has been muffled on the right side. On examination there is no bruising. Both his ears are obscured by a thin translucent layer of wax. On the right, Rinne's test demonstrates the tuning fork is easier to hear when pressed on the mastoid bone. On Weber's test the sound is heard best on the right hand side. What is the most likely diagnosis? Otosclerosis Base of skull fracture Otitis media Earwax Perforated eardrum
Tympanic membrane perforation is a relatively common complication from trauma to the skull. It is important to distinguish this from sensorineural hearing loss resulting from a base of skull fracture. Rinne's test her shows that there is a conductive hearing loss in the affected ear. Weber's test confirms that there is no sensorineural hearing loss on the right.
1768
A 45-year-old man presents with dizziness and right-sided hearing loss. Which one of the following tests would most likely indicate an acoustic neuroma? Jerky nystagmus Left homonymous hemianopia Tongue deviated to the left Fasciculation of the tongue Absent corneal reflex
Loss of corneal reflex - think acoustic neuroma
1769
A 74-year-old man presents with a 8-week history of right sided otalgia. This is associated with a sore throat and odynophagia. He smokes 20 cigarettes every day and is known to be a heavy drinker. On examination of the ear there are no abnormalities noted. What is the most likely cause of the otalgia? Eustachian tube dysfunction Acute otitis media Cholsteatoma Referred pain from nasopharyngeal carcinoma Mastoiditis
Otagia can be due to a primary or secondary cause. Primary otalgia is a result of pathology within the ear where as secondary otalgia occurs due to referred pain from an external source. Referred otalgia can occurs due to one of five neural pathways (cranial nerve V, cranial nerve VII, cranial nerve IX, cranial nerve X, and via the second and third spinal segments, C2 and C3). Therefore, many parts of the head and neck can refer pain back to the ears. Otalgia in the absence of any ear signs is a red flag for head and neck malignancy and must be investigated further. In this case the otalgia is likely to be explained by referred pain from the pharynx, and the pharynx must be assess for malignancy, particular due to the age of the gentleman and the risk factor profile.
1770
Systemic: cervical lymphadenopathy Local: otalgia unilateral serous otitis media Nasal obstruction, dsicharge and or epistaxis Cranial nerve palsies e.g. III-VI
?Nasopharyngeal carcinoma Squamous cell carcinoma of the naasopharynx Associated with EBV infection
1771
Theme: Parotid gland disorders A.Sialectasis B.Pleomorphic adenoma C.Bacterial parotitis D.Viral parotitis E.Sjogren's syndrome F.Adenoid cystic carcinoma G.Mucoepidermoid carcinoma H.Warthin's tumour I.Sarcoidosis Please select the most likely diagnosis for the scenario given. Each option may be used once, more than once or not at all. 52. A 50-year-old lady presents with symptoms of a dry mouth that has been present for the past few months. She also has a sensation of grittiness in her eyes. On examination she has a diffuse swelling of her parotid gland. There is no evidence of facial nerve palsy. 53. A 50-year-old female presents with bilateral parotid gland swelling and symptoms of a dry mouth. On examination she has bilateral facial nerve palsies. This improved following steroid treatment. 54. An 18-year-old boy presents with pancreatitis. He has bilateral painful parotid enlargement.
Sjogren's syndrome Most patients with Sjogren's present in the post menopausal years. Multi-system involvement is common. Sarcoidosis Sarcoid occurs bilaterally in 70% of cases and facial nerve involvement is recognised. Treatment is conservative in most cases although individuals with facial nerve palsy will usually receive steroids with good effect. Viral parotitis In a young adult with parotid swelling and pancreatitis/orchitis/reduced hearing/meningoencephalitis suspect mumps.
1772
Most common parotid neoplasm (80%) Proliferation of epithelial and myoepithelial cells of the ducts and an increase in stromal components Slow growing, lobular, and not well encapsulated Recurrence rate of 1-5% with appropriate excision (parotidectomy) Recurrence possibly secondary to capsular disruption during surgery Malignant degeneration occurring in 2-10% of adenomas observed for long periods, with carcinoma ex-pleomorphic adenoma occurring most frequently as adenocarcinoma
Benign pleomorphic adenoma or benign mixed tumour
1773
Second most common benign parotid tumor (5%) Most common bilateral benign neoplasm of the parotid Marked male as compared to female predominance Occurs later in life (sixth and seventh decades) Presents as a lymphocytic infiltrate and cystic epithelial proliferation May represent heterotopic salivary gland epithelial tissue trapped within intraparotid lymph nodes Incidence of bilaterality and multicentricity of 10% Malignant transformation rare (almost unheard of)
Warthin tumor (papillary cystadenoma lymphoma or adenolymphoma)
1774
Account for less than 5% of tumours Parotid Slow growing Consist of only one morphological cell type (hence term mono) Include; basal cell adenoma, canalicular adenoma, oncocytoma, myoepitheliomas
Monomorphic adenoma
1775
Should be considered in the differential of a parotid mass in a child Accounts for 90% of parotid tumours in children less than 1 year of age Hypervascular on imaging Spontaneous regression may occur and malignant transformation is almost unheard of
Haemangioma
1776
30% of all parotid malignancies Usually low potential for local invasiveness and metastasis (depends mainly on grade)
Mucoepidermoid carcinoma
1777
Parotid Unpredictable growth pattern Tendency for perineural spread Nerve growth may display skip lesions resulting in incomplete excision Distant metastasis more common (visceral rather than nodal spread) 5 year survival 35%
Adenoid-cystic carcinoma
1778
Often a malignancy occurring in a previously benign parotid lesion
Mixed parotid tumour
1779
Parotid tumour Intermediate grade malignancy May show perineural invasion Low potential for distant metastasis 5 year survival 80%
Acinic cell carcinoma
1780
Parotid Develops from secretory portion of gland Risk of regional nodal and distant metastasis 5 year survival depends upon stage at presentation, may be up to 75% with small lesions with no nodal involvement
Adenocarcinoma
1781
Large rubbery lesion, may occur in association with Warthins tumours Diagnosis should be based on regional nodal biopsy rather than parotid resection Treatment is with chemotherapy (and radiotherapy)
Lymphoma
1782
Diagnosing parotid masses
Plain x-rays may be used to exclude calculi Sialography may be used to delineate ductal anatomy FNAC is used in most cases Superficial parotidectomy may be either diagnostic or therapeutic depending upon the nature of the lesion Where malignancy is suspected the primary approach should be definitive resection rather than excisional biopsy CT/ MRI may be used in cases of malignancy for staging primary disease
1783
Autoimmune disorder characterised by parotid enlargement, xerostomia and keratoconjunctivitis sicca 90% of cases occur in females Second most common connective tissue disorder Bilateral, non tender enlargement of the gland is usual Histologically, the usual findings are of a lymphocytic infiltrate in acinar units and epimyoepithelial islands surrounded by lymphoid stroma Treatment is supportive There is an increased risk of subsequent lymphoma
Sjogren's
1784
Parotid involvement occurs in 6% of patients Bilateral in most cases Gland is not tender Xerostomia may occur Management of isolated parotid disease is usually conservative
Sarcoidosis
1785
Lymphoepithelial cysts occur almost exclusively in the parotid Typically presents as bilateral, multicystic, symmetrical swelling Risk of malignant transformation is low and management usually conservative
Parotid manifestation of HIV infection
1786
A 24-year-old man who is suffering from sinusitis asks about using Sudafed (pseudoephedrine). Which one of the following medications would make the use of Sudafed contraindicated? ## Footnote Sodium valproate Monoamine oxidase inhibitor Salbutamol Triptan Selective serotonin reuptake inhibitor
A monoamine oxidase inhibitor combined with pseudoephedrine could potentially cause a hypertensive crisis.
1787
A 7-year-old girl is brought to surgery due to a sore throat. She has a temperature of 39.2ºC and is not eating due to the pain, although she is tolerating fluids. She has had no other related symptoms such as a cough or a rash. Her heart rate is 120/min and auscultation of the chest is unremarkable. The tonsils are covered in exudate bilaterally. Examination of the ears is unremarkable. Other than supportive treatment, what is the most appropriate management? ## Footnote Erythromycin for 10 days Amoxicillin for 7 days Antibiotics are not indicated Phenoxymethylpenicillin for 10 days Aciclovir for 5 days
This girl has marked systemic upset and should be treated with antibiotics. A 7 or 10 day course of antibiotics is appropriate to ensure eradication of possible Streptococcus infection. Phenoxymethylpenicillin is the first-line antibiotic choice in the BNF
1788
You see a 3-year-old boy as a follow-up appointment. Two weeks ago he presented with left-sided otalgia associated with a purulent discharge. You prescribed amoxicillin and arranged to see him today. His mum reports that he is much better and says she has managed to keep the ear dry. On examination of the left side a perforation of the tympanic membrane is noted. What is the most appropriate action? Advise to keep ear dry and see in a further 4 weeks time Prescribe gentamicin ear drops to prevent infection + see in a further 6 weeks time Advise to keep ear dry and see in a further 12 weeks time Refer to ENT Prescribe prophylactic dose amoxicillin to prevent infection + see in a further 4 weeks time
When he presented initially with the perforation this boy was given amoxicillin which is consistent with NICE guidelines. There is no indication for continuing the antibiotics if the ear is dry. If there is still a perforation when the boy is reviewed in 4 weeks time (i.e. 6 weeks since the perforation occurred) then ENT referral should be considered.
1789
Management of perforated tympanic membrane
no treatment is needed in the majority of cases as the tympanic membrane will usually heal after 6-8 weeks. It is advisable to avoid getting water in the ear during this time it is common practice to prescribe antibiotics to perforations which occur following an episode of acute otitis media. NICE support this approach in the 2008 Respiratory tract infection guidelines myringoplasty may be performed if the tympanic membrane does not heal by itself
1790
A 44-year-old man asks for advice. He is due to go on a long bus journey but suffers from debilitating motion sickness. Which one of the following medications is most likely to prevent motion sickness? Cyclizine Chlorpromazine Metoclopramide Prochlorperazine Domperidone
Motion sickness - hyoscine \> cyclizine \> promethazine
1791
Management of motion sickness
Management the BNF recommends hyoscine (e.g. transdermal patch) as being the most effective treatment. Use is limited due to side-effects non-sedating antihistamines such as cyclizine or cinnarizine are recommended in preference to sedating preparation such as promethazine
1792
This 21-year-old woman has a history of recurrent epistaxis: ## Footnote © Image used on license from DermNet NZ What is the most likely underlying diagnosis? Idiopathic thrombocytopenic purpura Peutz-Jeghers syndrome Anorexia nervosa Combined oral contraceptive pill use Hereditary haemorrhagic telangiectasia
Osler Weber Rendu HHT
1793
What are the diagnostic criteria for HHT?
2= possible diagnosis 3 or more= definite diagnosis Epistaxis: spontaneous and recurrent nosebleeds Telangiectasis: multiple at characteristic sites: lips, oral cavity, fingers, nose Visceral lesions: e.g. GI, pulmonary AVM, hepatic AVM, spinal AVM Fhx of first degree relative with HHT
1794
The chest x-ray shows multiple pulmonary nodules representing arteriovenous malformations, the largest in the right mid-zone. The CT scan shows multiple hepatic arteriovenous malformations
1795
Which one of the following medications is most useful for helping to prevent attacks of Meniere's disease? Promethazine Prochlorperazine Betahistine Chlorphenamine Cinnarizine
Management ## Footnote ENT assessment is required to confirm the diagnosis patients should inform the DVLA. The current advice is to cease driving until satisfactory control of symptoms is achieved acute attacks: buccal or intramuscular prochlorperazine. Admission is sometimes required prevention: betahistine may be of benefit
1796
A 59-year-old man presents with recurrent attacks of vertigo and dizziness. These attacks are often precipitated by a change in head position and typically last around half a minute. Examination of the cranial nerves and ears is unremarkable. His blood pressure is 120/78 mmHg sitting and 116/76 mmHg standing. Given the likely diagnosis of benign paroxysmal positional vertigo, what is the most appropriate next step to help confirm the diagnosis? Epley manoeuvre Tilt table test Tympanometry MRI of the cerebellopontine angle Dix-Hallpike manoeuvre
This patient has classical symptoms of benign paroxysmal positional vertigo. A positive Dix-Hallpike manoeuvre is an appropriate next step and would help support the diagnosis. The change in blood pressure on standing is not significant.
1797
You review a 25-year-old man who has allergic rhinits. He has been using intranasal oxymetazoline which he bought from the local chemist for the past 10 days. What is the main side-effect of using topical decongestants for prolonged periods? Permanent loss of smell Infective sinusitis Post-nasal drip Tachyphylaxis Necrosis of the nasal septum
After using topical decongestants for prolonged periods increasing doses are needed to provide the same effect, a phenomenon known as tachyphylaxis.
1798
Facial 'fullness' and tenderness Nasal discharge, pyrexia or post-nasal drip leading to cough
Sinusitis
1799
Unilateral facial pain characterised by brief electric shock-like pains, abrupt in onset and termination May be triggered by light touch, emotion
Trigeminal neuralgia
1800
Pain typical occurs once or twice a day, each episode lasting 15 mins - 2 hours Clusters typically last 4-12 weeks Intense pain around one eye Accompanied by redness, lacrimation, lid swelling, nasal stuffiness
Cluster headache
1801
Tender around temples Raised ESR
Temporal arteritis
1802
A 60 year-old man presents with a two month history of nasal blockage on the right side, which is now beginning to disrupt his sleep. He has not noticed any bleeding but has had postnasal drip. On examination you see a polyp on the right side and an inflamed mucosa bilaterally. What is the most appropriate management? Start saline nasal douche and review in 6 weeks Start intranasal steroids and review in 6 weeks Start saline douche and intranasal steroid and review in 6 weeks Start antihistamine and intranasal steroid and review in 6 weeks Refer to ENT
This patient has a unilateral nasal polyp. Polyps due to rhinosinusitis are usually bilateral so it is important to refer this gentleman to be seen by an ENT doctor to exclude malignancy. If small bilateral nasal polyps are seen these can be treated in primary care with a saline nasal douche and intranasal steroids, but if they are causing significant obstruction patients should be referred to ENT.
1803
A 37 year old man presents to your clinic with otalgia. He was seen in the emergency department 2 days previously but was discharged with advice only. He has now had otalgia for 5 days. On examination, he has a temperature of 38.5ºC, and he has a red bulging ear drum on the right. How should you manage this gentleman? Advise on regular paracetamol and return if no better Start erythromycin Start penicillin V Start amoxicillin Start co-amoxiclav
This is a case of otitis media. Although 50% of these cases are viral, and 60% improve without antibiotics, guidelines would advocate treatment after a delay of 2-3 days if there is no improvement in symptoms. Especially in this case, where the gentleman has a temperature and therefore evidence of systemic involvement. Therefore, advising regular paracetamol is not correct in this case. Erythromycin is a useful alternative to patients who are penicillin allergic, and especially as a syrup in children (as it costs less that some alternatives!) but would not be first line in someone who can take penicillin. Penicillin V is the first line antibiotic for tonsillitis due to amoxicillin having the potential to cause a rash in cases of glandular fever. However, it is not generally used in otitis media. Amoxicillin is the correct first line medication for treating otitis media at 500mg TDS for 7 days. Co-amoxiclav is used as a second line agent if amoxicillin doesn't work, but wouldn't be used first line according to current guidelines.
1804
A 23-year-old woman presents one week after being prescribed a combined antibiotic and steroid spray for otitis externa. There has been no improvement in her symptoms and the erythema seems to have extended to the ear itself. What is the most appropriate treatment? ## Footnote Topical clotrimazole Oral flucloxacillin Topical ciprofloxacin Oral fluconazole Oral ciprofloxacin
The spreading erythema is an indication for oral antibiotics. Flucloxacillin is first-line.
1805
A 25 year-old man presents with a history of sudden hearing loss on the right side. He had no preceding coryzal illness, fevers, headache or ear pain. On examination his ear canal and tympanic membrane appear normal. Weber testing localises to the left side. What is the appropriate management? ## Footnote Refer routinely to ENT Watch and wait Refer urgently to ENT and start high dose oral steroids Start oral aciclovir and high dose steroids Start decongestant nasal spray and intranasal steroids
This man has sudden sensorineural hearing loss, which in the vast majority of cases is idiopathic. There is some evidence that high dose steroids (60mg/day) for seven days improves prognosis, so all patients should start treatment as soon as possible. ENT assessment should be arranged as soon as possible to allow pure tone audiometry testing and to arrange an MRI to exclude an acoustic neuroma. Intra-tympanic steroids can also be given if there is no response to oral steroids. Aciclovir is not routinely recommended as there is no evidence of benefit.
1806
A.Peripheral arterial disease B.Prolapsed disc C.Facet joint pain D.Perforated duodenal ulcer E.Leaking abdominal aortic aneurysm F.Pyelonephritis G.Ankylosing spondylitis H.Rheumatoid arthritis I.Crush fracture J.Spinal stenosis A 34-year-old man reports the sudden onset of back pain after bending over to tie his shoe laces. There is tenderness over the lumbar spine on examination and leaning back worsens the pain. Neurological examination and straight leg raising is normal
Although patients often give a history of bending prior to disc prolapse the normal straight leg raising makes this diagnosis less likely.
1807
May be acute or chronic Pain worse in the morning and on standing On examination there may be pain over the facets. The pain is typically worse on extension of the back
Facet joint
1808
Usually gradual onset Unilateral or bilateral leg pain (with or without back pain), numbness, and weakness which is worse on walking. Resolves when sits down. Pain may be described as 'aching', 'crawling'. Relieved by sitting down, leaning forwards and crouching down Clinical examination is often normal Requires MRI to confirm diagnosis
Spinal stenosis
1809
What are the Ottawa ankle criteria
Ankle XR only reqired if there is any pain in malleolar zone + 1 of: Bony tenderness at lateral malleolar zone Bony tenderness at the medial malleolar zone Inability to walk four weight bearing steps immediately after the injury and in the ED
1810
A 7-year-old boy is taken to the Emergency Department after falling during football. He complains of pain in his left wrist. The x-ray is shown below: © Image used on license from Radiopaedia What which one of the following best describes this injury? Greenstick fracture Buckle fracture Salter-Harris type 1 fracture Salter-Harris type 2 fracture Salter-Harris type 3 fracture
A typical buckle fracture is shown in this radiograph. This is a common fracture pattern in children due to the pliable nature of the bone. Buckle, or torus, fractures are incomplete fractures of the shaft of a long bone that is characterised by bulging of the cortex. They typically occur in children aged 5-10 years. As they are typically self-limiting they do not usually require operative intervention and can sometimes be managed with splinting and immobilisation rather than a cast.
1811
Softening of the cartilage of the patella Common in teenage girls Characteristically anterior knee pain on walking up and down stairs and rising from prolonged sitting Usually responds to physiotherapy
Chondromalacia patellae
1812
Seen in sporty teenagers Pain, tenderness and swelling over the tibial tubercle
Osgood-Schlatter disease | (tibial apophysitis)
1813
Pain after exercise Intermittent swelling and locking
Osteochondritis dissecans
1814
Medial knee pain due to lateral subluxation of the patella Knee may give way
Patellar subluxation
1815
More common in athletic teenage boys Chronic anterior knee pain that worsens after running Tender below the patella on examination
Patellar tendonitis
1816
A 10-year-old girl is brought to the Emergency Department after falling from a tree swing. She is complaining of pain in the left forearm. An x-ray is requested: ## Footnote © Image used on license from Radiopaedia What type of fracture is seen? Buckle fracture Greenstick fracture Salter-Harris type I Salter-Harris type II Salter-Harris type IV
The radiograph shows a fracture involving the palmar surface of the distal radius, with minimal dorsal angulation and no disruption of the dorsal cortex. The growth plate appears normal.
1817
Both sides of cortex are breached
Complete fracture
1818
Oblique tibial fracture in infants
Toddlers fracture
1819
Stress on bone resulting in deformity without cortical disruption
Plastic deformity
1820
Unilateral cortical breach only
Greenstick fracture
1821
Incomplete cortical disruption resulting in periosteal haematoma only
Buckle fracture
1822
Defective osteoid formation due to congenital inability to produce adequate intercellular substances like osteoid, collagen and dentine. Failure of maturation of collagen in all the connective tissues. Radiology may show translucent bones, multiple fractures, particularly of the long bones, wormian bones (irregular patches of ossification) and a trefoil pelvis.
Osteogenesis imperfecta
1823
Type 1 Osteogenesis imperfecta
Collagen is normal quality but insufficient quantity
1824
Type II OI
Poor collagen quantity and quality
1825
Type III OI
Collagen poorly formed, normal quantity
1826
Type IV OI
Sufficient collagen quantity but poor quality
1827
Bones become harder and more dense. Autosomal recessive condition. It is commonest in young adults. Radiology reveals a lack of differentiation between the cortex and the medulla described as marble bone.
Osteopetrosis
1828
A 65-year-old man presents with bilateral leg pain that is brought on by walking. His past medical history includes peptic ulcer disease and osteoarthritis. He can typically walk for around 5 minutes before it develops. The pain subsides when he sits down. He has also noticed that leaning forwards or crouching improves the pain. Musculoskeletal and vascular examination of his lower limbs is unremarkable. What is the most likely diagnosis? Inflammatory arachnoiditis Peripheral arterial disease Raised intracranial pressure Spinal stenosis Lumbar vertebral crush fracture
This is a classic presentation of spinal stenosis. Whilst peripheral arterial disease is an obvious differential the characteristic relieving factors of the pain and normal vascular examination point away from this diagnosis.
1829
What are the red flags for LBP?
Age \<20 or \>50 Hx of previous malignancy Night pain History of trauma Systemicallly unwell e.g. weight loss fever Altered neurology Incontinence or constipation
1830
Muscles innervated by median nerve LOAF
Lumbricals (third and fourth) Opponens pollicis Abductor pollicis brevis Flexor pollicis brevis
1831
He is a know intravenous drug user who has been commenced on a methadone rehabilitation programme around 2 weeks previously. He has no fixed abode and spends his night between various hostels. He has no significant past medical history. Although has previous admissions following various injuries such as stabbings. His observations are: heart rate 99/min, respiratory rate 16/min, blood pressure 98/75 mmHg, temperature 37.7º, Sats 99% on air. On examination he appears to be in pain and is lying flat on his back with his knees flexed. He is very tender over his back at L1 and L2 levels. He actively resists passive movement from his position of comfort and is unable to weight bear due to pain. Blood tests show raised inflammatory markers, lumbar spine and pelvic x-ray show no abnormality. He is requesting analgesia for his pain. What is the most likely cause of this mans symptoms? Atypical femoral neck fracture Discitis Malingering Vertebral osteomyelitits Psoas abscess
Psoas abscess is a collection within the psoas muscle. It is commonly missed or diagnosed late due to its numerous differential diagnoses and a high index of suspicion is required in those with risk factors. The psoas muscle extends from T12 - L5 caudally, inserting on the lesser trochanter of the femur. It can be of primary origin or a result of spread from local sources such as pyelonephritis or inflammatory bowel disease. Left untreated it can lead to septicaemia and multi organ failure. The most common causative organism is staphylococcus or streptococcus and risk factors for developing a primary abscess are related to causes of immunosupression such as HIV, cancer and diabetes. Being an intravenous drug user, previous surgery and tuberculosis also predispose to the condition. Pain is usually non specific initially but increases over several days. It is worth suspecting if there is no history of trauma or injury. Fever may be present but not always. Psoas irritation is evidenced when the position of comfort is the patient lying on their back with slightly flexed knees. Inability to weight bear or pain when moving the hip is usually evident. Investigations should include bloods to evidence infection and a complete septic screen if systemic inflammatory response syndrome criteria are met. Plain radiographs are not useful for identifying an abscess although are useful for ruling out differentials. CT abdomen may identify the abscess but MRI is the gold standard. Management is with antibiotic therapy +/- drainage. Alongside managing any predisposing risk factors if appropriate.
1832
What is the diagnostic intracompartmental pressure in compartment syndrome
\>20mmHg is abnormal \>40mmHg is diagnostic
1833
Treatment of compartment syndrome
This is essentially prompt and extensive fasciotomies In the lower limb the deep muscles may be inadequately decompressed by the inexperienced operator when smaller incisions are performed Myoglobinuria may occur following fasciotomy and result in renal failure and for this reason these patients require aggressive IV fluids Where muscle groups are frankly necrotic at fasciotomy they should be debrided and amputation may have to be considered Death of muscle groups may occur within 4-6 hours
1834
Associations of trigger finger
More common in women than men RA DM
1835
More common in thumb, middle or ring finger Initially stiffness and snapping when extending a flexed digit Nodule may be felt at base of affected finger
Tirgger finger
1836
Mx of trigger finger
Steroid injeciton is successful in the majority Surgery may be reserved for patients who have not responded to steroid injections
1837
You see an 81 year old lady with a history of diabetes, osteoarthritis and hypertension. She twisted her leg whilst getting out of a car and developed increasing pain weight bearing which has eased with simple analgesia. She also tells you she has a lump under her knee. On examination she has a 4cm non-tender lump just below the popliteal fossa which becomes tense on extending the leg. She has full power throughout. What is the most likely diagnosis? ## Footnote Deep vein thrombosis Popliteal artery aneurysm Sprain Baker's cyst Ruptured head of gastrocnemius
This describes the typical patient with a Baker's cyst. They are more likely to develop in patients with arthritis or gout and following a minor trauma to the knee. Foucher's sign describes the increase in tension of the Baker's cyst on extension of the knee. A DVT (deep vein thrombosis) needs to be considered because it can mimic a Baker's cyst. A DVT can also co-exist with a Baker's cyst and a low threshold for ultrasound should be considered.
1838
Knee pain. Patient is typically \> 50 years, often overweight Pain may be severe Intermittent swelling, crepitus and limitation of movement may occur
Osteoarthritis of the knee
1839
Knee pain associated with kneeling
Infrapatellar bursitis: Clergyman's knee
1840
Knee pain associated with more upright kneeling
Prepatellar bursitis: Housemaid's knee
1841
Knee pain May be caused by twisting of the knee, popping noise may have been noted Rapid onset knee effusion Positive draw test
ACL
1842
Knee pain May have been caused by anterior force applied to proximal tibia e.g. knee hitting dashboard during car accident
PCL
1843
Knee pain Tenderness over affected ligament Knee effusion
?Collateral ligament injury
1844
Knee pain May have been caused by twisting of the knee Locking and giving way are common feature Tender joint line
Meniscal lesion
1845
What is significant about anatomical vs surgical neck fractures of the proximal humerus
Anatomical neck fractures are rare, those that are displaced by \>1cm carry a risk of avascular necrosis to the humeral head
1846
What are the types of shoulder dislocation?
Glenohumeral dislocation Acromioclavicular dislocation: clavicle loses all attachment with scapula Sternoclavicular dislocation (uncommon)
1847
What are the types of glenohumeral dislocation?
Anterior Inferior Posterior Superior
1848
External rotation and abduction 35-40% recurrent Associated with greater tuberosity fracture, Bankart lesion, Hill-Sachs defect
Anterior dislocation
1849
What is Trough line sign
The trough line sign is a sign of posterior shoulder dislocation on AP films. In posterior dislocation, the anterior aspect of the humeral head becomes impacted against the posterior glenoid rim. With sufficient force, this causes a compression fracture on the anterior aspect of the humeral head. This compression fracture is analogous to the Hill-Sachs compression fracture seen with anterior shoulder dislocation of the glenohumeral joint. Frontal radiographs reveal two nearly parallel lines in the superomedial aspect of the humeral head.
1850
Trough sign
1851
Luxatio erecta
An inferior shoulder dislocation is the least common form of shoulder dislocation. The condition is also called luxatio erecta because the arm appears to be permanently held upward or behind the head, in fixed abduction.
1852
Luxatio erecta (inferior shoulder disloccation)
1853
A 75-year-old female presents with weakness of her left hand. On examination wasting of the hypothenar eminence is seen and there is weakness of finger abduction. Thumb adduction is also weak. Where is the lesion most likely to be? Common peroneal nerve Median nerve Radial nerve Anterior interosseous nerve Ulnar nerve
Ulnar nerve
1854
pain and tenderness localised to the lateral epicondyle pain worse on resisted wrist extension with the elbow extended or supination of the forearm with the elbow extended episodes typically last between 6 months and 2 years. Patients tend to have acute pain for 6-12 weeks
Lateral epicondylitis (tennis elbow)
1855
Features ## Footnote pain and tenderness localised to the medial epicondyle pain is aggravated by wrist flexion and pronation symptoms may be accompanied by numbness / tingling in the 4th and 5th finger due to ulnar nerve involvement
Medial epicondylitis (golfer's elbow)
1856
Most commonly due to compression of the posterior interosseous branch of the radial nerve. It is thought to be a result of overuse. Features ## Footnote symptoms are similar to lateral epicondylitis making it difficult to diagnose however, the pain tends to be around 4-5 cm distal to the lateral epicondyle symptoms may be worsened by extending the elbow and pronating the forearm
Radial tunnel syndrome
1857
Due to the compression of the ulnar nerve. Features ## Footnote initially intermittent tingling in the 4th and 5th finger may be worse when the elbow is resting on a firm surface or flexed for extended periods later numbness in the 4th and 5th finger with associated weakness
Cubital tunnel syndrome
1858
Swelling over the posterior aspect of the elbow. There may be associated pain, warmth and erythema. It typically affects middle-aged male patients.
Olecranon bursitis
1859
Def: De Quervain's tenosynovitis
De Quervain's tenosynovitis is a common condition in which the sheath containing the extensor pollicis brevis and abductor pollicis longus tendons is inflamed. It typically affects females aged 30 - 50 years old
1860
Features pain on the radial side of the wrist tenderness over the radial styloid process abduction of the thumb against resistance is painful Finkelstein's test: with the thumb is flexed across the palm of the hand, pain is reproduced by movement of the wrist into flexion and ulnar deviation
De Quervain's tenosynovitis
1861
Mx of tenosynovitis
Management analgesia steroid injection immobilisation with a thumb splint (spica) may be effective surgical treatment is sometimes required
1862
A 30-year-old woman has left knee ligament reconstruction surgery for a torn lateral collateral ligament. During recovery, she notices persistent weakness in her left leg and foot. On examination, she has weakness of dorsiflexion and eversion of the left foot (MRC power grade 2/5). There is a small patch of sensory loss over the first and second toes. What is the most likely diagnosis? ## Footnote L5 radiculopathy Tibial nerve palsy Compartment syndrome Right-sided stroke Common peroneal nerve palsy
Loss of dorsiflexion and eversion suggests a common peroneal nerve lesion as opposed to an L5 radiculopathy (in L5 radiculopathy, eversion tends to be spared while sensory involvement tends to be greater). This is before the recent risk factor of knee surgery is considered, making common peroneal nerve palsy the more obvious answer. NB common peroneal palsy spares inversion whilst l5 radiculopathy will have weakness of ankle inversion
1863
Foot drop weakness of foot dorsiflexion weakness of foot eversion weakness of extensor hallucis longus sensory loss over the dorsum of the foot and the lower lateral part of the leg wasting of the anterior tibial and peroneal muscles
Common peroneal nerve palsy
1864
A 57-year-old woman presents with a three month history of right-sided hip pain. This seems to have come on spontaneously without any obvious precipitating event. The pain is described as being worse on the 'outside' of the hip and is particularly bad at night when she lies on the right hand side. On examination there is a full range of movement in the hip including internal and external rotation. Deep palpation of the lateral aspect of the right hip joint recreates the pain. An x-ray of the right hip is reported as follows: Right hip: Minor narrowing of the joint space otherwise normal appearance What is the most likely diagnosis? Fibromyalgia Lumbar nerve root compression Osteoarthritis Greater trochanteric pain syndrome Meralgia paraesthetica
Greater trochanteric pain syndrome is now the preferred term for trochanteric bursitis. Whilst the x-ray shows joint space narrowing this is not an uncommon finding. Osteoarthritis would also be less likely given the palpable nature of the pain and relatively short duration of symptoms.
1865
Hip pain Pain exacerbated by exercise and relieved by rest Reduction in internal rotation is often the first sign Age, obesity and previous joint problems are risk factors
OA
1866
Hip pain Pain in the morning Systemic features Raised inflammatory markers
Inflammatory arthritis
1867
Hip pain Femoral nerve compression may cause referred pain in the hip Femoral nerve stretch test may be positive - lie the patient prone. Extend the hip joint with a straight leg then bend the knee. This stretches the femoral nerve and will cause pain if it is trapped
Referred lumbar spine pain
1868
Due to repeated movement of the fibroelastic iliotibial band Pain and tenderness over the lateral side of thigh Most common in women aged 50-70 years
Greater trochanteric pain syndrome (Trochanteric bursitis)
1869
Caused by compression of lateral cutaneous nerve of thigh Typically burning sensation over antero-lateral aspect of thigh
Meralgia paraesthetica
1870
Symptoms may be of gradual or sudden onset May follow high dose steroid therapy or previous hip fracture of dislocation
Avascular necrosis
1871
Common in pregnancy Ligament laxity increases in response to hormonal changes of pregnancy Pain over the pubic symphysis with radiation to the groins and the medial aspects of the thighs. A waddling gait may be seen
Pubic symphysis dysfunction
1872
An uncommon condition sometimes seen in the third trimester of pregnancy Groin pain associated with a limited range of movement in the hip Patients may be unable to weight bear ESR may be elevated
Transient idiopathic osteoporosis
1873
A 48-year-old woman presents with progressively worsening pain in the right shoulder over the past few weeks. She is generally fit and well but smokes 20 cigarettes/day. On examination there is diffuse mild tenderness over the lateral aspect of the right shoulder. The pain is recreated when abducting the shoulder to around 70-80 degrees. A shoulder x-ray is requested: ## Footnote © Image used on license from Radiopaedia What is the most likely diagnosis? Pancoast tumour Supraspinatus tendonitis Adhesive capsulitis Humeral head fracture Avascular necrosis
The x-ray shows calcification of the supraspinatus tendon consistent with prolonged inflammation. On examination the patient exhibits the classical 'painful arc' associated with this condition.
1874
What are the associations of talipes equinovarus?
Most commonly idiopathic. Associations include: ## Footnote spina bifida cerebral palsy Edward's syndrome (trisomy 18) oligohydramnios arthrogryposis
1875
A 22-year-old male presents to the emergency room with pain in the left knee following a twisting injury during a rugby match. He states that it has gradually swollen over the past 24 hours, and he is unable to fully extend it. On examination you note tenderness over the medial joint line, a joint effusion, and the joint is held in a flexed position. There is no laxity on valgus stress test. What is the most likely diagnosis? Medial meniscus tear Lateral meniscus tear Anterior cruciate ligament (ACL) tear Posterior cruciate ligament (PCL) tear Medial collateral ligament (MCL) tear
Gradual swelling of the knee is suggestive of effusion which often occurs due to meniscal injury. Tenderness over the medial joint line suggests a medial meniscus tear. An ACL or PCL tear would more commonly present with rapid joint swelling due to bleeding within the joint capsule (haemarthrosis). Isolated MCL injuries rarely cause a large effusion. In addition, the lack of laxity on the valgus stress test makes an MCL injury less likely.
1876
Sport injury Mechanism: high twisting force applied to a bent knee Typically presents with: loud crack, pain and RAPID joint swelling (haemoarthrosis) Poor healing Management: intense physiotherapy or surgery
Ruptured ACL
1877
Mechanism: hyperextension injuries Tibia lies back on the femur Paradoxical anterior draw test
Ruptured posterior cruciate ligament
1878
Mechanism: leg forced into valgus via force outside the leg Knee unstable when put into valgus position
Rupture of medial collateral ligament
1879
Rotational sporting injuries Delayed knee swelling Joint locking (Patient may develop skills to "unlock" the knee Recurrent episodes of pain and effusions are common, often following minor trauma
Menisceal tear
1880
Teenage girls, following an injury to knee e.g. Dislocation patella Typical history of pain on going downstairs or at rest Tenderness, quadriceps wasting
Chondromalacia patellae
1881
Most commonly occurs as a traumatic primary event, either through direct trauma or through severe contraction of quadriceps with knee stretched in valgus and external rotation Genu valgum, tibial torsion and high riding patella are risk factors Skyline x-ray views of patella are required, although displaced patella may be clinically obvious An osteochondral fracture is present in 5% The condition has a 20% recurrence rate
Dislocation of the patella
1882
2 types: i. Direct blow to patella causing undisplaced fragments ii. Avulsion fracture
Fractured patella
1883
Occur in the elderly (or following significant trauma in young) Mechanism: knee forced into valgus or varus, but the knee fractures before the ligaments rupture Varus injury affects medial plateau and if valgus injury, lateral plateau depressed fracture occurs Classified using the Schatzker system (see below)
Tibial plateau fracture
1884
What can be used to classify tibial plateau fractures?
Schatzker system
1885
Describe Schatzker Classification
Type 1: Vertical split of lateral condyle Fracture through dense bone, usually in the young, may be undisplaced or condylar fragment may be pushed in feriorly Type 2: Vertical split of the lateral condyle combined with an adjacent load bearing part of the condyle The wedge fragment (which may be of variable size), is displaced laterally; the joint is widened. Untreated, a valgus deformity may develop Type 3: Depression of the articular surface with intact condylar rim The split does not extend to the edge of the plateau. Depressed fragments may be firmly embedded in subchondral bone, the joint is stable Type 4 Fragment of the medial tibial condyle Two injuries are seen in this category; (1) a depressed fracture of osteoporotic bone in the elderly. (2) a high energy fracture resulting in a condylar split that runs from the intercondylar eminence to the medial cortex. Associated ligamentous injury may be severe Type 5 Fracture of both condyles Both condyles fractured but the column of the metaphysis remains in continuity with the tibial shaft Type 6 Combined condylar and subcondylar fractures High energy fracture with marked comminution
1886
Which option is not recommended during the management of compartment syndrome? Anticoagulation Keep limb level with the body Intravenous fluids Pain control Fasciotomy
Anticoagulation will worsen compartment syndrome.
1887
Associations of Dupuytren's
Dupuytren's contracture has a prevalence of about 5%. It is more common in older male patients and around 60-70% have a positive family history Specific causes include: manual labour phenytoin treatment alcoholic liver disease trauma to the hand
1888
A 16-year-old male presents with lower back pain of 5 months duration, worse at night, with morning stiffness. He finds the pain improved with exercise. There is no history of trauma. He is given a clinical diagnosis of ankylosing spondylitis. Which of the following findings on examination would be most associated with this diagnosis? Schober's test 4.0cm Development of scoliosis Cervical kyphosis Mitral valve incompetence Osteomyelitis
Schober's test \<5cm is suggestive of ankylosing spondylitis. This is an indication of reduced lumbar flexion. Schober's test is performed by identifying L5, and then marking 10cm above and 5cm below this point whilst the patient is stood upright. The patient is then asked to bend forwards to touch their toes whilst keeping their knees straight. If the distance between the points does not increase by 5cm (or the distance between the points originally marked is not more than 20cm in total), then it can be said that there is reduced flexion of the lumbar spine, which is a sign of ankylosing spondylitis. Thoracic kyphosis is an associated spinal deformity, alongside neck hyperextension. This may be referred to by some as the 'question mark' appearance. Aortic valve incompetence is associated with \<3% of cases.
1889
As of ank spond
Apical fibrosis Anterior uveitis Aortic regurgitation Achilles tendonitis AV node block Amyloidosis and cauda equina syndrome peripheral arthritis (25%, more common if female)
1890
Specific management of femoral and tibial fractures
Resus and Mx life threatening injuries first X-match Assess neurovascular status: especially distal pulses If open Abx and ATT Take to theatre urgently for debridement, washout and stabilisation Fixation methods: Intramedullary nail External fixation Plates and screws MUA with fixed traction for 3-4 months
1891
X-match how many units in tibial #?
2 units
1892
X-match how many units in #femur
4 units
1893
What are the specific complications of femoral and tibial fractures?
Hypovolaemic shock Neurovascular: SFA: swelling and check pulses Sciatic nerve Compartment syndrome Respiratory complications: Fat embolism ARDS Pneumonia
1894
Features of ankle ligament strain
Typically twisting inversion injury Strains anterior talofibular part of LCL Medial deltoid ligament strains are rare May be associated with malleolar avulsion fractures
1895
What is Weber classification of ankle injuries?
Relation of fibula # to joint line
1896
Outline Weber classificaiton of fibula #
A: below joint line B: at joint line C: above joint line
1897
Significance of Weber classification
Weber's B and C represent possible injury to the syndesmotic ligaments between tib and fib -\> instability
1898
What is this classificaiton system?
Weber Classification 􀁸 Relation of fibula # to joint line 􀁸 A: below joint line 􀁸 B: at joint line 􀁸 C: above joint line 􀁸 Weber’s B and C represent possible injury to the syndesmotic ligaments between tib and fib → instability
1899
Mx of Weber A
Boot or below knee POP
1900
Mx of Non-displaced Weber B/C
Below knee POP
1901
Mx of displaced Weber B/C
Closed reduction and POP if anatomical reduction achieved ORIF if closed reduction fails
1902
Important components of knee injury history
Mechanism Swelling: immediate vs overnight Pain/tenderness: joint line vs medial/lateral margins Locking: meniscal tear Giving way: instability following lgt injury
1903
Immediate swelling following knee injury
= haemarthrosis. # or torn cruciates
1904
Overnight swelling following knee injury
= effusion Meniscus or other ligamentous injury
1905
Locking following knee injury=
Meniscal tear
1906
Pain/tenderness over joint line following knee injury
Meniscal
1907
Pain/tenderness over med/lat knee margins=
Collateral ligaments
1908
1o knee haemarthrosis
Spontaneous bleeding: Coagulopathy: warfarin, haemophilia
1909
2o Knee haemarthrosis
Trauma ACL injury: 80% Patella dislocation: 10% Meniscal injury: outer third where it is vascularised (10%) Osteophyte #
1910
What is the unhappy triad of O'Donoghue MMA
MCL Medial meniscus ACL
1911
Mx of acutely injured knee
Full examination of acutely swollen knee after injury is difficult Take XR to ensure no #s: fluid level indicates a lipohaemarthrosis and indicates either a # or torn cruciate If no #-\> RICE + later re-examination If meniscal or cruciate injury suspected-\> MRI
1912
Features of knee arthroscopy
Direct vision of inside of knee joint by arthroscope Can examine knee under anaesthesia (reduced muscle tone) Meniscal tears can be trimmed or repaired
1913
Mx of Ruptured ACL
Conservative: Rest PT to strengthen quads and hamstrings Not enough stability for many sports Surgical: Gold-standard is autograft repair Usually semintendonosus +/- gracillis (can use patella tendon) Tendon threaded through heads of tibia and femur and held using screws
1914
Pathophysiology of OA
Softening of articular cartilage-\> fraying and fissuring of smooth surface-\> underlying bone exposure Subchondral bone becomes sclerotic with cysts Proliferation and ossification of cartilage in unstressed areas-\> osteophytes Capsular fibrosis-\> stiff joints
1915
DDx for OA
Septic Crystal Trauma
1916
XR changes in OA
Loss of joint space Osteophytes Subchondral cysts Subchondral sclerosis Deformity
1917
Bloods in OA
CRP may be elevated Ca, PO4, ALP all normal
1918
Rx of OA
MDT: GP, physio, OT, dietician, orthopod Conservative: Lifestyle: reduce weight, increase exercise PT: muscle strengthening OT: walking aids, supportive footwear, home modifications Medical: Analgesia: paracetamol + topical NSAIDs e.g. voiltarel Tramadol Joint injeciton: LA and steroids Surgical: Arthroscopic washout Realignment osteotomy: small area of bone cut out, useful in younger patients with medial knee OA. High tibial valgus osteotomy redistributes weight to lateral part of joint Arthroplasty Arthrodesis Novel techniques
1919
Mechanical back pain features
Soft tissue injury-\> dysfunction of whole spine-\> muscle spasm-\> pain May have inciting event e.g. lifting Young patients with no sinister features
1920
Mx of mechanical back pain
Conservative: Max 2d bed rest Education: keep active, how to lift/stoop PT Psychoscoial issues Warmth Medical: Analgesia: paracetamol +/- NSAIDS +/- codeine Muscle relaxant: low-dose diazepam (used ST)
1921
Def: disc prolapse
Herniation of nucleeus pulposus through annulus fibrosus
1922
Which spinal nerve roots most commonly compressed in disc herniation?
L5 (L4/L5 disc) S1 (L5/S1 disc)
1923
May present as severe pain on sneezing, coughing or twisting a few days after low back strain Lumbago: low back pain Sciatica: shooting radicular pain down buttock and thigh
=?Disc prolapse
1924
Limited spinal flexion and extension Free lateral flexion Lesague's sign
?Disc herniation
1925
What is Lesague's sign
Pain on straight leg raise ?Radiculopathy
1926
Location of disc herniation and significance
Lateral herniation= radiculopathy Central herniatoin= cauda equina syndrome
1927
Weak hallux extension +/- foot drop Weak inversion (helps distinguish from peroneal nerve palsy) Reduced sensation on inner dorsum of foot
L4/L5 root compression
1928
Weak floot plantarflexion and eversion Loss of ankle jerk Calf pain Reduced sensation over sole of foot and back of calf
L5/S1-\> S1 root compression
1929
Ix in disc prolapse
MRI (emergency if cauda equina)
1930
Mx of disc herniation
Brief rest, analgesia and mobilisation effective in \>90% Conservative: Brief rest Mobilisation/PT Medical: analgesia, transforaminal steroid injection Surgical: discectomy or laminectomy may be needed in cauda equina syndrome, continuing pain or muscle weakness
1931
Features of lumbar microdiscectomy?
Commonest procedure for disc prolapse Microscopic resection of the protruding nucleus pulposus Posterior approach with patient in prone position May be performed endoscopically
1932
Def: spondylolisthesis
Displacement of one lumbar vertebra on another Usually forward Usually L5 on S1
1933
Spondylolisthesis
1934
Causes of spondylolisthesis
Congenital malformation Spondylosis osteoarthritis
1935
Onset of pain usually in adolescence or early adulthood Worse on standing +/- sciatic, hamstring tightness, abormal gait
Spondylolisthesis
1936
Dx of sponylolisthesis
Plain radiography
1937
Rx of spondylolisthesis
Corset Nerve release Spinal fusion
1938
Def: spinal stenosis
Developmental predisposition +/- facet joint OA-\> generalised narrowing of lumbar spinal canal
1939
Aching or heavy buttock and lower limb pain on walking Rapid onset May c/o paraesthesia, numbness Pain eased by leaning forward e.g. on a bike Pain on extension
Spinal claudicaiton
1940
Ix in spinal stenosis
MRI
1941
Rx of spinal stenosis
Corsets NSAIDs Epidural steroid injection Canal decompression surgery
1942
Def: lordosis
Spine of a person with lordosis curves significantly inward at lower back
1943
1944
Def: kyphosis
Abnormally rounded upper back (more than 50 deg of curvature)
1945
Def: scoliosis
Sideways curve to the spine, often S-shaped or C-shaped
1946
Def: osteochondritis
Idiopathic condition in which bony centres of children/adolescents become temporarily softened due to osteonecrosis Bone hardens in new deformed position
1947
Radiography in osteochondritis
Initially: increased denisty/sclerosis then: patchy appearance
1948
Scheuermann's disease
Self-limiting skeletal disorder of childhood. Vertebrae grow unevenly in respect to the saggital plane. (posterior angle greater than anterior angle) Uneven growth results in wedging shape of vertebrae causing kyphosis.
1949
Scheueurmann's disease Autosomal dominant Vertebral tenderness and kyphosis XR: wedge-shaped thoracic vertebra
1950
Kohler's disease
Rare bone disorder of the foot found in young children (3-5). Caused by the navicular bone temporarily losing its blood supply. Undergoes avascular necrosis. Pain in mid-tarsal region-\> limp
1951
Kohler's disease
1952
Kienbochs disease
Kienböck's disease is a disorder of the wrist. It is named for Dr. Robert Kienböck, a radiologist in Vienna, Austria who described osteomalacia of the lunate in 1910.[1] It is breakdown of the lunate bone, a carpal bone in the wrist that articulates with the radius in the forearm. Specifically, Kienböck's disease is another name for avascular necrosis[2](death and fracture of bone tissue due to interruption of blood supply) with fragmentation and collapse of the lunate. This has classically been attributed to arterial disruption, but may also occur after events that produce venous congestion with elevated interosseous pressure.
1953
Kienboch's disease Lunate bone 􀁸 Adults 􀁸 Pain over lunate, esp. on active movement 􀁸 Impaired grip
1954
Friedberg's disease
Freiberg disease, also known as a Freiberg infraction, is a form of avascular necrosis in the metatarsal. It generally develops in the second metatarsal, but can occur in any metatarsal. Physical stress causes repeated microfractures where the middle of the metatarsal meets the growth plate. These restrict circulation to the end of the metatarsal, causing the necrosis. It is an uncommon condition, occurring most often in young women, athletes, and those with abnormally long metatarsals. Approximately 80% of those diagnosed are women.[1]
1955
Friedberg's disease 2nd/3rd metatarsal heads Around puberty Forefoot pain worse with pressure
1956
Panner disease
Panner disease is an osteochondrosis of the capitellum of the elbow. It causes pain and stiffness in the affected elbow and may limit extension. On radiographs, the capitulum may appear irregular with areas of radioluceny. Treatment is symptomatic, with a good prognosis. It is primarily seen in children between five and ten years old. The disease is named after the Danish radiologist Hans Jessen Panner
1957
Panner's disease Capitulum of humerus
1958
Perthes Disease
Legg–Calvé–Perthes disease (LCPD) is a childhood hip disorder initiated by a disruption of blood flow to the ball of the femur called the femoral head. Due to the lack of blood flow, the bone dies (osteonecrosis or avascular necrosis) and stops growing. Over time, healing occurs by new blood vessels infiltrating the dead bone and removing the necrotic bone which leads to a loss of bone mass and a weakening of the femoral head.[1] The bone loss leads to some degree of collapse and deformity of the femoral head and sometimes secondary changes to the shape of the hip socket. It is also referred to as idiopathic avascular osteonecrosis of the capital femoral epiphysis of the femoral head since the cause of the interruption of the blood supply of the head of the femur in the hip joint is unknown.
1959
Legg-Calve-Perthes Disease of right hip
1960
Featurs of Osgood Schlatter's
Tibial tuberosity apophysitis + patellar tendonitis Seen in children 10-14y/o M\>F 3:1 Associated with physical activity Pain below knee especially on quad contraction
1961
Tibial tuberosity apophysitis + patellar tendonitis Seen in children 10-14y/o M\>F 3:1 Associated with physical activity Pain below knee especially on quad contraction
Osgood-Shlatter's
1962
Osgood-Shlatters
1963
Tranction tendinopathy with calcification of proximal attachment of patellar tendon 􀁸 Children 8-10yrs
Singind Larsen's disease
1964
Sinding Larsen's disease
Tranction tendinopathy with calcification of proximal attachment of patellar tendon 􀁸 Children 8-10yrs
1965
Sinding Larsen's disease Tranction tendinopathy with calcification of proximal attachment of patellar tendon 􀁸 Children 8-10yrs
1966
Sever's disease
Calcaneal apophysitis 8-13 years Pain behind heel and limp
1967
Calcaneal apophysitis 8-13 years Pain behind heel and limp
Sever's disease
1968
Features of osteochondritis dissecans
Piece of bone overlying catrilage dissects off into the joint space Commonly knee (medial femoral condyle), also elbow, hip and ankle Young adult/adolescent Pain, swelling, locking, reduced ROM
1969
Piece of bone overlying catrilage dissects off into the joint space Commonly knee (medial femoral condyle), also elbow, hip and ankle Young adult/adolescent Pain, swelling, locking, reduced ROM
Osteochondritis dissecans
1970
Loose bodies, lucent crater on XR Mx with arthroscopic removal
Osteochondritis Dissecans
1971
Causes of avascular necrosis
or dislocation SCD, thalassaemia SLE Gaucher's Drugs: steroids, NSAIDs
1972
Apophysis
Natural swelling of bone for attachment of a muscle
1973
Enthesis
Connective tissue between tendon or ligament and bone. There are two types of entheses: Fibrous entheses and fibrocartilaginous entheses.
1974
Trimalleolar fracture
A trimalleolar fracture is a fracture of the ankle that involves the lateral malleolus, the medial malleolus, and the distal posterior aspect of the tibia, which can be termed the posterior malleolus. The trauma is sometimes accompanied by ligament damage and dislocation.[1]
1975
Bimalleolar fracture
A bimalleolar fracture is a fracture of the ankle that involves the lateral malleolus and the medial malleolus. Studies have shown[1] that bimalleolar fractures are more common in women, people over 60 years of age, and patients with existing comorbidities.[1]
1976
Borders of the anatomical snuffbox
Ulnar (medial border): tendon of extensor pollicis longus Radial (lateral) border: tendons of abductor pollicis longus and extensor pollicis brevis Proximal border: styloid process of the radius Floor: carpal bones: scaphoid and trapezium Roof: skin
1977
Contents of the anatomical snuffbox
Radial artery Superficial branch of radial nerve Cephalic vein
1978
Borders of the cubital fossa
Lateral border: medial border of brachioradialis Medial border: lateral border of pronator teres Superior border: line between the epicondyles of the humerus
1979
Contents of the cubital fossa Really Need Beer To Be At My Nicest
Lateral to medial: Radial Nerve Biceps Tendon Brachial Artery Median Nerve
1980
Borders of the carpal tunnel
Formed by two layers: a deep carpal arch and a superficial flexor retinaculum Carpal arch: Concave on palmar side Formed laterally by the scaphoid and trapezium tubercles Formed medially by the hook of hamate and pisiform Flexor retinaculum: Thick connective tissue Turns the carpal arch into the carpal tunnel Originates on the lateral side and inserts on the medial side of the carpal arch
1981
Contents of the carpal tunnel
9 tendons and median nerve
1982
Tendons in the carpal tunnel
1 FPL own sheath 4 FDP + 4 FDS shared sheath
1983
Contents of carpal tunnel
Median nerve 1 FPL 4 FDP 4 FDS
1984
Borders of the axilla
4 sides and a base with an opening at the apex Apex: lateral border of first rib, superior border of scapula and posterior border of clavicle Lateral wall: intertubercular groove of the humerus Medial wall: serratus anterior and thoracic wall Anterior wall: pec major and pec minor and subclavius Posterior wall: subscap, teres major, lat dorsi
1985
What are the passageways exiting the axilla
3 routes Main route: into the upper limb, immediately inferiorly and laterally Another via the quadrangular space: gap in the posterior wall of the axilla Clavipectoral triangle: opening in the anterior wall of the axilla bounded by pectoralis major, deltoid and clavicle
1986
Contents of the axilla
Axillary artery Axillary vein Brachial plexus Biceps brachii and coarcobrachialis Axillary lymph nodes
1987
What are the four muscles in the pectoral region?
Pec major, minor, serratus anterior, subclavius
1988
Function of pec major?
Adducts and medially rotates the upper limb Draws scapula anteroinferiorly
1989
Innervation of pec major
Lateral and medial pectoral nerves
1990
Action of pec minor
Stabilises the scapula by drawing it anteroinferiorly against the thoracic wall
1991
Innervation of pec minor
Medial pectoral nerve
1992
Action of serratus anterior
Rotates the scapula allowing the arm to be raised over 90 Holds scapula against the ribcage
1993
Innervation of serratus anterior
LTN
1994
Actions of subclavius
Anchors and depresses the clavicle
1995
Innervation of subclavius
Nerve to subclavius
1996
What is the division of muscles of the shoulder?
Extrinsic: originate from the torso and attach to bones of the shoulder Intrinsic: originate from scapula or clavicle and attach to the humerus
1997
What are the intrinsic muscles of the shoulder?
Deltoid, teres major Rotator cuff muscles
1998
Deltoid actions
Anterior fibres flex arm at the shoulder Posterior fibres extend arm at the shoulder Middle fibres are the major abductor of the arm, taking over from supraspinatus which abducts the first 15 degrees
1999
Innervation of Deltoid
Axillary nerve
2000
Action of Teres major
Adducts at the shoulder and internally rotates arm
2001
Innervation of teres major
Lower subscapular nerve
2002
What muscle is innervated by the thoracodorsal nerve?
Lat dorsi
2003
What muscles innervated by the dorsal scapular nerve?
Rhomboid Levator scapulae
2004
How are the extrinsic muscles of the shoulder organised?
Into a superficial and deep layer
2005
What are the superifical extrinsic muscles of the shoulder?
Trapezius Lat dorsi
2006
Action of trapezius
Elevate scapula and rotate it during abduction of the arm. Middle fibres retract scapula Lower fibres pull the scapula inferiorly
2007
Innervation of trapezius
Accessory nerve
2008
Action of lat dorsi
Extends, adducts and medially rotates the upper limb
2009
What are the deep muscles of the shoulder?
Levator scapulae Rhomboids
2010
What muscles are in the anterior compartment of the upper arm?
Biceps brachii Brachialis Coarcobrachialis
2011
What muscles are in the posterior compartment of the upper arm?
triceps
2012
Action of biceps brachii
Supination of forearm Flexes arm at elbow and at the shoulder
2013
Innervation of biceps brachii
Musculocutaneous nerve
2014
What spinal cord segment is tested by the biceps reflex?
C6
2015
Action of coracobrachialis
Flexion of the arm at the shoulder and weak adduciton
2016
Innervation of coracobrachialis
Musculocutaneous nerve
2017
Action of brachialis
Flexion at the elbow
2018
Innervation of brachialis
Musculocutanous nerve
2019
2020
Popeye sign
Rupture of biceps tendon
2021
Function of the triceps brachii
Extension of the arm at the elbow
2022
Innervation of triceps brachii
Radial nerve
2023
Triceps tendon tests which spinal segment?
C7
2024
How are the muscles in the anterior compartment of the forearm arranged?
Superficial Intermediate Deep
2025
General action of muscles in the anterior compartment of forearm?
Flexion at wrist and fingers, pronation
2026
What are the muscles in the superifical compartment of the forearm?
Flexor carpi ulnaris Palmaris Longus Flexor carpi radialis Pronator teres
2027
Action of FCU
Flexion and adduciton at wrist
2028
Innervation of FCU
Ulnar nerve
2029
Action of palmaris longus
Flexion at wrist NB this muscle is absent in 15% of the population
2030
Innervation of PL
Median nerve
2031
Action of FCR
Flexion and adduction at the wrist
2032
Innervation of FCR
Median nerve
2033
Action of pronator teres
Pronation of the forearm
2034
Innervation of pronator teres
Median nerve
2035
2036
Muscles in the intermediate compartment of the forearm
Flexor digitorum superficialis
2037
Action of flexor digitorum superficialis
Flexes the metacarpophalangeal joints and PIP at the 4 fingers and flexes the wrist
2038
Muscles in the deep compartment of the anterior forearm
FDP FPL Pronator quadratus
2039
Action of FDL
Flex the DIP of the fingers (only)
2040
Innervation of FDL
Medial half is innervated by the ulnar nerve Lateral half innervated by median nerve
2041
Action of FPL
Flexes the interphalangeal joint and MCP of the thumb
2042
Innervation of FPL
Median nerve (anterior interosseus branch)
2043
Action of pronator quadratus
Pronates the forearm
2044
Innervation of pronator quadratus
Median nerve (ant interosseus)
2045
How are the muscles in the posterior compartment of the forearm arranged?
Deep and superficial
2046
What are the superficial muscles of the posterior forearm
Extensor carpi radialis brevis and longus, extensor digitorum, extensor carpi ulnaris, extensor digitis minimi, brachioradialis, anconeus
2047
Action of brachioradialis
Flexes forearm
2048
Innervation of muscles in posterior compartment of forearm
Radial nerve
2049
What are the deep muscles of the posterior compartment of the forearm?
Supinator APL EPB EPL Extensor indices
2050
Action of supinator
Supinates the forearm
2051
How can muscles of the hand be classified?
The extrinsic muscles are located in the anterior and posterior compartments of the forearm. They control crude movements and produce a forceful grip. The intrinsic muscles of the hand are located within the hand itself. They are responsible for the fine motor functions of the hand.
2052
What is the innervation of the thenar muscles?
Median nerve
2053
What are the thenar muscles?
Opponens polllicis Abductor Pollicis brevis Flexor pollicis brevis
2054
Innervation of the hypothenar muscles?
Ulnar nerve
2055
What are the hypothenar muscles?
Opponens digiti minimi Abductor digiti minimi Flexor digiti minimi brevis
2056
Action of the lumbricals
Flex at the MCP joint and extend at the IP joints
2057
Innervation of the lumbricals
Medial two: ulnar nerve Lateral two: median nerve
2058
Action of dorsal interossei?
Abduct the fingers at the MCP
2059
Innervation of the interossei?
Ulnar nerve
2060
Action of the palmar interossei
Adducts the fingers at the MCP
2061
What are the two muscles not found in the hypothenar or thenar compartments and are not lumbricals or interossei?
Palmaris brevis Adductor pollicis Both innnervated by ulnar nerve
2062
Action of palmaris brevis
Wrinkles the skin of the hypothenar eminence and deepens the curvature of the hand
2063
Actions of adductor pollicis
Adductor of the thumb
2064
Causes of a limping child
DDH Transient synovitis Septic arthritis Perthes SUFE JIA/Still's Disease
2065
Def: DDH
Congenital hip deformity in which the femoral head is or can be completely/partially displaced
2066
Predisposing factors to DDH
Fhx Breech presentation Oligohydramnios
2067
Screening Asymmetric skin folds Limp/abnormal gait
DDH
2068
Ix in DDH
USS
2069
Mx of DDH
Maintain abduction Double nappies Pavlik harness Plaster hip spica Open reduction: derotation varus osteotomy
2070
What is the commonest cause of acute hip pain in children?
Transient synovitis
2071
2-12 years Sudden onset hip pain/limp Often following or with viral infection Not systemically unwell
Transient Synovitis
2072
Ix in transient synovitis
PMN and ESR/CRP normal -ve blood cultures May need joint aspiraiton and culture
2073
Mx of transient synovitis
Rest and analgesia Settles over 2-3d
2074
Def: Perthes disease
Osteochondritis of the femoral head 2o to AVN
2075
Insidiuous onset Hip pain initially then painless 10-20% bilateral
Perthes' disease
2076
Ix in Perthes' disease
XR normal intially increased density of femoral head Femoral head becomes fragmented and irregular Flattening and sclerosis is seen
2077
Mx of Perthes disease
Detected early and \< half femoral head affected- bed rest and traction More severe: maintain hip in abduction with plaster Femoral or pelvic osteotomy
2078
Def: SUFE
Postero-inferior displacement of femoral head epiphysis 10-15 years Fat and sexually undeveloped tall annd thin
2079
Groin pain Shortened, externally rotated leg All movements painful Can also be chronic or acute on chronic Fat and sexually underdeveloped or tall and thin 20% bilateral
SUFE
2080
Mx of acute SUFE
Reduce and pin ephiphysis
2081
Mx of chronic SUFE
In situ pinning as epihpyseal reduction risks AVN
2082
Complications of SUFE
Chondrolysis: breakdown of articular cartilage Increased risk with surgery
2083
Organisms in acute osteomyelitis
**Staph** Strep E Coli Pseudomonas Salmonella (SCD)
2084
What bacteria associated with acute osteomyelitis in sickle cell diseaes?
Salmonella
2085
RFs for acute osteomyelitis
Vascular disease Trauma SCD Immunosuppression e.g. DM Children: rich blood supply to growth plate therefore usually affects the metaphysis
2086
Pain tenderness, erythema, warmth, reduced ROM Effusion in neighbouring joints Signs of systemic infection
Acute OM
2087
Ix in osteomyelitis
Raised ESR/CRP Raised WCC +ve blood cultures in 60% XR changes take 10-14d MRI is sensitive and specific
2088
XR changes in osteomyelitis
Changes take 10-14d Haziness and reduecd bone density Sub-periosteal reaction Sequestrum and involucrum
2089
Mx of osteomyelitis
IV Abx: vanc and cefotaxime until MCS known Drain abscess and remove sequestra Analgesia
2090
What are the commonest bone tumours?
Bony mets
2091
Features of bone mets
Usually radiolucent except prostate is sclerotic Usually axial skeleton (contains red marrow) Present with pain or pathological fracture
2092
What malignancy metastasise to bone LTBKP
Lung Thyroid Breast Kidney Prostate
2093
Ground glass lytic lesion Shepherds crook deformity of proximal femur Usually long bones Ribs skull Mono-ostotic
Fibrous dysplasia
2094
Polyostotic fibrous dysplasia Precocious puberty (females) Cafe au lait spots
McCune Albright's
2095
Clinical features of fibrous dysplasia
0-30 F\>M Increased fracture risk Long bones, rib, skull Mono-ostotic
2096
Well defined lytic lesion in proximal metaphysis of humerus or femur Cortex can flll into cyst- fallen fragment \<20y/o Lump migrates down shaft from original bone plate site
Simple bone cyst
2097
Fibrous dysplasia Ground glass appearance
2098
Simple bone cyst Well-defined lytic lesion
2099
What are the tumour like non-neoplastic conditions of bone?
Fibrous dysplasia Simple bone cyst Aneurysmal bone cyst Fibrous cortical defect and non-ossifying fibroma
2100
Bone \<30y Painful MRI showing multiple fluid levels
Aneurysmal bone cyst
2101
Children, not painful, benign lesion Spontaneously regresses Seen in distal femur Proximal tibia Often multiple
Fibrous cortical defect
2102
Fibrous cortical defect
2103
What are the benign catilaginous neoplasms?
Osteochondroma Enchondroma/Chondromas Chondroblastoma
2104
Cartilage capped bony outgrowth Knee Commonest benign bone tumour May be related to previous bone trauma
Osteochondroma (exostosis)
2105
Oval lucencies with radiodense rim Endosteal scalloping Hands and feet
Enchondromas/chondromas
2106
Ollier disease
Multiple enchondromas
2107
Maffuci syndrome
Enchondromatosis and multiple soft tissue haemangiomas
2108
Radiolucent with sclerotic border Epiphysis Knee
Chondroblastoma
2109
Osteochondroma
2110
Enchondroma
2111
Chondroblastoma
2112
What is the significance of having mutliple enchondromas?
Have risk of malignant transformation
2113
Ollier disease
2114
Marfucci syndrome
2115
\>40 Pain and lump Arising de novo or from chondromas Located in pelvis or axial skeleton Lytic lesion Fluffy popcorn calcification
Chondrosarcoma
2116
Chondrosarcoma
2117
What are the malignant cartilaginous neoplasms?
Chondrosarcoma
2118
What are the benign bone-forming neoplasms
Osteoma Osteoid osteoma Osteoblastoma Giant Cell tumour/osteoclastoma
2119
Lump, usually solitary In skull and faical bones
Osteoma
2120
Osteoma
2121
Multiple osteomas
Gardner syndrome
2122
Gardner syndrome
2123
M\>F 2:1 Teens and 20s Severe nocturnal pain relieved by aspirin Hot on bone scan Lower limb/diaphyseal cortex Lytic lesion with central nidus and sclerotic rim
Osteoid osteoma
2124
Osteoid osteoma
2125
Similar to osteoid osteoma but pain unresponsive to aspirin Spine
Osteoblastoma
2126
20-40 After fusion of growth plate Knee Abutting joint surface Soap bubble appearance Solitary, expansile, lytic lesion
Giant Cell Tumour/osteocalstoma
2127
Osteoclastoma (Giant cell tumour)
2128
What are the malignant bone-forming neoplasms?
Osteosarcoma Ewing's Sarcoma
2129
Adolescents M\>F Commonest 1o bone tumour Pain, warm, bruit May arise 2o to Paget's Knee Metaphysis Periosteal elevation: Sunburst appearance Codman's triangle
Osteosarcoma
2130
Osteosarcoma (Codman triangle)
2131
Painful, warm, enlarging mass Systemic: fever, raised ESR, anaemia, raised WCC \<20 Long bone diaphysis Lytic tumour Onion-skin periosteal reaction
Ewing's sarcoma
2132
Ewing's Sarcoma
2133
Where do the roots of the roots of the brachial pleuxus leave the vertebral column?
Between scalenus anterior and medius
2134
Where do the divisions of the brachial plexus occur?
Under the clavicle, medial to the coracoid process
2135
Causes of brachial plexus injury
Direct e.g. shoulder girdle #, penetrating or iatrogenic injury. Indirect: e.g. avulsion or traction injuries
2136
What can be used to classify brachial plexus injuries?
Leffert Classification
2137
What are the components of the Leffert classificaiton
1. Open 2. Closed: a supraclavicular b infraclavicular 3. Radiation induced 4. Obstetric a upper b lower c mixed
2138
Abductors and external rotators paralysed Waiter's tip Loss of sensation in C5/C6
Erb's palsy (high brachial plexus injury)
2139
Paralysis of small hand muscles Claw hand Loss of sensation in C8/T1 dermatomes
Klumpke's paralysis
2140
Features of low radial nerve injury
Posterior interosseus nerve affected Site: #around elbow or forearm e.g. head of radius Loss of extension of CMC (finger drop) No sensory loss
2141
Features of high radial nerve injury
Site: #shaft of humerus where N is in radial groove Wrist drop Loss of sensation to dorsum of thumb Triceps functions nromally
2142
Wrist drop Loss of sensation to dorsum of thumb Triceps functions normally
High radial nerve injury
2143
Features of very high radial nerve lesions
Axilla e.g. crutches or saturday night palsy Paralysis of triceps and wrist drop
2144
Site of ulnar nerve lesions
Elbow: cubital tunnel Wrist: Guyon's canal
2145
What is Guyon's canal?
The ulnar canal or ulnar tunnel (also known as Guyon's canal or tunnel) is a semi-rigid longitudinal canal in the wrist that allows passage of the ulnar artery and ulnar nerve into the hand
2146
Intrinsic hand muscle paralysis-\> claw hand Lesion at elbow has less clawing as FDP is paralysed, decreasing flexion of 4th and 5th digits Sensory loss over little finger
Ulnar nerve lesion
2147
Tests for ulnar nerve palsy
Can't cross fingers for luck Froment's sign
2148
Features of injury to median nerve above the antecubital fossa
Can't flex index finger IPJs Can't flex terminal thumb phalanx Loss of sensation in median distribution
2149
median nerve injury at the wrist
Typically affects abductor pollicis brevis
2150
Nerve damage mechanism Accessory
Posterior triangle LN biopsy
2151
Nerve damage mechanism Sciatic
Posterior approach to hip
2152
Nerve damage mechanism Common peroneal
Legs in Lloyd davies position
2153
What is Lloyd davies position?
Lloyd-Davies position is a medical term referring to a common position for surgical procedures involving the pelvis and lower abdomen. The majority of colorectal and pelvic surgery is conducted with the patient in the Lloyd-Davies position. It is also known as the Trendelenburg position with legs apart.
2154
Nerve damage mechanism Long thoracic
Axillary node clearance
2155
Nerve damage mechanism Pelvic autonomic nerves
Pelvic cancer surgery
2156
Nerve damage mechanism Recurrent laryngeal nerves
During thyroid surgery
2157
Nerve damage mechanism Hypoglossal nerve
During carotid endaterectomy
2158
Nerve damage mechanism Ulnar and median nerves
During upper limb fracture repairs
2159
Damage to structure mechanism Thoracic duct
During thoracic surgery e.g. pneumonectomy, oesophagectomy
2160
Damage to structure mechanism Parathyroids
During difficult thyroid surgery
2161
Damage to structure mechanism Ureters
During colonic resections/gynaecological surgery
2162
Damage to structure mechanism Bowel perforation
Use of verres needle to establish pneumoperitoneum
2163
What is verres needle?
A Veress needle is a spring-loaded needle used to create pneumoperitoneum for laparoscopic surgery. Of the three general approaches to laparoscopic access, the Veress needle technique is the oldest and most traditional.
2164
Damage to structure mecahnism Bile duct injury
Failure to delineate Calot's triangle carefully and careless use of diathermy
2165
What is Calot's triangle?
Hepatobiliary triangle bordered by the cystic duct inferiorly, common hepatic duct medially and the inferior surface of the liver superiorly. Cystic artery lies within the triangle which is used to locate it during a laparoscopic cholecystectomy
2166
Damage to structure mecahnism Facial nerve
Always at risk during parotidectomy
2167
Damage to structure mecahnism Tail of pancreas
When ligating splenic hilum
2168
Damage to structure mecahnism Testicular vessels
During re-do open hernia surgery
2169
Damage to structure mecahnism Hepatic veins
During liver mobilisation
2170
Physiological disturbance mechanism Arrythmias following cardiac surgery
Susceptibility to hypokalaemia (\<4 in cardiac patients)
2171
Physiological disturbance mechanism Neurosurgical electrolyte disturbance
SIADH following cranial surgery causing hyponatraemia
2172
Physiological disturbance mechanism Ileus following GI sx
Fluid sequestration and loss of electrolytes
2173
Physiological disturbance mechanism Pulmonary oedema following pneumonectomy
Loss of lung volume makes patients very sensitive to fluid overload
2174
Physiological disturbance mechanism Anastomotic leak
Generalised sepsis causing mediastinitis or peritonitis depending on site of leak
2175
Physiological disturbance mechanism MI
May follow any type of sx and in addition to direct cardiac effects, the decreased CO may compromsie grafts etc.
2176
Identifying surgical complications: Intra-abdominal abscess/air/ anastomotic leak
CT scanning +luminal contrast
2177
Identifying surgical complications: Rectal anastomotic leak
Gastrograffin enema
2178
Identifying surgical complications: Ureteric injury Pancreatic injury
U+E Amylase
2179
Identifying surgical complications: Pericardial effusion
Echocardiogram if no pleural window made
2180
A 53-year-old gentleman is 1 week post right-hemicolectomy for colorectal cancer and formation of ileostomy. He complains of intermittent shortness of breath and an arterial blood gas sample was taken. The results showed the following; Normal range pH: 7.25(7.35 - 7.45) pO2: 11.1(10 - 14)kPa pCO2: 3.2(4.5 - 6.0)kPa HCO3: 11(22 - 26)mmol/l BE: -15(-2 to +2)mmol/l Normal range Na: 110135-145 mmol/l K: 33.5-5 mmol/l Given the above information, what should form part of the most likely differential diagnosis for this gentleman? Loss from high output stoma post-operatively Uraemia Lactic acidosis Hospital acquired pneumonia Pulmonary embolism
When considering acid-base disorders in post-operative patients, it is important to consider the potential side effects related to the specific procedure. In this case, this gentleman has an ileostomy for a stoma bag to drain bowel contents post-operatively. These patients may develop significant volume depletion, electrolyte and acid-base disturbances (metabolic acidosis) if the ileostomy output increases or if dietary intake is disrupted or altered. Hence, it is important to monitor fluid balance including stoma output in these patients.
2181
What are the considerations in selecting type of resection for rectal cancer?
Tumours located in the rectum can be surgically resected with either an anterior resection or an abdomino-perineal excision of rectum (APER). The technical aspects governing the choice between these two procedures can be complex to appreciate and the main point to appreciate for the exam is that involvement of the sphincter complex or very low tumours require APER. In the rectum a 2cm distal clearance margin is required and this may also impact on the procedure chosen. In addition to excision of the rectal tube an integral part of the procedure is a meticulous dissection of the mesorectal fat and lymph nodes (total mesorectal excision/ TME).
2182
Why is radiotherapy an option in rectal carcinoma?
In rectal cancer surgery involvement of the cirumferential resection margin carries a high risk of disease recurrence. Because the rectum is an extraperitoneal structure (until you remove it that is!) it is possible to irradiate it, something which cannot be offered for colonic tumours. This has a major impact in rectal cancer treatment and many patients will be offered neoadjuvent radiotherapy (both long and short course) prior to resectional surgery. Patients with T1 and 2 /N0 disease on imaging do not require irradiation and should proceed straight to surgery. Patients with T4 disease will typically have long course chemo radiotherapy. Those with T3 , N0 tumours may be offered short course radiotherapy prior to surgery. Patients presenting with large bowel obstruction from rectal cancer should not undergo resectional surgery without staging as primary treatment (very different from colonic cancer). This is because rectal surgery is more technically demanding, the anastomotic leak rate is higher and the danger of a positive resection margin in an unstaged patient is high. Therefore patients with obstructing rectal cancer should have a defunctioning loop colostomy.
2183
Site of cancer, type of resection, type of anastomosis Caecal, ascending or proximal transverse colon
Right hemicolectomy Ileo-colic
2184
Site of cancer, type of resection, type of anastomosis Distal transverse, descending colon
Left hemicolectomy Colo-colon
2185
Site of cancer, type of resection, type of anastomosis Sigmoid colon
High anterior resection Colo-rectal
2186
Site of cancer, type of resection, type of anastomosis Upper rectum
Anterior resection (TME) Colo-rectal
2187
Site of cancer, type of resection, type of anastomosis Low rectum
Anterior resection (Low TME) Colo-rectal +/- defunctioning stoma
2188
Site of cancer, type of resection, type of anastomosis Anal verge
APER None
2189
What is the choice of surgery in an emergency setting where the bowel has perforated
In the emergency setting where the bowel has perforated the risk of an anastomosis is much greater, particularly when the anastomosis is colon-colon. In this situation an end colostomy is often safer and can be reversed later. When resection of the sigmoid colon is performed and an end colostomy is fashioned the operation is referred to as a Hartmans procedure. Whilst left sided resections are more risky, ileo-colic anastomoses are relatively safe even in the emergency setting and do not need to be defunctioned.
2190
Colorectal screening programme features
60-74 years Every 2 years to all men and women
2191
Impact of colorectal screening programme on mortality?
16% reduction
2192
Colonoscopy following abnormal FOB, results
5/10 will have normal exam 4/10 will have polyps which may be removed due to premalignant potential 1/10 will have cancer
2193
Theme: Abdominal stomas A.End ileostomy B.End colostomy C.Loop ileostomy D.Loop colostomy E.End jejunostomy F.Loop jejunostomy G.Caecostomy A 56-year-old man is undergoing a low anterior resection for carcinoma of the rectum. It is planned to restore intestinal continuity. A 23-year-old man with uncontrolled ulcerative colitis is undergoing an emergency sub total colectomy. A 63-year-old women presents with large bowel obstruction. On examination she has a carcinoma 10cm from the anal verge.
The correct answer is Loop ileostomy Colonic resections with an anastomosis below the peritoneal reflection may have an anastomotic leak rate (both clinical and radiological) of up to 15%. Therefore most surgeons will defunction such an anastomosis to reduce the clinical severity of an anastomotic leak. A loop ileostomy will achieve this end point and is relatively easy to reverse. End ileostomy Following a sub total colectomy the immediate surgical options include an end ileostomy or ileorectal anastomosis. In the emergency setting an ileorectal anastomosis would be unsafe. The correct answer is Loop colostomy Large bowel obstruction resulting from carcinoma should be resected, stented or defunctioned. The first two options typically apply to tumours above the peritoneal reflection. Lower tumours should be defunctioned with a loop colostomy and then formal staging undertaken prior to definitive surgery. An emergency attempted rectal resection carries a high risk of involvement of the circumferential resection margin and is not recommended
2194
Def: stoma
Bringing of lumen or visceral contents onto the skin With bowel stomas, the method and site will be determined by the bowel affected. In practice small bowel stomas should be spouted so that their irritant contents are not in contact with the skin Colonic stomas do not need to be spouted
2195
Types and features of stoma Gastrotomy
Gastric decompression or fixation Feeding Commonly sited in the epigastrium
2196
Types and features of stoma Loop jejunostomy
Seldom used as very high output May be used following emergency laparotomy with planned early closure Any location according to need
2197
Types and features of stoma Percutaneous jejunostomy
Usually performed for feeding purposes and sited in the proximal bowel Usually LUQ
2198
Types and features of stoma Loop ileostomy
Defunctioning of colon e.g. following rectal cancer surgery Does not decompress colon if ileocaecal valve competent Usually RIF
2199
Types and features of stoma End ileostomy
Usually folllowing complete excision of colon or where ileo-colic anastomosis is not planned May be used to defunciton colon but reversal is more difficult Usually RIF
2200
Types and features of stoma End colostomy
Where a colon is diverted or resected and anastomosis is not primarly achievable or desirable Either L or RIF
2201
Types and features of stoma Loop colostomy
To defunction a distal segment of colon Since both lumens are present, the distal lumen acts as a vent May be located in any region of the abdomen depending on colonic segment used
2202
Types and features of stoma Caecostomy
Stoma of last resort where loop colostomy is not possible RIF
2203
Types and features of stoma Mucous fistula
To decompress a distal segment of bowel following colonic diversion or resection Where closure of a distal resection margin is not safe or achievable May be located in any region of the abdomen according to clinical need
2204
A 50-year-old man is admitted to hospital with a 5 day history of worsening abdominal pain. Over the past 24 hours the pain has become very severe. On examination his pulse is 110/min, blood pressure 110/62 mmHg and temperature 37.7ºC. Bloods show the following: Hb10.5 g/l Platelets452 \* 109/l WBC16.3 \* 109/l CRP263 mg/l The abdominal film is shown below: What is the most likely underlying disorder? Perforated diverticulum Sigmoid volvulus Ulcerative colitis Spontaneous bacterial peritonitis Crohn's disease
This patient had toxic megacolon secondary to underlying ulcerative colitis - note the dilated transverse colon. The abdomen demonstrates a markedly dilated transverse colon (9 cm) with impression of slight dilatation of the descending colon with some 'thumb printing' in the wall. No free subphrenic gas is seen. They went on to have a subtotal colectomy
2205
A 54 year old man is referred to clinic with change in bowel habit, blood in his stools, lethargy and weight-loss. A colonoscopy is ordered which shows a high rectosigmoid mass. Which operation would be most appropriate? Pancolectomy Abdominoperineal resection Left hemicolectomy Posterior resection Anterior resection
This man's tumour is in the rectum and sigmoid colon. Therefore, removing only the colon (left hemicolectomy or pancolectomy) is not a valid management option. For tumours that are in the distal 8cm of the rectum, an abdominoperoneal resection is the option of choice. In this procedure, the anus, rectum and distal sigmoid are removed and the remaining sigmoid is brought out to the surface as a permanent colostomy. For tumours in the proximal part of the rectum (as in this case), an anterior resection is performed and after removal of the tumour, the remaining sigmoid is anastomosed to the lower rectum. The approach is anterior (through the abdominal wall), giving the procedure its name. Once upon a time the procedure was done with a posterior approach (posterior resection), but this has fallen out of favour.
2206
A 58-year-old gentlemen presents to your clinic complaining of 4 weeks of altered bowel habit, with some per rectal bleeding which is mixed in with his stool, he also complains of tenesmus following defecation and has lost 6 kilos of weight in the last 8 weeks. You decide to do a PR examination. You feel a mass on the posterior wall of the rectum around 10 cm from the anal verge, it is 9cm in diameter and feels irregular. You are highly concerned that this may be a rectal cancer and order an urgent suspected cancer review and urgent colonoscopy. If your suspicions are correct what is the most likely diagnosis? Squamous cell carcinoma Gastrointestinal stromal tumour Secondary lymphoma Adenocarcinoma Carcinoid tumour
More than 90% of colorectal cancers are adenocarcinomas
2207
Sigmoid volvulus associations
older patients chronic constipation Chagas disease neurological conditions e.g. Parkinson's disease, Duchenne muscular dystrophy psychiatric conditions e.g. schizophrenia
2208
Caecal volvulus associations
all ages adhesions pregnancy
2209
Mx of sigmoid volvulus
Rigid sigmoidoscopy with rectal tube insertion
2210
Mx of caecal volvulus
Usually operative R hemicolectomy often needed
2211
Relative proportions of different types of volvulus
Simoid (80%) Caecal (20%)
2212
A 59-year-old woman is admitted to hospital after developing an infection of a non-functioning left kidney, Intravenous antibiotics are given and a nephrostomy tube is inserted. During her recovery she starts to develop a distended abdomen and complains of nausea and abdominal pain. An abdominal film is requested: © Image used on license from Radiopaedia What is the cause of the abdominal distension? Bowel perforation Intussusception Bacterial peritonitis Caecal volvulus Subcutaneous emphysema
Small bowel obstruction is clearly visible on this film (note the valvulae conniventes, mucosal folds, that cross the full width of the bowel) secondary to caecal volvulus. Note the left nephrostomy tube in-situ.
2213
Theme: Colonic resections ## Footnote A.End ileostomy B.Loop ileostomy C.Ileo anal pouch D.Loop colostomy E.Pan proctocelectomy F.Left hemicolectomy G.Right hemicolectomy H.Hartmann's procedurce I.Anterior resection with covering loop ileostomy A 75-year-old man requires resection of an obstructing carcinoma of the splenic flexure. A patient presenting with a large bowel obstruction from a low rectal cancer. A 45-year-old man presents with a carcinoma 10cm from the anal verge, he has completed a long course of chemoradiotherapy and has achieved downstaging with no evidence of threatened circumferential margin on MRI scanning.
Carcinoma of the splenic flexure requires a left hemicolectomy. This patient should be defunctioned-definitive surgery should wait until staging is completed. A loop ileostomy will not satisfactorily decompress an acutely obstructed colon. Low rectal cancers that are obstructed should not usually be primarily resected. The obstructed colon that would be used for anastomosis would carry a high risk of anastomotic dehisence. In addition, as this is an emergency presentation, staging may not be completed, an attempted resection may therefore compromise the circumferential resection margin, with an associated risk of local recurrence Low rectal cancer is usually treated with a low anterior resection. Contraindications to this include involvement of the sphincters (unlikely here) and poor sphincter function that would lead to unsatisfactory function post resection. Most colorectal surgeons defunction resections below the peritoneal reflection as they have an intrinsically high risk of anastomotic leak. A loop ileostomy provides a safe an satisfactory method of defunctioning these patients. A contrast enema should be performed prior to stoma reversal.
2214
A 72-year-old male is recovering from a partial colectomy that he had 3 days ago. The patient complains of worsening pain at the wound site. On closer examination there is pink serous discharge, separation of the wound edges and bowel can be seen protruding. The patient has no other obvious symptoms. How should this patient immediately be managed? ## Footnote Cover the area with dry gauze and apply pressure Pack the wound and begin intravenous fluids Start sepsis six protocol Non-urgent senior review Call for senior help urgently
Wound dehiscence is a post-operative complication in which a wound ruptures along the surgical incision site. In this case, deep dehiscence has occurred as bowel can be seen protruding. This is an emergency and senior help should be called for immediately. Non-urgent senior review should be considered for superficial dehiscence. Applying pressure with dry gauze is inappropriate immediate management for this patient. However, a large sterile swab soaked in 0.9% saline can be used while waiting for senior help to arrived. Packing the wound can be considered for superficial dehiscence but is an inappropriate immediate management for this patient. Sepsis six protocol is a possibility and the patient's vital signs should be recorded after senior help has been called for.
2215
What are the NICE criteria for urgent referral to CRC services
\>40 with unexplained weight loss and abdo pain \>50 with unexplained rectal bleeding \>60 with IDA or change in bowel habit Tests show occult blood in faeces
2216
Who should FOBT be offered to?
\>50 with unexplained abdo pain or weight loss \<60 with change in bowel habit or IDA \>60 who have anaemia even in absence of IDA
2217
When should an urgent CRC referral be considered?
Rectal or abdo mass UNexplained anal mass or ulceration \<50 with rectal bleeding and any of: abdo pain change in bowel habit weight loss IDA
2218
The most common type of inherited colorectal cancer: Familial adenomatous polyposis Li-Fraumeni syndrome Hereditary non-polyposis colorectal carcinoma Fanconi syndrome Peutz-Jeghers syndrome
HNPCC
2219
What are the 3 types of colon cancer?
sporadic (95%) hereditary non-polyposis colorectal carcinoma (HNPCC, 5%) familial adenomatous polyposis (FAP, \<1%)
2220
HNPCC features
HNPCC, an autosomal dominant condition, is the most common form of inherited colon cancer. Around 90% of patients develop cancers, often of the proximal colon, which are usually poorly differentiated and highly aggressive. Currently seven mutations have been identified, which affect genes involved in DNA mismatch repair leading to microsatellite instability. The most common genes involved are: MSH2 (60% of cases) MLH1 (30%)
2221
What are the Amsterdam criteria for HNPCC?
at least 3 family members with colon cancer the cases span at least two generations at least one case diagnosed before the age of 50 years
2222
FAP mutation
delta FAP
2223
A 65-year-old female is admitted to your surgical ward for an elective hemicolectomy tomorrow due to Duke's B colonic cancer. You are carrying out her admission assessment and notice her full blood count (FBC) demonstrates a microcytic anaemia with haemoglobin of 58 g/L. Her previous FBC 3 months earlier showed Hb 88 g/L. Haematinic blood tests show that the cause of the microcytosis is iron deficiency. What is the most appropriate management of her anaemia? Iron transfusion (e.g. Ferinject) Pre-operative blood transfusion Oral iron supplementation (e.g. ferrous sulphate) Post-operative blood transfusion No need to correct anaemia as removal of tumour will resolve iron loss
A haemoglobin of 58 g/L will need to be corrected prior to surgery and this will only be achieved in such a short time frame by arranging a blood transfusion. Iron transfusions or oral iron supplements would be recommended over a longer time frame of weeks to months had this been detected earlier.
2224
Special preparation for surgery Thyroid
Vocal cord check
2225
Special preparation for surgery Parathyroid
Consider methylene blue to identiffy gland
2226
Special preparation for surgery Sentinal node biopsy
Radioactive marker/patent blue dye
2227
Special preparation for surgery Surgery involving thoracic duct
Several methods have been described that vary from a high fat diet the evening before that includes heavy cream or ice cream.8 and 9 Some have advocated for enteral fat to continue during the intraoperative period via a nasogastric tube, nasoduodenal feeding tube, gastrostomy tube, or feeding jejunostomy.8 and 9 This will create a high-volume flow of chyle and allow the surgeon to identify the thoracic duct clearly.
2228
Special preparation for surgery: Phaeo
Will require alpha and beta blockade
2229
Specail preparation for surgery: Carcinoid tumours
Will require covering with octreotide
2230
Specail preparation for surgery: Colorectal cases
Bowel preparation
2231
Special preparation for surgery: Thyrotoxicosis
Lugols iodine/ medical therapy
2232
What are the average proportions of colorectal cancer location?
Location of cancer (averages) rectal: 40% sigmoid: 30% descending colon: 5% transverse colon: 10% ascending colon and caecum: 15%
2233
CRC in terms of other cancers?
3rd most common in UK Second most common cause of cancer deaths
2234
Duke's classification: A
Tumour confined to mucosa (90%)
2235
Duke's classification: Duke B
Tumour invading bowel wall (70% 5y survival)
2236
Duke's classification: C
LN metastases (45%)
2237
Duke's classification: Dukes D
Distant mets (6%)
2238
What is the most common extra-intestinal feature in both CD and UC?
Arthritis
2239
In which IBD is episcelritis more common?
CD
2240
In which IBD is uveitis more common?
UC
2241
What are the extraintestinal manifestations common to both Crohn's and UC that are related to disease activity?
Arthritis: pauciarticular, asymmetric Erythema nodosum Episcleritis Osteoporosis
2242
What are the extraintestinal manifestation of Crohn's and UC common to both unrelated to disease activity
Polyarticular symmetric arthritis Uveitis Pyoderma gangrenosum Clubbing PSC
2243
What is Frimann Dahl's sign?
three dense lines converging towards the site of obstruction (Frimann Dahl's sign) in keeping with sigmoid volvulus.
2244
TNM classification in CRC T
Tx Primary tumour cannot be assessed T0 No evidence of primary tumour Tis Carcinoma in situ: intraepithelial or invasion of lamina propria T1 Tumour invades submucosa T2 Tumour invades muscularis propria T3 Tumour invades through the muscularis propria into the pericolorectal tissues T4a Tumour penetrates to the surface of the visceral peritoneum T4b Tumour directly invades or is adherent to other organs or structures
2245
TNM classification in colon cancer Regional lymph nodes (N)
NX Regional lymph nodes cannot be assessed N0 No regional lymph node metastasis N1 Metastasis in 1-3 regional lymph nodes N1a Metastasis in 1 regional lymph node N1b Metastasis in 2-3 regional lymph nodes N1c Tumour deposit(s) in the subserosa, mesentery, or non-peritonealised pericolic or perirectal tissues without regional nodal metastasis N2 Metastasis in 4 or more lymph nodes N2a Metastasis in 4-6 regional lymph nodes N2b Metastasis in 7 or more regional lymph nodes
2246
TNM classification in colon cancer Distant metastasis (M)
M0 No distant metastasis M1 Distant metastasis M1a Metastasis confined to 1 organ or site (eg, liver, lung, ovary, non-regional node) M1b Metastases in more than 1 organ/site or the peritoneum
2247
Features of Li Fraumeni?
Autosomal dominant Consists of germline mutations to p53 tumour suppressor gene High incidence of malignancies particularly sarcomas and leukaemias Diagnosed when: \*Individual develops sarcoma under 45 years \*First degree relative diagnosed with any cancer below age 45 years and another family member develops malignancy under 45 years or sarcoma at any age
2248
Features of BRCA1 and 2 Remember BRCA1 is counterintuitive
Carried on chromosome 17 Linked to developing breast cancer (60%) risk. Associated risk of developing ovarian cancer (55% with BRCA 1 and 25% with BRCA 2).
2249
Lynch Syndrome
Autosomal dominant Develop colonic cancer and endometrial cancer at young age 80% of affected individuals with get colonic and or endometrial cancer High risk individuals may be identified using the Amsterdam criteria
2250
Gardners syndrome
Autosomal dominant familial colorectal polyposis Multiple colonic polyps Extra colonic diseases include: skull osteoma, thyroid cancer and epidermoid cysts Desmoid tumours are seen in 15% Mutation of APC gene located on chromosome 5 Due to colonic polyps most patients will undergo colectomy to reduce risk of colorectal cancer Now considered a variant of familial adenomatous polyposis coli
2251
A 64 year old woman presents to her GP with a 2 month history of abdominal pain and diarrhoea. She describes it as severe, central pain and says that it is worse after eating. Her past medical history consists of hypertension, hypercholesterolaemia and a previous myocardial infarction. Which investigation is most likely to be diagnostic? Capsule endoscopy MR angiogram CT abdomen US renal tract Barium studies
This lady is an arteriopath as evidenced by her past medical history. The pain she describes - severe, central and worse after eating, with associated diarrhoea is classic of mesenteric ischaemia - worse when the gut is working to digest food. The most appropriate investigation to confirm the diagnosis would be a magnetic resonance angiogram of the mesenteric vasculature.
2252
Where is mesenteric ischaemia more likely to occur?
Mesenteric ischaemia is primarily caused by arterial embolism resulting in infarction of the colon. It is more likely to occur in areas such as the splenic flexure that are located at the borders of the territory supplied by the superior and inferior mesenteric arteries.
2253
abdominal pain rectal bleeding diarrhoea fever bloods typically show an elevated WBC associated with acidosis In an arteriopath
Mesenteric ischaemia
2254
What are the predisposing factors for mesenteric ischaemia?
Increasing age AF other causes of emboli e.g. endocarditis CV disease risk factors Cocaine
2255
A 72-year-old male has been diagnosed with rectal carcinoma. He is due to undergo a lower anterior resection. The aim of the resection is to restore intestinal continuity. Which is the most appropriate type of stoma? Loop colostomy End ileostomy Loop ileostomy Caecostomy Total colectomy
Loop ileostomy is a method to divert bowel contents away from a distal anastomosis. It is often indicated in rectal cancers. Reversal of the ileostomy restores bowel continuity and improves the patient's overall quality of life.
2256
A 36-year-old lady with a past history of Crohn's disease presents with painful bleeding per rectum. She tells you that the bleeding occurs after defaecation and it is bright red. What is the most likely cause of the bleeding? ## Footnote Fissure in ano Haemorrhoid Haemorrhagic perianal abscess Rectal cancer Recto-uterine fistula
Pain on passing faeces accompanied by bleeding post-defaecation is suggestive of a diagnosis of fissure in ano. Thrombosed haemorrhoids may also present with painful PR bleeding but in this scenario a fissure is more likely. This young lady has a background of Crohn's disease and that patients with Crohn's disease are more susceptible to fissure formation. Rectal cancer can present with rectal bleeding but would be unlikely in a 36-year-old. Recto-uterine fistulas typically cause faecal incontinence rather than bleeding. A perianal abscess would cause perianal pain and may be accompanied by pyrexia.
2257
What is the dentate line?
The pectinate line (dentate line) is a line which divides the upper two thirds and lower third of the anal canal. Developmentally, this line represents the hindgut-proctodeum junction.
2258
A 76-year-old patient undergoes a right hemicolectomy for bowel cancer. 4 days post-operative you are on-call and are asked to review him by one of the nurses as she is concerned about the patient's blood pressure. On examination the patient is clammy, confused, heart rate 115 bpm, blood pressure 80/50 mmHg, urine output is 10 mls per hour and temperature is 38.6ºC. His wound is clean and dry, and his abdomen is non-peritonitic. Chest examination is clear. Heart sounds normal. Peripheral lines appear intact with no phlebitis. The patient does not have a urinary catheter. You perform an urgent arterial blood gas which demonstrates a normal gas exchange, haemoglobin 12.5 g/L, lactate of 5.4 µmol/L, and creatinine of 331 µmol/L. You fluid resuscitate him and arrange immediate imaging. Which imaging modality would be best in this situation? ## Footnote Plain abdominal x-ray CT abdomen with contrast CT angiogram US abdomen MRI abdomen
This is a clinical picture of severe sepsis (i.e. sepsis with one or more organ dysfunction) and clearly points to an intra-abdominal origin as other sources of infection are unremarkable. The ABG is consistent with sepsis but has also impaired renal function (creatinine 331 µmol/L) and therefore intravenous contrast would be unwise due to the risk of developing contrast nephropathy. As such a CT abdomen would not be advisable and a CT angiogram is not warranted as there isn't any suspicion of haemorrhage. An anastomotic leak is unlikely as the patient's abdomen would be peritonitic. Plain abdominal x-ray would not detect a source of infection and an MRI is not going to be possible 4 days post-operative due to the use of metal surgical clips. The best modality would therefore be ultrasound abdomen as this would be able to detect an intra-abdominal collection.
2259
Theme: Surgery for inflammatory bowel disease A.Proctectomy B.Anterior resection C.Panproctocolectomy D.Panproctocolectomy and ileoanal pouch E.Sub total colectomy F.Right hemicolectomy Please select the most appropriate surgical modality for treating the inflammatory bowel disease scenarios described. Each option may be used once, more than once or not at all. 45. A 22-year-old man presents with his first presentation of ulcerative colitis. Despite aggressive medical management with steroids, azathioprine and infliximab his symptoms remain unchanged and he has developed a megacolon. 46. A 22-year-old lady has a long history of severe perianal Crohns disease with multiple fistulae. She is keen to avoid a stoma. However, she has progressive disease and multiple episodes of rectal bleeding. A colonoscopy shows rectal disease only and a small bowel study shows no involvement with Crohns. 47. A 22-year-old man has a long history of ulcerative colitis. His symptoms are well controlled with steroids. However, attempts at steroid weaning and use of steroid sparing drugs have repeatedly failed. He wishes to avoid a permanent stoma.
In patients with fulminant UC a sub total colectomy is the safest treatment option. The rectum will be left in situ as resection of the rectum in these acutely unwell patients carries an extremely high risk of complications. Severe rectal Crohns that has developed complications such as haemorrhage and multiple fistulae is usually best managed with proctectomy. Although a diverting stoma may reduce the risk of local sepsis it is unlikely to reduce the bleeding. She is keen to conserve a rectum, however, an ileoanal pouch in this setting is unwise. In patients with UC where medical management is not successful, surgical resection may offer a chance of cure. Those patients wishing to avoid a permanent stoma may be considered for an ileoanal pouch. However, this procedure is only offered in the elective setting.
2260
What is an absolute indication for proctocolectomy in UC?
Longstanding UC is associated with a risk of malignant transformation. Dysplastic transformation of the colonic epithelium with associated mass lesions is an absolute indication for a proctocolectomy.
2261
What is the management of poorly controlled colitis that presents as an emergency and fails to respond to medical therapy?
Emergency presentations of poorly controlled colitis that fails to respond to medical therapy should usually be managed with a subtotal colectomy. Excision of the rectum is a procedure with a higher morbidity and is not generally performed in the emergency setting. An end ileostomy is usually created and the rectum either stapled off and left in situ, or, if the bowel is very oedematous, may be brought to the surface as a mucous fistula.
2262
What are the complications of ileoanal pouch?
Anastomotic dehiscence Pouchitis Poor physiological function with seepage and soiling
2263
What are the restorative options in UC post sx?
Restorative options in UC include an ileoanal pouch. This procedure can only be performed whilst the rectum is in situ and cannot usually be undertaken as a delayed procedure following proctectomy.
2264
What is a consideration regarding surgical treatment of Crohn's?
Surgical resection of Crohns disease does not equate with cure, but may produce substantial symptomatic improvement. Indications for surgery include complications such as fistulae, abscess formation and strictures. Extensive small bowel resections may result in short bowel syndrome and localised stricturoplasty may allow preservation of intestinal length. Staging of Crohns will usually involve colonoscopy and a small bowel study (e.g. MRI enteroclysis).
2265
Sx mx of severe perianal and or rectal crohn's?
Severe perianal and / or rectal Crohns may require proctectomy. Ileoanal pouch reconstruction in Crohns carries a high risk of fistula formation and pouch failure and is not recommended.
2266
Considerations regarding mx of crohn's in its most common disease site?
Terminal ileal Crohns remains the commonest disease site and these patients may be treated with limited ileocaecal resections. Terminal ileal Crohns may affect enterohepatic bile salt recycling and increase the risk of gallstones.
2267
A 67-year-old man presents to the Emergency department with sudden-onset sharp abdominal pain radiating to his back. His observations on arrival include: heart rate 110 beats per minute, blood pressure 102/67 mmHg, respiratory rate 30 breaths per minute, oxygen saturations 94% on air and temperature 37.4ºC. What is the most important first step in the management of this patient? Abdominal x-ray Immediate contrast CT of the abdomen Immediate fluid resuscitation to keep blood pressure \>120/80mmHg Patient should go straight to theatre Urine dip
This man most likely has a ruptured abdominal aortic aneurysm and is showing signs of shock. This carries a very high mortality and he should therefore be taken immediately to theatre. Diagnosing a ruptured abdominal aortic aneurysm requires a high index of suspicion and if suspected, it is inappropriate to waste time on imaging. Whilst it is important to gain intravenous access and treat shock, systolic blood pressure should be maintained \<100mmHg to avoid rupturing any contained leak.
2268
A 60-year-old man is investigated for intermittent claudication. He is referred to the local vascular unit and a diagnosis of peripheral arterial disease is made. His blood pressure is 128/78 mmHg and his fasting cholesterol 5.8 mmol/l. Following recent NICE guidelines which of the following medications should he be taking? Antiplatelet + statin + ACE inhibitor Statin Antiplatelet + statin + long-acting nitrate Antiplatelet + statin + beta-blocker Antiplatelet + statin
As this patient has established cardiovascular disease he should be taking a statin, regardless of the baseline cholesterol. The 2010 NICE guidelines on clopidogrel changed the previous advice that all patients with established cardiovascular disease should be taking aspirin, unless there is a contraindication. NICE propose that clopidogrel is now used first-line following an ischaemic stroke and also in peripheral arterial disease.
2269
Mx of PAD
Treat comorbidites All patients with established CVD should be taking a statin Clopidogrel should be used first line in patients with PAD in preference to aspirin Exercise training has been shown to ahve significant benefits Severe PAD or critical limb iscahemia may be treated by: Angioplasty Stenting Bypass surgery Other drugs that are licensed for PAD include naftidrofuryl oxalate: vasodilator sometimes used for patients with poor QoL Cilostazol: PDE III inhibitor with both antiplatelet and vasodilator effects (not recommended by NICE)
2270
Oesophageal TNM staging Tumour
T1- the tumour is confined to the submucosa T2- the tumour has grown into (but not through) the muscularis propria T3- the tumour has grown into (but not through) the serosa T4- the tumour has penetrated through the serosa and the peritoneal surface. If extending directly into other nearby structures (such as other parts of the bowel or other organs/body structures) it is classified as T4a. If there is perforation of the bowel, it is classified as T4b.
2271
Oesophageal TNM staging Nodes
N0- no lymph nodes contain tumour cells N1- there are tumour cells in up to 3 regional lymph nodes N2- there are tumour cells in 4 or more regional lymph nodes
2272
Oesophageal TNM staging Mets
Metastases M0- no metastasis to distant organs M1- metastasis to distant organs
2273
A 67-year-old man with a 10-year history of gastro-oesophageal reflux disease is investigated for dysphagia. An endoscopy shows an obstructive lesion highly suspicious of oesophageal cancer. What is the biopsy most likely to show? Squamous cell carcinoma Normal squamous epithelium Adenocarcinoma Leiomyoma Metaplastic columnar epithelium
Oesophageal adenocarcinoma is associated with GORD or Barrett's
2274
Usually follows long term use and is usually painless with non obstructive features Often due to hepatic dysfunction and fatty liver which may occur with long term TPN usage.
TPN associated jaundice
2275
A 60-year-old male smoker underwent endoscopy for recurrent dyspepsia despite Helicobacter Pylori eradication. A mass was noted around the oesophagogastric junction. What is the most appropriate modality for staging the primary tumour? MRI Non-contrast CT CT with oral contrast only Positron emission tomography (PET) Endoscopic ultrasound
Oesophageal cancer is the eighth most common cancer worldwide and the thirteenth most common in the UK. It is 20 times more common in China but its incidence is rising in the western world. Risk factors include smoking, alcohol and obesity. In addition, squamous cell carcinoma is linked to achalasia and coeliac disease, while adenocarcinoma occurs in the setting of Barrett's oesophagus. Flexible upper GI endoscopy is the diagnostic investigation of choice and a minimum of eight biopsies should be obtained. CT is an acceptable staging modality and should be used routinely to identify metastatic disease. However, it requires the use of intravenous and oral contrast (unlike the options given above). Endoscopic ultrasound provides superior axial resolution to CT and is the most accurate way of determining the depth of spread of a malignant tumour through the oesophageal wall. PET is not routinely used as a staging modality in oesophageal carcinoma.
2276
A 39-year-old overweight female undergoes an elective laparoscopic cholecystectomy for gallstone disease. Day 1 post-operatively you are asked to review her by the nurse in charge. The patient is complaining of severe right upper quadrant pain. On examination she is tachycardic, but normotensive and apyrexial. Her right upper quadrant is tender to palpation but there is no evidence of jaundice. The intra-abdominal drain in-situ has a small volume of green liquid draining from it. What post-operative complication is most likely? Intra-abdominal collection Biliary leak Intra-abdominal haemorrhage Perforated viscus Ileus
Right upper quadrant tenderness and bilious fluid in the intra-abdominal drain would suggest a bile leak following the cholecystectomy. As the patient is apyrexial and normotensive an intra-abdominal collection or haemorrhage would be unlikely. A perforation is a recognised complication of a laparoscopic cholecystectomy however the patient would normally develop peritonitis, as oppose to localised right upper quadrant tenderness. Finally, an ileus would not causes right upper quadrant pain or bilious fluid in the drain.
2277
What is the gingko leaf sign?
Subcutaneous (surgical) emphysema which is a known complication of laparoscopic surgery. If the anterior chest wall is affected air can outline the pectoralis major muscle, giving rise to the 'ginkgo leaf' sign.
2278
You are asked to review a 65-year-old woman who has become breathless on the surgical ward. Earlier in the day she had a laparoscopic cholecystectomy for gallstone disease. A chest x-ray has already been obtained: ## Footnote © Image used on license from Radiopaedia What complication has developed? Pneumothorax Intestinal perforation resulting in pneumoperitneum Subcutaneous emphysema Pulmonary embolism Acute respiratory distress syndrome
This radiograph demonstrates subcutaneous (surgical) emphysema which is a known complication of laparoscopic surgery. If the anterior chest wall is affected air can outline the pectoralis major muscle, giving rise to the 'ginkgo leaf' sign.
2279
What are some complications of laparoscopy?
General risks of anaesthetic Vasovagal reaction e.g. bradycardia in response to abdominal distension Extra-peritoneal gas insufflation: surgical emphysema Trauma to GIT Injury to BVs: Common iliacs, deep IEA
2280
A 65-year-old man with a history of dyspepsia is found to have a gastric MALT lymphoma on biopsy. What treatment should be offered? ## Footnote Gastrectomy Laser ablation None CHOP chemotherapy H. pylori eradication
Overview associated with H. pylori infection in 95% of cases good prognosis if low grade then 80% respond to H. pylori eradication Features paraproteinaemia may be present
2281
A.Lymphoma B.Gastrinoma C.Insulinoma D.Glucagonoma E.Phaeochromocytoma F.Carcinoid syndrome G.Vasoactive Intestinal Peptide secreting tumour H.Pancreatic adenocarcinoma Please select the most likely diagnosis for the scenario given. Each option may be used once, more than once or not at all. A 65-year-old male attends surgical out patients with epigastric discomfort. He has recently been diagnosed with diabetes by the GP and is a heavy smoker. An OGD is normal. A 50-year-old male presents with recurrent episodes of abdominal pain and diarrhoea. Blood tests reveal mild iron deficiency anaemia and an upper GI endoscopy demonstrates multiple ulcers in the first part of the duodenum. An obese 40-year-old male presents with episodes of anxiety, confusion and one convulsive episode. CT brain is normal. An abdominal CT scan shows a small 1.5cm lesion in the head of the pancreas.
The dominant differential diagnosis should be of pancreatic adenocarcinoma in this setting. Glucagonomas are very rare and may be associated with a bullous rash. Diarrhoea, abdominal pain and multiple ulcers should raise the suspicion of Zollinger Ellison syndrome cause by gastrinoma. These episodes are due to hypoglycaemia. Insulinomas are normally solitary tumours and may not be seen by radiological imaging. Resection is the treatment of choice.
2282
Ix in pancreatic adenocarcinoma?
Investigation ## Footnote ultrasound has a sensitivity of around 60-90% high resolution CT scanning is the investigation of choice if the diagnosis is suspected
2283
What is purstcher retinopathy?
Purtscher retinopathy is a hemorrhagic and vasoocclusive vasculopathy, which, in 1912, was first described as a syndrome of sudden blindness associated with severe head trauma. These patients had findings of multiple white retinal patches and retinal hemorrhages that were associated with severe vision loss Since its original description, Purtscher retinopathy has been associated with traumatic injury, primarily blunt thoracic trauma and head trauma, and numerous nontraumatic diseases. Purtscher-like retinopathy is seen in diverse conditions, including acute pancreatitis; fat embolization; amniotic fluid embolization; preeclampsia; hemolysis, elevated liver enzymes, and low platelets (HELLP) syndrome; and vasculitic diseases, such as lupus.
2284
Characteristic fundus findings of Purtscher retinopathy. Multiple cotton-wool spots surround the optic nerve after blunt thoracic trauma.
2285
Tumour antigens: S-100
Melanoma Scwhwannomas
2286
Tumour antigen: Bombesin
SCLC Gastric cancer Neuroblastome
2287
A 45-year-old male with a history of heavy alcohol intake presents with acute onset epigastric pain radiating to the right side. On examination his sclera are yellow and his abdomen is tender in the right upper quadrant with localised guarding. Observations are: Heart rate 95/min, blood pressure 80/50 mmHg, saturation 99% on 2L, temperature 39.5ºC, Glasgow coma score 14/15 (confused speech). Which of the following diagnoses would explain this set of signs and symptoms? ## Footnote Cholecystitis Pancreatitis Gallbladder empyema Ascending cholangitis Perforated peptic ulcer
Reynolds Pentad (jaundice, right upper quadrant pain, fever/rigors, shock and altered mental status) is associated with ascending cholangitis. This patient would need adequate resuscitation before further investigation of biliary tree with USS/MRCP for common bile duct stones +/- ERCP.
2288
A 65-year-old lady is undergoing an OGD for investigation of dysphagia. She is known to have achalasia. A mass is seen in the middle third of the oesophagus. There is no other pathology identified past this point. What is the most likely type of cancer? Adenocarcinoma of the oesophagus Squamous cell carcinoma of the oesophagus MALT tumour Direct invasion from lung neoplasm Benign tumour of the oesophagus
Whilst Barrett's oesophagus increases the risk of oesophageal adenocarcinoma, achalasia increases the risk of squamous cell carcinoma of the oesophagus.
2289
Why is sensation over the thenar area spared in carpal tunnel syndrome?
Palmar cutaneous branch of the median nerve travels superficially to the flexor retinaculum
2290
Causes of carpal tunnel syndrome WRIST
F\>M 1o/ idiopathic 2o Water: pregnancy, hypothyroidism Radial: # Inflamation: RA/gout Soft tissue swelling: lipomas, acromegaly, amyloidosis Toxic: DM, EtOH
2291
Tingling/ pain in thumb, index and middle fingers Pain worse at night or after repetitive actions Relieved by shaking/ flicking Clumsiness
Carpal tunnel syndrome
2292
What are the signs of carpal tunnel syndrome
Reduced sensation over lateral 3.5 fingers Reduced 2 point touch discrimination: early sign of irreversible damage Wasting of thenar eminence: late sign of irreversible damage Phalen's Flexing Tinnel's Tapping
2293
Phalen's
The patient is asked to hold their wrist in complete and forced flexion (pushing the dorsal surfaces of both hands together) for 30–60 seconds. The lumbricals attach in part to the flexor digitorum profundus tendons. As the wrist flexes, the flexor digitorum profundus contracts in a proximal direction, drawing the lumbricals along with it. In some individuals, the lumbricals can be "dragged" into the carpal tunnel with flexor digitorum profundus contraction. As such, Phalen's maneuver can moderately increase the pressure in the carpal tunnel via this mass effect, pinching the median nerve between the proximal edge of the transverse carpal ligament and the anterior border of the distal end of the radius. By compressing the median nerve within the carpal tunnel, characteristic symptoms (such as burning, tingling or numb sensation over the thumb, index, middle and ring fingers) conveys a positive test result and suggests carpal tunnel syndrome. Because not all individuals will draw the lumbricals into the carpal tunnel with this maneuver, this test cannot be perfectly sensitive or specific for carpal tunnel syndrome
2294
Reverse Phalen's
This test is performed by having the patient maintain full wrist and finger extension for two minutes. The reverse Phalen's test significantly increases pressure in the carpal tunnel within 10 seconds of the change in wrist posture and the carpal tunnel pressure has the tendency to increase throughout the test's duration. In contrast, the change in carpal tunnel pressure noted in the standard Phalen's test is modest and plateaus after 20 to 30 seconds.
2295
Tinel's
Tinel's sign is a way to detect irritated nerves. It is performed by lightly tapping (percussing) over the nerve to elicit a sensation of tingling or "pins and needles" in the distribution of the nerve. It takes its name from French neurologist Jules Tinel (1879–1952).[1][2][3] For example, in carpal tunnel syndrome where the median nerve is compressed at the wrist, Tinel's sign is often "positive" causing tingling in the thumb, index, middle finger and the radial half of the fourth digit. Tinel's sign is sometimes referred to as "distal tingling on percussion" or DTP. This distal sign of regeneration can be expected during different stage of somatosensory recovery.[4] Although most frequently associated with carpal tunnel syndrome, Tinel's sign is a generalized term, and can also be positive in tarsal tunnel syndrome, or in ulnar nerve impingement at the wrist (Guyon's canal syndrome), where it affects the other (ulnar) half of the fourth digit and the fifth digit.
2296
Ix in carpal tunnel syndrome
Not usually performed Nerve conduction studies USS
2297
Mx of carpal tunnel
Conservative: Mx of underlying cause Wrist splints: neutral position, especially at night Medical: Local steroid injections Surgical: Carpal tunnel decompression by division of the flexor retinacuum
2298
Cx of carpal tunnel Sx
Scar formation: high risk for hypertrophied or keloid Scar tenderness: up to 40% Nerve injury: palmar cutaneous branch of the median nerve; motor branch to the thenar muscles Failure to relieve symptoms
2299
What are some other locations of median nerve entrapment?
Pronator syndrome Anterior interossesous syndrome
2300
What is pronator syndrome
Entrapment of the median nerve between two heads of pronator teres
2301
What is anterior interosseus syndrome?
Compression of the anterior interosseous branch of the median nerve by deep head of pronator teres Muscle weakness only: pronator quadratus, FPL, radial half of FDP
2302
Def: Dupuytren's contracture
Progressive, painless fibrotic thickening of palmar fascia
2303
Patient in Dupuytren's
M\>F Middle age/elderly Skin puckering and tethering Fixed flexion contracture of ring and little fingers. Often bilateral and symmetrical MCP and IP joint flexion
2304
Dupuytren's conracture
2305
Associations of Dupuytren's BAD FIBERS
Bent penis: Peyronies AIDS DM FH: D Idiopathic: commonest Booze: ALD Epilepsy (+ epilepsy meds- phenytoin) Reidel's thyroiditis and other fibromatoses e.g. Ledderhose disease, Retroperitoneal fibrosis Smoking
2306
Peyronie's
Peyronie's disease or Peyronie disease (/peɪroʊˈniː/), also known as induratio penis plastica (IPP)[1] or chronic inflammation of the tunica albuginea (CITA), is a connective tissue disorder involving the growth of fibrous plaques[2] in the soft tissue of the penis affecting an estimated 5% of men.[3] Specifically, scar tissue forms in the tunica albuginea, the thick sheath of tissue surrounding the corpora cavernosa causing pain, abnormal curvature, erectile dysfunction, indentation, loss of girth and shortening.[4][5][6][7] A variety of treatments have been used, but none have been especially effective.
2307
Ledderhose disease
Plantar fascial fibromatosis, also known as Ledderhose's disease, Morbus Ledderhose, and plantar fibromatosis, is a relatively uncommon[1] non-malignant thickening of the feet's deep connective tissue, or fascia. In the beginning, where nodules or cords start growing along tendons of the foot[citation needed], the disease is minor. Eventually, however, the cords thicken, the toes stiffen and bend, and walking becomes painful. The disease is named after Dr. Georg Ledderhose, a German surgeon who described the condition for the first time in 1894.[2][3] A similar disease is Dupuytren's disease, which affects the hand and causes bent hand or fingers.
2308
Mx of Dupuytren's
Conservative: PT/ exercise Fasciectomy: e.g. when hand can't be placed flat on table Z-shaped scars prevent contracture However can damage ulnar nerve, usually recurs
2309
DDx for Dupuytren's
Skin contracture: old laceration or burn Tendon fibrosis, trigger finger Ulnar N palsy
2310
Trigger finger features
Tendon nodule which catches on proximal side of tendon sheath-\> triggering on forced extension-\> fixed flexion deformity Usually ring and middle fingers Associated with RA Rx: steroid injection or sx
2311
Def: ganglion
Smooth multilocular cystic swellings Mucoid degeneration of joint capsule or tendon sheath May be in communication with joint capsules/tendons
2312
90% located on dorsum of wrist Subdermal, fixed to deeper structures Limits plane of movement May cause pain or nerve pressure symptoms
Ganglion
2313
Mx of ganglion
50% disappear spontaneously Aspiration +/- steroid and hyaluronidase injection Sx excision
2314
DDx for ganglion
Lipoma Fibroma Sebaceous cyst
2315
Ganglion
2316
Entrapment of lat cutaneous nerve of thigh beetween ASIS and inguinal ligament Pain +/- paraesthesia on lateral thigh No motor deficit Increased risk with obesity Can occasionally be damaged during lap hernia repair
Meralgia paraesthetica
2317
Predominantly young women Patellar aching after prolonged sitting or climbing stairs Pain on patellofemoral compression Ix: no abnormality on X ray Rx: vastus medialis strengthening
Chondromalacia patellae
2318
Popliteal swelling arising between the medial head of gastrocnemius and semimebranosus muscle Herniation from joint synovium Usually 2o to OA Rupture: acute calf pain and swelling (NB ?DVT)
Baker's cyst
2319
Clarke's test
In medicine, Clarke's test is a component of knee examination which may be used to test for patellofemoral pain syndrome, or anterior knee pain. It is not a standard part of the knee examination but is used to diagnose anterior knee pain where the history indicates this as the likely pathology. The patient is asked to actively contract the quadriceps muscle while the examiner's hand exerts pressure on the superior pole of the patella, so trying to prevent the proximal movement of the patella. While it can produce some discomfort even in normal people, the reproduction of the symptoms suggest pain of patello-femoral origin.[1]
2320
Baker's cyst
2321
Great toes deviates laterally at MTP joint Pressure of MTP against shoe-\> bunion Increased weight bearing at 2nd metatarsal head: transfer metatarsalgia, hammer toe Aetiology: pointed shoes Wearing high heels Mx: Conservative: Bunion pads, plast wedge between great and second toes Metatarsal osteotomy
Hallux valgus
2322
2323
Hallux valgus
2324
Pain from pressure on an interdigital neuroma between the metatarsals Pain radiates to medial side of one toe and lateral side of another
Morton's metatarsalgia/Neuroma
2325
A runner presents with heel pain. On examination, there is diffuse tenderness which is worse 2cm distal to the medial calcaneal tuberosity. Although the patient has stopped running for the past week, pain is worse when they walk on their toes and when they are on their feet for a long period at work. What is the most likely diagnosis? Achilles tendonitis Plantar fasciitis S1 radiculopathy Morton's neuroma Subcalcaneal bursitis
This is typical of plantar fasciitis which is the most common cause of heel pain in adults. Pain in Achilles tendonitis is at the calcaneal insertion of the tendon or further up the tendon depending on the area affected. Thompson's test excludes rupture of the tendon. S1 radiculopathy would cause sensory loss along the lateral aspect of the foot and may lead to reduced dorsiflexion of the foot. Morton's neuroma is a thickening of the tissue around the nerve usually between the 3rd and 4th toes. Pain tends to be on the ball of the foot. Subcalcaneal bursitis presents with pain at the point of Achilles tendon insertion, and on the back and bottom of the heal. Plantar fasciitis is more common and would give the specific area of tenderness mentioned.
2326
Thompson test (aka Simmonds)
The Thompson test is diagnostic for a complete tear of the Achilles tendon. The Thompson Test: When the tendon is intact, and the calf is squeezed, the ankle will plantar flex . The test is positive when the right ankle doesn't plantar flex when the calf is squeezed,
2327
What is the most common cause of heel pain in adults?
Plantar fasciitis Pain usually worse around the medial calcaneal tuberosity Mx: Rest feet where possible Wear shoes with good arch support and cushioned heels Insoles and heel pads may be helpful
2328
A 28-year-old male presents to the emergency room with severe pain in the right knee following an injury during a football match. He states that he was tackled from behind, and then felt a 'pop' and severe pain which was followed by rapid swelling of the joint. On examination there is a right sided knee effusion and a positive Lachman test. What is the most likely diagnosis? Medial collateral ligament (MCL) rupture Lateral collateral ligament (LCL) rupture Anterior cruciate ligament (ACL) rupture Posterior cruciate ligament (PCL) rupture Meniscal tear
Rapid joint swelling is suggestive of haemoarthrosis which can occur due to ACL or PCL rupture. The mechanism of injury suggests rupture of the ACL. A positive Lachman tests is also very suggestive of an ACL injury. An LCL injury most commonly occurs due to direct blows to the medial aspect of the leg which puts strain on the LCL ligament. The classical symptoms would be a slow developing joint effusion and lateral joint line tenderness. Similarly, an MCL injury most commonly occurs due to direct blows to the lateral aspect of the leg which results in strain on the MCL ligament. The classical symptoms would be a slow developing joint effusion and medial joint line tenderness. Meniscal tears often occur due to twisting injuries. They are associated with delayed knee swelling and joint locking.
2329
A 33-year-old woman presents with back pain which radiates down her right leg. This came on suddenly when she was bending down to pick up her child. On examination straight leg raising is limited to 30 degrees on the right hand side due to shooting pains down her leg. Sensation is reduced on the dorsum of the right foot, particularly around the big toe and foot dorsiflexion is also weak. The ankle and knee reflexes appear intact. A diagnosis of disc prolapse is suspected. Which nerve root is most likely to be affected? L2 L3 L4 L5 S1
L5 lesion features = loss of foot dorsiflexion + sensory loss dorsum of the foot
2330
A 75-year-old lady presents to the emergency room after falling onto her left elbow. She has marked bruising and tenderness of the left upper arm. On examination, you note a left wrist drop. What is the most likely injury? Fracture of the proximal humerus Supracondylar fracture of humerus Colle's fracture Smith's fracture Fracture of the shaft of the humerus
This example describes an injury of the humerus with associated radial nerve damage. The radial nerve is most susceptible to damage from a fracture of the shaft of the humerus. Supracondylar fracture of humerus is most commonly associated with ulnar nerve damage. Fracture of the proximal humerus is most commonly associated with axillary nerve damage. Colle's fracture and Smith's fracture are fractures of the distal radius. These fractures are not in keeping with the upper limb examination findings.
2331
Mx of talipes equinovarus
ponseti method: manipulation and progressive casting starting sooon after birth (6-10w). Achilles tenotomy required in around 85% of cases Night-time braces applied until child is 4 years old
2332
Sensory loss over anterior thigh Weak quadriceps Reduced knee reflex Positive femoral stretch test
L3 nerve root compression
2333
Sensory loss anterior aspect of knee Weak quadriceps Reduced knee reflex Positive femoral stretch test
L4 nerve root compression
2334
Sensory loss dorsum of foot Weakness in foot and big toe dorsiflexion Reflexes intact Positive sciatic nerve stretch test
L5 nerve root compression
2335
Sensory loss posterolateral aspect of leg and lateral aspect of foot Weakness in plantar flexion of foot Reduced ankle reflex Positive sciatic nerve stretch test
S1 nerve root compression
2336
Femoral nerve stretch tset
Femoral nerve stretch test (Mackiewicz sign[1]) - for the FNST the patient lies prone, the knee is passively flexed to the thigh and the hip is passively extended; the test is positive if the patient experiences anterior thigh pain. This test is usually strongly positive in patients with protrusions at L2–L3 and L3–L4, slightly positive or negative in L4–L5 disc protrusions and negative in cases with a lumbosacral protrusion.
2337
Sciatic nerve stretch test
The therapist raises the leg, keeping the knee straight. The therapist moves the ankle into a dorsiflexed position which lengthens the nerve. If there are no neural symptoms (tingling, shooting pain or tight, restricted feeling throughout the back of the leg), then the therapist may ask the patient to raise the head to further increase the stretch.
2338
A 47-year-old female presents as she is concerned about elbow pain. She has just spent the weekend painting the house. On examination there is localised pain around the lateral epicondyle and a diagnosis of lateral epicondylitis is suspected. Which one of the following movements would characteristically worsen the pain? Resisted thumb flexion Thumb extension Flexion of the elbow Pronation of the forearm with the elbow flexed Resisted wrist extension with the elbow extended
Lateral epicondylitis: worse on resisted wrist extension/supination whilst elbow extended
2339
A 5-year-old boy is seen in the Minor Injury Unit after falling in the playground. His mother observed the fall and describes him falling on an outstretched hand. The x-ray is shown below ## Footnote © Image used on license from Radiopaedia What which one of the following best describes this injury? Colles' fracture Salter-Harris type 1 fracture Salter-Harris type 2 fracture Buckle fracture Greenstick fracture
Buckle, or torus, fractures are incomplete fractures of the shaft of a long bone that is characterised by bulging of the cortex. They typically occur in children aged 5-10 years. As they are typically self-limiting they do not usually require operative intervention and can sometimes be managed with splinting and immobilisation rather than a cast.
2340
Def: talipes equinovarus
Inverted and plantar flexed foot Usually diagosed on newborn exam M \> F 2:1 1:1000 births Idiopathic most commonly Associated with spina bifida, cerebal palsy, Edward's, oligohydramnios, arthrogryposis
2341
Hip pain in adults A.Inflammatory arthritis B.Trochanteric bursitis C.Pubic symphysis dysfunction D.Osteoarthritis E.Meralgia paraesthetica F.Avascular necrosis G.Transient idiopathic osteoporosis H.Referred lumbar spine pain I.Perthes' disease J.Slipped upper femoral epiphysis For each one of the following scenarios please select the most likely diagnosis: A 43-year-old woman complains of right hip pain. During the examination the patient lies on her left side and the right hip is extended with a straight leg. Flexing the knee then recreates the pain
This is a femoral nerve stretch test
2342
A 50-year-old woman presents with pain in the right forefoot for the past three months. The pain is worse around the third inter-metatarsophalangeal space and is described as a burning which is brought on by walking. There is no history of trauma and the patient does not do any regular exercise. Her alcohol intake is 28 units per week. On examination she complains of tenderness in the middle of the forefoot and her symptoms are recreated by squeezing the metatarsals together. What is the most likely diagnosis? Metatarsal stress fracture Gout Alcohol-related peripheral neuropathy Plantar fasciitis Morton's neuroma
Morton's neuroma
2343
forefoot pain, most commonly in the third inter-metatarsophalangeal space worse on walking. May be described as a shooting or burning pain. Patients may feel they have a pebble in their shoe Mulder's click: one hand tries to hold the neuroma between the finger and thumb. The other hand squeezes the metatarsals together. A click may be heard as the neuroma moves between the metatarsal heads there may be loss of sensation distally in the toes
Morton's neuroma
2344
Body composition of 70kg man Proprotion intracellular Proprotion extracellular Components and volumes of extracellular?
Total water: 60% of 70kg= 42l 2/3rds intracellular: 28l 1/3rd extracellular: 14l Plasma 3l Interstitial 10l Transcellular 1l
2345
What are Starling's forces?
Osmotic pressure Hydrostatic pressure
2346
Def: osmotic pressure?
Pressure which needs to be applied to prevent the inflow of water across a semipermeable membrane i.e. the ability of a solute to attract water Oncotic pressure: form of osmotic pressure exerted by proteins
2347
Def: Hydrostatic pressure
Pressure exerted by a fluid at equilibrium due to the force of gravity
2348
What drives the distribution of fluid between the ECF and ICF?
Driven by differences in osmotic pressure only
2349
What determines the distribution of fluid within the ECF?
Determined by Starling's forces: capillary and interstitial oncotic pressure capillary and interstitial hydrostatic pressure Filtration coefficient (capillary permeability)
2350
Starling equation for fluid
The four Starling’s forces are: hydrostatic pressure in the capillary (Pc) hydrostatic pressure in the interstitium (Pi) oncotic pressure in the capillary (pc ) oncotic pressure in the interstitium (pi ) The balance of these forces allows calculation of the net driving pressure for filtration. Net Driving Pressure = [( Pc - Pi ) - ( pc - pi )]
2351
3rd space losses lead to?
Reduction in ECF e.g. bowel obstruction-\> reduced fluid reabsorption-\> 3rd space loss Peritonitis-\> ascites-\> 3rd space loss
2352
Daily fluid input/output?
40ml/kg/d
2353
What is minimum urine output?
0.5ml/kg/h ~30ml/h
2354
Na requirement?
1.5-2 mmol/kg/d= 100mmol/d
2355
K requirement
1mmol/kg/d= 60mmol/d
2356
Daily requirement- fluid regimens? Normal
3L dex-saline with 20mM K in each bag (i.e. Hartmann's) or 1l NS + 2l dex with 20mM K in each bag Each bag over 8h= 125ml/hr
2357
What other losses need to be replaced in fluid homeostasis?
Vomiting and diarrhoea NGT Drains Fever (+500ml for each oC) Tachypnoea High-output stomas
2358
What does CVP indicate?
RV preload and depends on venous return and CO
2359
Raised CVP seen in?
Increased circualting volume Reduced CO i.e. pump failure
2360
Reduced CVP seen in?
Reduced circulating volume
2361
Normal CVP
5-10 cm H2O
2362
Considerations regarding CVP readings
Single reading is not as useful as serial measurements before and after fluid challenge Unchanged- hypovolaemic Increase that reverses after 30 mins: euvolaemic Sustained raise \>5cm: overload/failure Passive leg raising may be more useful than fluid challenge in determining the response to fluids. Sustained increase in CVP suggests heart failure
2363
Types of Crystalloid
NS 5% dextrose Dextrose-Saline Hartmann's
2364
Features of NS
0.9% NaCL= 9g/L 15mM NaCL pH: 5-6 Use normal daily fluid requirements + replace losses
2365
Features of 5% dextrose
Contains 50g dextrose/l Used for normal daily fluid requirements
2366
Features of dextrose-saline
Contains 4% dextrose= 4-g/l 0.18% NaCl= 31mM Used for normal daily fluid requirements
2367
Contents of Hartmann's/Ringer's lactate
Na 131mM Cl: 111mM K: 5mM Ca 2.2mM Lactate/HCO3: 29mM
2368
Uses of Hartmann's / Ringer's lactate
Resuscitation in trauma patients Maintenance
2369
What is the Parkland Formula
The Parkland formula is a burn formula used to estimate the amount of replacement fluid required for the first 24 hours in a burn patient so as to ensure they remain hemodynamically stable.[1] The milliliter amount of fluid required for the first 24 hours -usually Ringer's lactate- is four times the product of the body weight and the burn percentage (i.e. body surface area affected by burns).[2] The first half of the fluid is given within 8 hours from the burn incident, and the remaining over next 16 hours. Only area covered by second-degree burns or greater is taken into consideration, as first-degree burns do not cause hemodynamically significant fluid shift to warrant fluid replacement.[3] The Parkland formula is mathematically expressed as:[2] V = 4 ⋅ m ⋅ ( A ⋅ 100 ) {\displaystyle V=4\cdot m\cdot (A\cdot 100)} where mass is in kilograms (kg), area as a percentage of total body surface area, and volume is in milliliters (mL). For example, a person weighing 75 kg with burns to 20% of his or her body surface area would require 4 x 75 x 20 = 6,000 mL of fluid replacement within 24 hours. The first half of this amount is delivered within 8 hours from the burn incident, and the remaining fluid is delivered in the next 16 hours.[4]
2370
pH of Hartmann's
pH=6.5 but Harmann's is an alkalinising solution Lactate is not an acid in itself it's a conjugate base Lactate metabolised in liver -\> HCO3 production
2371
Problems with crystalloid fluids
Give 1l NS-\> 210ml remaining IV Give 1L D5W-\> 70ml remaining IV Acidosis or electrolyte disturbances Fluid overload
2372
What are colloids?
Contain large molecular weight molecules e.g. gelatin, dextrans Idea is to preserve oncotic pressure and thus remain intravascular
2373
Give examples of colloid and categories
Synthetic: Gelofusin Volpex Haemaccel Voluven Natural: Albumin Blood
2374
Problems with colloid
Can interfere with cross-matching therefore take blood for cross matching before using Anaphylaxis Volume overload
2375
How to assess fluid status
Hx: balance chart, surgery, other losses, thirsty Impression: drowsy, alert Inspect: drips, drains, stomas, catheter Examination
2376
What components of hydration can be assessed through examination?
IV volume Tissue perfusion End-organ perfusion
2377
Indicators of IV volume
CRT HR BP lying and standing JVP
2378
Indicators of tissue perfusion
Skin turgor Oedema: ankle, pulmonary, ascites Mucus membranes
2379
Indicators of end-organ perfusion
UO, raised U + Cr Consciousness Lactate
2380
Other tests to assess fluid status
PCWP CVP
2381
What is PCWP
The pulmonary wedge pressure or PWP, or cross-sectional pressure (also called the pulmonary arterial wedge pressure or PAWP, pulmonary capillary wedge pressure or PCWP, pulmonary venous wedge pressure or PVWP, or pulmonary artery occlusion pressure or PAOP), is the pressure measured by wedging a pulmonary catheter with an inflated balloon into a small pulmonary arterial branch.[1] Physiologically, distinctions can be drawn among pulmonary artery pressure, pulmonary capillary wedge pressure, pulmonary venous pressure and left atrial pressure, but not all of these can be measured in a clinical context.[2] Noninvasive estimation techniques have been proposed. Essentially an indirect measure of left atrial pressure
2382
What are the issues with post-operative fluids
Raised ADH, raised aldosterone, raised cortisol-\> Na and H2O conservation Increased K: tissue damage, transfusion, stress hormones
2383
Solutions to issues with post-operative fluids?
Use UO (aim \>30ml/h) to guide fluid replacement, may need to reduce maintenance fluids to 2l for first 24h post op Avoid K supplementation for first 24h post op
2384
What is the problem with fluids in cardiac/renal failure? And the solution
RAS activation-\> Na and H2O retention Avoid fluids with Na-\> 5% dextrose
2385
Issue with fluids in bowel obstruction
Patients have significant third space losses of both water and electrolytes Likely to need significantly more than standard daily requirments
2386
Fluid regimen in bowel obstruction
0.9% NS with 20-40mm KCL added to each bag Titrate rate of fluid therapy to clinical findings on serial examination Serial U+Es guide electrolyte replacement
2387
Fluids in pancreatitis
Inflammation- significant fluid shift into the abdomen Patients require aggressive fluid resuscitiation and maintenance Inser urinary catheter and consider CVP monitoring 0.9% NS with 20-40mm KCL Keep UO \>30 Serial U+Es guide electrolyte replacement
2388
Ileal fluid composition
Na: 130mM Cl: 110mM K: 10mM HCO3: 30mM Normal output: 10-15ml/Kg/d= 700ml/d High output= 1000ml/d Ileum will adapt to limit fluid and electrolyte losses
2389
Fluids in ileostomy
0.9% saline and KCl Daily requirements + replace losses titrated to UO Serial U+Es guide electrolyte replacement
2390
High output ileostomy
\>1000ml/d
2391
Rx treatment of high output ileostomy
Antimotility: loperamide, codeine phosphate Antisecretory: omeprazole
2392
Causes of reduced UO post-op
Post-renal: Commonest cause, blocked/malsited catheter or acute urinary retention Pre-renal: hypovolaemia Renal: NSAIDs, gentamicin Anuria normally= blocked or malsited catheter Oliguria: inadeqauate fluid replacement
2393
Mx of reduced UO post op
Collect info: Op Hx, Obs chart, drug chart Examine patient: fluid status, palpable bladder, inspect drips, drains etc. Action: flush with 50mL NS, fluid challenge
2394
Def: refeeding syndrome
Life-threatening metabolic complication of refeeding via any route after prolonged period of starvation
2395
Pathophysiology of refeeding syndrome
Reduced carbs-\> catabolic state, reduced insulin, fat and protein catabolism and depletion of intracellular PO4 Refeeding: increased insuin in response to carbs and increased cellular PO4 uptake Result is hypophosphataemia which can lead to: rhabdo respiratory insufficiency arrhythmias shock seizures
2396
Ions deranged in Refeeding Consultancy company
KPMG (all reduced)
2397
Patients at risk of refeeding syndrome
Malignancy AN Alcoholism GI surgery Starvation
2398
Prevention of refeeding syndrome
Identify and monitor at-risk patients Liaise with dietician
2399
Rx of refeeding syndrome
Identify at risk patients in advance Parenteral and oral PO4 supplementation Rx complications
2400
How to assess Nutrition
Clinically: Hx: weight loss, diet Examination: skin fat, dry hair, pressure sores, chelitis, Weight and BMI (\<20) Anthropometric Skin-fold thickness Arm circumference Ix Albumin Transthyretin (prealbumin) Phosphate
2401
Daily nutritional requirements
per kg: 20-40kCal Carbs: 2g Fat: 3g Protein 0.5-1g Nitrogen: 0.2-0.4g
2402
Delivery of enteral nutrition
PO is best, consider semi-solid diet if risk of aspiration Other options include NGT PEG Jejunostomy Build up feeds gradually to prevent diarrhoea
2403
PEG tube
2404
jejunostomy feeding
2405
Feed options for enteral nutrition
Oral supplements Polymeric e.g. osmolite, jevity. Intact proteins, starches and long chain FAs Disease specific: e.g. redcued branch chain AAs in hepatic encephalopathy Elemental e.g. simple AAs and oligo/monosaccharides, require minimal digestion and used if abormal GIT e.g. in Crohn's
2406
indications for enteral nutrition
Catabolic: sepsis, burns, major Sx Coma/ITU Malnutrition Dysphagia: stricture, stroke
2407
Cx of NGT
Nasal trauma Malposition or tube blockage
2408
Cx of feeding
Feed intolerance-\> diarrhoea Electrolyte imbalance Aspiration Refeeding syndrome
2409
Parenteral nutrition
May be total or used to supplement enteral feeding Combined with H2O to deliver total daily requirements
2410
Indications for(T)PN
Prolonged obstruction or ileus (\>7d) High output fistula Short bowel syndrome Severe Crohn's Severe malnutrition Severe pancreatitis Unable to swallow e.g. oesophageal Ca
2411
Delivery of TPN
Delivered centrally as high osmolality is toxic to veins ST: CV catheter LT: Hickmann or PICC line Sterility is essential, use line only for PN
2412
Monitoring of parenteral nutrition
Standard: weight, fluid balance and urine glucose daily. Zn, MG weekly Initially: blood glucose, FBC, U+E, PO4 daily. LFTs 3/w Once stable: blood glucose, FBC, U+E +PO4, 3/w LFTs weekly
2413
Contents of TPN
2000kCal: 50% fat, 50% carbs 10-14g nitrogen Vitamins, minerals and trace elements
2414
Cx of TPN
Line related: Pneumothorax/haemothorax Cardiac arrythmia Line sepsis Central venous thrombosis: PE or SVCO Feed-related: Villous atrophy of GIT Electrolyte disturbance: refeeding syndrome, hypercapnea from excessive CO2 production Hyperglycaemia and reactive hypoglycaemia Line sepsis: increased risk with TPN Vitamin and mineral deficiencies Liver disease: Fatty liver is usually a more long term complication of TPN, though over a long enough course it is fairly common. The pathogenesis is due to using linoleic acid (an omega-6 fatty acid component of soybean oil) as a major source of calories.[10][11] TPN-associated liver disease strikes up to 50% of patients within 5–7 years, correlated with a mortality rate of 2–50%. Onset of this liver disease is the major complication that leads TPN patients to requiring an intestinal transplant
2415
2416
2417
2418
Where is the facet for attachment of PCL?
Facet for attachment of the posterior cruciate ligament – Found on the medial wall of the intercondylar fossa, it is a large rounded flat face, where the posterior cruciate ligament of the knee attaches
2419
Facet for attachment of anterior cruciate ligament
Found on the lateral wall of the intercondylar fossa, it is smaller than the facet on the medial wall, and is where the anterior cruciate ligament of the knee attaches.
2420
2421
2422
2423
Where is the common peroneal nerve found on the fibula?
Proximal end On the posterolateral surface
2424
What are the proximal tarsal bones?
Talus and calcaneus
2425
What is the main function of the talus?
Transmit forces from the tibia to calcaneus
2426
What are the intermediate tarsal bones?
Navicular: articulates with the talus posteriorly, the cuneiform bones anteriorly and the cuboid bone laterally. Attachment on plantar surface for the attachment of tibialis posterior
2427
What are the distal group of tarsal bones?
Cuboid and three cuneiforms
2428
2429
What are the stabilising factors at the hip joint?
Acetabulum Fibrocartilaginous collar Iliofemoral, pubofemoral and ischiofemoral ligaments also provide a degree of stability
2430
What are the movements that can be carried out at the hip joint?
Flexion Extension Abduction Adduction Lateral rotation Medial rotation
2431
What determines the degree of flexion at the hip joint?
Knee flexion, knee flexion relaxes the hamstring muscles and increases the range of flexion
2432
Hilton's law
Hilton's law, espoused by John Hilton in a series of medical lectures given in 1860–1862,[1] is the observation that in the study of anatomy, the nerve supplying the muscles extending directly across and acting at a given joint also innervate the joint.[2] For example, the musculocutaneous nerve supplies the elbow joint of humans with pain and proprioception fibres. It also supplies coracobrachialis, biceps brachii, brachialis, and the forearm skin close to the insertion of each of those muscles.
2433
What are the movements that can take place at the knee joint?
Extension Flexion Lateral rotation Medial rotation
2434
Why is the lateral ligament more likely to be sprained at the ankle?
Lateral ligament is weaker than medial ligament Lateral ligament resists inversion
2435
What is a Pott's fracture?
Term used to describe a bimalleolar or trimalleolar fracture ## Footnote Forced eversion pulls on the medial ligaments, producing an avulsion fracture of the medial malleolus. The talus moves laterally, breaking off the lateral malleolus. The tibia is then forced anteriorly, shearing off the distal and posterior part against the talus.
2436
Pott's (trimalleolar fracture)
2437
Primary survery in trauma
Address problems in 1o survey in ABCDE order
2438
1o survey Airway
Check for airway compromsie: Ask pt question Stridor Orofacial inury or burns Visualise airway and use suction if necessar Manoeuvres to open airway: Jaw thrust Adjuncts if compromsie/potential compromised NPA: gag reflex present OPA: no gag refelex (stop tongue swallowing) Emergency airways: Needle circothyroidotomy or surgical cric Definitive airways: no risk of aspiration ETT Tracheostomy
2439
1o survery: C spine
Maintain in-line cervical support to keep neck stable Place pt in hard collar and sandbags with tape
2440
1o survery Breathing
Start 15l O2 via non-rebreathe mask (Hudson) Inspection of chest RR and chest expansion Position of trachea Breath sounds, vocal resonance Perucssion ABG
2441
Respiratory distress Raised JVP and reduced BP Tracheal deviation and displaced apex Reduced air entry and reduced vocal resonance Hyper-resonant to percussion
Tension pneumothorax
2442
Rx: tension pneumothorax
Insert large bore venflon into 2nd ICS MCL Insert ICD later
2443
Mx of open sucking chest wounds
Convert to closed wounds by covering with damp occlusive dressing stuck down on both sides
2444
1o survery: Circulation
Two large bore cannulae: 14G/16G in each ACF FBC, U+E, X-match (6U), clotting, VBG Assess: Inspection: pale, sweaty, active bleeding Vascular status: BP, HR, JVP, heart sounds, cardiac monitoring End-orgna: consciousness, UO Sites of haemorrhage: CAP: use pelvic binder Floor Mx: if haemodynamic compromsie give 2l warm Hartmann's stat Consider further colloid/blood Inesrt CVP and catheter (after PR) to guide resus
2445
How to assess response to fluids
Use UO, lactate, BP
2446
Rapid respsonse to fluid resus?
Usually \<20% loss Slow fluid response to maintenance if haemodynamically stable
2447
Transient response to fluid resus
20-40% loss On-going losses or inadequate resus
2448
No response to fluid resus
Exsanguinating haemorrhage-\> theatre Consider non-haemorrhagic shock: tamponade, pnuemothorax
2449
Assessing disability
AVPU or GCS PEARL
2450
Exposure Assessment
Completely undress patient Perform leg roll and PR: feel for high riding prostate (urethral rupture) Look for bleeding Prevent hypothermia
2451
At end of primary survery?
Repate primary survery again
2452
2o survery: Hx
Allergies Medications PMHx Last ate/ drunk Events
2453
Examination in 2o survery
Head to toe Examine every system
2454
Ix in 2o survery
Trauma series: C spine: lat and peg CXR Pelvis FAST (focusseed assessment with sonogrpahy in trauma) CT: when patient is stable
2455
Assessing C-spine radiographs: views
Lateral AP Open-mouth Peg view
2456
For adequacy of C-spine assessment
Need C7-T1 junction visualised May need swimmer's view with abducted arm
2457
What are the 4 lines of alignment to assess in C-spine
Anterior vertebral bodies Anterior vertebral canal Posterior vertebral canal Tips of spinous processes
2458
Assessment of bones in C-spine radiograph
Shapes of bodies Laminae Processes
2459
Assessment of cartilage in c-spine
IV discs should be equal height
2460
Assesment of C-spine radiograph: soft tissue
Width of soft tissue shadow anterior to upper vertebrae should be 50% of vertebral width
2461
C-spine assessment- systematic: lateral
C-spine systematic approach - Normal Lateral 1 Coverage - All vertebrae are visible from the skull base to the top of T2 (T1 is considered adequate) - If T1 is not visible then a repeat image with the patient's shoulders lowered or a 'swimmer's' view may be necessary Alignment - Check the Anterior line (the line of the anterior longitudinal ligament), the Posterior line (the line of the posterior longitudinal ligament), and the Spinolaminar line (the line formed by the anterior edge of the spinous processes - extends from inner edge of skull) - GREEN = Anterior line - ORANGE = Posterior line - RED = Spinolaminar line Bone - Trace the cortical outline of all the bones to check for fractures Note: The spinal cord (not visible) lies between the posterior and spinolaminar lines
2462
-spine systematic approach - Normal Lateral 2 Disc spaces - The vertebral bodies are spaced apart by the intervertebral discs - not directly visible with X-rays. These spaces should be approximately equal in height Pre-vertebral soft tissue - Some fractures cause widening of the pre-vertebral soft tissue due to pre-vertebral haematoma - Normal pre-vertebral soft tissue (asterisks) - narrow down to C4 and wider below - Above C4 ≤ 1/3rd vertebral body width - Below C4 ≤ 100% vertebral body width Note: Not all C-spine fractures are accompanied by pre-vertebral haematoma - lack of pre-vertebral soft tissue thickening should NOT be taken as reassuring Edge of image - Check other visible structures
2463
C spine systmatic assessment AP
C-spine systematic approach - Normal AP Coverage - The AP view should cover the whole C-spine and the upper thoracic spine Alignment - The lateral edges of the C-spine are aligned (red lines ) Bone - Fractures are often less clearly visible on this view than on the lateral Spacing - The spinous processes (orange) are in a straight line and spaced approximately evenly Soft tissues - Check for surgical emphysema Edges of image - Check for injury to the upper ribs and the lung apices for pneumothorax
2464
C-spine assessment odontoid peg
C-spine normal anatomy - Open mouth view This view is considered adequate if it shows the alignment of the lateral processes of C1 and C2 (red circles) The distance between the peg and the lateral masses of C1 (asterisks) should be equal on each side Note: In this image the odontoid peg is fully visible which is not often achievable in the context of trauma due to difficulty in patient positioning
2465
C2 odontoid peg fracture - Lateral view The C2 bone 'ring' is incomplete due to a fracture The odontoid peg is displaced posteriorly
2466
C2 'hangman' fracture - Lateral view Loss of alignment at C2/C3 with anterior displacement of C2 (large arrow) Following the cortical outline of C2 (white line) reveals discontinuity due to a fracture
2467
Bilateral perched facets - Lateral view (Same patient as image below) Loss of alignment of all three lines at C5/C6 with 'perching' of the C5 facet on the C6 facet (ring) No fracture is visible The pre-vertebral soft tissue is widened due to a haematoma Bilateral perched facets - AP view (Same patient as image above) There is widening of space between the C5 and C6 spinous processes (SP) with loss of normal alignment Again no fracture is demonstrated Note The spinal canal lies between the posterior (Orange) and spinolaminar (Red) lines Derangement of the spinal canal due to this injury results in a high incidence of spinal cord injury
2468
Clinical clearance for C-spine injury crieria
NEXUS criteria
2469
NEXUS Criteria
Focal neurologic deficit Midline spinal tenderness Altered level of consciousness Intoxication present Distracting injury If no to all of the above, C-spine can be cleared clinically
2470
Method for clinical clearance of c-spine
Examine for brusing or deformity Palpate for deformity and tenderness Ensure pain-free active movement
2471
Indications for radiological C-spine clearance
Patient doesn't meet criteria for clinical clearance
2472
Radiographical C-spine clearance
Radiograph initially: clear if normal radiograph and clinical exam CT C-spine if abnormal radiograph or clinical exam
2473
How can haemorrhagic shock be classified?
By degree of blood loss There is a correlation clinically between volume loss and clinical manifestation
2474
What proportion of body mass is circulating blood volume?
7%
2475
Classes of haemorrhagic shock
1: 0-15% loss: 750ml 2: 15-30% loss 750-1500ml 3: 30-40% loss 1500-2000,l 4: \>40% loss \>2000ml
2476
Haemorrhagic shock, what grade? RR normal HR normal BP normal UO normal Mental Normal
1: 0-15%
2477
Haemorrhagic shock, what grade? RR \>20 HR \>100 BP normal UO \<30 Anxious ++
2 15-30%
2478
Haemorrhagic shock, what grade? RR \>30 HR \>20 BP reduced UO 5-20 Confused
3 30-40%
2479
Haemorrhagic shock, what grade? RR \>35 HR \>140 BP reduced ++ UO \<5 Lethargic
4 \>40%
2480
Def: neurogenic shock
Disruption of symapthetic nervous system
2481
Causes of neurogenic shock
Spinal anaesthesia Hypoglycaemia Cord inury above T5 Closed head injuries
2482
Presentation of neurogenic shock
Hypotension Bradycardia Warm extremities
2483
Mx of neurogenic shock
Vasopressors: vasopressors and noradrenaline Atropine: reverse bradycardia
2484
Def: spinal shock
Acute spinal cord transection Loss of all voluntary and reflex activity below the level of injury
2485
Trauma Hypotonic paralysis Loss of sensation Bladder retention
?Spinal shock
2486
DDx for life-threatening Chest injuries ATOM FC
Airway obstruction Tension pneumothorax Open pneumothorax (sucking) Massive haemothorax Flail chest Cardiac tamponade
2487
Def: massive haemothorax
Accumulation of \>1.5l of blood in chest cavity Usually caused by disruption of hilar vessels
2488
Signs of chest wall trauma Reduced BP Reduced expansion Reduced breath sounds and vocal resonance Stony dull percussion
Massive haemothorax
2489
Mx of massive haemothorax?
X-match 6u Large-bore chest drain with heparinised saline for autotransfusion Thoracotamy if \>1.5ml or \>200ml/h
2490
Massive haemothorax
2491
Def: flail chest
Anterior or lateral # of \>2 adjacent ribs in 2 places Flail segment moves paradoxically with respiration Reduced oxygenation: due to underlying pulmonary contusion and reduced ventilation of affected segment
2492
Ix in flail chest
CXR/CT chest: pulmonary contusion (white) Serial ABGs: Reduced PaO2:FiO2 ratio
2493
Rx flail chest
O2 Good analgesia: PCA, epidural Persistant respiratory failure: PPV
2494
Flail chest
2495
Def: cardiac tamponade
Disruption of myocardium or great vessles-\> blood in pericardium-\> reduced filing and contraction-\> shock Usually results from penetrating trauma
2496
Raised JVP/distended neck veins Reduced BP Muffled heart sounds SBP fall of \>10mmHg on inspiration Kussmaul's sign: raised JVP on inspiration Intensely restless patient
Cardiac tamponade
2497
What is Beck's triad
Seen in Cardiac tamponade: Raised JVP/distended neck veins Reduced BP Muffled heart sounds
2498
What is pulsus paradoxus
Seen in cardiac tamponade SBP fall of \>10mmHg on inspiration Normally during inspiration, systolic blood pressure decreases ≤10 mmHg.,[1] and pulse rate goes up slightly. This is because inspiration makes intra-thoracic pressure more negative relative to atmospheric pressure. The negative pressure in the thorax increases venous return, so more blood flows into the right side of the heart. However, the decrease in intra-thoracic pressure also expands the compliant pulmonary vasculature. This increase in pulmonary blood capacity pools the blood in the lungs, and decreases pulmonary venous return, so flow is reduced to the left side of the heart. Also, the increased systemic venous return to the right side of the heart expands the right heart and directly compromises filling of the left side of the heart. Reduced left-heart filling leads to a reduced stroke volume which manifests as a decrease in systolic blood pressure. The decrease in systolic blood pressure leads to a faster heart rate due to the baroreceptor reflex, which stimulates sympathetic outflow to the heart. Although it might be tempting to expect during inspiration that the increased volume of the right ventricle causes the septum to bulge dramatically into the left ventricle, this is unlikely under normal physiologic conditions, as there is still a large pressure gradient between the right and left ventricles during inspiration. However, during cardiac tamponade, this is the case. Here, pressure equalizes between all of the chambers of the heart.[4] This means that there is a zero-sum game, and as the right ventricle gets more volume, it can push the septum into the left ventricle and therefore reduce the volume of the left ventricle. This additional loss of volume of the left ventricle that only occurs with equalization of the pressures (as in tamponade) allows for the further reduction in volume, so cardiac output is reduced, leading to a further decline in BP. However, in situations where the left ventricular pressure remains higher than the pericardial sac (most frequently from coexisting disease with an elevated left ventricular diastolic pressure), there is no pulsus paradoxus
2499
Kussmaul's sign
Raised JVP on inspiration Seen in Cardiac tamponade amongst other conditiosn Ordinarily the JVP falls with inspiration due to reduced pressure in the expanding thoracic cavity and the increased volume afforded to right ventricular expansion during diastole. Kussmaul sign suggests impaired filling of the right ventricle due to a poorly compliant myocardium or pericardium. This impaired filling causes the increased blood flow to back up into the venous system, causing the jugular vein distension (JVD) and is seen clinically in the internal jugular veins becoming more readily visible.
2500
Ix in cardiac tamponade
US: FAST or TTE CXR: enlarged pericardium CVP \>12mmHg ECG: low voltage QRS with electrical alternans
2501
low voltage QRS with electrical alternans, tachycardic
Cardiac tamponade
2502
Massive pericardial effusion Massive pericardial effusion produces a triad of… Low voltage Tachycardia Electrical alternans Electrical alternans is… when consecutive, normally-conducted QRS complexes alternate in height. produced by the heart swinging backwards and forwards within a large fluid-filled pericardium. Patients with this ECG pattern need to be immediately assessed for clinical and echocardiographic evidence of tamponade.
2503
Mx of cardiac tamponade
Pericardiocentesis: spinal needle in R subxiphoid space aiming at 45o towards R tip of left scapula Thoracotamy may be needed
2504
Which ribs are usually # in trauma
Usually 5th-9th ribs of upper 4 ribs= high energy trauma
2505
2o survery chest injuries
Rib# Sternal# Pulmonary contusion Myocardial contusion Contained aortic disruption Diaphragmatic injury Oesophageal disruption Trachoebronchial disruption
2506
Cx if rib #
Pneumothorax Lacerate thoracic or abdominal viscera
2507
Rx rib #
Good analgesia NSAIDs + opioids Intrapleural analgesia Intercostal block
2508
Features of sternal #
Usually MVA driver vs steering wheel Risk of mediastinal injury
2509
Rx sternal #
Analgesia, admit, observe Cardiac monitor Troponin: rule out myocardial contusion
2510
Features of pulmonary contusion
Usually due to rapid deceleration injury or shock waves May-\> ARDS
2511
Dyspnoea, haemopytsis, resp failure following Trauma
?Pulmonary contusion
2512
Ix in ?pulmonary contusion
CXR: opacification Serial ABGs: reduced PaO2: FiO2 ratio
2513
Rx pulmonary contusion
O2, ventilate if necessary
2514
Direct blunt trauma over precordium ECG: abnormal arrythmias Troponin raised
?Myocardial contusion
2515
Rx in myocardial contusion
Bed rest, cardiac monitoring, Rx arrythmias
2516
Rapid deceleration injury (80% immediately fatal) Initially stable but-\> hypertensive CXR: wide mediatsinum, deviation of NGT Requries cardiothroacic consult
?Contained aortic disruption
2517
Penetrating injury below 5th rib or high energy compression CXR: visceral herniation, CT
Diaphragmatic injury
2518
Usually penetrating trauma-\> mediastinitis Ix: CXR: pneumoediastinum, surgical emphysema
Oesophageal disruption
2519
Persistent pneumothorax Pneumomediastinum
Tracheobronchial disruption
2520
Mechanisms of abdominal trauma
Penetrating: All require exploration as tract may be deeper than it appears Blunt: Have a high index of suspicion for taking to theatre
2521
Specific Ix in abdominal trauma
Urine dip: Heamturia suggests injury to renal tract FAST scan Diagnostic peritoneal lavage
2522
Features of FAST scan
Replacing DPL in most centres Check for fluid in abdomen, pelvis and pericardium Can be extended to look for pneumothoraces
2523
Areas examined in FAST scan
Perihepatic space (Morrison's pouch) Perisplenic space Pericardium Pelvis 90% sensitive
2524
Features of diagnostic peritoneal lavage
Insert urinary catheter and NGT (decompression to minimise risk of injury) Midline incision through skin and fascia @ 1/3rd distance from umbilicus to pubic symphysis (arcuate line) Carefully dissect to peritoneum and insert a urinary catheter Instil 10ml/kg warmed Hartman's Drain fluid back into bag and send sample to lab +ve= \>100,000 RBCs/mm, bile/intestinal contents
2525
Advantages and disadvanatges of DPL
98% sensitive for intra-abdominal haemorrhage Useful if FAST unavailable May be better for identifying injury to hollow viscus Unable to identify retroperitoneal injury
2526
What are the indications for emergency laparotomy in abdo tauma
Unexplained shock Peritonism: rigid or silent abdomen Evisceration: bowel or omentum Radiological evidence of intraperitoneal gas Radiological evidence of ruptured diaphragm Gunshot wounds +VE DPL or CT
2527
Aim of damage control surgery
Early Mx of abdominal trauma should focus on damge control to limit physiological stress Control haemorrhage: ligation and packing Control contamination: stabilise in ITU
2528
Kehr's Sign
Shoulder tip pain 2o to blood in peritoneal cavity Left Kehr's is classic symptom of ruptured spleen
2529
Classification of splenic inury (AAST)
1: capsular tear 2: tear + parenchymal injury 3: tear up to hilum 4: complete fracture
2530
Mx of splenic injury
Haemodynamically unstable: laparotomy Stable 1-3: observation in HDU Stable 4: consider laparotomy: suture lac or partial/complete splenectomy
2531
Mx of liver injury
Conservative if capsule is intact Suture laceration Partial hepatectomy Packing
2532
Mx of bowel injury
Resection may be required
2533
Mx of bladder injury
Often associated with pelvic injury Intraperitoneal rupture requires laparoscopic repair with urethral and suprapubic drainage Extraperitoneal rupture can be treated conservatively with urethral drainage Give prophylactic Abx
2534
Classification of urethral injury
Anterior Posterior
2535
Anterior urethral injury
Injury to spongy urethra (penile + bulbar) Occur following straddling injuries or instrumentation
2536
Posterior injury to urethra
Membranous urethra Occur following pelvic #s
2537
Often associated with pelvic fracture Blood in urethral meatus or scrotum Perineal brusing High-riding prostate Inability to micturate and palpable bladder
?Urethral injury
2538
Ix in urethral injury
Retrograde urethrogram
2539
Mx of urethral injury
Suprapubic catheter Surgical repair
2540
Contained aortic dissection
2541
Pneumomediastinum
2542
Epidemiology of head injury
Head injury alone or in combination with other injuries is the commonest cause of trauma death (50%)
2543
Def and classification of 1o brain injury
Occcurs at time of injury and is a result of direct or indirect injury to brain tissue Diffuse: Concusison/ mild TBI: temporary reduction in brain function. Headache, confusion, visual symptoms, amnesia Diffuse axonal injury: Shearing forces disrupt axons. May lead to coma and persistent vegetative state. Autonomic dysfunction: fever, HTN, seating Focal: Contusion e.g. coup and contra-coup, may have focal neurological deficit Intracranial haemorrhage: EDH, SDH, SAH, ICH and laceration
2544
Def and causes of 2o brain injury
Occurs after 1o injury Hypoxia Hypercapnoea Hypotension Raised ICP Infection
2545
What is the Monroe-Kelly Doctrine
Cranium is a rigid box. Therfore total volume of intracranial contents must remain constant if ICP is not to change. Increase in a volume of one constitutent leads to a compensatory reduciton in another e.g. CSF, bloods (especially venous) These mechanisms can compensate for a volume change of around 100ml before ICP increases As autoregulation feails, ICP raipidly-\> herniation
2546
Features of Cerebral Blood Flow and ICP
CBF proportion to CPP x radius of vessels CPP= MABP-ICP Raised ICP-\> reduced CPP-\> Reduced CBF Reduced CBF-\> autoregulatory-\> vasodilation-\> increased volume-\> increased ICP Need to prevent or attenuate this vicious cycle by ventilating to normocapnoea IV fluid to normovolaemia Mannitol bolus acutely
2547
How does ventilating to normocapnoea neuroprotect
Ventilate to low normocapnia [end - tidal CO2 of 30 mmHg, 4.0KPa]. This equates to a PaCO2 of approximately 4.5KPa in normal individuals. This minimises the risk of cerebral vasodilation (high PaCO2) and cerebral vasoconstriction (low PaCO2)
2548
Cushing's Triad What does it suggest
HTN Bradycardia Irregular breathing Imminent herniation
2549
What are the typical clinical criteria for use of mannitol or hypertonic saline
Unilateral or bilateral pupil dilation in association with GCS \<8 Progressive hypertension and bradycardia in association with GCS \<8
2550
Key points in head injury Hx
LOC Amnesia: anterograde worse N+V Fits Focal neurology Mechanisms Drugs e.g. antiplatelets, warfarin
2551
RFs: for burns
Age: children and elderly Co-morbidities: epilepsy, CVA, dementia, mental illness Occupation
2552
How can burns be classfiied?
Superficial Partial thickness Full thickness
2553
Features of superficial burn
Erythema Painful e.g. sunburn
2554
Features of partial thickness burns
Heal within 2-3w if not complicated Superficial: No loss of dermis Painful Blisters Deep: Loss of dermis but adnexae remain Healing from adenexae e.g. follicles V painful
2555
Features of full thickness burns
Complete loss of dermis Charred, waxy, white, skin Anaesthetic Heal from edges-\> scar
2556
Early Cx of burns
Infection: loss of barrier funciton, necrotic tissue, SIRS Hypovolaemia: loss of fluid in skin and increased capillary permeability Metabolic distrubance: raised K, raised myoglobin, Raised Hb-\> AKI Compartment syndrome: circumferential burns Peptic ulcers: Curling's ulcers Pulmonary: laryngeal oedema, CO poisoning, ARDS Renal and hepatic impariment
2557
Intermediate Cx of burns
VTE Pressure sores
2558
Late Cx of burns
Scarring Contractures Psychological problems
2559
Assessment of burns: Wallace Rule of 9s
Head and neck: 9% Arms: 9% Torso 18% front and back Legs: 18% each Perineum 1% Palms 1% May also use Lund and Browder charts
2560
General principles of burn managements
Based on ATLS principles Specific concerns with burns: secure airway, manage fluids, prevent infection
2561
Airway in burns:
Examine for respiratory burns: soot in oral or nasal cavity, burnt nasal hairs, hoarse voice/stridor Flexible laryngoscopy can be helpful Conider early intubation and dexamethasone
2562
Breathing in burns
100% O2 Exclude constricting burns Look for signs of CO poisoning e.g. headache, N+V, confusion, cherry red appearance ABG: COHb level, SpO2 unreliable if CO poisoning
2563
Circulation in burns
Fluids losses may be huge 2x large bore cannulae in each ACF Bloods: FBC, U+E, G+S, X match Start 2l warmed Hartmann's immediately. Formula guide additional fluid requirements in burns patients
2564
Parkland formula in burns
1st 24h 4x weight (kg) x % burn=ml Hartmann's in 24h Replace fluid from time of burn Give half in 1st 8h Best guide is UO: 30-50ml
2565
Alternative burns fluid formula
Muir and Barclay, relates to albumin as fluid replacement Parkland formula is preferred by British Burns Association
2566
Mx of Burns
Analgesia: morphine Dress partial thickness burns: biological e.g. cadaveric skin synthetic cream e.g. flamazine \*silver sulfadiazine + sterile film Full thickness burns: tangential excision debridement, split thickness skin grafts Circumferential burns may require escharotomy to prevent compartment syndrome Anti-tetanus toxoid Consider prophylactic Abx esp. pseudomonas
2567
Def: hypothermia
Core (rectal) T \<35
2568
What are the 4 mechanisms of body heat loss
Radiation: 60% Conduction: 15% direct contatct, primary means is cold water immersion Convection: 15% Evaporation: 10%
2569
Aetiological classification of hypothermia
1o: environental exposure 2o: change in temperature set point e.g. age-related, hypothyroidism, autonomic neuropathy
2570
Features of mild hypothermia
32-35 deg Shivering Tachycardia Vasoconstriction Apathy
2571
Features of moderate hypothermia
28-32 deg Dysrhythmia, bradycardia, hypotension J waves Reduced reflexes, dilated pupils, reduced GCS
2572
Features of severe hypothermia
\<28 deg VT-\> VF-\> cardiogenic shock Apnoea Non-reactive pupils Coagulopathy Oliguria Pulmonary oedema
2573
2574
Ix in hypothermia
Rectal/ear temperature FBC, U+E, glucose TFTs, blood gas ECG: J waves between QRS and T wave, arrythmias
2575
Mx of hypothermia
Cardiac monitor Warm IVI 0.9% saline Urinary catheter Consider Abx for prevention of pneumonia routine if temp \<32 and \>65 Slowly rewarm: reheating too qucikly-\> peripheral vasodilation and shock Aim for 0.5 deg /hr Passive external: blankets, warm drinks Active external: warm water or warmed air Active internal: mediastinal lavage and CPB (severe hypothermia only)
2576
Cx in hypothermia
Arrhythmias Pneumonia Coagulopathy ARF
2577
Features of oesophageal anatomy
25cm long mucscular tube (40cm from GOJ to lips) Starts at level of cricoid cartilage (C6) Lies in the visceral compartment of the neck Runs in posterior mediastinum and passes through right crus of diaphragm at T10 Continues before entering the cardia
2578
Level of cricoid cartilage?
C6
2579
Level of oesophagus passing through diaphragm
Right crus T10
2580
3 locations of oesophageal narrowing?
Level of cricoid Posterior to left main bronchus and aortic arch LOS
2581
How is the oesophagus divided?
Into 3rds reflecting change in musculature from striated to mixed to smooth
2582
What is the level of bronchoaortic oesophageal constriction?
T4
2583
What is the Z line?
Where the oesophagus changes from squamous epithelium to gastric columnar aka squamocolumnar junction
2584
Def: dysphagia
Concious difficulty in swallowing
2585
Def: aphagia
Complete inability to swallow
2586
Def: odynophagia
Painful swallowing
2587
How can dysphagia be classified?
Considered from the point of its chronciity to be acute, chronic, or progressive
2588
How can the causes of dysphagia be classified?
Inflammatory Neurological/motility disorders Mechanical obstruction
2589
Inflammatory causes of dysphagia
Tonsillitis, pharyngitis Oesophagitis: GORD, candida Oral candidiasis Apthous ulcers
2590
Neurological/motility causes of dysphagia
Local: Achalasia Diffuse oesophageal spasm Nutcracker oesophagus Bulbar/pseudobulbar palsy (CVA, MND) Systemic: Systemic sclerosis/CREST MG
2591
Mechanical causes of dysphagia
Luminal: FB Large food bolus Mural: Benign stricutre: Web, oesophagitis, Trauma (e.g. OGD) Malignant stricture: pharynx, oesopgaus, gastric Pharyngeal pouch Extra mural: Retrosternal goitre Rolling hiatus hernia Lung Ca Mediastinal LNs e.g. lymphoma Thoracic aortic aneurysm
2592
Ix in dypshagia
Upper GI endoscopy Ba swallow Manometry
2593
Pathophysiology of achalasis
Degeneration of myenteric plexus (Auerbach's)-\> decresed peristalsis with failure of LOS to relax
2594
Causes of achalasia
1o/idiopathic: commonest 2o: Chagas (T. cruzi)
2595
Dysphagia: liquids then solids Regurgitation esp @ night Substernal cramps Weight loss
?Achalasia
2596
Cx of achalasia
Oesophageal SCC in 3-5%
2597
Ix in achalasia
Ba swallow: dialted tapering oesophagus, Brid's beak Manometry: failure of relaxation and reduced peristalsis CXR: widened mediatsinum, double heart border OGD: exclude malignancy
2598
Oesophageal achalasia Bird's beak
2599
Mx of achalasia
Medical: CCBs, nitrates Interventional: botox injection, endoscopic balloon dilatation Surgery: Heller's cardiomyotomy eith peroral, endoscopic
2600
Def: Zenker's diverticulum
Pharyngeal pouch Outpouching between crico and thyropharyngeal components of the inferior pharyngeal constrictor at an area of weakness known as Killian's dehiscence Defect usually occurs posteriorly but swelling usually bulges to left side of neck Food debris-\> pouch expansion-\> oesophageal compression-\> dysphagia
2601
Regurgitation Halitosis Gurgling sounds
Pharyngeal Pouch (Zenker's diverticulum)
2602
Rx of Pharyngeal pouch
Excision Endoscopic stapling
2603
Features of diffuse oesophageal spasm
Intermittent severe chest pain +/i dysphagia Barium swallow shows corkscrew appearance Diffuse esophageal spasm (DES) is a condition characterized by uncoordinated contractions of the esophagus, which may cause difficulty swallowing (dysphagia) or regurgitation. In some cases, it may causes symptoms such as chest pain, similar to heart disease. The cause of DES remains unknown. Certain abnormalities on x-ray imaging are commonly observed in DES, such as a "corkscrew" or "rosary bead esophagus", although these findings are not unique to this condition. Specialized testing called manometry can be performed to evaluate the motor function of the esophagus, which can help identify abnormal patterns of muscle contraction within the esophagus that are suggestive of DES. The treatment of DES consists primarily of medications, such as acid suppressing agents (like proton pump inhibitors), calcium channel blockers, hyoscine butylbromide, or nitrates. In only extremely rare cases, surgery may be considered. People with DES have higher incidences of gastroesophageal reflux disease (GERD) and anxiety.
2604
"corkscrew" or "rosary bead esophagus",
Diffuse oesophageal spasm
2605
DOS Pathology Aetiology is unknown but may be related to loss of inhibitory neurones in the distal oesophagus. Radiographic features Fluoroscopy only 60% of barium swallows will be abnormal \<5% will show "corkscrew oesophagus" or "rosary bead oesophagus" where normal peristalsis is interrupted by many tertiary (non-propulsive) contractions occurring in the distal oesophagus nonperistaltic contractions, pushing contrast in two directions, can be seen (sometimes the only feature) 5 sacculations and pseudodivertucula may be seen 5
2606
Features of nutcracker oesophagus
Intermittent dysphagai +/- chest pain Increased contraction pressure with normal peristalsis Nutcracker esophagus, or hypertensive peristalsis, is a disorder of the movement of the esophagus characterized by contractions in the smooth muscle of the esophagus in a normal sequence but at an excessive amplitude or duration. Nutcracker esophagus is one of several motility disorders of the esophagus, including achalasia and diffuse esophageal spasm. It causes difficulty swallowing, or dysphagia, to both solid and liquid foods, and can cause significant chest pain; it may also be asymptomatic. Nutcracker esophagus can affect people of any age, but is more common in the sixth and seventh decades of life. The diagnosis is made by an esophageal motility study (esophageal manometry), which evaluates the pressure of the esophagus at various points along its length. The term "nutcracker esophagus" comes from the finding of increased pressures during peristalsis, with a diagnosis made when pressures exceed 180 mmHg; this has been likened to the pressure of a mechanical nutcracker. The disorder does not progress, and is not associated with any complications; as a result, treatment of nutcracker esophagus targets control of symptoms only.[1][2]
2607
Features of Plummer Vinson Syndrome
Severe IDA-\> hyperkeratinsiation of upper 3rd of oesophagus-\> web formation Premalignant: 20% risk of SCC
2608
Causes of oesophageal rupture
Iatrogenic (85-90%): endoscopy, biopsy, dilatation Violent emesis: Boerhaave's syndrome Carcinoma Caustic ingestion Trauma: surgical emphysema +/- pneumothorax
2609
Odynophagia Mediastinitis: tachypnoea, dyspnoea, fever, shock Surgical emphysema
?Oesophageal rupture
2610
Mx of iatrogenic oesophageal rupture
PPI NGT Abx
2611
Mx of other causes of oesophageal rupture
ABC PPI ABx ANtifunglas Debridement and formation of oesophagocutaneous fistula with T-tube
2612
A 65-year-old man presents with severe epigastric pain radiating to his back. He states that the pain is 9/10 severity. He has associated nausea and vomiting. Serum amylase is raised. You suspect a diagnosis of acute pancreatitis. How would you initially manage his acute pain? ## Footnote IV morphine in 1-2mg boluses until comfortable IM pethidine IV morphine 10mg STAT Regular paracetamol Regular paracetamol and ibuprofen
This patient has severe pain which will likely need an opiate to settle. IV morphine titrated in 1-2mg boluses until comfortable would be a sensible first choice. Regular paracetamol would also be sensible as this would be opioid sparing, however this would not be the first choice for initially managing severe acute pain.
2613
WHO Analgesic ladder structure
nitially peripherally acting drugs such as paracetamol or non-steroidal anti-inflammatory drugs (NSAIDs) are given. If pain control is not achieved, the second part of the ladder is to introduce weak opioid drugs such as codeine or dextropropoxyphene together with appropriate agents to control and minimise side effects. The final rung of the ladder is to introduce strong opioid drugs such as morphine. Analgesia from peripherally acting drugs may be additive to that from centrally-acting opioids and thus, the two are given together.
2614
The World Federation of Societies of Anaesthesiologists (WFSA) Analgesic Ladder for management of acute pain
Severe pain and may need controlling with strong analgesics with local anaesthetic blocks and peripherally acting drugs Second rung on postoperative pain ladder is restoration of oral route and strong opioids may no longer be required with adequate analgesia obtained using combinations of peripherally acting agents and weak opioids Final step is when pain can be controlled with peripherally acting agents alone
2615
Feautes of local anaesthetics
Infiltration of a wound with a long-acting local anaesthetic such as Bupivacaine Analgesia for several hours Further pain relief can be obtained with repeat injections or by infusions via a thin catheter Blockade of plexuses or peripheral nerves will provide selective analgesia in those parts of the body supplied by the plexus or nerves Can either be used to provide anaesthesia for the surgery or specifically for postoperative pain relief Especially useful where a sympathetic block is needed to improve postoperative blood supply or where central blockade such as spinal or epidural blockade is contraindicated.
2616
Features of spinal anaesthesia
Provides excellent analgesia for surgery in the lower half of the body and pain relief can last many hours after completion of the operation if long-acting drugs containing vasoconstrictors are used.
2617
Side effects of spinal anaesthesia
Hypotension Sensory and motor block Nausea Urinary retention
2618
Features of epidural anaesthesia
An indwelling epidural catheter inserted. This can then be used to provide a continuous infusion of analgesic agents. It can provide excellent analgesia. They are still the preferred option following major open abdominal procedures and help prevent post operative respiratory compromise resulting from pain.
2619
Disdavanatges of epidural
- Disadvantages of epidurals is that they usually confine patients to bed, especially if a motor block is present. In addition an indwelling urinary catheter is required. Which may not only impair mobility but also serve as a conduit for infection. They are contraindicated in coagulopathies.
2620
Features of transversus abdominal plane block
In this technique an ultrasound is used to identify the correct muscle plane and local anaesthetic (usually bupivicaine) is injected. The agent diffuses in the plane and blocks many of the spinal nerves. It is an attractive technique as it provides a wide field of blockade but does not require the placement of any indwelling devices. There is no post operative motor impairment. For this reason it is the preferred technique when extensive laparoscopic abdominal procedures are performed. They will then provide analgesia immediately following surgery but as they do not confine the patient to bed, the focus on enhanced recovery can begin sooner.
2621
Disadvanatges of TAP
The main disadvantage is that their duration of action is limited to the half life of the local anaesthetic agent chosen. In addition some anaesthetists do not have the USS skills required to site the injections.
2622
Give some examples of strong opioids
Morphine Pethidine Tramadol Buprenorphine Methadone Diamorphine Fentanyl Hydromorphone Oxycodone Used for severe pain arising from deep or visceral structures
2623
Features of morphine
Short half life and poor bioavailability. Metabolised in the liver and clearance is reduced in patients with liver disease, in the elderly and the debilitated Side effects include nausea, vomiting, constipation and respiratory depression. Tolerance may occur with repeated dosages
2624
Features of pethidine
Synthetic opioid which is structurally different from morphine but which has similar actions. Has 10% potency of morphine. Short half life and similar bioavailability and clearance to morphine. Short duration of action and may need to be given hourly. Pethidine has a toxic metabolite (norpethidine) which is cleared by the kidney, but which accumulates in renal failure or following frequent and prolonged doses and may lead to muscle twitching and convulsions. Extreme caution is advised if pethidine is used over a prolonged period or in patients with renal failure.
2625
Mild opioids
Codeine Dihydrocodeine
2626
Features of paracetamol
Inhibits prostaglandin synthesis. Analgesic and antipyretic properties but little anti-inflammatory effect It is well absorbed orally and is metabolised almost entirely in the liver Side effects in normal dosage and is widely used for the treatment of minor pain. It causes hepatotoxicity in over dosage by overloading the normal metabolic pathways with the formation of a toxic metabolite.
2627
Features of NSAIDs
Analgesic and anti-inflammatory actions Inhibition of prostaglandin synthesis by the enzyme Cyclooxygenase which catalyses the conversion of arachidonic acid to the various prostaglandins that are the chief mediators of inflammation. All NSAIDs work in the same way and thus there is no point in giving more than one at a time. . NSAIDs are, in general, more useful for superficial pain arising from the skin, buccal mucosa, joint surfaces and bone. Relative contraindications: history of peptic ulceration, gastrointestinal bleeding or bleeding diathesis; operations associated with high blood loss, asthma, moderate to severe renal impairment, dehydration and any history of hypersensitivity to NSAIDs or aspirin.
2628
Management of neuropathic pain
First line: Amitriptyline (Imipramine if cannot tolerate) or pregabalin Second line: Amitriptyline AND pregabalin Third line: refer to pain specialist. Give tramadol in the interim (avoid morphine) If diabetic neuropathic pain: Duloxetine
2629
Diabetic patients and preop care
Diabetic patients have greater risk of complications. Poorly controlled diabetes carries high risk of wound infections. Patients with diet or tablet controlled diabetes may be managed using a policy of omitting medication and checking blood glucose levels regularly. Diabetics who are poorly controlled or who take insulin will a require variable rate intravenous insulin infusion. Potassium supplementation should also be given. Diabetic cases should be operated on first.
2630
Contraindications to COCP
The decision of whether to start a women on the combined oral contraceptive pill is now guided by the UK Medical Eligibility Criteria (UKMEC). This scale categorises the potential cautions and contraindications according to a four point scale, as detailed below: UKMEC 1: a condition for which there is no restriction for the use of the contraceptive method UKMEC 2: advantages generally outweigh the disadvantages UKMEC 3: disadvantages generally outweigh the advantages UKMEC 4: represents an unacceptable health risk
2631
UKMEC 3
more than 35 years old and smoking less than 15 cigarettes/day BMI \> 35 kg/m^2\* family history of thromboembolic disease in first degree relatives \< 45 years controlled hypertension immobility e.g. wheel chair use carrier of known gene mutations associated with breast cancer (e.g. BRCA1/BRCA2)
2632
UKMEC 4
more than 35 years old and smoking more than 15 cigarettes/day migraine with aura history of thromboembolic disease or thrombogenic mutation history of stroke or ischaemic heart disease breast feeding \< 6 weeks post-partum uncontrolled hypertension current breast cancer major surgery with prolonged immobilisation
2633
Medical patients at risk of VTE
if mobility significantly reduced for \>= 3 days or if expected to have ongoing reduced mobility relative to normal state plus any VTE risk factor (see below)
2634
Surgical patients at risk of VTE
if total anaesthetic + surgical time \> 90 minutes or if surgery involves pelvis or lower limb and total anaesthetic + surgical time \> 60 minutes or if acute surgical admission with inflammatory or intra-abdominal condition or if expected to have significant reduction in mobility or if any VTE risk factor present (see below)
2635
What are the options for post-procedure VTE prophylaxis
Dabigatran Fondaparinux LMWH Rivaroxaban Apixaban
2636
When can the post-operative procedure VTE prophylaxis be started?
dabigatran, started 14 hours after surgery fondaparinux, started 6 hours after surgery LMWH, started 6-12 hours after surgery rivaroxaban, started 6-10 hours after surgery. apixaban
2637
Length of VTE prophylaxis Elective hip
28-35d
2638
Length of VTE prophylaxis Elective knee
10-14d
2639
Length of VTE prophylaxis Hip #
28-35d
2640
A 43-year-old lady with a metallic heart valve has just undergone an elective paraumbilical hernia repair. In view of her metallic valve, she is given unfractionated heparin perioperatively. How should the therapeutic efficacy be monitored, assuming her renal function is normal? Therapeutic monitoring is not required Measurement of APTT Measurement of INR Measurement of Prothromin time None of the above
Unlike low molecular weight heparins that do not require monitoring unfractionated heparin does require monitoring, this is done by measuring the APTT.
2641
MOA standard heparin
Activates antithrombin III. Forms a complex that inhibits thrombin, factors Xa, IXa, Xia and XIIa
2642
MOA LMWH
Activates antithrombin III. Forms a complex that inhibits factor Xa
2643
Monitoring of unfractionated heparin
APTT
2644
Monitoring of lMWH
Anti-factor Xa (although routine monitoring not required)
2645
MOA HIT
immune mediated - antibodies form against complexes of platelet factor 4 (PF4) and heparin these antibodies bind to the PF4-heparin complexes on the platelet surface and induce platelet activation by cross-linking FcγIIA receptors usually does not develop until after 5-10 days of treatment despite being associated with low platelets HIT is actually a prothrombotic condition features include a greater than 50% reduction in platelets, thrombosis and skin allergy treatment options include alternative anticoagulants such as lepirudin and danaparoid
2646
What electrolyte disturbance can be caused by both unfractionated and LMWH?
Hyperkalaemia ?through inhibition of aldosterone secretion
2647
A 78-year-old man is due to have an anterior resection for colorectal carcinoma. He is currently on clopidogrel. He has been on clopidogrel for the past 6 months due to the insertion of a drug eluting stent during primary percutaneous coronary intervention for a STEMI. When should you advise him to stop taking his clopidogrel? ## Footnote 3 days before surgery 5 days before surgery 7 days before surgery 10 days before surgery 14 days before surgery
The BNF states that for elective procedures, where an antiplatelet effect is not needed, clopidogrel should be discontinued 7 days before surgery. The indication for clopidogrel is important, and if related to cardiovascular disease, discontinuation of clopidogrel therapy should only be considered after discussion with the patients cardiologist.
2648
Features of clopidogrel
Clopidogrel is an antiplatelet agent used in the management of cardiovascular disease. It was previously used when aspirin was not tolerated or contraindicated but there are now a number of conditions for which clopidogrel is used in addition to aspirin, for example in patients with an acute coronary syndrome. Following the 2010 NICE technology appraisal clopidogrel is also now first-line in patients following an ischaemic stroke and in patients with peripheral arterial disease.
2649
MOA clopidogrel
Antagonist of P2Y12 adenosine diphosphate R, inhibiting platelet activaton
2650
What is clopidogrel's drug class
Clopidogrel belongs to a class of drugs known as thienopyridines which have a similar mechanism of action. Other examples include: prasugrel ticagrelor ticlopidine
2651
Clopidogrel +PPI
May make clopidogrel less effecive Generally this seems to be with omeprazole and esomeprazole Other PPIs such as lansoprazole are ok
2652
Non-immune mediated blood trasnfusion reactions
Hypocalaceamia CCF Infections Hyperkalaemia
2653
A 75-year-old man comes into the orthopaedic ward for an elective hip replacement. He has been assessed for venous thromboembolism (VTE) prophylaxis. Apart from the operation and his age he does not have any additional risk factors and he does not have any risk factors for bleeding. What is the recommended VTE prophylaxis measures for this gentleman? TED stockings TED stockings + dalteparin sodium started at least 6 hours post-operation TED stockings + dalteparin sodium started the morning of surgery Dalteparin sodium started at least 6 hours post-operation Dalteparin sodium stared the morning of surgery
NICE recommends that patients who will undergo an elective hip replacement have both mechanical and pharmacological methods of venous thromboembolism (VTE) prophylaxis. TED stockings should be administered and the patient should wear them once they have been admitted. As long as there are not contraindications, such as bleeding risk, pharmacological VTE prophylaxis is administered after surgery. Dalteparin sodium, a low molecular weight heparin, is started 6 hours after surgery. Other pharmacological methods can also be used.
2654
A 77-year-old male is day 1 post-op TURP for benign prostatic hyperplasia. You are bleeped by the nurses as the patient has spiked a temperature. Observations are: Respiratory rate 16/min, saturations 95% on air, Blood pressure 120/70 mmHg, Heart rate 70 bpm, temperature 38.3ºC, Glasgow coma score 15/15. On arrival the patient is lying in bed. He reports feeling well in himself. On examination there is reduced air entry in the lungs bilaterally. Post op bloods show: Hb119 g/l Platelets245 \* 109/l WBC10.2 \* 109/l CRP89 mg/l What is the most appropriate next step? Commence IV antibiotics Inform the on-call registrar Organise a CXR and take blood cultures Encourage the patient to mobilise and engage in deep breathing exercises Commence high flow oxygen through a non-rebreathe mask
This is a case of post-operative pyrexia which is a very common finding for junior doctors on a surgical firm. This questions tests the ability to know the common causes of post-operative pyrexia and the time frames they are likely to occur within. From the given vignette it is testing the user to identify a clinically stable patient with no evidence of focal infection (CRP commonly raised post-op, chest likely collapsed bilaterally following a general anaesthesia) but who presents with an isolated temperature spike. These findings are in keeping with post-surgical inflammation/atelectasis given the stable picture. It is importan to be able to clinically synthesise the history, examination and clinical picture (I.e. 24 hours post TURP - a relatively low risk procedure) and be guided by this in further management instead of performing blanket investigations (i.e. CXR, blood cultures) for an isolated temperature spike 24 hours post-op. Chest physiotherapy with mobilisation and breathing exercises would help manage post-op lung atelectasis which is a very common post-op complication; especially within the first 24 hours. If the patient were to become unwell (I.e. infective symptoms, further temperature spikes, development of SIRS) they would then need further review and investigations based on the clinical picture. Benign temperature spikes in the first 24 hours after surgery due to atelectasis is a common presentation. Treatment involves mobilisation, chest physiotherapy and saline nebulisers for excessive secretions. Ongoing temperature spikes or infective symptoms would warrant further investigation.
2655
A 49-year-old man is having an elective repair of a right-sided inguinal hernia under general anaesthetic. What is the most appropriate advice to give him about eating and drinking before the operation? ## Footnote He should be nil-by-mouth from midnight before his operation No food or clear fluids for 6 hours before his operation No food for 6 hours and no clear fluids for 4 hours before his operation No food for 6 hours and no clear fluids for 2 hours before his operation No food for 6 hours and no clear fluids for 1 hour before his operation
The Royal College of Anaesthetists recommend that patients should have no food for 6 hours before the induction of general anaesthesia. Patients should be allowed to drink water or other clear fluids until 2 hours before the induction of general anaesthesia. This is to reduce the likelihood of pulmonary aspiration of gastric contents.
2656
Adverse effects of halothane
Hepatotoxicity Myocardial depression Malignant hyperthermia
2657
Adverse effects of thiopental
Laryngospasm
2658
After a complicated revision of a total hip replacement, an 80-year-old lady receives two units of packed red cells. Which drug should be prescribed between the units? Furosemide Paracetamol Cetirizine Hydrocortisone Platelets
Although packed red cells have a higher haematocrit than blood, transfusion of two units or more can result in fluid overload. Therefore, furosemide should be prescribed to be given between every other unit, if two or more units are given. Paracetamol can be used if there is a non-haemolytic febrile reaction to the transfusion. Cetirizine and hydrocortisone are used in cases of an anaphylactic reaction to the transfusion. Platelets may be given in cases of major haemorrhage, alongside packed red cells.
2659
Packed red cells
Used for transfusion in chronic anaemia and cases where infusion of large volumes of fluid may result in cardiovascular compromise. Product obtained by centrifugation of whole blood.
2660
Platelet rich plasma
Usually administered to patients who are thrombocytopaenic and are bleeding or require surgery. It is obtained by low speed centrifugation.
2661
Platelet concentrate
Prepared by high speed centrifugation and administered to patients with thrombocytopaenia.
2662
Fresh frozen plasma
Prepared from single units of blood. Contains clotting factors, albumin and immunoglobulin. Unit is usually 200 to 250ml. Usually used in correcting clotting deficiencies in patients with hepatic synthetic failure who are due to undergo surgery. Usual dose is 12-15ml/Kg-1. It should not be used as first line therapy for hypovolaemia.
2663
Cryoprecipitate
Formed from supernatant of FFP. Rich source of Factor VIII and fibrinogen. Allows large concentration of factor VIII to be administered in small volume.
2664
SAG-Mannitol Blood
Removal of all plasma from a blood unit and substitution with: Sodium chloride Adenine Anhydrous glucose Mannitol Up to 4 units of SAG M Blood may be administered. Thereafter whole blood is preferred. After 8 units, clotting factors and platelets should be considered.
2665
Methods of Warfarin reversal
Stop Warfarin 2. Vitamin K (reversal within 4-24h) IV takes 3-6h to work (at least 5mg) Oral can take 24h to be clinically effective 3. FFP Used less commonly now as first line 30ml/kg need to give at least 1l fluid in 70kg person (therfore not appropriated in fluid overload Need blood group Only used if human prothrombin complex is not available 4. Human prothrombin complex (reversal within 1 hour) Bereplex 50u/kg Rapid action but factor 6 short t1/2, therefore give with vit K
2666
A 50-year-old diabetic woman is admitted to the day surgery unit for an elective incision and drainage of a groin abscess. Her diabetes is usually well controlled on metformin. What should be done with regard to her diabetic control? ## Footnote Stop metformin, restart 48 hours after surgery Continue her normal regimen Admit the day before surgery and commence variable rate insulin infusion Commence variable rate insulin infusion on the day of surgery Stop metformin for 2 weeks and delay surgery
This patient is an orally controlled diabetic and therefore is unlikely to need a sliding scale regimen unless it is particularly major surgery, which an incision and drainage is not. If the patient was undergoing significant surgery, then they would usually be admitted the night before, and commenced on a variable rate infusion. Delaying surgery is not normally advised unless there are significant contraindications. This type of surgery is likely to be a day case and therefore she can continue on her normal metformin regimen.
2667
normal haemoglobin level associated with a microcytosis. In patients not at risk of thalassaemia
this should raise the possibility of polycythaemia rubra vera which may cause an iron-deficiency secondary to bleeding.
2668
A 22-year-old female is extubated following an uncomplicated laparoscopic appendicectomy. However, no respiratory effort is made and she is re-intubated and ventilated. She is monitored in the intensive care unit and all observations are normal. She is weaned from the ventilator 24 hours later successfully. What complication has occurred? Misplacement of the endotracheal tube in intubation Suxamethonium apnoea Opioid toxicity Malignant hyperpyrexia Overdose of propofol
A small subset of the population has an autosomal dominant mutation, leading to a lack of the specific acetylcholinesterase in the plasma which acts to break down suxamethonium, terminating its muscle relaxant effect. Therefore, the effects of suxamethonium are prolonged and the patient needs to be mechanically ventilated and observed in ITU until the effects of suxamethonium wear off. Opioid toxicity causes respiratory depression but is unlikely to be extreme enough to cause no respiratory effort in the monitored conditions of an anaesthetic. Misplacement of the endotracheal tube would cause hypoxia with a respiratory acidosis soon after intubation and potentially a pneumothorax ipsilaterally with collapse contralaterally. A propofol overdose would cause a fall in blood pressure. Malignant hyperpyrexia would manifest with a rise in temperature, rise in blood pressure, muscle spasm, type II respiratory failure and metabolic acidosis and arrhythmias.
2669
Suxamethonium
Depolarising neuromuscular blocker Inhibits action of acetylcholine at the neuromuscular junction Degraded by plasma cholinesterase and acetylcholinesterase Fastest onset and shortest duration of action of all muscle relaxants Produces generalised muscular contraction prior to paralysis Adverse effects include hyperkalaemia, malignant hyperthermia and lack of acetylcholinesterase
2670
Atracurium
Non depolarising neuromuscular blocking drug Duration of action usually 30-45 minutes Generalised histamine release on administration may produce facial flushing, tachycardia and hypotension Not excreted by liver or kidney, broken down in tissues by hydrolysis Reversed by neostigmine
2671
Vecuronium
Non depolarising neuromuscular blocking drug Duration of action approximately 30 - 40 minutes Degraded by liver and kidney and effects prolonged in organ dysfunction Effects may be reversed by neostigmine
2672
Pancuronium
Non depolarising neuromuscular blocker Onset of action approximately 2-3 minutes Duration of action up to 2 hours Effects may be partially reversed with drugs such as neostigmine
2673
A 72-year-old gentleman is about to undergo an elective hernia repair. He has mild asthma which is well-controlled using a salbutamol inhaler PRN, on average about once per week. His asthma causes no limitation to his daily activity. What is his ASA (American Society of Anesthesiologists) status? ASA 3 ASA 1 ASA 5 ASA 2 ASA 4
An ASA (American Society of Anesthesiologists) score is an indicator of a patient's fitness for surgery. A patient is classified as ASA 2 if they have a mild systemic disease without any functional limitations. Examples include (but not limited to): current smoker, social alcohol drinker, pregnancy, obesity (30 \< BMI \< 40), well-controlled diabetes mellitus or hypertension, and mild lung disease.
2674
ASA classificaiton Normal healthy patient
ASA I
2675
ASA classification A patient with mild systemic disease e.g. current smoker, socal EtOH, pregnancy, obesity \<30, well controlled DM, HTN, mild lung disease
ASA II
2676
ASA classificaiton A patient with severe systemic disease Examples include (but not limited to): poorly controlled Diabetes Mellitus/Hypertension, COPD, morbid obesity (BMI 40), active hepatitis, alcohol dependence or abuse, implanted pacemaker, moderate reduction of ejection fraction, End Stage Renal Disease (ESRD) undergoing regularly scheduled dialysis, history (\>3 months) of Myocardial infarction, Cerebrovascular accidents
ASA III
2677
ASA classification A patient with severe systemic disease that is a constant threat to life
ASA IV recent (\< 3 months) of Myocardial infarction, Cerebrovascular accidents, ongoing cardiac ischaemia or severe valve dysfunction, severe reduction of ejection fraction, sepsis, DIC, ARD or ESRD not undergoing regularly scheduled dialysis
2678
ASA V A moribund patient not expected to survive without the operation
ruptured abdominal/thoracic aneurysm, massive trauma, intra-cranial bleed with mass effect, ischaemic bowel in the face of significant cardiac pathology or multiple organ/system dysfunction
2679
ASA VI
A declared brain-dead patient whose organs are being removed for donor purposes
2680
Theme: Blood product ordering prior to surgery A.No group and save or cross-match required B.Group and save C.Cross-match 2-6 units depending on local protocols D.Cross-match 8-12 units depending on local protocols E.Transfuse 2 units prior to operation regardless of haemoglobin For each of the following procedures select the most appropriate preparation with respect to ordering blood products: Laparoscopic cholecystectomy Total gastrectomy Elective lower segment caesarean section
G+S X-match 2-6u dependant on local protocols G+S
2681
A 69-year-old man has just undergone laparoscopic abdominal surgery for appendicitis. There was minimal blood loss. He weighs 75 kg. He initially does not feel able to drink as he is nauseous from the anaesthetic. His pre-operative bloods were normal. What fluid should initially be prescribed to initiate a maintenance regime and how fast should it be given? ## Footnote 500 ml 0.9% sodium chloride at 100 ml/hr 500 ml 0.9% sodium chloride at 150 ml/hr 500 ml 0.9% sodium chloride STAT 500 ml Gelofusine at 72.5 ml/hr 1 L 0.9% sodium chloride at 50 ml/hr
This patient has just left theatre and will require fluids. Oral fluids should be initiated as soon as possible but if a patient is unable to drink then maintenance fluids should be prescribed through the IV route. Sodium chloride is a recommended fluid to be used for maintenance. Maintenance fluids should be prescribed at a rate of 30 ml/kg/24hr. Amount: 75 kg X 30 ml = 2250 mL in a 24 hour period Rate: 2500 / 24 = 93.75 ml/hr. Initially prescribe 500 ml and then reassess the patients fluid status and ability to drink. So prescribe 500 ml at a rate of 100 ml/hr.
2682
What is the maximum safe dose of Lidocaine?
3mg/kg Available pre-mixed with adrenaline which increases the duration of aciton and reduces blood loss secondary to vasoconstriction Should never be used near extremities due to risk of ischaemia
2683
Give some examples of non-absorbable suture material
Slik Novafil Prolene Ethilon
2684
Give some examples of absorbable sutures
Vicryl Dexon PDS
2685
When should non-absorbable sutures be removed from face?
3-5d
2686
When should non-absorbable sutures be removed from scalp, limbs, chest
7-10d
2687
When should non-absorbable sutures be removed from hand, foot, back
10-14d
2688
A 55-year-old gentleman has been admitted to the surgical assessment unit with acute abdominal pain, worse in right iliac fossa, and associated nausea and mild fever. Your surgical registrar suspects an appendicitis and arranges an urgent US scan of his abdomen. This is consistent with acute appendicitis and your surgical registrar asks you to prepare the patient for theatre. As you are reviewing his blood results you notice his platelet count is 87x10^9/L. On questioning the patient tells you he has idiopathic thrombocytopenic purpura (ITP). He is due for theatre in 4 hours. What is the most appropriate management of his pre-operative thrombocytopenia? Fresh frozen plasma Monitor for intra-operative bleeding Cryoprecipitate Start eltrombopag (thrombopoietin receptor agonist) Intravenous immunoglobulin (IVIG)
Patients who are not actively bleeding and have a platelet count of \> 80x10^9/L do not require any immediate management of their ITP pre-operatively and can be monitored intra-operatively. When treatment is required urgently this normally involves corticosteroids +/- IVIG. Eltrombopag is used in chronic ITP but requires 10-14 days to have an outcome on platelet count. Finally, cryoprecipitate and fresh frozen plasma are not indicated for the treatment of ITP.
2689
A 68-year-old man is undergoing a total hip replacement. He has a past medical history of ischaemic heart disease. During surgery he becomes hypotensive (blood pressure of 65/35 mmHg) with a pulse rate of 85 beats per minute. He has peripheral IV access. What is the most appropriate treatment? Adrenaline Dobutamine Cardioversion Noradrenaline Metaraminol
Drugs used to increase blood pressure in intra-operative hypotension can be broadly divided into those which are predominantly vasopressors and those which are positive inotropes (although there is a significant overlap). In this case, the patient has a normal heart rate and therefore a vasopressor such as metaraminol would be the most sensible choice. Metaraminol is primarily an alpha 1-adrenergic receptor agonist which causes systemic arteriole vasoconstriction, thereby increasing mean arterial blood pressure. Phenylephrine and metaraminol have dominant actions on alpha 1 receptors. Therefore these drugs are most suitably classed as vasopressors. Dobutamine is a powerful beta 1 receptor agonist which acts on the myocardium to increase myocardial contractility and heart rate. Doputamine is therefore most suitably named a positive inotrope. It is important to remember that there is often a significant overlap in properties of these agents, and noradrenaline, dopamine, and adrenaline have mixed alpha 1 and beta 1 receptor agonist properties and are therefore both positive inotropes and vasopressors.
2690
A 68-year-old lady is due to have a cholecystectomy for gallstone disease. She is on warfarin and her last INR two weeks ago was 2.7. When should you advise her to stop taking her warfarin? 3 days before surgery 1 day before surgery 5 days before surgery 10 days before surgery 14 days before surgery
In general, warfarin is usually stopped 5 days before planned surgery, and once the person's international normalized ration (INR) is less than 1.5 surgery can go ahead. Warfarin is usually resumed at the normal dose on the evening of surgery or the next day if haemostasis is adequate.
2691
Causes of addisonian crisis
Sepsis or surgery causing an acute exacerbation of chronic insufficiency Adrenal haemorrahge e.g. Waterhouse-Friedrichsen Steroid withdrawal
2692
Mx of Addisonian crisis
100mg IM or IV 1L NS infused over 30-5mins or with dextrose if hypogylcaemic Continue hydrocortisone 6 hourly until patient is stable. No fludrocortisone is necessary because high cortisol exerts weak MC action Oral replacement may begin after 24h and reduced to maintenance over 3-4d
2693
Epidemiology of oesophageal cancer
12/100000 (increassing due to increased Barret/s) 50-70y M\>F 5:1 Iran, Transkei, China
2694
RFs for oesophageal cancer?
EtOH Smoking Achalasia GORD-\> Barrett;s Plummer Vinson Fatty Diet Reduced Vit A and C Nitrosamine exposure
2695
Relative prevalences of the different kinds of oesophageal cancer
65% adenocarcinoma 35% SCC
2696
Oesophageal cancer Lower 3rd GORD-\> Barrett's-\> Dysplasia-\> Ca
Adenocarcinoma
2697
Oesophageal cancer Upper and middle 3rd Associated with EtOH and smoking Commonest type worldwide
SCC
2698
Progressive dysphagia: solids-\> liquids often altering dietary habit Weight loss Retrosternal chest pain Lymphadenopathy
Oesopageal carcinoma
2699
Oesophageal cancer with hoarsenss due to recurrent laryngeal nerve invasion Cough +/- aspiration pneumonia Location
Likely Upper 3rd
2700
Spread of oesophageal carcinoma
Direct extension, lymphatics and blood 75% of patients have mets at diagnosis
2701
Ix in oesophageal Ca
Bloods: FBC: anaemia LFTs: hepatic mets, albumin Dx: Upper GI endsocopy: biopsy Ba swallow, not often used, apple core stricture Staging: CT EUS Laparoscopy/mediastinoscopy: mets
2702
Apple core appearance Oesophageal carcinoma
2703
TNM Staging Oesophagus
􀁸 Tis: carcinoma in situ 􀁸 T1: submucosa 􀁸 T2: muscularis propria (circ / long) 􀁸 T3 adventicia 􀁸 T4: adjacent structures 􀁸 N1: regional nodes 􀁸 M1: distant mets
2704
MDT mx of oesophageal carcinoma
Upper GI surgeon and gastro Radiologist Pathologist Oncologist Specialist nurses Macmillan nurses Palliative care
2705
Surgical approach to oesophageal carcinoma
Only 25-30% have resectable tumours May be offered neo-adjuvant chemo before surgery to downstage tumour e.g. cisplatin + 5FU Approaches@ Ivor-Lewis McKeown Hiatal
2706
Ivor Lewis Oesophagectomy
2 stage approach In the Ivor Lewis esphagectomy, the esophageal tumor is removed through an abdominal incision and a right thoracotomy (a surgical incision of the chest wall). The esophagogastric anastomosis (reconnection between the stomach and remaining esophagus) is located in the upper chest.
2707
McKeown Oesophagectomy
Three stage Abdominal + R thoractomoy and left neck incision Used for lesions higher in the oesophagus Cervical anastomosis
2708
Px of oesophageal resection
Stage dependant 15% 5y
2709
Palliative approach to oesophageal carcinoma LAASAR
Majority of patients Laser coagulation Alcohol injeciton and reduce ascites (spironolactone) Stenting and secretion reduction e.g. hyoscine patch Analgesia e.g. fentanyl patch RTx: external or brachytherapy Referral: palliative care team Macmillan nurses Px: 5y \<5% Median: 4mo
2710
Benign tumours of oesophagus
Leiomyoma Lipoma Haemangioma Benign polyps
2711
Pathophysiology of GORD
LOS dysfunciton-\> reflux of gastric contents-\> oesophogaitis
2712
RFs: for GORD
Hiatus hernia Smoking EtOH Obesity Pregnancy Drugs: anti-AChM, nitrates, CCBs, TCAs Iatrogenic: Heller's myotomy
2713
Symptoms of GORD
Oesophageal: Retrosternal pain: heartburn Related to meals Worse lying down and stooping Relieved by antacids Belching Regurgitation Acid brash, water brash Odynophagia Extra-oesophageal Nocturnal asthma Chronic cough Laryngitis, sinusitis
2714
Cx of GORD
Oesophagitis Ulceration: rarely-\> haematemesis, melaena, reduced Fe Benign stricture: dysphagia Barrett's oesophagus: intestinal metaplasia of squamous epithelium-\> dysplasia-\> adenocarcinoma Oesophageal adenocarcinoma
2715
Ix in GORD
Isolated symptoms don't need Ix Bloods: FBC CXR: hiatus hernia may be seen OGD if fulfil criteria Ba swallow: hiatus hernia, dysmotility 24h pH testing + manometry
2716
Hiatus hernia retrocardiac opacity with air-fluid level
2717
Indications for OGD in GORD ALARMS
If \>55yrs Persistent symptoms despite Rx Anaemia Loss of weight Anorexia Recent onset progressive symptoms Melaena Swallowing difficulty
2718
What is the grading system for oesophagitis
Los Angeles grade A to D Grade A: one or more mucosal breaks no longer than 5 mm, none of which extends between the tops of the mucosal folds. Grade B: one or more mucosal breaks more than 5 mm long, none of which extends between the tops of two mucosal folds. Grade C: mucosal breaks that extend between the tops of two or more mucosal folds but which involve \<75% of the mucosal circumference Grade D: mucosal breaks which involve ≥75% of the mucosal circumference
2719
Rx in GORD
Conservative: Reduce weight Raise head of bed Small regular meals \>3h before bed Stop smoking and EtOH Avoid hot drinks and spicy food Stop drugs: NSAIDs, anti-AChM, nitrates, CCB, TCAs Medical: OTC antacids: Gaviscon, Mg Triscillate 1. Full dose PPI for 102mo Lansoprazole 30mg OD 2. No response-\> double dose PPI BD 3. No response add H2RA: Ranitidine 300mg Control, low dose acid suppression PRN Step down to lowest effective dose Surgical: Nissen fundoplication
2720
Indications for surgical Mx of GORD
Severe symptoms Refractory to medical therapy Confirmed reflux
2721
Nissen fundoplication
Aim: prevent reflux Repair diaphragm Can be open or lap Mobilise gastric fundus and wrap around lower oesophagus Close any diaphragamtic hiatus
2722
Cx of Nissen fundo
Gas-bloat syndrome: inability to belch/vomit Dysphagia if wrap too tight
2723
Alternatives to Nissen
Lap insertion of magnetic bead band With the patient under general anaesthesia, an implant is placed so that it encircles the distal oesophagus at the gastro-oesophageal junction. The implant is then secured in place. The implant consists of a ring of interlinked titanium beads, each with a weak magnetic force which holds the beads together to keep the distal oesophagus closed. When the patient swallows, the magnetic force is overcome, allowing the ring to open. After swallowing, magnetic attraction brings the beads together and the distal oesophagus is again closed. MRI is contra-indicated after this procedure. NICE currently recommends that the evidence on the safety and efficacy of laparoscopic insertion of a magnetic bead band for GORD is limited in quantity. Therefore, this procedure should only be used with special arrangements for clinical governance, consent and audit, or for research
2724
What are the indications for continuous PPI therapy
Patients with documented NSAID induced ulcer who must consitinue with NSAIDs Patients with severe reflux oesophagitis Patients with complicated reflux disease
2725
What are the different types of hiatus hernia
Sliding (80%) Rolling (15) Mixed (5%)
2726
Features of Sliding hiatus hernia
80% GOJ slides up into chest Often associated with GORD
2727
Thin little old lady Confused Distended AF
Think Rolling/ paraoesophageal hiatus hernia
2728
Features of rolling hiatus hernia
GOJ remains in abdomen but bulge of stomach rolls into chest alongside oesophagus LOS remains intact so GORD uncommon Can lead to strangulation
2729
Ix in hiatus hernia
CXR: gas bubble and fluid level in chest Ba swallow OGD: assess for oesphagitis 24pH and manometry to exclude dysmotility or achalasia
2730
Rx in hiatus hernia
Lose weight Treat reflux Surgery if intractable symptoms despite medical Rx Should repair rolling hernia due to risk of strangulation (even if asymptomatic)
2731
Hiatus hernia
2732
Epigastric pain Before meals and at night Relieved by eating
Duodenal ulcer
2733
Epigastric pain Worse on eating (weight loss) Relieved by antacids
Gastric ulcer
2734
RFs for PUD
H. pylori NSAIDs, steroids Smoking EtOH Stress GU Cushing's ulcers: head injury Curling's ulcers: burns
2735
Pathology of PUD
Punched out ulcers Usualy background of chronic inflammation DU: 4x commoner than GU, 1st part of duodenum GU: lesser curvature of gastric antrum
2736
Cx of PUD
Haemorrhage: Haematemesis or melaeana IDA Perforation: peritonitis Gastric outflow obstruction Vomiting, colic, distension Malignancy: Incresed risk with H. pylori infection Actual malignant transformation probably doesn't occur
2737
Ix in PUD
Bloods: FBC, urea (raised in UGI haemorrhage) C13 breath test or stool antigen test (C13 as test of eradication) OGD: Stop PPIs 2w before Biopsy ulcers to check for malignancy (only necessary with gastric) Gasrtin levels if Zollinger-Ellison suspected
2738
Mx of PUD
Conservative: Lose weight Stop smoking and reduce EtOH Avoid hot drinks and spicy food Stop drugs: NSAIDs, steroids OTC antacids Medical: OTC antacids: Gaviscon, Mgtriscillate Aimed at H pylori eradication: PAC500 or PMC250 If not H. pylroi induced: PPI
2739
PAC500 H pylori eradication triple therapy:
PPI: lansoprazole mg/BD 1g amoxicllin BD Clarithromycin 500BD
2740
PMC250 H prylori eradication
PPI Metronidazole Clarithromycin
2741
PPI standard dose
Lansoprazole 30mg/d
2742
H2RA standard dose
300mg nocte
2743
Surgical concepts in treatment of PUD
No acid- no ulcer Acid secretion is stimulated by gastrin from antral G cells and vagus nerve
2744
What are the surgical options for PUD
Rarely used Vagotomy Antrectomy with vagotomy Subtotal gastrectomy with Roux en Y
2745
Features of truncal vagotomy
Reduce acid secretion directly and via reduced gastrin Prevents pyloric sphincter relaxation Must be combined with pyloroplasty (widening of pylorus) or gastroenterostomy
2746
Features of selective vagotomy
Vagus nerve only denervated where it supplies lower oesophagus and stomach Pylorus left intact
2747
Features of antrectomy with vagotomy
Distal half of stomach removed Anastomosis: Billroth 1: directly to duodenum Billroth 2: to small bowel loop with duodenal stump oversown
2748
Physical cx with sx for PUD
Ca: increased risk of gastric Ca Reflux or billious vomiting (improves with time) Abdominal fullness Stricture Stump leakage
2749
Metabolic Cx of PUD sx
Dumping syndrome: Abdo distension, flushing, N/v, fainting, sweating Early: osmotic hypovolaemia Late: reactive hypoglycaemia Blind loop syndrome: malbasorption, diarrhoea Overgrowth of bacteria in duodenal stump Vitamin deficiency: Reduced parietal cells-\> B12 deficiency Bypassing proximal SB-\> Fe and folate deficiency Osteoporosis Weight loss: malabsroption of reduced calorie intake
2750
pH testing GORD
pH \<4 for \>4hrs
2751
Pathophysiology of perforated peptic ulcer
Perforated duodenal ulcer is commonest 1st part of duodenum: highest acid concentration Anterior perforation-\> air under diaphragm Posterior perforation can erode into GDA-\> bleed 3/4 of duodenum is retroperitoneal therefore no air under diaphragm if perforated Perforated GU Perforated Gastric Ca
2752
Sudden onset severe pain beginning in the epigastrium and then becoming generalised Peritonitis
Perforated peptic ucler
2753
DDx perforated peptic ulcer
Pancreatitis Acute cholecystitis AAA MI
2754
Ix in perforated peptic ulcer
Bloods; FBC, U+E, amylase, CRP, G+S, clotting ABG: mesenteric ischaemia Urine dipstick Erect CXR: must be erect for 15 minutes first Air under diaphragm seen in 70% False positive in Chilaiditi's sign AXR: Rigler's: aire on both sides of bowel wall
2755
Chailadati syndrome
Chilaiditi syndrome is a rare condition when pain occurs due to transposition of a loop of large intestine (usually transverse colon) in between the diaphragm and the liver, visible on plain abdominal X-ray or chest X-ray.
2756
Chest X-ray showing obvious Chilaiditi's sign, or presence of gas in the right colic angle between the liver and right hemidiaphragm.
2757
Subdiaphragmatic air
2758
2759
Mx of perforated peptic ulcer
ABC: NBM Aggressive fluid resusc: urinary catheter +/- CVP line Analgesia: 5-10mg/2h max +/- cyclizine Abx: cef and met NGT Conservative: May be considered if patient is not peritonitic Careful monitorig, fluid + Abx Omentum may seal perforation preventing operation in 50% Surgical: Laparotomy DU: abdominal washout and omental patch repair GU: excise ulcer and repair defect Partial/gastrectomy may be required Send specimen for histo: exclude Ca Test and treat: 90% perforated PU associated with H. pylori
2760
Cause of gastric outlet obstruction
Late complication of PUD-\> fibrotic stricturing Gastric Ca
2761
Hx of bloating, early satiety and nausea Copious projectile non bilious vomiting a few hours after meals Contains stale food Epigastric distension and succusion splash Adult
Gastric outlet obstruction
2762
Ix in gastric outlet obstruction
ABG: hypochloraemic, hypokalaemic metabolic alkalosis AXR: dilated gastric air bubble, air flud level, collapsed distal bowel OGD Contrast meal
2763
Rx in gastric outlet obstruction
Correct metabolic abnormality: 0.9% NS and KCl Benign: Endoscopic balloon dilatation Pyloroplasty or gastroenterostomy Malignant: Stenting Resection
2764
6-8w old Projectile vomiting minutes after feed RUQ mass: olive Visible peristalsis
Py Sten
2765
Dx in Py sten?
Test feed: palpate mass and see peristalsis Hypochloraemic hypokalaemic metabolic alkalosis USS
2766
Mx of py sten
Resus and correct metabolic abnormality NGT Ramstedt pyloromyotomy: divide muscularis propria
2767
Epidemiology of gastric cancer
23/100000 50y/o M\>F Increased in Japan, Eastern Europe, China, SAm
2768
RF for gastric cancer
Atrophic gastritis (intestinal metaplasia): pernicious anaemia/AI gatritis. H. pylori Diet: high in nitrates: smoked pickled salted. Metabolised to carcinogenic nitrosamines in GIT Smoking Blood group A Low SEC Familial: cadherin abnormality Partial gastrectomy
2769
Pathology of gastric cancer
Mainly adenocarcinomas Usually located on gastric antrum H. pylroi may -\> MALTOMA
2770
How can gastric cancer be classified?
By depth of invasion: Early gastric Ca: mucosa or submucosa Late gastric cancer: muscularis propria breached Microscopic appearanace: Intestinal: bulky glandular tumours, heaped ulceration Diffuse: infiltravive with signet ring morphology
2771
Anatomy of alimentary canal
4 basic tissue layers: Mucosa Submucosa Muscularis Serosa
2772
Where is Aurbach's plexus?
Myenteric plexus
2773
Where is Meissner's plexus
Submucosal plexus
2774
2775
What can be used to classify late gastric carcinoma?
Bormann Classification
2776
Outline Bormann classificaiton
Polypoid/fungating Excavating Ulcerating and raised Linitis plastica: leather bottle like thickening with flat rugae
2777
Usually presents late Weight loss and anorexia Dyspepsia: epigastric or retrosternal pain/discomfort Dysphagia N/V
Gastric Ca
2778
Signs of gastric Ca
Anaemia Epigastric mass Jaundice Ascites Hepatomegaly Virchow's node (Troisier's sign) Acanthosis nigricans
2779
Cx of gastric carcinoma
Perforation Upper GI bleed Gastric outlet obstruction: succession splash
2780
Succession splash
Succussion splash is a sloshing sound heard through the stethoscope during sudden movement of the patient on abdominal auscultation. It reflects the presence of gas and fluid in an obstructed organ, as in gastric outlet obstruction. Physical examination can show an abdominal succussion splash, which is elicited by placing the stethoscope over the upper abdomen and rocking the patient back and forth at the hips. Retained gastric material greater than three hours after a meal will generate a splash sound and indicate the presence of a hollow viscus filled with both fluid and gas. An example would be a gastric outflow obstruction as pyloric stenosis, with abdominal succussion splash
2781
Spread of gastric carcinoma
Within stomach: linitis plastica Direct invasion: pancreas Lymphatic: Virchow's node Blood: liver and lung Transcoelomic: Ovaries: Krukengerg tumour Sister Mary Joseph nodule: umbilical mets
2782
Krukenburg tumour
Transcoelomic spread to ovaries associated with gastric Ca and signet ring morphology
2783
Sister Mary Joseph Nodule
Palpable node bulging in the umbilicus
2784
Sister Mary Joseph Nodule
2785
Trosier's Sign
Virchow's node (or signal node) is a lymph node in the left supraclavicular fossa (the area above the left clavicle). It takes its supply from lymph vessels in the abdominal cavity. The finding of an enlarged, hard node (also referred to as Troisier's sign) has long been regarded as strongly indicative of the presence of cancer in the abdomen, specifically gastric cancer, that has spread through the lymph vessels. It is sometimes called the signal node or sentinel node for the same reason. Despite this, the concept is not directly related to the sentinel node procedure sometimes used in cancer surgery, and it is also unrelated to the "sentinel gland" of the greater omentum.[citation needed] It is named after Rudolf Virchow (1821–1902), the German pathologist who first described the gland and its association with gastric cancer in 1848.[1] The French pathologist Charles Emile Troisier noted in 1889 that other abdominal cancers, too, could spread to the node
2786
Ix in gastric carcinoma
Bloods: FBC: anaemia LFTs and clotting Imaging: CXR: mets USS: liver mets Gastroscopy and biopsy Ba meal Staging: Endoluminal US CT/MRI Diagnostic laparoscopy
2787
Mx of gastric carcinoma
Medical palliation: Analgesia e.g. fentanyl patch PPI Secretion control CTx: epirubicin, 5FU, cisplatin Palliative care team package Surgical palliation Pyloric stenting Bypass procedures Curative surgery Can be resected endoscopically Partial or total gastrectomy with roux en Y to prevent bile reflux Spleen and part of pancreas may be removed
2788
Roux en Y
In general surgery, a Roux-en-Y anastomosis, or Roux-en-Y, is a surgically created end-to-side anastomosis, most commonly performed for weight loss or to remove a malignancy. Typically, it is between stomach and small bowel that is distal (or further down the gastrointestinal tract) from the cut end. The name is derived from the surgeon who first described it (César Roux)[1] and the stick-figure representation. Diagrammatically, the Roux-en-Y anastomosis looks a little like the letter Y. Typically, the two upper limbs of the Y represent (1) the proximal segment of stomach and the distal small bowel it joins with and (2) the blind end that is surgically divided off, and the lower part of the Y is formed by the distal small bowel beyond the anastomosis. Roux-en-Ys are used in several operations and collectively called Roux operations.[1] When describing the surgery, the Roux limb is the efferent or antegrade limb that serves as the primary recipient of food after the surgery, while the hepatobiliary or afferent limb that anatamoses with the biliary system serves as the recipient for biliary secretions, which then travel through the residual stomach from the liver and into the Roux limb to aid digestion. The altered anatomy can contribute to indigestion following surgery
2789
Px in gatric carcinoma
5y 10% Sx: 20-50%
2790
Benign gastric neoplasms
Benign polyps: adenomas Leiomyoma Lipoma Haemangioma Schwannoma
2791
Malignant additional gastric neoplasms
Lymphoid Carcinoid GIST
2792
GIST
Gastrointestinal stromal tumour Commonest mesenchymal tumour of the GIT \>50% occur in the stomach
2793
Epidemiology of GIST
M=F 60y Increased with NF1
2794
Pathology of GIST
Airse from intestinal cells of cajal located in muscularis propria Pacemaker cells On OGD: well demarcated spherical ams with central punctum
2795
Presentation of GIST
Mass effects: abdo pain, obstruction Ulceration: bleeding
2796
Poor Px in GIST
Size Extra-gastric location Raised mitotic index
2797
Mx of GIST
Medical: Unresectable, recurrent or metastatic disese Imatinib: seletive RtkI Surgical: Resection
2798
Def: carcinoid tumours
Diverse group of neuroendocrine tumours of enterochromaffin cell origin May secrete multiple horomones 10% occur in stomach
2799
Features of gastric carcinoid tumours
Atrophic gastritis-\> reduced acid produciton-\> raised gastrin-\> ECL hyperplasia-\> carcinoid tumour Gastrinomas may also-\> carcinoid
2800
What is the most common site of extranodal lymphoma?
Gastric lymphoma
2801
Features of gastric lymphoma
Most commonly MALToma due to chronic H. pylori gastritis H. pylroi eradication can be curative
2802
Pathophysiology of ZE syndrome
Gastrin-secreting tumour (gastrinoma) most commonly found in the small intestine or pancreas Increased gastrin-\> raised HCL-\> PUD + chronic diarrhoea Diahrroea is a consequence of pancreatic enzymes ECL proliferation can -\> carcinoid tumours 60-90% of gastrinomas are malignant 25% associated with MEN1
2803
Abdominal pain and dyspepsia Chronic diarrhoea/steatorrhoea Refractory PUD
ZE syndrome
2804
Ix in ZE syndrome
Raised gastrin with raised ++HCl (pH\<2) MRI/CT Somatostatin R scintigraphy
2805
Rx in ZE syndrome
High dose PPI Sx: Tumour resection May do subtotal gastrectomy wtih Roux en Y
2806
Benefits of bariatric surgery?
Sustained weight loss Symptom improvement: sleep apnoea Mobility HTN DM
2807
Indications for bariatric surgery
All criteria must be met: BMI \>40 or \>35 with significant co-morbidities that could improve with weight Failure of non-surgical mx to achieve and maintain clinically beneficail weight loss for 6m Fit for Sx and anaesthesia Integrated programm providing guidance on diet, physical activity, psychosocial concerns and lifelong medical monitoring Well informed and motivated patient If BMI \>50 sx is first line Rx
2808
Surgical approaches: bariatric
Laparoscopic gastric banding Roux-en-Y Gastric Bypass
2809
Laparoscopic Gastric Bypass
Inflatable silicone band around proximal stomach-\> small pre-stomach pouch Limits food intake Slows digestions At 1y 46% mean XS weight loss
2810
Roux en Y Gastric Bypass
Oesophagojejunostomy allows bypass of stomach, duodenum and proximal jejunum Alters secretion of hormones influencing glucose regulation and perception of hunger/satiety Greater weight loss and lower reoperation rates
2811
Cx of Roux-en-Y gastric bypass
Dumping syndrome Wound infection Hernias Malabsorption Diarrhoea Mortality: 0.5%
2812
a large vacuole of mucin which displaces the nucleus to one side
Signet ring cells
2813
Patients with inter current illness (e.g. diabetes, organ failure) Patient of systemically unwell Gallbladder inflammation in absence of stones High fever
Acalculous cholecystitis
2814
A 34-year-old male is admitted with central abdominal pain radiating through to the back and vomiting. The following results are obtained: Amylase1,245 u/dl Which one of the following medications is most likely to be responsible? Phenytoin Sodium valproate Metoclopramide Sumatriptan Pizotifen
Sodium valproate induced pancreatitis is more common in young adults and tends to occur within the first few months of treatment. Asymptomatic elevation of the amylase level is seen in up to 10% of patients
2815
Drugs causing acute pancreatitis
Azathioprine Mesalazine (\*pancreatitis is 7 times more common in patients taking mesalazine than sulfasalazine) Didanosine Bendroflumethiazide Furosemide Pentamidine Steroids VPA
2816
Which of the following is the most sensitive blood test for diagnosis of acute pancreatitis? Amylase Lipase C-peptide Trypsin Trysinogen
Lipase The serum amylase may rise and fall quite quickly and lead to a false negative result. Should the clinical picture not be concordant with the amylase level then serum lipase or a CT Scan should be performed.
2817
An 83-year-old female, with a history of osteoporosis, presented to the emergency department with a suspected hip fracture. She is generally frail and has a background of dementia, ischaemic heart disease and chronic obstructive pulmonary disease. There is no history of hip pain due to osteoarthritis but she does walk with the aid of a walking stick. She received an x-ray, which shows a displaced subcapital fracture of the femur. What is the most likely surgical treatment option for this type of fracture? Dynamic hip screw Hemiarthroplasty Kirschner wires Intramedullary nail Total hip replacement
A subcapital fracture is the commonest type of intracapsular fracture of the proximal femur. The intertrochanteric line is the line connecting the greater and lesser trochanters. Any fracture proximal to that line is classed as intracapsular, while any fracture distal is classed as extracapsular. Since the blood supply is threatened in intracapsular fractures, as a general rule: ## Footnote Intracapsular femoral fracture - hemiarthroplasty extracapsular femoral fracture - dynamic hip screw A hemiarthroplasty is favoured over a total hip replacement in this situation as the patient is: frail, with a background of chronic health problems no history of hip osteoarthritis
2818
Def: hernia
Protrusion of a viscus or part of a viscus through the walls of its containing cavity into an abnromal position
2819
def: reducible hernia
Sac can be returned to the abdominal cavity either spontaneously or with manipulation
2820
def: irreducible hernia
Sac cannot be returned despite pressure or maniupulation
2821
def: strangulated hernia
Blood supply of contents is compromised due to pressure at the neck of the hernia
2822
def: sliding hernia
Part of the sac is formed by bowel e.g. caecum or sigmoid, take care when excising sac
2823
def: Maydl's hernia
Herniating double loop of bowel. Strangulated portion may reside as a single loop inside the abdomen
2824
Maydl's hernia
2825
Def: Maydl's hernia
Herniating double loop of bowel. Strangulated portion may reside as a single loop inside the abdomen
2826
def: Littre's hernia
Hernia sac containing strangulated Meckel's diverticulum
2827
Def: Richter's hernia
Only part of circumference of bowel is within sac. Most commonly seen with femoral hernias. Can strangulate without obstructing
2828
Def: Amyand's hernia
Inguinal hernia containing strangulated appendix
2829
def: Pantaloon
Simultaneous direct and indirect hernia
2830
Herniotomy
Excivision of hernial sac
2831
Herniorrhaphy
Suture repair of hernia defect
2832
Hernioplasty
Mesh repair of hernial defect
2833
Epidemiology of inguinal hernia
3% of adults will require hernioplasty 4% of male neonates will have hernia M\>F 9:1 (due to testes descent) Majority present in 50s
2834
Pathology of inguinal hernia
Commoner on R (?damage to ilioinguinal N and appendicectomy-\> muscle weakness) 5% are bilateral 8-15% present as emergency with strangulation/obstruction
2835
Aetiology of inguinal hernias
Congenital Acquired
2836
Congenital inguinal hernias
Patent processus vaginalis Should obliterate following descent of the testes If it stays patent, it may fill with Fluid-\> hydrocele Bowel/omentum-\> indirect hernia
2837
Acquired causes of inguinal hernia
Mainly things which raise IAP Chronic cough: COPD, asthma Prostatism Constipation Severe muscular effort e.g. heavy lifting Previous incision/repair Ascites/ obesity Appendicectomy
2838
Classification of inguinal hernias
Indirect Direct
2839
What is the most common type of inguinal hernia?
Indirect (80%), commoner in young
2840
Features of indirect inguinal hernia
Congenital patent processus vaginalis Emerge through deep ring Same 3 coverings as cord and descend into the scrotum Can strangulate
2841
Features of direct hernia
20%: commoner in elderly Acquired Emerge through Hesselbach's triangle Can acquire internal and external spermatic fascia Rarely descend into the scrotum Rarely strangulate
2842
Borders of Hesselbach's trianagle
Inguinal ligament as base Inferior epigastric vessels as the lateral border Lateral border of rectus sheath as medial border FC Hesselbach: German anatomist and surgeon
2843
Direct inguinal hernia occur through which structure?
Hesselbach's triangle
2844
Layers of the abdominal wall
Skin Camper's fascia: fatty Scarpa's fascia: membranous External olbique Internal oblique Nerves and vessels Transversus abdominis Transversalis fascia Pr-peritoneal fat Parietal peritoneum
2845
Location of deep inguinal ring
1.5cm above femoral pulse or mid-point of inguinal ligament (ASIS-\> PT)
2846
Contents of the inguinal canal
Ilioinguinal N and spermatic cord in males Ilioinguinal nerve, genital branch of genitofemoral nerve and round ligament of uterus in females
2847
Course of the ilioinguinal nerve
Enters canal directly through the anterior wall, does not pass through the deep ring Exits through the superficial ring
2848
Function of the ilioinguinal nerve
Supplies skin at the root of the penis and the scrotum and small area of skin on the upper thigh
2849
Contents of the spermatic cord Rule of 3s
3 layers of fascia: External spermatic: from external oblique Cremasteric: from internal oblique Internal spermatic: from transversalis fascia 3 arteries: Testicular: from aorta Cremasteric: from inferior epigastric Artery of vas: from inferiror vesciular artery 3 veins: Pampiniform plexus-\> R drains into IVC, left to left renal Cremasteric vein Vein of vas 2 nerves: Nerve to cremaster from genito-femoral nerve Sympathetic fibres from T10-T11 ilioinguinal N (is on the cord) 3 other structures: Vas deferens Lymphatics of the testes-\> para aortic nodes Obliterated processus vaginalis
2850
Layers of fascia in spermatic cord
External speramtic fascia: from external oblique Cremasteric fascia: from internal oblique Internal spermatic fascia: from transversalis fascia
2851
Arteries of the spermatic cord
Testicular: from aorta Cremasteric: from inferior epigastric Artery of vas: from the inferior vesicular arteries
2852
Veins of the spermatic cord
Pampiniform plexus-\> R-\> IVC, L-\> LRV Cremasteric vein Vein of vas
2853
Nerves of spermatic cord
Ilioinguinal on the cord Nerve to cremaster: from genitofemoral nerve Sympathetic fibres from T10-T11
2854
Additional structures in the spermatic cord
Vas deferens Lymphatics of the testes (drain to para-aortic nodes) Obliterated processus vaginalis
2855
Features of inferior epigastric vessels
Arise from EIA immediately superior to inguinal ligament Can be seen passing deep to the posterior wall Sac arising laterally= indirect Sac arising medially= direct
2856
Structure of the inguinal canal
4cm long Floor: inguinal ligament Roof: arching fibres of the internal olbique and transversus abdominis Anterior: external oblique aponeurosis and internal oblique for lateral 3rd Posterior: transveralis fascia and conjoint tendon for medial 3rd Laterally: deep ring Medially: pubic tubercle
2857
Conjoint tendon=
Combined insertion of internal oblique and trasnversus abdominis into pubic crest and pectineal line
2858
Where does the rectus sheath end?
Below arcuate line
2859
Ix in inguinal hernias
US if Dx in doubt
2860
Lump in groin which may descend into scrotum Exacerbated by crying Commonly obstruct Child
Indirect inguinal hernia
2861
Lump in groin exacerbated by straining/cough May be clear precipitating event Dragging pain radiating to groin May present with obstruction/strangulation Adult
Inguinal hernia ?direct
2862
Key questions in hernia hx
Reducible? Ever episodes of obstruction/strangulation Predisposing factors: cough, straining, lifting Occupation and social circumstances
2863
Mx of hernia
Non-surgical: Rx RFs: cough, constipation Lose weight Truss Surgical: Tension-free mesh (e.g. Lichenstein repair) better cf. suture repair (\<2% vs 10% recurrence) Open approach can be done under LA or GA Lap approach allows bilateral repair and improved cosmesis. Also preferred for recurrent hernias 1o unilateral repairs should be open Children only require sac excision (herniotomy)
2864
Early Cx of hernia repair
Haematoma/seroma formation (10%) Intra-abdominal injury (lap) Infection: 1% Urinary retention
2865
Late cx of hernia repair
Recurrence (\<2%) Iscaehmic orchitis: 0.5% Chronic groin pain/paraesthesia: 5%
2866
Def: femoral hernia
Protrusion of viscus through the femoral canal
2867
Epidemiology of femoral hernia
F\>M **Inguinal hernias are still more comon in F** Middle aged and elderly
2868
Aetiology of femoral canal
Acquired: raised intra-abdominal pressure Femoral canal larger in females due to shape of pelvis and changes in its configuration due to childbirth
2869
Neck inferior and lateral to pubic tubercle Cough impulse Often irreducible (due to tight borders) Commonly present with obstruciton or strangulation Tender, red and hot Abdo pain, distension, vomiting, constipation
?Femoral hernia
2870
Mx of femoral hernia
50% risk of strangulation within 1m Require urgent surgery Elective or Emergency
2871
Elective femoral hernia repair
Lockwood Approach Low incision over hernia with herniotomy and herniorrhaphy: suture inguinal ligament to pectineal ligament
2872
2873
Emergency femoral hernia repair
High approach in inguinal region to allow inspection and resection of non-viable bowel Then herniotomy and herniorrhaphy Vertical incision
2874
Anatomy of femoral sheath
In the femoral triangle, femoral artery vein and lymphatics are enclosed within femoral sheath Sheath is contiuous superiorly with transversalis fascia Each structure has its own compartment Most medial compartment is the femoral canal
2875
Borders of the femoral canal
Anterior: inguinal ligaemnt Posterior: pectineal ligament (ligament of Cooper and pectineus) Medially: lacunar ligament and pubic bone Laterally: femoral vein Contents: fat and Cloquet's node
2876
Cloquet's node
Cloquet's node (or gland) is a lymph node[1][2] found in the inguinal region. It is named for French surgeon Jules Germain Cloquet.[3][4] It can be considered the superiormost deep inguinal lymph nodes or inferiormost external iliac lymph nodes.[
2877
Def: incisional hernia
Hernia arising through a previously acquired defect
2878
Epidemiology of incisional hernia
6% of surgical incisions
2879
Categorisation of RFs for incisional hernia
Pre-operative Intra-operative Post-operative
2880
Pre-operative RFs for incisional hernia
Increased age Obesity or malnutirtion Comorbidities: DM, renal failure, malignancy Drugs: steroids, chemo, RTx
2881
Intra-operative RFs for incisional hernia
Surgical technique/skill (major factor) Too small suture bites Inappropriate suture material Incision type e.g. midline Placing drains through wounds
2882
Post-operative RFs for incisional hernia
Raised IAP: chronic cough, post-op ileus, straining Infection Haematoma
2883
Mx of incisional hernia
Sx not appropriate for all patients Must balance risk of operation and recurrence with risk of obstruction/strangulation and patient choice Usually broad-necked, therefore low risk of strangulation
2884
Mx of incisional hernia
Conservative: Manage RFs e.g. constipation, cough Weight loss Elasticated corset or truss Surgical: Pre-op: Optimise cardiorespiratory funciton Encourage weight loss Nylon mesh repair: open or lap
2885
Features of umbilical hernias
Congenital 3% of LBs Defect in umbilical scar
2886
RFs for umbilical hernia
Afro-caribbean Trisomy 21 Congenital hypothyroidism
2887
Mx of umbilical hernia
Usually resolves by 2-3y Mesh repair if no closure Can recur in adults: pregnancy or gross ascites
2888
Features of paraumbilical hernia
Acquired: middle aged obese men Defect through linea alba just above or below umbilicus Small defect-\> omentum, often strangulates
2889
RFs for paraumbilical hernia
Chronic cough Straining
2890
Mx of paraumbilcal repair
Mayo (double breast linea alba with sutures)/ mesh repair
2891
Feature of epigastric hernia
Young M\>F Pea-sized swelling caused by defect in linea alba above umbilicus Usually contains omentum: can strangulae
2892
Mx of epigastric hernia
Mesh repair
2893
Features of Spigelian hernia
Hernia through linea semilunaris Hernia lies between layers of abdo wall Palpable mass more likely to be colon Ca
2894
Features of obturator hernia
Old aged F\>M Sac protrudes through obturator foramen Pain on inner aspect of thigh or knee Frequently present obstructed/strangulated
2895
Features of lumbar hernia
Middle-aged M\>F Typically following loin incisions Hernia through superior/inferior lumbar triangles
2896
Features of sciatic hernia
Hernia through LSF Usually presents as SBO + gluteal mass
2897
Gluteal hernia
Hernia through GSF Usually presents as SBO + gluteal mass
2898
Anatomy of the rectum
12cm Sacral promontory to levator ani muscle 3 tenia coli fuse around the rectum to form a continuous muscle layer
2899
Anatomy of the anal canal
4cm Levator ani muscle to anal verge Upper 2/3rd of the canal: lined by columnar epithelium Insensate Superior rectal artery and vein Internal iliac nodes Lower 1/rd of the canal: Lined by squamous epithelium Sensate Middle and inferior rectal arteries and veins Superficial inguinal nodes
2900
What is the dentate line?
Squamomucosal junciton between columnar epithelium of upper 2/3rd of anal canal and lower 1/3rd which is lined by squamous epihtelium
2901
What is the white line
Where anal canal becomes true skin
2902
What are the anal sphincters?
Internal External
2903
Features of internal anal sphincter
Thickening of rectal smooth muscle Involuntary control
2904
Features of external anal sphincter
Three rings of skeltal muscle: deep, superficial, subcutaenous Voluntary control
2905
What is the anorectal ring
Deep segment of external sphincter which is continuous with puborectalis muscle (part of levator ani) Palpable on PR: 5cm from anus Demarcates junction between the anal canal and rectum Must be preserved to maintain continence
2906
Def: perianal haematoma
Subcutaneous bleeding from a burst venule caused by straining or passage of hard stool Also called an external pile: misnomer
2907
Tender blue lump at the anal margin Pain worsened by defacation or movement
Perianal haematoma
2908
Rx of perianal haematoma
Analgesia and spontaenous resolution Evacuation under LA
2909
Young anxious men Crampy anorectal pain, worse at night Unrelated to defecation Associated with trigeminal neuralgia
Proctalgia fugax
2910
Rx in proctalgia fugax
Reassurance GTN cream
2911
Features of perineal warts
Commonly seen in MSM HPV Syphillis
2912
Condylomata accuminata
HPV Rx: podophyllin paint, cryo, surgical excision
2913
Condylomata lata
Syphillis Rx: penicllin
2914
Causes of pruritus ani
50% idiopathic Poor hygiene Haemorrhoids Anal fissure Anal fistula Fungi, worms Crohn's Neoplasia
2915
Def: haemorrhoids
Disrupted and dilated anal cushions
2916
Pathophysiology of haemorrhoids
Anal cushion: mass of spongy vascular tissue Positioned at 3, 7, and 11 o' clock where the three major arteries that feed the vascular plexuses feed the anal canal Gravity, straining-\> engorgement and enlargement of anal cushions Hard stool disrupts connective tissue around cushions Cushions protrude and can be damaged by hard stool-\> bright red capillary bleeding Haemorrhoids arise above dentate line therefore **NOT PAINFUL** May be gripped by anal sphincter-\> thrombosis, strangulated piles are acutely painful. May ulcerate or infarct
2917
Causes of haemorrhoids
Constipation with prolonged straining Venous congestion may contribute Pregnancy, abdominal tumour, portal HTN
2918
Internal haeomorrhoid classification
Grade 1: never prolapse 2nd: prolapse on defecation but spontaneously reduce 3rd: prolapse on defecation but require digital reduction 4th: remain permanently prolapsed
2919
Fresh painless PR bleeding: bright red, on paper, on stool, may drip into pan Pruritus ani Lump in perianal area Severe pain= thrombosis
Haemorrhoids
2920
Examination in haemorrhoids
Full abdo exam palpating for masses Inspect perianal area: masses, recent bleeding DRE: can't palpate piles unless thrombosed Rigid sig to ideitify higher rectal pathology Proctoscopy: also allows Rx
2921
DDx in haemorrhoids
Perianal haematoma Fissure Abscess Tumour (must exclude in all cases)
2922
Mx of haemorrhoids
Conservatve: Increase fibre and fluid intake Stop straining at stool Medical: Topical preparations: anusol (hydrocortisone), topical analgesics Laxatives: lactulose, fybogel Interventional: Injection scleropathy Barron's banding Cryotherapy Infrared coagulation Bipolar diathermy Surgical: Haemorrhoidectomy
2923
Injection scleropathy
Injection sclerosant (5% phenol in Almond oil) Injection above dentate line SE: impotence, prostatisi
2924
Barron's banding
Haemorrhoid intervention: thrombosis and separation SE: bleeding, infection
2925
SE cryotherpay for haemorrhoids
Watery discharge3 post procedure
2926
What is most effective outpatient haemorrhoid rx
Band ligation
2927
Surgical options for haemorrids
Haemorrhoidectomy: Excision of piles and ligation of vascular perdicles Lactulose and metronidazole 1w pre-op Discharge with laxatives post-op Haemorrhoid artery ligation can also be used
2928
SE of haemorrhoidectomy
Bleeding Stenosis
2929
Mx of thrombosed piles
Analgesia Ice-packs Stool softeners Bed rest with elevate foot of bed Pain usually resolves in 2-3w Hamoerrhoidectomy is not usually necessary
2930
Def: anal fissure
Tear of squamous epithelial lining in lower anal canal
2931
Causes of anal fissure
Mostly trauma 2o to the passage of hard stool Associated with constipation Spasm of internal anal sphincter contributes to pain and ischaemia-:\> poor healing Commoner in women Rarer causes often lead to multiple +/- lateral fissures: crohn's, herpes, anal ca
2932
Intense anal pain, especially on defecation, may prevent patients from passing stools Fresh rectal bleeding, mostly on paper
Anal fissure
2933
Examination findings in anal fissure
PR often impossible Midline ulcer seen, usually posteriorly at 6 o'clock May be anterior May be a mucosal tag: sentinal pile, usually at 6 o'clock Groin LNs suggest complicating factor e.g. HIV
2934
Anal fissure with sentinal skin pile
2935
Mx of recurrent, chronic or difficult to Rx anal fissures
EUA
2936
Mx of fissure in ano
Conservative: Soaks in warm bath Toileting and dietary advice Medicals: Lactulose + fybogel Topical: resolution in 75: lignocaine, GTN, diltiazem Botulinum injeciton Surgical: Lateral partial sphincterectomy
2937
Surgical Mx of anal fissure
Lateral partial sphincterectomy Division of internal anal sphincter at 3 o'clock Pre-op anorectal US and mannometry Lord's operation is no longer used due to high rates of incontinence (anal dilatation under anaesthesia)
2938
Cx of lateral partial sphincterectomy
Minor feacal/flatus incontinence Perianal abscess
2939
Def: anal fistula
Abnromal connection between ano-rectal canal and the skin
2940
Pathogenesis of anofistula
Usually occurs 2o to perianal sepsis Blockage of intramuscular glands-\> abscess Abscess discharges to form a fistula
2941
Associations of fistula in ano
Crohn's Diverticular disease Rectal Ca Immunosuppression
2942
Classficiation of anal fistula
Parks Classificaiton inter-sphincteric (~70%): fistula crosses the intersphincteric space and does not cross the external sphincter trans-sphincteric (25%): fistula crosses from the intersphincteric space, through the external sphincter and into the ischiorectal fossa supra-sphincteric (5%): fistula passes superiorly into the intersphincteric space, and over the top of the puborectalis muscle then descending through the iliococcygeus muscle into the ischiorectal fossa and then skin extra-sphincteric (1%): fistula crosses from perineal skin through the ischiorectal fossa and levator ani muscle complex into the rectum (i.e. is outside the external anal sphincter)
2943
What is Goodsall's rule
Determines the path of an anal fistula tract Internal opening of the fistula is dependant on where the fistula is located relative to the anal clock and the transverse anal line If the internal opening is anterior to the transverse anal line, there will be a usually simple direct radial fistulous tract If the internal opening is posterior to the transverse anal line, there will be a tortusous and often more complex fistulous tract that enters posteriorly in the midline (6 o'clock) Exception: anterior fistulas lying more than 3cm from the anus which may have a curved track that opens into the posterior midline of the anal canal
2944
2945
2946
Persitent anal discharge Perianal pain or discomfort
?anal fistula
2947
Examination may visualise external opening: may be pus Induration around fistula on DRE Proctoscopy may reveal internal opening
anal fistula
2948
Ix in anal fistula
MRI Endoanal US
2949
Rx of anal fistula
Extent of fistula must be delineated by probing the fistula @ EUA Approach varies dependant on whether the fistula is high or low
2950
Mx of low anal fistula
Fistulotomy and excision Laid open to heal by 2o intention
2951
Mx of high anal fistula
Fistulotomy could damage the anorectal ring Suture: a seton: passed through fistula and gradually tightened over months. Stimulates fibrosis of tract. Scar tissue holds sphincter together
2952
Pathogenesis of peri-anal sepsis/abscess
Anal gland blockage-\> infection-\> abscess e.g. E. Coli, bacteroides May develop from skin infections e.g. sebaceous gland or hair follcile Staphs
2953
Associations of peri-anal sepsis/abscess
Crohn's DM Malignancy
2954
Classficaiton of peri-anal abscesses
Perianal: 45% discrete local red swelling close to the anal verge Ischiorectal \<30%: systemic upset, extremely painful on DRE Intersphincteric/intermuscular: \>20% Pelvirectal/supralevator: 5% Systemic upset bladder irritaiton
2955
2956
Throbbing perianal pain, worse on sitting Occasionally a purulent anal discharge Perianal mass or cellulitic area Fluctuant mass on PR septic signs
?Peri-anal abscess
2957
Rx in perianal abscess
Abx may suffice if instigated early Most cases require EUA with I&D Wound packed Heals by second intention Daily dressing for 7-10d Look for anal fistula which complicates 30% of abscesses
2958
Different types of wound healing
Primary intention: healing of clean wound without tissue loss, i.e. edges brought together Secondary intention: wound allowed to granulate, resulting in broader scar Teritary intention: intially, cleaned debrided, purposely left open.
2959
Def: pilonoidal sinus
Pilonoidal: nest of hair Sinus: blind ending tract, lined either by epithelial or granulation tissue which opens onto an epithelial surface
2960
Pathophysiology of pilnoidal sinus
Hair works way beneath skin-\> foreign body reaction-\> abscess formation usually occurs in the natal cleft
2961
RFs for pilnoidal sinus
M\>F 4:1 Mediterranean, Middle east, Asians Often overweight with poor personal hygiene Occupation with lots of sitting
2962
Persistent discharge or purulent or clear fluid Recurrent pain Abscesses Natal cleft
Pilonidal sinus
2963
Rx in pilonidal sinus
Conservative: Hygiene advice Shave/remove hair from affected area Surgical: I&D of abscesses Elective sinus excision: methylene blue to outline tract. Recurrence in 4-15%
2964
Epidemiology of anal carcinoma
Relatively uncommon 250-300 caes per year in UK
2965
Pathology of anal carcinoma
80% are SCCs, others: melanomas, adenocarcinomas Anal margin tumours Anal canal tumours
2966
Features of anal margin tumours
Well differentatied keratinising lesions Common in men Good Px
2967
Features of anal canal tumours
Arise above dentate line Poorly differentiated, non-keratinising Commoner in women Worse prognosis
2968
Spread of anal carcinoma
Above dentate line-\> internal iliac nodes Below dentate line-\> inguinal nodes
2969
Aetiology of anal carcinoma
HPV 16, 18, 31, 33 is important factor Increased incidence in MSM Increased incidence if perianal warts
2970
Perianal pain and bleeding Pruritus ani Faecal incontinence May-\> rectovaginal fistula
Anal carcinoma
2971
Faecal incontinence in anal carcinoma
70% have sphincter involvement at presentation Important RED FLAG
2972
Examination findings in anal carcinoma
Palpable lesion in only 25%, +/- palpable inguinal nodes
2973
Ix in anal carcinoma
FBC: ACD Endoanal US Rectal EUA and biopsy CT/MRI to assess pelvic spread
2974
Rx of anal carcinoma
ChemoRTx: most patients. 50% 5y Sx: reserved for Tumours that fail to respond GI obstruction Small anal margin tumours without sphincter involvement
2975
Def: rectal prolapse
Protrusion of rectal tissue through the anal canal
2976
Classification of rectal prolapse
Type 1: mucosal prolapse Partial prolapse of redundant mucosa Commoner in children, especially in CF Essentially large piles, same Rx Type 2: Full thickness prolapse Commoner cf. type 1 Usually elderly females with poor O+G hx
2977
Mass extruding from rectum on defecation May reduce spontaneously or require manual reduction May become oedmeatous and ulcerated, pain and bleeding Faecal soiling Associated with vaginal prolapse and urinary incontinennce
Rectal prolapse
2978
Examination findings in rectal prolapse
Visibile prolapse: brought out on straining +/- excoriation and ulceration Reduced sphincter tone on PR Associated with uterovaginal prolapse
2979
Ix in rectal prolapse
Sigmoidoscopy to exclude proximal lesions Anal manometry Endoanal US MRI
2980
Rx partial rectal prolapse
Phenol injection Rubber band ligation Delorme's procedure
2981
Delorme's procedure
A Delorme's procedure aims to repair the prolapse. This operation involves the surgeon remov- ing some of the prolapsed lining of the rectum (mucosa) and reinforcing the muscle of the rectum by placating stitches. This is done via the anus. No external incision is needed.
2982
Mx of complete rectal prolapse
Conservative: Pelvic floor exercises Stool softeners Sx: Abdominal appraoach: Rectopexy, lap or open. Mobilised rectum fixed to sacrum with mesh Perineal appraoch: Delorme's procedure
2983
Relative proportion of small bowel neoplasms
35% benign 65% malignant (2% of GI malignancies)
2984
Benign small bowel neoplasms
Lipoma Leiomyoma Neurofibroma Haemangioma Adenomatous polyps (FAP, Peutz-Jehgers)
2985
Malignant small bowel neoplasms
Adenocarcinoma (40% of malignant tumours) Carcinoid (40%) Lymphoma (especially with coeliac disease: EATL) Gastrointestinal stromal tumours
2986
Presentation of small bowel neoplasms
Often non-specific symptoms so present late N/V, obstruction Weight loss and abdominal pain Bleeding Jaundice from biliary obstruction or liver mets
2987
Imaging in small bowel neoplasms
AXR: SBO Ba follow through CT Endocscopy: Push enteroscopy Capsule enteroscopy
2988
Def: carcinoid tumours
Diverse group of neuroendocrine tumours of enterochromaffin cell origin capable of producing 5HT May be derived from foregut: resp tract Midgut: stomach, ileum, appendix Hindgut: colorectum
2989
What can carcinoid tumours secrete
5HT Vasoactive intestinal peptide Gastrin Glucagon Insulin ACTH Hindgut tumours rarely secrete 5HT
2990
What does carcinoid syndrome suggest?
Bypass of FPM and is strongly associated with metastatic disease
2991
With what condition are carcinoid tumours associated?
10% with MEN1
2992
Sites of caricnoid tumours
Appendix: 45% Ileum: 30% Colorectum: 20% Stomach: 10% Elsewhere in GIT Bronchus: 10% Cosider all as malignant
2993
What is the most common site of carcinoid tumours?
Appendix
2994
Features of carcinoid syndrome FIVE HT
Flushing: paroxysmal, upper body +/- wheals Intestinal: diarrhoea Valve fibrosis: TR and PS whEEze: bronchoconstriction Hepatic involvement: bypassed FPM Tryptophan deficiency: pellagra (3Ds)
2995
Local presentation of carcinoid tumours
Appendicits Intussuception or obstruction Abdominal pain
2996
Ix in carcinoid tumours
Increased urine 5-hydroxyindoleacetic acid: 5HT metabolite Raised plasma chromogranin A CT/MRI: find primary
2997
Rx in carcinoid tumour
Symptoms: octreotide or loperamide Curative: tumours are very yellow Give octerotide to avoid carcinoid crisis
2998
Pathophysiology of carcinoid crisis?
Tumour outgrows blood supply or is handled too much-\> massive mediator release Leads to vasodilatoin, hypotension, bronchoconstriction, hyperglycaemia
2999
Rx in carcinoid crisis?
High-dose octreotide
3000
Px in carcinoid tumours
Median survival is 5-8y ~3y if mets present
3001
Def: acute appendicits
Inflammation of the vermiform appendix ranging from oedema to ischaemic necrosis and perforation
3002
Epidemiology of appendicitis?
Incidence: 6% lifetime incidence, commonest surgical emergency Rare \<2y. Maximal peak during childhood, decreases thereafter
3003
Pathogenesis of appendicitis
Obstruction of the appendix: faceolith most commonly lymphoid hyperplasia post-infection Tumour e.g. caecal Ca, carcinoid Worms e.g. Ascaris lumbicoides, Schisto Gut organisms-\> infection behind obstruction Leads to oedema, ischaemia, necrosis, perforation Peritonitis Abscess Appendiceal mass
3004
Pattern of abdominal pain in appendicits?
Early inflammation-\> appendiceal irritation: Visceral pain is not well localised cf. somatic pain Nociceptive info travels in the sympathetic afferent fibres that supply the viscus Pain is refrred to the dermatome corresponding toth e spinal cord level of these sympathetic fibres Append= midgut= lesser splanch (T10/11)= umbilical pain Late inflammation-\> parietal peritoneum irritation Pain localised to RIF
3005
Symptoms of acute appendicits
Colicky abdominal pain. Central-\> localised in RIF. Worse with movement Anorexia Nausea (vomiting is rarely prominent) Constipation/diarrhoea
3006
Colicky abdominal pain. Central-\> localised in RIF. Worse with movement Anorexia Nausea (vomiting is rarely prominent) Constipation/diarrhoea
Appendicits
3007
Signs of appendicits
Low grade pyrexia: 37.5-38,5 Increased HR, shallow breathing Foetor oris Guarding and tenderness @ McBurney's point: +ve cough/percussion tenderness Appendix may be palpable in RIF Pain PR suggests pelvic appendix
3008
Low grade pyrexia: 37.5-38,5 Increased HR, shallow breathing Foetor oris Guarding and tenderness @ McBurney's point: +ve cough/percussion tenderness Appendix may be palpable in RIF Pain PR suggests pelvic appendix
Acute appendicits
3009
McBurney's point
1/3rd from ASIS to the umbilicus
3010
Blumberg's sign
Blumberg's sign, also referred to as rebound tenderness, is a clinical sign that is elicited during physical examination of a patient's abdomen by a doctor or other health care provider. It is indicative of peritonitis. It refers to pain upon removal of pressure rather than application of pressure to the abdomen.
3011
Rovsing's sign
Pressure in LIF-\> more pain RIF Appendicits
3012
Psoas sign
Pain on extending the hip: retrocaecal appenidix
3013
Cope Sign
Flexion + internal rotation of R hip-\> pain Appendix lying close to obturator internus
3014
DDx for appendicits
Surgical: Cholecystitis Diverticulitis Meckel's diverticulitis Gynae: Cyst accident: torsion, rupture, haemorrhage Salpingitis/PID Medical: Mesenteric adenitis UTI Crohn's
3015
Ix in appendicitis
Dx is primarily clinical Bloods: FBC, CRP, amylase, G+S. clotting Urile: Sterile pyruia may indicate bladder irritation Ketones: anorexia Exclude UTI **Beta HCG** Imaging: USS: exclude gynae path. Visualise inflamed appendix CT: can be used Diagnostic lap
3016
Mx of appendicits
Fluids Abx: cef 1.5mg + met 500g IV TDS Analgesia: paracetamol, NSAIDs, codeine phosphate Certain dx-\> appendicectomy Uncertain dx-\> active observation
3017
Cef + met doseages
cef 1.5g met 500g IV TDS
3018
Cx of appendicitis
Appendix mass Apppendix abscess Perforation
3019
Appendiceal mass
Inflammed appendix with adherent covering of omentum and small bowel
3020
Dx of appendix mass
US or CT
3021
Mx of appendix mass
Initially: Abx and NBM Resolution of mass-\> interval appendicectomy Exclude a colonic tumour: colonoscopy
3022
Features of appendix abscess
Results if appendix mass doesn't resolve Mass enlarges, patient deterioirates
3023
Mx of appendix abscess
Abx + NBM CT guided percutaneous drainage If no resolution, sx may involve right hemicolectomy
3024
Features of appendicits-\> perforation
Commoner if faecolith present and in young children (as dx is often delayed) Deteriorating patient with peritonitis
3025
Epidemiology of UC Prev Age Sex
100-200/100,000 30s F\>M
3026
Aetiology of UC
Concordance= 10% Smoking protective TH2 mediated
3027
Epdiemiology of Crohn's Prev Age Sex
50-100,000 20s F\>M
3028
Aetiology of Crohns
Concordance= 70% Smoking increases risk TH1/Th17 mediated
3029
Macroscopic appearance of UC
Found in rectum and colon +/- backwash ileitis Contiguous No strictures
3030
IBD Found in rectum and colon +/- backwash ileitis Contiguous No strictures
UC
3031
Macroscopic appearance of Crohn's
Found mouth to anus, especially terminal ileum Skip lesions Strictures present
3032
IBD Found mouth to anus, especially terminal ileum Skip lesions Strictures present
Crohn's
3033
Microscopic apperance of UC
Mucosal inflammation Shallow and broad ulceration No fibrosis No granulomas Marked pseudopolyps No fistulae
3034
IBD Mucosal inflammation Shallow and broad ulceration No fibrosis No granulomas Marked pseudopolyps No fistulae
UC
3035
Microscopic appearance of Crohn's
Transmural inflammation Deep, thin, serpiginious ulceration-\> cobblestone mucosa Marked fibrosis Granulomas present Minimal pseudopolyps Fistulae present
3036
IBD Transmural inflammation Deep, thin, serpiginious ulceration-\> cobblestone mucosa Marked fibrosis Granulomas present Minimal pseudopolyps Fistulae present
Crohn's
3037
Systemic features of UC and crohn's
Fever, malaise, anorexia, weight loss in active disease
3038
Diarrhoea Blood +/- mucus PR Abdominal discomfort Tenesmus, faecal urgency IBD
UC
3039
Diarrhoea (not usually bloody) Abdominal pain Weight loss IBD
Crohn's
3040
Abbdominal signs of UC
Fever Tender, distended abdomen
3041
Abdominal signs of Crohn's
Apthous ulcers Glossitis Abdominal tenderness RIF mass Perianal abscesses, fistulae, tags Anal/rectal strictures
3042
How can the extraintestinal signs of IBD be classified?
Skin Eyes Joints HPB Other
3043
Skin manifestations of IBD
Clubbing Erythema nodosum Pyoderma gangrenosum (esp. UC)
3044
Eye manifestations of IBD
Iritis Conjunctivitis Episcleritis Scleritis
3045
Joint manifestations of IBD
Arthritis (non-deforming, asymmetrical) Sacroilitis Ank spond
3046
HPB manifestations of IBD
PSC and cholangiocarcinoma (esp. UC) Gallstones (esp. Crohn's) Fatty liver
3047
Other extra-intestinal manifestations of IBD
Amyloidosis Oxalate renal stones (esp. Crohn's)
3048
Cx of UC
Toxic megacolon Bleeding Malignancy Cholangiocarcinoma Strictures-\> obstruction Venous thrombosis
3049
Features of toxic megacolon
Diameter \>6cm Risk of perforation
3050
Malignancy in UC
CRC in 15% with pancolitis for 20y Cholangiocarcinoma also a risk
3051
Cx of CD
Fistulae Strictures-\> obstruction Abscesses Malabsorption Toxic megacolon and Ca may occur although this is less common than in UC
3052
Fistulae in Crohn's
Entero-enteric/colonic-\> diarrhoea Enterovescial-\> frequency, UTI Enterovaginal Perianal-\> pepperpot anus
3053
Abscess in crohn's
Abdominal Anorectal
3054
Malabsorption in Crohn's
Fat-\> steatorrhoea, gallstones B12-\> megaoloblastic anaemia Vit D-\> osteomlacia Protein-\> oedema
3055
Ix in UC
Bloods Stool Imaging Ileocolonoscopy and regional biopsy
3056
Bloods in UC
FBC: reduced Hb, raised WCC LFT: reduced albumin Raised CRP/ESR Blood cultures
3057
Stool in UC
MCS: exclude campy, shigella, salmonella CDT: C d.iff may complicate or mimic
3058
Imaging in UC
AXR: megacolon (\>6cm) CXR: perforation CT Ba/gastrograffin enema: Lead pipe: no haustra Thumbprinting: mucosal thickening Pseudopolyps: regenerating mucosal island
3059
Ileocolonoscopy and regional biopsy in UC:
Baron Score
3060
Ba
Lead pipe colon UC
3061
Dilated transverse colon noted. The abdomen demonstrates markedly dilated transverse colon (9 cm) with impression of slight dilatation of the descending colon with some" thumb printing" in the wall (consistent with mucosal inflammation in the clinical circumstances). No free subphrenic gas is seen. UC
3062
Baron score
n endoscopic scoring system devised for ulcerative colitis, which has been used in clinical practice as the modified Baron score: • Normal—normal mucosa; inactive disease. • Mild—erythema; decreased vascular pattern. • Moderate—marked erythema; loss of vascular pattern; mucosal friability. • Severe—spontaneous bleeding; ulceration.
3063
What can be used to grade the severity of UC?
Truelove and Witts criteria
3064
Components of Truelove and Witts criteria
Bowel movements PR bleeding Pyrexia (\>37.8) HR (\>90) Anaemia ESR
3065
Truelove and Witts criteria: Mild UC
\<4 bm Small PR bleeding No pyrexia HR \<90 Anaemia not present ESR \<30
3066
Truelove and Witts criteria Moderate UC
4-6bm Between mild and severe PR bleed No pyrexia No HR \>90 No anaemia ESR \<30
3067
Truelove and Witts criteria Severe UC
?6 bm Large PR bleed Pyrexic \>37.8 HR \>90bpm Hb \<10.5 ESR \>30
3068
Mx of acute severe UC
Resus: admit, IV hydration, NBM IV hydrocortisone 100mg QDS + PR (can consider adding IV ciclosporin if not improvement) Transfuse if required Thromboprophlyaxis Monitoring Abx not routinely recommended may be used in megacolon, peforation, uncertain Dx
3069
Monitoring in acute severe UC
Bloods: FBC, ESR, CRP, U+E Vitals and stool chart Twice daily examination +/- AXR
3070
Acute complications of acute severe UC
Perforation Bleeding Toxic megacolon VTE
3071
Mx of acute severe UC If improvement
Switch to oral prednisolone and a 5-ASA (e.g. mesalazine) Taper pred after full remission
3072
Mx of acute severe UC, no improvement
Rescue therapy On day 3: stool freq \>8, or CRP \>45 Predicts 85% chance of needing a colectomy during admission Medical: ciclosporin, infliximab or visilzumab (anti T cell) Surgical
3073
Oral therapy to induce remission in mild/mod UC
1st line: 5-asas e.g. mesalazine 2nd line: oral pred
3074
Topical therapies to induce remission in mild/moderate UC
Mainly used for left-sided disease Proctitis: suppositories More proximal disese: enemas or foams 5 ASA +/- steroids (pred or budenoside)
3075
Additional therpapy for mild-moderate UC disease
Can add pred to 5-ASA Oral tacrolimus can be added Steroid sparing agents include: azathioproine or mercaptopurine Infliximab: steroid-dependant patients
3076
Maintaining remission in UC
1st line: 5-ASA PO: sulfasalzine or mesalazine Topical can be used in proctitis 2nd line: Azathioprine or mercaptopurine Relapsed on ASA or are steroid dependent. Give 6-mercaptopurine if azathioprine intolerant 3rd line: Infliximab/ adalimumab
3077
Indications for emergency surgery in UC
Toxic megacolon Perforation Massive haemorrhage Failure to respond to medical Rx
3078
Surgery in UC
20% require surgery at some stage 30% with colitis require surgery within 5y
3079
Emergency surgical procedures in UC
Total/subtotal colectomy with end ileostomy +/- mucus fistula Followed after 3m by either completion proctectomy and ileal pouch anal anastomosis or end ileostomy. Or ileorectal anastomosis Panproctocolectomy and permanent end ileostomy Acute colitis op mortality: 7% (30% if perforated)
3080
Indications for elective surgery in UC
Chronic symptoms despite medical therapy Carcinoma or high grade dysplasia
3081
Elective surgical procedures in UC
Panproctocolectomy with end ileostomy or ileal pouch anal anastomosis Total colectomy with IRA (ileorectal anastomosis)
3082
Cx of UC sx
Abdominal: SBO Anastomotic stricture Pelvic abscess Stoma: Retraction Stenosis Prolapse Dermatitis Pouch: Pouchitis Reduced female fertility Faecal leakage
3083
Rx in pouchitits
Metronidazole and cipro
3084
Ix in Crohn's disease
Bloods Stool Imaging Endoscopy
3085
Bloods in Crohns'
FBC: anaemia, raised WCC LFT: hypoalbuminaemia Raised CRP/ESR Haematinics: Fe B12 folate Blood cultures
3086
Stool in CD
MCS: exclude campy, shigella, salmonella CDT
3087
Imaging in Crohn's
AXR: obstruction, sacroileitis CXR: perforation MRI: assess pelvic disease and fistula. Assess disease severity Small bowel follow thourgh or enterocylsis: Skip lesions Rose-thorn ulcers Cobllestoning: ulceration and mural oedema String sign of Kantor: narrow terminal ileum Endoscopy: Ileocolonsocopy and regional biopsy Wireless capsule endoscopy Small bowel enteroscopy
3088
Severity markers of acute Crohn's attack: bloods
FBC LFT CRP/ESR
3089
Assessment of severe attack in CD
Temperature (increased) HR (increased) ESR (raised) CRP (raised) WCC (raised Albumin (reduced)
3090
String sign of Kantor
Narrow terminal ileus
3091
String sign of Kantor
3092
Mx of severe Crohn's attack
ABC, NBM, IV hydration Hydrocortisone IV + PR if rectal disease Abx: metronidazole PO or IV Thromboprophylaxis: LMWH Dietician review: Elemental diet Consider TPN Monitoring: vitals and stool chart, daily examination
3093
Mx of severe crohn's attack, improvement
Switch to oral pred 40mg/d
3094
Mx of severe crohns, no improvement
Rescue therapy Methotrexate +/- infliximab Surgical
3095
Inducing remisison in mild/moderate CD Supportive
High fibre diet Vitamin supplements
3096
Oral therapy in CD, remission induction
1st line: prednisolone 2nd line: budenoside or sulfasalazine Add on treatment Consider azathioprine or mercaptopurine addition to pred or budenoside Consider adding methotrexate in those unable to tolerate azathioprine or in whom TPMT activity is deficient Biologic: Infliximab/ adalimumab
3097
Perianal disease in CD
Occurs in 50% Ix: MRI and EUA Rx: oral abx: metronidazole immunosuppression +/- infliximab Local surgery +/- seton insertion
3098
Maintaining remission in CD
1st line: azathioprine or mercaptopurine 2nd line: methotrexate 3rd line: infliximab/adalimumab
3099
Sx in CD
50-80% need \>1 operation in their life Never curative Should be as conservative as possible
3100
Emergency sx indications in CD
Failure to respond to medical Rx Intestinal obstruction or perforation Massive haemorrhage
3101
Elective sx indications in CD
Abscess or fistula Perianal disease Chronic ill health Carcinoma
3102
Surgical procedures in CD
Limited resection e.g. ileocaecal Stricturoplasty Defunction distal disease with temproray loop ileostomy
3103
Cx of CD sx
Stoma complications Enterocutaneous fistulae Anastamotic leak or stricture
3104
Def: short gut
\<1-2m small bowel
3105
Features of short gut syndrome
Steatorrhoea ADEK and B12 malabsorption Bile acid depletion-\> gall stones Hyperoxaluria-\> renal stones
3106
Rx in short gut syndrome
Dietician Supplements or TPN Loperamide
3107
General medical mx of bowel obstruction: Resuscitate
ABC Drip and suck IV fluids: aggressive as patient may be v dehydrated NGT: decompress upper GIT, stops vomiting, prevents aspiration Catheterise: moinotr UO
3108
General medical Rx of bowel obstruction Therapy
Analgesia: may require strong opioid Abx: cef + met if strangulation or peforation Gastrograffin study: oral or via NGT Consider need for parenteral nutrition
3109
General medical Rx of bowel obstruction Monitoring
Regular clinical examination is necessary to ensure that the patient is not deteriorating Change in distension, pain or tenderness, HR or RR Repeat imaging and bloods Non-operative mx succesful in 80% of patients with SBO without peritonitis Pts with LBO are more likely to need sx
3110
Indications for Sx in bowel obstruction
Closed loop obstruction Obstructing neoplasm Strangulation/perforation-\> sepsis/peritonitis Failure of conservative mx (up to 72h)
3111
Principles of surgical management of bowel obstruction
Aim to treat cause Typically involves resection of obstructing lesion Colon has not been cleaned, therefore most surgeons utilise a proximal ostomy post-resection Patients with substantial comorbidity or unresectable tumours may be offered bypass procedures Endoscopically placed expanding metal stents offer palliation or a bridge to surgery allowing optimisation
3112
Surgical procedures in bowel obstruction
Must consent patient for possible resection +/- stoma SBO: adhesiolysis LBO: Hartman's Colectomy and 1o anastomosis and on table lavage Palliative bypass procedure Transverse loop colostomy or loop ileostomy Caecostomy
3113
What proportion of volvulus is sigmoid
80%
3114
Pathophysiology of sigmoid volvulus
Long mesentry with narrow base predisposes to torsion Usally due to sigmoid elongation 2o to chronic constipation Increased risk in neuropsych patients: MS, PD, psychiatric as disease Rx interferes with intestinal motility Leads to closed loop obstruction
3115
Commoner in males Often eldelry, constipated, co-morbid patients Massive distension with tympanic abdomen
Sigmoid volvulus
3116
Sigmoid volvulus Coffee bean sign
3117
What can differentiate radiographically between sigmoid volvulus and caecal volvulus
Ahaustral wall and the lower end pointing to the pelvis
3118
Mx of sigmoid volvulus
Often relieved by sigmoidoscopy and flatus tube insertion Monitor for signs of bowel ischaemia Sigmoid colectomy occassionally required: failed endoscopic decompression bowel necrosis Often recurs: elective sigmoidectomy may be needed
3119
Features of caecal volvulus
Associated with congenital malformation where caecum is not fixed in the RIF Only 10% of patients can be detorsed with colonoscopy therefore typically requires sx Right hemi with 1o ileocolic anastomosis Caecostomy
3120
Caecal volvulus Despite the varying positions of the distended cecum, the plain radiographic features of a caecal volvulus are characteristic, and the caput caecum can typically be identified. The colonic haustral pattern is generally maintained in contradistinction to a sigmoid volvulus although some effacement may be present if ischemia develops.
3121
Triad in gastro-oesophageal obstruction
Vomiting-\> retching with regurgitation of saliva Pain Failed attempts to pass an NGT
3122
RFs for gastric volvulus
Congenital: Bands Rolling/paraoesophageal hernia Py Sten Acquired Gastric/oesophageal sx Adhesions
3123
Ix in gastric volvulus
Gastric dilatation Double fluid level on erect films
3124
Mx of gastric volvulus
Endoscopic manipulation Emergency laparotomy
3125
Adynamic bowel 2o to the absence of normal peristalsis Usually SBO Reduced or absent bowel sounds Mild abdominal pain: not colicky
Paralytic ileus
3126
Causes of paralytic ileus
Post-op Peritonitis Pancreatitis or any localised inflammation Poisons/Drugs: AntiAChM e.g. TCAs Pseudo-obstruction Metabolic: hypokalaemia, hyponatraemia, hypomagnesaemia, uraemia Mesenteric ischaemia
3127
Prevention of paralytic ileus
Reduced bowel handling Laparoscopic approach Peritoneal lavage after peritonitis Unstarched gloces
3128
Mx of paralytic ileus
Conservative drip and suck Mx Correct any underlying causes e.g. drugs, metabolic abnormalities Consider need for parenteral nutrition Exclude mechanical cause if protracted
3129
Clinical signs of mechanical obstruction without obstructing lesion Usually distension only: no colic
Colonic pseudo-obstruction/ Ogilvie's syndrome
3130
Cause of pseudo-obstruction
Aetiology unknown Associated with elderly, cardiorespiratory disorders, pelvic sx e.g. hip arthroplasty, trauma
3131
Ix in colonic pseudo-obstruction
Gastrograffin enema to exclude mechanical cause
3132
Mx of Ogilvie's syndrome
Neostigmine: anti-cholinesterase Colonoscopic decompression: 80% successful
3133
Epidemiology of CRC
3rd commonest cancer 2nd commonest cause of cancer death Age: peak in 60s Sex: rectal Ca commoner in men Geo: Western disease
3134
Pathophysiology of CRC Colonic adenomas
Benign precursors to CRC Characterised by dysplastic epithelium Malignant potential increases with size, dysplasia and villous component
3135
Classificaiton of colonic adenomas
Tubular: small, pedunculated, tubular glands Villous: large, sessile, covered by villi Tubulovillous: mixture
3136
Presentation of colonic polyps
Typically asymptomatic Large polyps can bleed-\> IDA Villous adenomas can lead to hypokalaemia and hypoproteinaemia
3137
APC role in CRC
Negative regulator of beta-catenin (component of WNT pathway) APC binds to and promotes beta catenin degradation mutAPC leads to increased beta catenin-\> incrased tx of genes that promote cell proliferation Proliferation-\> mutation of other genes which promote growth and prevent apoptosis e.g. KRAS (proto-oncogen) p53 (TSG)
3138
Adenoma-\> carcinoma sequence
First hit: mutation of one APC copy Second hit: mutation of second APC copy-\> adenoma formation Additional mutations in adenoma-\> malignant transformation
3139
Other aetiological factors in CRC
Diet: reduced fibre, increased refined carbs IBD: CRC in 15% with pancolitis for 20y Familial: FAP, HNPCC, Peutz-Jehgers Smoking Genetics: one 1st degree relaticve= 1/10 risk (no relative 1/50) NSAIDs/Aspirin: protective
3140
Pathology of CRC
95% adenocarcinoma Others: lymphoma, GIST, carcinoid
3141
Locations of CRC
Rectum: 35% Sigmoid: 25% Caecum and ascending colong: 20% Transverse: 10% Descending: 5%
3142
Most common location of CRC
Rectosigmoidal
3143
Spread of CRC
Local Lymphatic Blood (liver, lungs) Transcoelomic
3144
Altered bowel habit PR mass (60%) Obstruction (25%) Bleeding/mucus PR Tenesmus old man
Left CRC
3145
Symptoms of left sided CRC
Altered bowel habit PR mass (60%) Obstruction (25%) Bleeding/mucus PR Tenesmus old man
3146
Anaemia Weight loss Abdominal pain Old man
Right sided CRC
3147
Symptoms of right sided CRC
Anaemia Weight loss Abdominal pain Old man
3148
Symptoms common to CRC on both sides of colon
Abdominal mass perforation haemorrhage fistula
3149
Palpable mass: per abdomen or PR Perianal fistulae Hepatomegaly Anaemia Signs of obstruction
?CRC
3150
Examination findings in CRC
Palpable mass: per abdomen or PR Perianal fistulae Hepatomegaly Anaemia Signs of obstruction
3151
A 75-year-old man attends the surgical assessment unit prior to an elective Hartmann's procedure in 7 days due to bowel cancer. He has a past medical history of atrial fibrillation, hypertension and previous cerebrovascular accident. Your registrar asks you to review him prior to his procedure next week. You notice that he is currently taking warfarin and his INR today is 2.6. His remaining blood tests are normal. What is the most appropriate management for his anticoagulation peri-operatively? Stop his warfarin Continue his warfarin at the current dose as his INR is within therapeutic range Stop his warfarin and commence treatment dose low molecular weight heparin Initiate an unfractionated heparin continuous infusion Stop his warfarin and commence aspirin
Managing anticoagulation peri-operatively is challenging and depends on the reasons for and agent used to anti-coagulate. Each patient should have a venous thromboembolic risk assessment undertaken to consider risk factors for thromboembolism versus bleeding. In this scenario the patient is at high risk of thromboembolic disease (previous CVA, known AF) but also significant bleeding due to major abdominal surgery. Therefore the best option is a shorter acting anticoagulant (e.g. low molecular weight heparin) given at treatment dose whilst withholding warfarin. This would then be withheld the evening before surgery, and mechanical prophylaxis used.
3152
What is the maximum safe volume of lidocaine 1% that may be used during minor surgery on an average sized adult? 10 ml 30 ml 50 ml 20 ml 5 ml
20ml
3153
You are the on-call doctor and are called to see a 45 year old lady who is 1 day post-appendicectomy because she has become acutely short of breath. She has just been given a dose of co-amoxiclav for a chest infection infection. She is now breathless with a respiratory rate of 30 breaths per minute and has a heart rate of 125 beats per minute. Her blood pressure is 87/52mmHg and saturations on air are 87%. The nurse is applying oxygen as you make your assessment. What should be the first step in your management? Give oral prednisolone Perform an arterial blood gas Give intramuscular adrenaline Give intravenous fluids Give nebulised salbutamol
The history here (sudden onset respiratory distress after a penicillin-containing antibiotic) is of anaphylaxis. Giving 0.5mg IM adrenaline 1:1000 as Resuscitation Council UK guidelines for anaphylaxis is the most sensible option.
3154
Features of propofol
Rapid onset of anaesthesia Pain on IV injection Rapidly metabolised with little accumulation of metabolites Proven anti emetic properties Moderate myocardial depression Widely used especially for maintaining sedation on ITU, total IV anaesthesia and for daycase surgery
3155
Features of sodium thiopentone
Extremely rapid onset of action making it the agent of choice for rapid sequence of induction Marked myocardial depression may occur Metabolites build up quickly Unsuitable for maintenance infusion Little analgesic effects
3156
Features of ketamine
May be used for induction of anaesthesia Has moderate to strong analgesic properties Produces little myocardial depression making it a suitable agent for anaesthesia in those who are haemodynamically unstable May induce state of dissociative anaesthesia resulting in nightmares
3157
Features of etomidate
Has favorable cardiac safety profile with very little haemodynamic instability No analgesic properties Unsuitable for maintaining sedation as prolonged (and even brief) use may result in adrenal suppression Post operative vomiting is common
3158
A 65-year-old female is admitted for an elective total hip replacement of the right hip. On admission she is given thigh-length anti-embolism stockings to wear before surgery and until she regains mobility. It is hospital policy to also use a low molecular weight heparin for postoperative thromboprophylaxis. According to NICE guidelines, when should this be initiated? 6-12 hours before surgery 1-4 hours after surgery Immediately after surgery 6-12 hours after surgery 30 minutes - 1 hour after surgery
For elective total hip replacement surgery NICE recommend commencing a low molecular weight heparin 6-12 hours after surgery.
3159
What are some procedures in which prophylactic antibiotics are recommended
* Cataract surgery (reduces the risk of endophthalmitis) * Appendicectomy * Colorectal surgery * Caesarean section * Abdominal/vaginal hysterectomy * Transurethral resection of the prostate * Arthroplasty * Hip fracture * 3rd/4th degree perineal tear repair
3160
What are some procedures where prophylactic antibiotics are not normally recommended
* Tonsillectomy * Inguinal hernia repair * Laparoscopic removal of ectopic pregnancy * Assisted delivery (e.g. forceps) * Evacuation of incomplete miscarriage
3161
A 45-year-old lady, with a past medical history of rheumatoid arthritis, is scheduled to have a laparoscopic cholecystectomy. What imaging should be performed pre-operatively? Anteroposterior and lateral cervical spine radiographs CT cervical spine Hand radiographs Anteroposterior and lateral cervical spine, plus hand, radiographs Anteroposterior cervical spine radiographs
Atlantoaxial subluxation is a rare complication of rheumatoid arthritis, but important as it can lead to cervical cord compression. Anteroposterior and lateral cervical spine radiographs preoperatively screen for this complication, ensuring the patient goes to surgery in a C-spine collar and the neck is not hyperextended on intubation. Radiographs of the hands are useful in diagnosis, but not necessary pre-operatively. CT scanning of the cervical spine is not necessary for screening pre-operatively, but may be useful is any abnormalities are picked up.
3162
You are the foundation doctor covering surgery. You are asked to review a 77 year old patient (75kg) who is post right hemicolectomy for bowel cancer. The patient is hypotensive (87/40 mmHg), tachycardic (128 bpm) and has a urine output of 25 mls per hour . His only past medical history is hypertension. You conduct a fluid assessment. He appears dry with sunken eye balls and reduced skin turgor. You want to conduct a fluid challenge to assess his response. What is the most appropriate fluid to px? 1 Litre of gelofusin 1 Litres 0.9% normal saline over 8 hours 500 mls 0.9% normal saline STAT 500 mls 0.9% normal saline over 8 hours 250 mls 0.9% normal saline STAT
In patients with no clinical signs or documentation of heart failure a 500 ml prescription of normal saline delivered STAT is the recommended fluid challenge. You must remember to reassess the patient to decide whether to prescribe another 500 mls. 250 mlx of 0.9% Normal Saline would be appropriate in patients with evidence of heart failure. This does not put as much strain on their physiology and risk the patient devoting worsening cardiac failure.
3163
Why is Hartmanns/Ringers lactate preferred as postoperative fluids?
In the UK the GIFTASUP guidelines (see reference below) were devised to try and provide some consensus guidance as to how intravenous fluids should be administered. A decade ago it was a commonly held belief that little harm would occur as a result of excessive administration of normal saline and many oliguric post operative patients received enormous quantities of IV fluids. As a result they developed hyperchloraemic acidosis. With greater understanding of this potential complication the use of electrolyte balanced solutions (Ringers lactate/ Hartmans) is now favored over normal saline. In addition to this solutions of 5% dextrose and dextrose/saline combinations are now generally not recommended for surgical patients.
3164
An 85-year-old female with multiple comorbidities is scheduled to receive a bowel resection in her local hospital. She attends a pre-operative assessment clinic with the senior anaesthetist to discuss her suitability for surgery and arrange any pre-operative investigations required. In whom do NICE recommend should receive a chest X-ray as part of their pre-operative assessment? Patients over the age of 65 Patients with a degree of renal impairment Patients with hypertension Not routinely recommended Patients with diabetes
Chest x-rays are now not routinely recommended before surgery. Patients over the age of 65 may need an ECG before major surgery. Patients with renal disease may need a full blood count and an ECG depending on their ASA grade even before intermediate surgery. Patients with hypertension do not need any specific investigations pre-operation. Patients with diabetes may need an ECG before intermediate surgery.
3165
Steroid cover: minor surgery
25mg hydrocortisone at induction, then resume normal medication post-operatively
3166
Steroid cover: moderate surgery
Usual dose pre-operatively Then 25mg hydrocortisone at induction followed by 25mg IV every 8 hours for 24h Continue normal pre-operative dose afterwards
3167
Steroid cover: major surgery
Usual dose of steroids preoperatively 50mg IV hydrocortisone at induction Followed by 50mg IV evey 8h for 48-72h. Continue infusion until patient has started light eating, then restart normal pre-operative dose
3168
Causes of addisonian crisis
sepsis or surgery causing an acute exacerbation of chronic insufficiency (Addison's, Hypopituitarism) adrenal haemorrhage eg Waterhouse-Friderichsen syndrome (fulminant meningococcemia) steroid withdrawal
3169
Mx of Addisonian crisis
Hydrocortisone 100mg IM or IV 1L NS over 30-60 mins + dextrose if hypoglycaemic Cotninue hydrocortisone 6hly until patient is stable Oral replacement may begin after 24h and be reduced to maintenance over 3-4d
3170
What is the most common ADR in PRC infusion
Pyrexia
3171
What is the most common ATR following FFP infusion
Urticaria
3172
Features of NG feeding
Usually administered via fine bore naso gastric feeding tube Complications relate to aspiration of feed or misplaced tube May be safe to use in patients with impaired swallow Often contra indicated following head injury due to risks associated with tube insertion
3173
Features of naso-jejunal feeding
Avoids problems of feed pooling in stomach (and risk of aspiration) Insertion of feeding tube more technically complicated (easiest if done intra operatively) Safe to use following oesophagogastric surgery
3174
Features of feeding jejunostomy
Surgically sited feeding tube May be used for long term feeding Low risk of aspiration and thus safe for long term feeding following upper GI surgery Main risks are those of tube displacement and peritubal leakage immediately following insertion, which carries a risk of peritonitis
3175
Features of PEG
Combined endoscopic and percutaneous tube insertion May not be technically possible in those patients who cannot undergo successful endoscopy Risks include aspiration and leakage at the insertion site
3176
Features of TPN
The definitive option in those patients in whom enteral feeding is contra indicated Individualised prescribing and monitoring needed Should be administered via a central vein as it is strongly phlebitic Long term use is associated with fatty liver and deranged LFT's
3177
A 32-year-old male is receiving a blood transfusion after being involved in a road traffic accident. A few minutes after the transfusion he complains of loin pain. His observations show temperature 39 oC, HR 130bpm and blood pressure is 95/40mmHg. What is the best test to confirm his diagnosis? USS abdomen Direct Coomb's test Blood cultures Blood film Sickle cell test
The diagnosis is of an acute haemolytic transfusion reaction, normally due to ABO incompatibility. Haemolysis of the transfused cells occurs causing the combination of shock, haemoglobinaemia and loin pain. This may subsequently lead to disseminated intravascular coagulation. A Coomb's test should confirm haemolysis. Other tests for haemolysis include: unconjugated bilirubin, haptoglobin, serum and urine free haemoglobin. Note that delayed haemolytic reactions are normally associated with antibodies to the Rh system and occur 5-10 days after transfusio
3178
What are the contraindications to day surgery?
Day surgery is suitable theoretically for any procedure in which GA time is \<1hr severe dementia severe learning disabilities ASA III and above (unless conditions can be optimised and stabilised pre-operatively) BMI (body mass index) 32 kg/m^2 and above diabetes type I (if sliding scale commenced) infection at the site of surgery social factors uncontrolled pain or nausea expected post-operatively
3179
Theme: Anaesthetic agents A.Halothane B.Propofol C.Ketamine D.Etomidate E.Sodium thiopentone F.Flumazenil G.Naloxone H.Sevoflurane Please select the drug which most closely matches the description given. Each option may be used once, more than once or not at all. An agent which reverses the action of midazolam An agent which is associated with hepatotoxicity An anaesthetic agent which has anti emetic properties
Flumazenil Flumazenil antagonises the effects of benzodiazepines by competition at GABA binding sites. Since may benzodiazepines have longer half lives than flumazenil patients still require close monitoring after receiving the drug. An agent which is associated with hepatotoxicity Halothane Halothane is hepatotoxic. Despite this it remains in mainstream use. It should be avoided in patients with hepatic dysfunction, and scavengers should be used in theatres as accumulation of the drug may be injurious to theatre staff. The correct answer is Propofol Propofol is rapidly metabolised and has mild/ moderate anti emetic properties. It is the agent of choice in most day case operations for this reason.
3180
High T with RIF pain
More typical of conditiosn such as mesenteric adenitis rather than appendicitis
3181
SBO features on AXR
Maximum normal diameter= 35mm Valvulae conniventes extend all the way across
3182
LBO features on AXR
Maximum normal diamter= 55mm Haustra extend about a third of the way acrosS
3183
Sudden onset loin to groin pain Colicky in nature Associated with macro or microscopic haematuria
Renal colic
3184
Dx of renal colic
CT KUB is most sensitive and specific diagnostic test
3185
Mx of renal colic
Stones \<5mm will pass within 4w of symptom onset More intensive and urgent treatment required in presence of ureteric obstruciton, renal developmental abnormality or previous renal transplant. Ureteric obstruction due to stones + infection is a surgical emergency.
3186
Stone burden of less than 2cm in aggregate
Lithotripsy
3187
Stone burden of less than 2cm in pregnant females
Ureteroscopy
3188
Complex renal calculi and staghorn calculi
Percutaneous nephrolithotomy
3189
Ureteric calculi less than 5mm
Manage expectantly
3190
Features of shockwave lithotripsy
A shock wave is generated external to the patient, internally cavitation bubbles and mechanical stress lead to stone fragmentation. The passage of shock waves can result in the development of solid organ injury. Fragmentation of larger stones may result in the development of ureteric obstruction. The procedure is uncomfortable for patients and analgesia is required during the procedure and afterwards.
3191
Features of ureteroscopy
A ureteroscope is passed retrograde through the ureter and into the renal pelvis. It is indicated in individuals (e.g. pregnant females) where lithotripsy is contraindicated and in complex stone disease. In most cases a stent is left in situ for 4 weeks after the procedure.
3192
Features of percutaneous nephrolithotomy
In this procedure access is gained to the renal collecting system. Once access is achieved, intra corporeal lithotripsy or stone fragmentation is performed and stone fragments removed.
3193
A 72-year-old man presents to the Emergency Department. Whilst walking back from a friends house he slipped on some ice and fell backwards, landing on his right arm and banging his head on the kerb in the process. His past medical history includes atrial fibrillation for which he takes bisoprolol and warfarin. A routine INR taken four days ago was 2.2. There are no signs of any external injury to his right arm or scalp. What is the most appropriate course of action with relation to his head injury? ## Footnote Arrange a CT head scan to be performed within 8 hours Discharge with standard head injury advice Admit for 24 hours of observation Admit for 8 hours of observation Discharge with standard head injury advice + advise he stops warfarin for 5 days
For patients (adults and children) who have sustained a head injury with no other indications for a CT head scan and who are having warfarin treatment, perform a CT head scan within 8 hours of the injury. A provisional written radiology report should be made available within 1 hour of the scan being performed.
3194
Def: anal fissure
Anal fissures are longitudinal or elliptical tears of the squamous lining of the distal anal canal. If present for less than 6 weeks they are defined as acute, and chronic if present for more than 6 weeks. Around 90% of anal fissures occur on the posterior midline
3195
A 24-year-old man presents due to severe pain when defecating for the past 2 weeks. He has occasionally noted some blood on the toilet paper when wiping himself. On examination a tear is seen on the posterior midline of the anal verge. Which one of the following should not be recommended as a treatment option? ## Footnote Bulk-forming laxatives Application of lubricant prior to defecation Topical steroids Dietary advice Paracetamol
Topical steroids have been shown in studies to be of little benefit in treating anal fissures
3196
Abdominal swelling: History of malignancy/previous operations Vomiting Not opened bowels recently 'Tinkling' bowel sounds
Intestinal obstruction
3197
Abdominal swelling History of alcohol excess, cardiac failure
Ascites
3198
Abdominal swelling History of prostate problems Dullness to percussion around suprapubic area
Urinary retention
3199
Abdominal swelling: Older female Pelvic pain Urinary symptoms Raised CA125 Early satiety/bloating
Ovarian cancer
3200
A 22-year-old man has undergone an inguinal hernia repair. Seven days later he presents with an erythematous and tender wound that is discharging a purulent material. What is the most likely cause? Infection with Staphylococcus aureus Discharging haematoma Infection with Pseudomonas Infection with Streptococcus pyogenes Infection with Bacteroides
In this setting Staphylococcus aureus Infection is the most likely cause. In the UK between 2010 and 2011 the commonest cause of wound infection was enterobacter infections (usually following cardiac or colonic surgery). 23% of infections were due to Staph aureus, which fits the scenario above. Infection with the other organisms including strep pyogenes was much rarer.
3201
You are the foundation doctor on call for the surgical ward. A 65 year old male is six hours post thyroidectomy. You are bleeped and asked to review this gentlemen because of worsening stridor. As you arrive at the bedside the nurse hands you the patients notes. When reviewing the notes, it is apparent the operation was uneventful. The surgeons notes describe adequate intra-operative haemostasis and closure using sutures. What is the most appropriate management for this patient? Intramuscular 1:10,000 Adrenaline Call anaesthetist and request immediate intubation Urgent removal of sutures and call for senior help Reassure patient Nebulised hypertonic saline
Post operative stridor in patients who have undergone neck surgery is a life threatening emergency. Using an ABCDE approach, this patient has potentially compromised airway and breathing. Each patient undergoing head and neck surgery is returned to the ward with a suture blade. In the event of a post operative bleed. If a bleed occurs, the pressure behind the suture line increases and the trachea becomes compressed resulting in stridor. Therefore 3 is the answer becuase immediate removal of the pressure will relieve the stridor. Senior assistance will be required as this patient will require further surgery for haemostasis. Intubation will improve this patients airway and breathing, however taken in the clinical context removal of the compression is the correct answer. For those individuals who chose 1, this is not anaphylaxis. There are no predisposing factors in the question. Moreover to treat anaphylaxis you prescribe 1:1000 intramuscular adrenaline not 1:10,000. Nebulised hypertonic saline will not be of any use in this patient.
3202
Head injury: Immediate CT head if
GCS \< 13 on admission GCS \< 15 2h after admission Suspected open or depressed skull fracture Suspected skull base fracture (panda eyes, Battle's sign, CSF from nose/ear, bleeding ear) Focal neurology Vomiting \> 1 episode Post traumatic seizure Coagulopathy
3203
Contact neurosurgeon following head injury if
Persistent GCS \< 8 or = 8 Unexplained confusion \> 4h Reduced GCS after admission Progressive neurological signs Incomplete recovery post seizure Penetrating injury Cerebrospinal leak
3204
If C-spine injury suspected? When is CT c-spine preferred?
If a c-spine injury is suspected a 3 view c-spine x-ray is indicated. CT c-spine is preferred if: - Intubated - GCS \<13 - Normal x-ray but continued concerns regarding c-spine injury
3205
A 76-year-old woman with a history of atrial fibrillation presents with abdominal pain and bloody diarrhoea. On examination her temperature is 37.8ºC, pulse 102 / min and respiratory rate 30 / min. Her abdomen is tender with generalised guarding. Blood tests reveal the following: Hb10.9 g/dl MCV76 fl Plt348 \* 109/l WBC23.4 \* 109/l Na+141 mmol/l K+5.0 mmol/l Bicarbonate14 mmol/l Urea8.0 mmol/l Creatinine118 µmol/l What is the most likely diagnosis? Diverticulitis Mesenteric ischaemia Campylobacter infection Ruptured abdominal aortic aneurysm Ulcerative colitis
The low bicarbonate points to a metabolic acidosis - highly suggestive of mesenteric ischaemia.
3206
A 78-year-old gentleman presents to the emergency department with a 3 hour history of lower back pain. It is achey in nature and a 6/10 on the pain scale. On examination he has some tenderness on palpation. His blood pressure is 100/70 mmHg despite 500ml fluid bolus and his heart rate is 110/min. What's the most likely diagnosis? Kidney stone Spinal cancer Ischaemic colitis Osteoporotic fracture Abdominal Aortic Aneurysm (AAA)
Any elderly gentleman that presents with back pain needs a ultrasound scan to exclude a AAA before any other diagnosis is considered, especially if they have haemodynamic instability.
3207
A 48 year old man presents to the Emergency Department with severe abdominal pain which has developed over the previous four hours. He opened his bowels earlier today and has had no problems passing water. He has been unwell recently with coryzal symptoms and a cough. He has been seen by his GP and not commenced on any antibiotics as it is a likely viral upper respiratory tract infection. His past medical history includes idiopathic atrial fibrillation for which is is currently taking warfarin. He has never had any abdominal surgery. His observations are: heart rate 110/min, respiratory rate 14/min, blood pressure 98/75 mmHg, temperature 37.4º, Sats 99% on air. On examination he is in obvious pain. Inspection reveals a discoloured purple non-demarcated area to the left of the umbilicus. Palpation of the abdomen demonstrates tenderness localised to a firm non-pulsatile mass just to the left of the midline at the level of the umbilicus. There is no guarding or rigidity. Bowel sounds are present. What is the most likely cause of this mans symptoms? Aortic aneurysm Strangulated hernia Abdominal wall haematoma Constipation Mesenteric ischaemia
Abdominal wall (rectus sheath) haematoma can occur following trauma, either directly to the abdominal wall or iatrogenic trauma from surgery, or can be spontaneous following excessive straining of the rectus muscle. This can occur during prolonged valsalva manoeuvres experienced with strenuous excesses or, in this case, coughing.
3208
Difficulty swallowing, dysphagia to both liquids and solids and sometimes chest pain Usually caused by failure of distal oesphageal inhibitory neurones Diagnosis is by pH and manometry studies together with contrast swallow and endoscopy Treatment is with either botulinum toxin, pneumatic dilatation or cardiomyotomy
Achalasia
3209
Spectrum of oesophageal motility disorders Caused by uncoordinated contractions of oesphageal muscles May show "nutcracker oesophagus" on barium swallow Symptoms include dysphagia, retrosternal discomfort and dyspepsia
Diffuse oseophagea spasm
3210
Commonest approach to the abdomen Structures divided: linea alba, transversalis fascia, extraperitoneal fat, peritoneum (avoid falciform ligament above the umbilicus) Bladder can be accessed via an extraperitoneal approach through the space of Retzius
Midline incision
3211
Parallel to the midline (about 3-4cm) Structures divided/retracted: anterior rectus sheath, rectus (retracted), posterior rectus sheath, transversalis fascia, extraperitoneal fat, peritoneum Incision is closed in layers
Paramedian incision
3212
Similar location to paramedian but rectus displaced medially (and thus denervated) Now seldom used
Battle insicsion
3213
Incision under right subcostal margin e.g. Cholecystectomy (open)
Kocher's
3214
Incision in right iliac fossa e.g. Appendicectomy
Lanz
3215
Oblique incision centered over McBurneys point- usually appendicectomy (less cosmetically acceptable than Lanz
Gridiron incision
3216
Rooftop incision
Gable
3217
Transverse supra pubic, primarily used to access pelvic organs
Pfannenstiel's
3218
Groin incision e.g. Emergency repair strangulated femoral hernia
McEvedy's
3219
Extraperitoneal approach to left or right lower quadrants. Gives excellent access to iliac vessels and is the approach of choice for first time renal transplantation.
Rutherford Morrison
3220
3221
Disseminated infection with Chlamydia. Usually seen in females. Consists of evidence of pelvic inflammatory disease together with peri-hepatic inflammation and subsequent adhesion formation.
Fitz-Hugh Curtis syndrome
3222
Boas sign
Boas' or Boas's sign is hyperaesthesia (increased or altered sensitivity) below the right scapula can be a symptom in acute cholecystitis (inflammation of the gallbladder).[1] It is one of many signs a medical provider may look for during an abdominal examination.[2] Originally this sign referred to point tenderness in the region to the right of the 10th to 12th thoracic vertebrae.[3] It is less than 7% sensitive.[4][5]
3223
Murphy's sign
Classically, Murphy's sign is tested for during an abdominal examination; it is performed by asking the patient to breathe out and then gently placing the hand below the costal margin on the right side at the mid-clavicular line (the approximate location of the gallbladder). The patient is then instructed to inspire (breathe in). Normally, during inspiration, the abdominal contents are pushed downward as the diaphragm moves down (and lungs expand). If the patient stops breathing in (as the gallbladder is tender and, in moving downward, comes in contact with the examiner's fingers) and winces with a 'catch' in breath, the test is considered positive. In order for the test to be considered positive, the same maneuver must not elicit pain when performed on the left side.
3224
A.Multiple endocrine neoplasia type I B.Multiple endocrine neoplasia type II C.Gardner's syndrome D.Lynch Syndrome E.Kartagener's syndrome F.Von Recklinghausen's disease Please select the most likely condition for the disease process described. Each option may be used once, more than once or not at all A 5-year-old boy presents with recurrent episodes of sinusitis. The casualty staff are surprised to find his liver lying in the left upper quadrant of the abdomen A 22-year-old man presents with carcinoma of the caecum. His brother died from colorectal cancer aged 25 and his father died from the disease aged 30. A tall 32-year-old lady presents with a diffuse neck swelling a carcinoma of the thyroid medullary type is diagnosed.
This is a case of Kartagener's syndrome. The primary problem is of immotile cilia syndrome. When associated with situs inversus Kartagener's syndrome is diagnosed. This is a case of Lynch syndrome HNPCC. It is transmitted in an autosomal dominant fashion. This is a case MEN type IIb. It is associated with phaeochromocytomas and is transmitted in an autosomal dominant pattern if inherited. All MEN II tend to have medullary carcinoma of the thyroid as a presenting feature
3225
A 25-year-old female presents to surgery with a 2 week history of painless rectal bleeding. Inspection of perineum and rectal examination is unremarkable. Proctoscopy reveals haemorrhoidal cushions at the left lateral and right anterior position. What is the most important component of management? Sitz baths Topical nitrate Fibre supplementation Improving anal hygiene Application of lubricant prior to defecation
Fibre supplementation has been shown to be as effective as injection sclerotherapy in some studies
3226
A 60-year-old retired man who lives alone and was previously a publican for 40 years is due to have a low anterior resection for a rectal adenocarcinoma. His preoperative blood tests including full blood count, clotting screen and liver function tests were markedly normal other than a moderately raised gamma-glutamyl transpeptidase and mean cell volume. During the operation the surgeon encounters significant blood loss when going through the abdominal wall. The bleeding has no obvious source, making ligation and coagulation very difficult. The operation is abandoned before entering the abdominal cavity. Blood tests taken during the operation show a normal activated partial thromboplastin time (APTT), prothrombin time (PT) and international normalised ratio (INR). What is the most likely cause of the excessive bleeding from the options below? Bud chiari syndrome Thrombocytopaenia Venous portal hypertension Disseminated intravascular coagulation Haemophilia A
The patients social history suggests they have worked in an environment serving alcohol for many years, though this does not mean they were a heavy drinker the raised gamma-glutamyl transpeptidase alludes to this. As a result of heavy drinking the patient has a degree of liver cirrhosis and therefore portal hypertension. This has caused raised venous pressure in the veins of the abdomen. This explains why a source of the bleeding is difficult to identify during the operation, as is typical of extensive venous bleeds. Arterial bleeds are pulsatile in nature and tend to clearly spout from their source. Thrombocytopenia - Would be shown by a low platelet count in the pre-operative full blood count. Disseminated intravascular coagulation - This would cause a prolonged PT and APTT Haemophilia A - This would cause a prolonged APTT Bud Chiari Syndrome - This could also be a cause of portal hypertension, though it is far rarer than cirrhosis. Von Willebrand Disease would be important to rule out in a patient such as this. As it is relatively common, and PT and APTT can both be norm
3227
Dx of mesenteric infarction
Arterial pH and lactate Arterial phase CT scanning is the most sensitive test
3228
Mx of mesenteric infarction
Immediate laparotomy and resection of affected segments, in acute embolic events SMA embolectomy may be needed.
3229
A 62-year-old man with no significant past medical history presents with a right sided groin lump which he noticed whilst having a shower. It has been present for 2 weeks and disappears when he lies down. It never causes him any discomfort and there are no other gastrointestinal symptoms of note. Examination reveals an small reducible swelling in the right groin consistent with an inguinal hernia. What is the most appropriate management? Refer for fitting of a truss Refer to vascular surgeon Routine referral for surgical repair Advise no action as will probably improve with time Fast-track referral to colorectal service
This patient has an asymptomatic inguinal hernia. Studies looking at conservative management tend to find that many patients become symptomatic and eventually have surgery anyway. As this patient is medically fit most clinicians would refer for surgical repair.
3230
A 62-year-old man has fallen over climbing some rocks on a beach and struck his head. On initial presentation, he has a GCS of 15, no signs of basal skull fracture, no neurological symptoms and no vomiting. He has a history of atrial fibrillation and diabetes, for which he takes verapamil, warfarin and metformin. Which of the following is the most appropriate next step? CT head scan within 1 hour CT head scan within 8 hours MRI head scan within 1 hour MRI head scan within 8 hours Discharge the patient and tell him to return if further symptoms develop
CT imaging of the head is currently the primary investigation of choice for detecting clinical important brain injuries in the acute setting. For safety, logistic and resource reasons MRI is not the investigation of choice in this setting. NICE recommends that patients who are taking warfarin who suffer a head injury should receive a CT head scan within 8 hours, even without further indications. If the patient has any indications for a CT head scan within 1 hour, this would obviously take precedence.
3231
A 71-year-old man has fallen off his bike and hit his head. According to a friend at the scene, he was unconscious for less than a minute after falling. At the time he was cycling slowly on a path beside a canal. On initial assessment, he has some bruising on his upper and lower limbs, has a Glasgow coma score (GCS) of 15, and no neurological deficit. He has not vomited or had a seizure since the accident, which he was able to describe to you. He is taking antihypertensives but otherwise has no notable medical history. Which of the following would be the most appropriate next step? Perform a CT head scan within 1 hour Perform a CT head scan within 8 hours Perform a MRI head scan within 1 hour Perform a MRI head scan within 8 hours Discharge the patient and tell him to return if further symptoms develop
NICE recommends that patients who suffer a head injury with loss of consciousness or amnesia, and who are aged over 65 years old, should have a CT head scan within 8 hours. If the patient had an indication for a CT head scan within 1 hour, obviously this would take precedence. The indications for CT head scan within 1 hour and within 8 hours, are found below.
3232
A 53-year-old man presents with an ulcerated mass at the anal verge. A biopsy is taken and the histology demonstrates as squamous cell carcinoma. Infection with which of the viruses below is most likely to have contributed to the development of the condition? Human papillomavirus 7 Human immunodeficiency virus 1 Human immunodeficiency virus 2 Human papillomavirus 16 Human T-lymphotropic virus 1
Infection with human papilloma virus 16 is a risk factor for the development of intra epithelial dysplasia of the anal skin with subsequent increased risk of invasive malignancy.
3233
A.E-coli and bacteroides B.Staphylococcus aureus C.Streptococcus viridians D.Staphylococcus epidermidis E.Klebsiella F.Clostridium tetani G.Clostridium difficile H.None of the above A 32-year-old women undergoes mastectomy and latissimus dorsi flap reconstruction for breast cancer, to provide optimal cosmesis a McGhan implant is placed under the myocutaneous flap. Three weeks post operatively the patient continues to suffer from recurrent wound infections that have proved resistant to multiple courses of antibiotics. A 68-year-old man with diabetes presents with an area of necrosis of the perineum at the base of the scrotum, there is some surrounding erythema. He is systemically unwell and hypotensive. A 68-year-old women with previous rheumatic fever is admitted with pyrexia of unknown origin. Her blood cultures are unhelpful but transoesophageal echocardiography reveals vegetations on the mitral valve.
The correct answer is Staphylococcus epidermidis This tends to colonise plastic devices and forms a biofilm which allows colonisation with other bacterial agents. It is notoriously difficult to eradicate once established and the usual treatment is removal of the device. -coli and bacteroides This is likely to be Fournier's Gangrene. A number of agents are implicated. E-coli and bacteroides are the most commonly isolated organisms. The key point is that both aerobic and anaerobic organisms must be present and only A has this option. Streptococcus viridians This is the most common organism affecting previously abnormal heart valves
3234
During a surgical ward round you are asked to request a nurse cleans a patient's surgical wound when the dressing is changed. The patient is 36 hours post surgery. According to NICE guidelines, what is the most appropriate substance to use to clean the wound? Iodine solution Sterile saline Patient may shower Alcohol swabs Sterile water
NICE recommend the following regarding postoperative wound cleansing: Use sterile saline for wound cleansing up to 48 hours after surgery. Advise patients that they may shower safely 48 hours after surgery. Use tap water for wound cleansing after 48 hours if the surgical wound has separated or has been surgically opened to drain pus.
3235
A.Anastamotic leak B.Chyle leak C.Air leak D.Biliary leak E.Deep vein thrombosis F.Portal vein thrombosis G.Biliary obstruction Please select the most likely complication for the scenario given. Each option may be used once, more than once or not at all. A 67-year-old female undergoes an oesophagogastrectomy for carcinoma of the distal oesophagus. She complains of chest pain. The following day there is brisk bubbling into the chest drain when suction is applied. A 20-year-old man has a protracted stay on ITU following a difficult appendicectomy for perforated appendicitis with pelvic and sub phrenic abscesses. He has now deteriorated further and developed deranged liver function tests. A 63-year-old man undergoes an Ivor - Lewis oesophagogastrectomy for carcinoma of the distal oesophagus. The following day a pale opalescent liquid is noted to be draining from the right chest drain.
Air leak Damage to the lung substance may produce an air leak. Air leaks will manifest themselves as a persistent pneumothorax that fails to settle despite chest drainage. When suction is applied to the chest drainage system, active and persistent bubbling may be seen. Although an anastomotic leak may produce a small pneumothorax, a large volume air leak is more indicative of lung injury. Portal vein thrombosis Such marked intra-abdominal sepsis may well produce coagulopathy and the risk of portal vein thrombosis. Chyle leak Damage to the lymphatic duct may occur during this procedure and some surgeons administer a lipid rich material immediately prior to surgery to facilitate its identification in the event of iatrogenic damage.
3236
Difference between mesenteric ischaemia and ischaemic colitits
you can also see the Hx which risk factors do the patient present with. CAD risks are more likely for mes ischemia. This particular pt has afib, a strong risk for emboli. dec in blood flow (eg decomp CHF, prolonged shock, dehydration) accompanied w abd pain and bloody diarrhea, will point to ischemic colitis.
3237
Theme: Tumour markers A.Invasive ductal carcinoma of the breast B.Prostate cancer C.Gastric cancer D.Ovarian cancer E.Colorectal cancer F.Pancreatic adenocarcinoma G.Seminoma testicular cancer H.Non-seminomatous testicular cancer I.Hepatocellular carcinoma For each tumour marker please select the most likely underlying malignancy. Each option may be used once, more than once or not at all. Raised beta-human chorionic gonadotropin with a raised alpha-feto protein level
The correct answer is Non-seminomatous testicular cancer A raised alpha-feto protein level excludes a seminoma
3238
A 65-year-old woman presents to the Emergency Department with lower abdominal pain and vomiting. On further questioning she has not opened her bowels for the past 2 days and feels bloated. A CT of her abdomen is requested: © Image used on license from Radiopaedia What is the most likely diagnosis? Diverticulitis Small bowel obstruction secondary to a strangulated inguinal hernia Linitis plastica of the stomach Large bowel obstruction secondary to volvulus Ovarian cancer with associated ovarian torsion
The CT shows multiple dilated loops of small bowel. CT is more sensitive than radiographs and will also demonstrate the cause in around 80% of cases. There are variable criteria for maximal small bowel obstruction, but 3.5 cm is a conservative estimate of dilated bowel. Note the protrusion of small bowel through the inguinal ring
3239
Medical indications for circumcision
phimosis recurrent balanitis balanitis xerotica obliterans paraphimosis
3240
How can the symptoms of BPH be categorised
Voiding symptoms: weak or intermittenet flow, straining, hesitancy, terminal dribbling, incomplete emptying Storage symptoms: urgency, frequency, urgency incontinence and nocturia Post micturition: Dribbling Cx: UTI, retention, obstructive uropathy
3241
Mx of BPH
Watchful waiting Rx: Alpha 1 antagonists 5 alpha reductase inhibitor Medical therapy of prostatic symptoms trial: (MTOPS) advocated combination therapy Sx: TURP
3242
E.g. of alpha-1 antagonists
Tamsulosin Afluzosin
3243
MOA alpha 1 antagonists
Decrease smooth muscle tone (prostate and bladder)
3244
Efficacy of alpha1 antagonists in BPH
Considered first line Improve symptoms in 40% of men
3245
Adverse effects of alpha1` anatgonists
Dizziness Postural hypotension Dry mouth Depression
3246
E.g. 5 alpha-reductase inhibtors
Block the conversion of testosterone to DHT (testosterone known to induce BPH)
3247
Efficacy of 5-alpha RIs
unlike alpha-1 antagonists causes a reduction in prostate volume and hence may slow disease progression. This however takes time and symptoms may not improve for 6 months. They may also decrease PSA concentrations by up to 50%
3248
Adverse effects of 5aRIs
ED Reduced libido Ejaculation problems Gynaecomastia
3249
Gallbladder location
Tip of the 9th costal cartilage
3250
Location of arcuate line
Half way between the umbilicus and pubic crest
3251
Transpyloric plane of Addison, location
L1 vertebra 9th Costal cartilage
3252
What structures are found on the transpyloric plane of Addison?
Pylorus Fundus of the gallbladder Origin of SMA Duodojejunal junction Neck of pancreas Hila of kidneys Formation of portal vein
3253
Location of the supracristal plane
L4/L5 Also location of bifurcation of the aorta
3254
Causes of hepatomegaly Smooth without jaundice
CCF Cirrhosis Lymphoreticular disease Budd Chiari Amyloid
3255
Causes of hepatomegaly Smooth with jaundice
Hepatitis Biliary tract obstruction Cholangitis Portal pyaemia
3256
Causes of hepatomegaly Irregular without jaundice
2o mets Macronodular cirrhosis Polycystic disease Primary HCC
3257
Causes of hepatomegaly Irregular with jaundice
Extensive 2o mets Cirrhosis Localised swellings: Reidel's lobe Hydatid cyst Liver abscess
3258
Why is it the spleen?
LUQ to RIF mass Notch Moves with respiration Dull to precussion Cannot get above it Not ballotable
3259
Massive kidneys in PACES?
Polycystic kidneys
3260
Stoma examination
Look- location, parastomal hernia Stoma: stoma itself, colour, surface ect. Bag + contents and surroundings Abdomen Ask to inspect perineum Palpate around and inside the stoma: need gloves and KY jelly Site Calibre Number of lumens Funcitoning Healthy
3261
How to tell the difference between periumbilical and umbilical hernia
Paraumbilical are crescenteric Umbilical are hemispherical
3262
Key clinical defect between hernia and diverification of the recti
There will be no palpable defect in diverification whereas with hernia, can palpate defect
3263
What is the rule of PR bleeding
Bright fresh rectal bleeding- visible with proctoscope: haemorrhoids Dark mixed in bleeding: upper GI/right colon
3264
If pathology stays in what type of stoma? Hartmann's=
= defunctioning Pathology taken out
3265
Low colorectal anastomosis type of stoma
Loop ileostomy
3266
What is the benefit of loop ileostomy vs loop colostomy
Loop ileostomy: - High output stoma + easy to make, easy to reverse Loop colostomy: - Tend to prolapse - Harder to reverse + Not high output
3267
Difference between feeding and NG tube
Feeding tube: into jejunum, can be guided under radiology Used in high output stomas Longer term than NGT
3268
Cx of NGT
LT use can lead to oesophageal stenosis
3269
Graded TEDs mecahnisms
Decreasing pressure up to knee Compress blood upwards Used in combination with calf exercises
3270
Female with urinary retention?
?Pelvic malignancy
3271
Male or female cause of postrenal obstruction
Megarectum i.e. constipation
3272
Why are tracheostomies used over ET tubes in ITU
Larynx is barrier to weaning from ventilation. Easier to wean from LT ITU ventilation or patients with elective maxfax sx
3273
What can central line be used to monitor in addition to presssure
Central venous O2: if \>75% patient adequately filled
3274
Suction drains shouldn't be used in?
Abdomen due to risk of fistula Can be used following breast sx etc
3275
Midline laparotomy and bilateral vertical groin incisisions in vascular
Aortobifemoral bypass graft
3276
Oblique LIF scar (Rutherford morrison scar) in vascular exam
Access to retroperitoneal iliac artery
3277
Midline laparotomy scar with externsion into 5th intercostal space=
Thoracolaparotomy Used for approaches to aort above the renal artery
3278
Oblique incicision anteriror to sternocleidomastoid
Access to carotid for carotid endarterectomy
3279
Bilateral groin incisions with rigid tube across pubic symphysis
Femorofemoral crossover graft
3280
Axillo bifemoral graft
Access axillary artery with cross over to both femorals
3281
Aortobifemoral bypass graft
Blockage in aorta or iliacs
3282
Scar on the inside of the leg running from 2cm lateral and inferior to pubic tubercle, one handsbreath below the knee and 2 centres anterior to medial malleolus
= long saphenous vein harvest scar.
3283
Definition of critical icshaemia (3 things)
Greater than two weeks duration (otherwise acute) Rest pain or tissue loss Ankle pressure of less than 40mmHg or \<0.6ABPI
3284
Relation between aneurysms
1 popliteal aneurysm 50% chance of having another 1 popliteal aneurysm 10% chance of infrarenal aneurysm
3285
How did the 5.5cm figure come around for AAA threhold
Small aneurysm trial showed that sureillance is safe for patients under 5.5cm
3286
Thoracic outlet syndrome
Can be due to an additional cervical rib, can be due to overgrowth of scalene, can be due to prolonged abudction e.g. violinists, cellists Can be classified as: Venous: upper limb DVT and long term swelling: heparinise Arterial: raynauds, claudication, embolisation Neurological: pain, radiculopathy
3287
How to remember stages of shock Game of tennis
0-15 15-30 30-40 Game
3288
Best arterial bypass prosthesis of choice in a young patient for fem-pop bypass
Autlogous saphenous vein
3289
Most common perforation site of duodenum
First due to exposure to acid
3290
Clinical signs of #
Pain Swelling Crepitus Deformity Adjacent structural injury: nerves/vessels/ligament/tendons
3291
Two types of displacement in#?
Translation (lateral): proximal/distal. ant/post. medial/lateral Angulation: internal/external rotation. dorsal/volar/ varus/valgus
3292
Different types of external fixation
Monoplanar (i.e. in one plane) Multiplaner e.g. circular ext fixation
3293
When is external fixation used?
When there is extensive soft tissue injury or complex periarticular fracture.
3294
External fixation and infection
100% of external fixators are infected. Pins get infected but controllable, prevents infection in the bone. Allows control of infection
3295
Classification of surgical complications
Immediate Early Late under these, local and general
3296
Cx of fractures
General (early or late): Fat embolus DVT Infection Prolonged immobility: UTI Specific: Neurovascular injuery Muscle/tissue injury Non/malunion Compartment synrome Local infection Degenerative change Reflex sympathetic dystrophy AVN Growth disturbance
3297
XR in orthopaedics
Weight bearing views
3298
OA how to phrase weight loss
Coming down the stairs is like 5x your body weight. If you lose 5kg- like reducing 25kg of strain on knee
3299
Def: frozen shoulder
Pain in all ranges of movement with a normal shoulder xray. (mostly external rotation is limited)
3300
Causes of post THR pain
Adductor weakness/rupture Leg length discrepancy Prosthesis failure Infection
3301
Constant dysuria with negative MSU
Red flag, require cystoscopy
3302
What is the main cause of bladder cancer?
Smoking
3303
Anticoagulation and haematuria
Doesn't exclude underlying cause May mean presentation is earlier
3304
Cytotoxic associated with bladder cancer
Cyclophosphamide
3305
How to classify haematuria
Micro and macroscopic
3306
How to classify haematuria anatomically
Upper UT: Kidney stones TCC of renal pelvis RCC Inury to kidney: tear Medical causes e.g. nephritis... TB Ureter: luminal: stone mural: tumour e.g. malignant stricture or urothelial Lower urinary tract Bladder: stone, tumour, injury to bladder Prostate: distended veins over large prostate, prostatitis, prostate cancer Urethra Testes
3307
beta naphthylamine dye
Bladder Ca
3308
Cytotoxic drug causing haematuria
Cyclophosphamide
3309
TWR indications for haematuria
All frank haematuria Persistent haematuria with dysuria in the absence of UTI Micro/macrohaematuria with LUTS Female retention with pain and haematuria
3310
Microscopic haematuria ix in TWR
Renal bladder/ USS
3311
Frank haematuria TWR Ix
CT urogram
3312
USS in urology
Noninvasive Differentiates between cyst and solid (tumour) Any evidence of hydronephrosis
3313
What is a CT urogram
Examination of KUB before and after IV contrast material. Cotrol CT, 5 and 15 min scans. Picks up urothelial filling defects. Instead of IV pyelogram
3314
What is a CT KUB?
Non contrast CT scan of the kidneys, ureturs and bladder Dx of renal stones which show up as white within the urinary trract Taken at 2.5mm cuts
3315
What is a triple phase CT scan?
Scan used to further evaluate renal tumours Non contrast: look for fat in tumour (to ensure not angiomyolipoma) Arterial: contrast enhancement Venous phase Examines location of tumour, size, renal vein involvement, any LNs or distant mets. Always comment on presence/absence/state of contralateral kidney
3316
Who needs a cystoscopy
Smokers Occupational exposure to chemicals/dyes History of persistent dysuria History of phenacitin abuse Hx of pelvic Rtx Cyclophosphamide exposure
3317
What is the false negative rate on renal biopsy?
11%
3318
Initial Mx of TCC bladder
TURBT R/V stage and grade
3319
What is HexFix
Allows examination of bladdder under blue light Red patch shows TCC in situ Enhances view
3320
=Staging of TCC bladder
CIS Ta: confined to mucosa T1: in the lamina propria T2: in the muscularis propria T3: into perivesical fat
3321
Layers of bladder
Mucosa Submucosa Muscularis propria Pervivesical fat
3322
Mx of T1G3 bladder tumour
Intravescial immunotherapy: BCG Close cystoscopic surveillance Ultimately radical cystectomy
3323
Features of bladder CIS
Present with bladder pain and dysruia If untreated for 2y: 50% develop invasive TCC Treated with intravesical BCG with radical cystectomy for those who fail to respond
3324
TCC: velvet in bladder
CIS
3325
Treatment of TCC of upper tract
Nephroureterectomy (kidney, ureteur and cuff of bladder) Ureteroscopy and laser for low grade tumours in unfit patients/solitary kidneys
3326
Why are patients with upper tract TCC at increased risk of bladder recurrence?
Urine carries malignant cells down to bladder 20-40% incidence of bladder TCC
3327
Presentation of renal cancer
Usually an incidental finding on abdo USS
3328
Classical triad in RCC
Haematuria Loin pain Palpable mass Late presentaiton
3329
Stauffer Syndrome
Stauffer syndrome is a constellation of signs and symptoms of liver dysfunction that arise due to presence of renal cell carcinoma, and, more rarely, in connection with other malignant neoplasms, though the specific pathogenesis is currently unknown. It is named for Dr. Maurice Stauffer, a gastroenterologist at the Mayo Clinic in Rochester, MN. The hepatic abnormalities are not due to tumor infiltration of the liver or intrinsic liver disease; they instead reflect the presence of a paraneoplastic syndrome.[1] Stauffer syndrome causes abnormal liver function tests, especially those that reflect the presence of cholestasis, i.e. abnormal bile flow. Hepatosplenomegaly may also be observed. The symptoms and signs resolve if the renal cell carcinoma (or another associated tumor) is successfully ablated
3330
Paraneoplastic in RCC
High clacium LFTs (stauffer syndrome)
3331
RCC staging
Stage 1 \<7cm Stage 2: \>7cm Stage 3: Invading into renal vein or into Gerota's fascia Stage IV: to other organs/LNs
3332
What is Gerota's fascia
Fascia covering kidney
3333
Renal mass \<3cm
Treated conservatively: active surveillance, total/partial nephrectomy, radiofrequency ablation or cryotherapy AKA Small renal mass (SRM)
3334
Mx of renal cancer: organ confined
Radical nephrectomy: lap or open Lap unless massive
3335
Absolute indications for partial nephrectomy in RCC
Solitary Bilateral renal mass Renal impairment
3336
Renal stones different types
85% calcium 15% combination or uric acid (radiolucent) cystine and struvite Struvite stones: combination of Mg, NH3 and P: occur in infected urine
3337
Bacterial causes of staghorn calculus
Urease producing bacteria: Staghorn calculi are composed of struvite (MAP, magnesium ammonium phosphate) and are usually seen in the setting of recurrent urinary tract infection with urease producing bacteria (e.g. Proteus, Klebsiella, Pseudomonas and Enterobacter).
3338
Renal colic + T
Indication for admission
3339
Renal colic NSAID
Rectal diclofenac
3340
Renal stone threshold for treatment
\<5mm have an 80% chance of passing spontaneously
3341
How to divide lower UT symptoms
Storage symptoms: Weak stream Straining Hesitancy Terminal dribbling Incomplete emptying Voiding: Urgency Frequency Nocturia Incontinence Post micturition dribbling
3342
Mx of bladder outflow obstruction
Treatment: alpha blockers: relax neck of bladder e.g. alfusoin, tamsulosin 5 alpha reductase inhibitor e.g. finasteride (takes 6m) Can be used in combination: combidart Surgical: TURP Enulceation of prostate If very large: open prostatectomy (Millin's prostatectomy) Freyer's prostatectomy (transvesicular) used if patient has a stone with the prostate
3343
Assessment of prostate
DRE PSA Flow rate US prostate (MRI is used more and more) Bone scan if ?mets
3344
Time limit on TURP
\<1 hour To prevent turp syndrome
3345
Normal PSA
\<4
3346
Staging of prostate cancer
Can be biopsied transrectally or transperineal. Stage 1: confined to periphery Stage 2: in both lobes May not be palpable Stage 3: multiple and palpable LN Stage 4: in contiguous organs Palpable
3347
Mx of prostate Ca
Active surveillance Hormone treatment RTx/Brachytherapy Sx: radical prostatectomy Cryotherapy/HIFU
3348
Doubling time for testicular cancer
10d Seen same day Painless enlarging lump in body of testes
3349
Approach to orchidectomy
Inguinal: The inguinal orchiectomy is a necessary procedure if testicular cancer is suspected. While it is possible to remove a testicle through an incision in the scrotum, this is not done when cancer is suspected because it disrupts the natural lymphatic drainage patterns. Testicular cancer usually spreads into the lymph nodes inside the abdomen in a predictable manner. Cutting the skin in the scrotum may disrupt this and cancer may spread to the inguinal lymph nodes, making surveillance and subsequent operations more difficult.
3350
Mx of nonseminoma post orchidectomy
Chemo BEP/CHOP may need retroperitoneal LN dissection One of the problems is retrograde ejaculation so need to consent
3351
2 way catheter used for
Drainage
3352
3 way catheter
Used for irrigation/haematuria/post TURP/TURBT Coude tipped, allow irrigation to prevent clot causing outflow obstruction
3353
Colours on urinary catheters
Used to size them Green is the smallest
3354
Purpose of JJ stent
Hollow tube: urine drains through and around Ureter stops peristalsing and dilates- can allow the uretur to become suitable for ureteroscopy
3355
Nephrostomy insertion
Antegrade: from above Retrograde: from below
3356
Flexible cystoscopy
Inspection or urethra and bladder under LA
3357
Rigid cystoscopy
Inspection of urethra and bladder under GA
3358
Cystoscopy and retrograde pyelogram
Contrast examination of ureter
3359
Cystoscopy and insertion of JJ stent
Under GA: obstructed ureter
3360
PCNL
Percutaenous nephrolithotomy (insertion of a scope directly into the kidney to laser stones in the kdiney): GA
3361
Simple nephrectomy
Removal of non functioning kidney: lap or open
3362
Radical nephrectomy
Removal of kidney for cancer: kidney/perinephric fat and adrenal gland
3363
Ix in CRC
Bloods: FBC: Hb LFTs: mets Tumour marker: CEA Imaging: CXR: lung mets USS liver: mets CT and MRI: staging, MRI best for rectal Ca and liver mets Endoanal US: staging rectal tumours Ba/gastrograffin enema: apple-core lesion Endoscopy + biopsy: Flexi sig: 65% of tumors accessible Colonoscopy
3364
Apple-core sign CRC
3365
What system is used to stage CRC
Dukes (Sir Cuthbert Dukes: St Mary's Pathologist)
3366
Duke's CRC staging
A: confined to bowel wall :90% B: through bowel wall but no LNs: 60% C: Regional LNs: 30% D: Distant mets: \<10% 5ys
3367
TNM staging of CRC
Tis: carcinoma in situ T1: submucosa T2: muscularis propria T3: subserosa T4: through serosa to adjacent organs N1: 1-3 nodes N2: \>4 nodes
3368
Grading of CRC
Grading from low to high based on cell morphology Dysplasia, mitotic index, hyperchromatism
3369
Mx of CRC principles
MDT Confirm Dx Stage with CT or MRI 60% amenable to radical Sx
3370
Sx for CRC
Use ERAS pathway Pre-operative bowel prep (except R sided lesions) e.g. Kleen Prep (macrogol: osmotic laxative) the day before and phosphate enema in the AM Consent for stoma Stoma nurse consult for siting
3371
Principles of CRC
Excision depends on lymphatic drainage which follows the arterial supply Mobility of bowel and blood supply at cut ends is also important Hartmann's often used if obstruction Laparoscopic approach is the standard of care
3372
TWR for CRC
\>40y reporting rectal bleeding with change in bowel habit persisting for \>6w \>60 with retal bleeding for \>6w without change in bowel habit \>60 with change in bowel habit without rectal bleeding Of any age with right lower abdominal mass consistent with involvement of large bowel Of any age with palpable rectal mass (intraluminal and not pelvic, if pelvic requires referral to uro or gynae) Men of any age with unexplained IDA and Hb \<11 Non-menstruating women with unexplained IDA and Hb \<10
3373
Sx mx of Rectal Ca
Neoadjuvant RTx may be used to reduced local recurrence and increase 5y survival Anterior resection AP resection + total mesorectal excision
3374
Anterior resection in rectal Ca
Tumour 4-5cm from anal verge Defunction with loop ileostomy
3375
AP resection in rectal Ca
\<4cm from anal verge
3376
Total mesorectal excision in rectal Ca
For tumours of the middle and lower third Aims to reduce recurrence Increased anastomotic leak and feacal incontinence
3377
Sigmoid Ca Sx
High anterior resection or sigmoid colectomy
3378
Left CRC Sx
Left hemicolectomy
3379
Transverse CRC Sx
Extended right hemicolectomy
3380
Caecal/right CRC
Right hemicolectomy
3381
3382
3383
Other Rx in CRC
Local exision: e.g. transanal endoscopic microsurgery Bypass surgery: palliation Hepatic resection: if single lobe mets Stenting: palliation or bridge to surgery in obstruction CTx
3384
CTx in CRC
Adjuvant 5-FU for Duke's C reduces mortality by 25% i.e. LN +ve patients High grade tumour Palliation of metastatic disease
3385
NHS Screening for CRC FOB
Introduced in 2006 60-75y Home FOB every 2y: 1/50 have +ve FOB Colonoscopy if +ve: 1/10 have Ca Lindholm et al BJS: screening reduced risk of dying from CRC by 25%
3386
CRC screening: Flexi sig
Introduced inn 2011/12 One off screen at 55 Atkin et al Lancet: Reduced CRC incidence by 33% Reduced CRC mortality by 43%
3387
FAP cause
Autosomal dominant APC gene on 5q21
3388
100-1000s adenomas by 16y Mainly in large bowel Also stomach and duodenum (near ampulla) 100% develop CRC, often by 40y May be associated with congenital hypertrophy of the retinal pigment epithelium
Familial Adenomatous Polyposis
3389
\<100 adenomas Later CRC (\>50y)
Attenuated FAP
3390
Gardner's Syndrome TODE
FAP variant Thyroid tumours Osteomas of the mandible, skull and long bones Dental abnormalities: supernumerary teeth Epidermal cysts
3391
Turcots
Variant of FAP In addition: CNS tumours medullo and glioblastomas
3392
Mx of FAP
Prophylactic colectomy before 20y Total colectomy + IRA: requires life long stump surveillance Proctocolectomy: IPAA Remain at risk of Ca in stomach and duodenum, require endoscopic screening
3393
What is the commonest cause of hereditary CRC?
HNPCC
3394
Pathology of HNPCC
AD Mutation of MMR enzymes e.g. MSH2 on Chr 2p Commonest cause of hereditary CRC: 3% of all CRC
3395
Lynch 1 presentation
HNPCC right sided CRC
3396
Lynch 2 presentation
CRC + gastric, endometrial, prostate, breast
3397
Lynch 1 vs 2
1 is familial colon cancer 2 is associated with other Ca of the GIT and reproductive tissue
3398
Dx of HNPCC 3, 2, 1
Amsterdam II criteria 3 or more relatives with an associated cancer (CRC, endometrial, small intestine, uretur or renal pelvis) 2 or more successive generations involved At least 1 diagnosed \<50y/o 1 should be a first degree relative of the other 2 FAP should be exluded Tumours should be verified via pathologic examination
3399
Pathology of Peutz-Jehgers
AD STK11 mutation
3400
10-15y/o Mucocutaneous hyperpigmentation: macules on palms, buccal mucosa Multiple GI hamartomous polyps: intussuception, haemorrhage CRC, pancreas, breast, lung, ovaries, uterus
Peutz-Jehgers
3401
Peutz Jehgers
3402
What are the different types of GI poylps
Inflammatory pseudopolyps Hyperplastic polyps Hamartomatous Neoplastic
3403
Inflammatory pseudopolyps=
Regnerating islands of mucosa in UC
3404
Hyperplastic polyps=
Piling up of goblet cells and absorptive cells Serrated surface architecture No malignant potential
3405
Piling up of goblet cells and absorptive cells Serrated surface architecture No malignant potential
Hyperplastic polyps
3406
Tumour like growths composed of tissues present at site where they develop Sporadic or part of familial syndromes
Hamartomous polyps
3407
Solitary hamartoma in children Cherry on a stalk appearance
Juvenile polyp
3408
Tubular or villous adenomas Usually asymptomatic May have blood/mucus PR, tenesmus
Neoplastic polyps
3409
Autosomal dominant \>10 hamartomatous polyps Increased CRC risk: need surveilance and polypectomy
Juvenile polyposis
3410
Autosomal dominant Macrocephaly and skin stigmata Intestinal hamartomas Increased risk of extra-intestinal Ca
Cowden syndrome
3411
How can the causes of acute mesenteric ischaemia be classified?
Arterial Non occlusive Venous Other
3412
Arterial mesenteric ischaemia
Thrombotic (35%), embolic (35%)
3413
Non-occlusive mesenteric acute mesenteric ischaemia
Splanchnic vasoconstriction e.g. 2o to shock
3414
Other causes of mesenteric ischaemia
Trauma, vasculitis, strangulation
3415
What is the most common cause of acute mesenteric ischaemia?
Arterial (70%) (non-occlusive-20%, VT- 5%)
3416
What is the triad of acute mesenteric iscahemia
Acute severe abdominal pain +/- PR bleed Rapid hypovolaemia-\> shock No abdominal signs
3417
Nearly always small bowel Acute severe abdominal pain +/- PR bleed Rapid hypovolaemia-\> shock No abdominal signs Degree of illness \>\>\> clinical signs May by in AF
?acute mesenteric ischaemia
3418
Ix in acute mesenteric iscahemia
Bloods: Raised Hb: plasma loss Raised WCC Raised amylase Persistent metabolic acidosis: raised lactate Imaging: AXR- gasless abdomen Arteriography/CT/MRI angio
3419
Cx of acute mesenteric ischaemia
Septic peritonitis SIRS-\> MODS
3420
Mx of acute mesenteric ischaemia
Fluids Abx: gent + met LMWH Laparotomy: resect necrotic bowel
3421
Cause of chronic small bowel ischaemia
Atheroma + low flow state e.g. LVF
3422
Severe colicky post-prandial abdominal pain (gut claudication) PR bleeding Malabsorption Weight loss
Chronic small bowel ischaemia
3423
Mx of chronic small bowel ischaemia
Mx: angioplasty
3424
Cause of chronic large bowel ischaemia
Follows low flow in IMA territory
3425
Lower, left sided abdominal pain Bloody diarrhoea Pyrexia Tachycardia
?Chronic large bowel ischaemia
3426
Ix in chronic large bowel ischaemia
Raised WCC Ba enema: thumb-printing MR angiography
3427
Cx of chronic large bowel ischaemia
May-\> peritonitis and septic shock Strictures in the LT
3428
Mx of chronic large bowel ischaemia
Usually conservative: fluids and Abx Angioplasty and endovascular stenting
3429
What are the common/important causes of lower GI bleed
Rectal: haemorrhoids, fissure Diverticulitis Neoplasm
3430
What are the causes of lower GI bleed
Important: Rectal: haemorrhoids, fissure Diverticulitis Neoplasm Other: IBD Infection: shigella, campylobacter, C diff Polyps Large upper GI bleed (15% of lower GI bleeds) Angio: dysplasic, ischaemic colitis, HHT
3431
Ischaemic colitis=
Colonic ischaemia
3432
Ix in lower GI bleed
FBC, U+E, LFT, x-match, clotting, amylase Stool: MCS Imaging: AXR erect CXR Angiography: necessary if no source on endoscopy Endoscopy
3433
Endoscopy in lower GI bleed
1st: Rigid proctoscopy/sigmoidoscopy 2nd: OGD 3rd: colonoscopy: difficult in major bleeding
3434
Mx of Lower GI bleed
ABC Urinary catheter Abx if evidence of sepsis or perf PPI if upper GI bleed Keep bed bound: need to pass stool may be large bleed-\> collapse Stool chart Diet: keep on clear fluids (allows colonoscopy) Surgery: only if unremitting, massive bleed
3435
Features of colonic angiodysplasia
Submucosal AV malformation 70-90% occur in right colon Can affect anywhere in GIT
3436
Presentation of angiodysplasia
Elderly Fresh PR bleeding
3437
Mx of angiodysplasia
Exlcude other dx: PR, Ba enema, colonoscopy Mesenteric angiorgraphy or CT angiography Tc-labelled RBC scan: indentify active bleeding
3438
Rx of angiodysplasia
Embolisation Endoscopic laser electrocoagulation Resection
3439
Benign tumour of mature adipocytes Sarcomatous change probably doesn't occur Liposarcomas arise de novo
Lipoma
3440
Occur anywhere fat can expand i.e. not scalp or palms. Include spermatic cord, submucosa Soft Subcutaneous Imprecise margin Fluctuant
Lipoma
3441
Soft Subcutaneous Imprecise margin Fluctuant
3442
Mx of lipomas
Non-surgical Surgical excision
3443
Diseases causing lipomas
Dercum's disease/Adiposis dolorosa Familial Mutliple Lipomatosis Madelung's Disease Bannayan-Zonana Syndrome
3444
Dercum's disease
Multiple painful lipomas Associated with peripheral neuropathy Obese, postmenopausal women Dercum's disease was first described at Jefferson Medical College by neurologist Francis Xavier Dercum in 1892
3445
Familial Multiple Lipomatosis
is a rare condition that is characterized by multiple lipomas on the trunk and extremities. As the name suggests, FML is diagnosed when multiple lipomatosis occurs in more than one family member, often over several generations. The lipomas associated with FML are usually painless, but may impact quality of life as they can be numerous and large.[1][2] Although the condition appears to be passed down through families in an autosomal dominant manner, the underlying genetic cause is currently unknown.[3]Treatment is based on the signs and symptoms present in each person. Surgical excision may be necessary if the tumors interfere with movement and/or daily life.[1][2
3446
Madelung's disease
Benign symmetric lipomatosis (also known as Benign symmetric lipomatosis of Launois–Bensaude, Madelung's disease, multiple symmetric lipomatosis, and cephalothoracic lipodystrophy) is a cutaneous condition characterized by extensive symmetric fat deposits in the head, neck, and shoulder girdle area.[1] The German surgeon Otto Wilhelm Madelung was the first to give a detailed description of the disorder. This condition is very rare, with an estimated incidence rate of 1 in 25,000, and affects males up to 30 times more frequently than females.[2] The cause of the disease remains unknown, but its incidence strongly correlates with alcohol abuse; abstinence from alcohol prevents disease progression. Defects in the adrenergic-stimulated lipolysis and accumulation of embryological brown fat have also been reported. Cosmetic disfigurement due to the fat deposition in the cervicothoracic region results in a "pseudoathletic appearance", resembling the Italian statue Warrior of Capestrano and carvings of Queen of Punt (Egypt).[3] Traditionally the treatment is mainly surgical, consisting of the removal of the lipomas, although recent study has proposed liposuction and phosphatidylcholine injection as possible alternatives.[4]
3447
Madelung's disease
3448
Bannayan-Zonana Syndrome
Multiple lipomas Macrocephaly Haemangiomas AD
3449
Epithelial lined cyst containing keratin Occur at sites of hair growth: scalp, face, neck chest and back Not soles or palms Central punctum Firm Smooth Intradermal
Sebaceous cyst
3450
What are the two subtypes of sebaceous cyst
Epidermal cyst: arise from hair follicle infundibulum Trichilemmal cyst/Wen Arise from hair follicle epithelium Often multiple May be AD
3451
Central punctum Firm Smooth Intradermal
Sebaceous cyst
3452
Cx of sebaceous cysts?
Infection: pus discharge Ulceration Calcification
3453
Large ulcerating trichilemmal cyst on the scalp Resembles an SCC
Cock's Peculiar Tumour
3454
Mx of sebaceous cyst
Non-surgical or with excision
3455
Cock's peculiar tumour
3456
Cystic swelling related to a synovial lined structure: joint, tendon Myxoid degeneration of fibrous tissue Contain thick, gelatinous material
Ganglion
3457
Can be found anywhere 90% on dorsum of hand or wrist Dorsum of ankle May be a scar from recurrence Weakly transilluminable Soft Subcutaneous May be tethered to a tendon
Ganglion
3458
DDx for ganglion
Bursae Cystic protrusion from synovial cavity of arthritic joint
3459
Mx of ganglion
Non-surgical: Aspiration followed by 3w of immobilisation Surgical excision: Recurrence can be 50% Risk of neurovascular damage
3460
Ganglion
3461
Benign hyperplasia of basal epithelial layer Hyperkeratosis: keratin layer thickening Acanthosis: prickle layer thickening
Seborrhoeic keratosis
3462
Stuck on appearance Dark brown Greasy
Seborrheic keratosis
3463
Mx of seborrheic keratosis
Nonsurgical
3464
Seborrheic keratosis
3465
Benign nerve sheath tumour arising from schwann cells
Neurofibroma
3466
Solitary or multiple Pedunculated nodules Fleshy consistency Pressure can-\> paraesthesia Examin the eyes (?Lisch), the axilla(freckling) and the CNs (esp. 8) BP
Neurofibroma
3467
Mx of neurofibroma
Surgical excision only indicated if malignant growth suspected Local regrowth is common
3468
Overgrowth of all the layers of the skin with a central vascular core Pedunculated Flesh coloured Fibroepithelial polyp
Papilloma
3469
Mx of papilloma
Excision and diathermy to control bleeding
3470
Rapidly growing capillary haemangioma Most commonly on hands face, gums and lips Bright red hemispherical nodule May have serous/purulent discharge Soft on palpation Bleed very easily
Pyogenic granuloma NB neither pyogenic nor a granuloma
3471
Additional features of pyogenic granuloma
Possibly associated with previous trauma More common in pregnancy
3472
Mx of pyogenic granuloma
Curettage with diathermy at the bases
3473
Pyogenic granuloma
3474
Epidermal lined cyst deep to the skin Smooth spherical swelling Sites of embryological fusion Scar from recurrence Soft Non-tender Subcutaneous
Dermoid cyst
3475
Dermoid cyst
3476
Classification of dermoid cysts
Congenital/inclusion: Developmental inclusion of epidermis along lines of skin fusion Midline of neck and nose Medial and lateral ends of eyebrows Acquired/implantation: Implantation of epidermis in dermis Often 2o to trauma e.g. piercing
3477
Mx of congenital dermoid cyst
CT to establish extent Surgical excision
3478
Acquired dermoid cyst
Surgical excision
3479
What to ask an adult with a dermoid cyst
Have you always had it Trauma
3480
Benign neoplasm of dermal fibroblasts Can occur anywhere Mostly on the lower limbs of young to middle-aged women Small, brown, pigmented nodule Firm, woody feel characteristic Intradermal: mobile over deep tissue
Dermatofibroma
3481
Dermatofibroma
3482
DDx for dermatofibroma
Melanoma, BCC Requires excision and histology
3483
Benign overgrowth of hair follicle cells Cytologically similar to well-differentiated SCCs Fast-growing Dome-shaped with a keratin plug Intradermal
Keratoacanthoma
3484
Keratoacnathoma
Typically regress As it cannot be clinically differentaited from SCC with reliability they require surgical treatment
3485
Epdiemiology of malignant melanoma
F\>M: 1.5:1 10000/yr and 2000 deaths/yr Increased 80% over past 20y
3486
ABCDE of melanoma
Asymmetry Border: irregular Colour: \>1 Diameter: \>6m Evolving/elevation
3487
RFs for MM
Sunlight especially intesnse exposure in early years Low Fitzpatrick skin type Increased no of common moles +ve FH Increased age Immunosuppression
3488
How can MM be classified?
Superficial spreading Lentigo maligna melanoma Acral lentiginous Nodular melanoma Amelanotic
3489
Most common type of MM
Superficail spreading
3490
MM Irregular borders, colour variation Commonest in caucasians Grow slowly, metastasise late= better Px
Superficial spreading melanoma
3491
Superficial spreading melanoma
3492
MM Often elderly patients Face or scalp
Lentigo maligna melanoma
3493
Lentigo Maligna melanoma
3494
MM Asians/blakcs Palms, soles, subungual (with Hutchinson's sign)
Acral lentiginous MM
3495
Hutchinson's sign in hands
Melanonychia: important sign of subungual melanoma
3496
Acral lentigionous melanoma
3497
MM All sites Younger age, new lesion Invade deeply and metastasis early=poor Px
Nodular melanoma
3498
Nodular Melanoma
3499
MM Atypical appearance-\> delayed dx
Amelanotic melanoma
3500
Amelanotic melanoma
3501
Staging of MM
Breslow depth Clark's staging
3502
Breslow depth
Thickness of tumour to deepest point of dermal invasion \<1mm= \>75% 5ys 4mm= 50% 5ys
3503
Clark's staging
MM Stratifies depth by 5 anatomical levles Stage 1: epidermis Stage 5: SC fat
3504
MM mets
Liver Eye
3505
Mx of MM
Excision and 2o margin excision depending on Breslow depth +/- lymphadenectomy +/- adjuvant chemo: may use isolated limb perfusion
3506
Poor pxic indicators in MM
Male sex (more tumours on trunk cf. females) Increased mitosis Satellite lesions
3507
Ulcerated lesion with hard, raised everted edges found on sun exposed areas
Squamous cell carcinoma
3508
Causes of SCC skin
Sun exposure: scalp, face, ears, lower leg May arise in chronic ulcers: Marjolin's ulcer Xeroderma pigmentosa
3509
Xeroderma pigmentosa Increased risk of SCC skin
3510
Evolution of SCC skin
Solar/actinic keratosis-\> Bowen's-\> SCC LN spread is rare
3511
SCC
3512
Irregular crusty warty lesions With pre-malignant potential Found on sun exposed areas
Actinic keratosis
3513
Pre-malignant potential of AK
1% /y
3514
Actinic keratoses
3515
Mx for Actinic keratoses
Cautery Cryotherapy 5-FU Imiquimod Photodynamic phototherapy
3516
Red/brown scaly plaques Typically on the legs of older women
Bowen's disease= SCC in situ
3517
Bowen's disease
3518
Rx of Bowen's disease
As for AK
3519
Commonest cancer Pearly nodule with rolled telangiectactic edge May ulcerate Typically on face in sun-exposed area above line from tragus-\> angle of mouth
BCC
3520
Behaviour of BCC
Low-grade malignancy-\> very rarely metastasies Locally invasvie
3521
Rx BCC
Ecision: Mohs- complete circumferential margin assessment using frozen section histology Cryo/radio may be used
3522
BCC
3523
Dx of neck lumps: general approach
85% of neck lumps are LNs: especially if present \<3w Infection: EBV, tonsilitis, HIV Ca: lymphoma or mets 8% are goitres 7% other e.g. sebaceous cyst or lipoma
3524
Ix in neck lumps
Clinical assessment Imaging: USS Cyto/histology: aspiration or biopsy
3525
Borders of the anterior triangle
Anterior margin of SCM Midline Ramus of the mandible Roof: investing fascia Floor: prevertebral fascia
3526
Pulsatile causes of anterior triangle neck lump
Carotid artery aneurysm Tortuous carotid artery Carotid body tumour
3527
Non pulsatile causes of anterior triangle neck lump
Branchial cysts Laryngocele Goitre Parotid tumour: lump in postero superior area
3528
Borders of the submandibular tirangle
Mental process Ramus of the mandible Line between the two angles of the mandible
3529
Causes of submandibular triangle lumps
Salivary stone Sialadenitis Salivary tumour
3530
Margins of the posterior triangle of the neck
Posterior margin of SCM Anterior margin of trapezius Middle 1/3rd of clavicle
3531
Causes of posterior triangle neck lumps
LNs Cervical ribs Pharyngeal pouch Cystic hygromas Pancoast's tumours
3532
Midline lump \<20y
Thyroglossal cyst Dermoid cyst
3533
Midline lump \>20y
Thyroid isthmus mass Ectopic thyroid tissue
3534
Def: branchial cyst
Embryological remnant 2nd branchial cleft
3535
Age \<20y Anterior margin of SCM at junction of upper and middle 3rd May become infected-\> abscess May be associated with a fistula Lined by squamous epithelium Contain "glary fluid" with cholesterol crystals
Branchial cysts
3536
Branchial cyst
3537
Rx of branchial cyst
Med: Abx for infection Sclerotherapy with OK-432 can be used Sx: Definitive Rx May be difficult due to proximity of carotids
3538
Small opening in lower 3rd of neck on anterior margin of SCM Between tonsillar fossa and anterior border of SCM May discharge mucus
Branchial sinus or fistula
3539
Features of chemodectoma
Carotid body tumour Very rare Located @ carotid bifurcation Detect pO2, pCO2 and H+
3540
Just anterior to upper 3rd of SCM Pulsatile Move laterally but not vertically May be bilateral Pressure may-\> dizziness and syncope Mostly bengin (5% malignant)
Chemodectoma
3541
Ix in chemodectoma
Doppler or angio: splaying of bifurcation
3542
Rx in chemodectoma
Extirpation by vascular surgeon
3543
Cystic dilatation of the laryngeal saccule Congenital or acquired Exacerbated by blowing
Laryngocele
3544
Common \<20y Found at junctions of emryological fusion Neck midline, lateral angles of eyebrow, under tongue Contains ectodermal elements: hair follciles, sebaceous glands Rx: excision
Dermoid Cyst
3545
Cyst formed from persistent thyroglossal duct Path of thyroid descent from base of tongue
Thyroglossal cyst
3546
Can be located anywhere between foramen caecum and the thyroid: usually just inferior to the hyoid (subhyoid or just above, suprahyoid) Fluctuant lump that moves up with tongue protrusion Can become infected-\> fistula
Thyroglossal cyst
3547
Infected thyroglossal cyst
3548
Def: cervical ribs
Overdevelopment of transverse process of C7 Occur in 1:150
3549
Mostly asymptomatic Hard swelling in posterior triangle of the neck Reduced radial pulse on abduction and external rotation of the arm Can-\> vascular symptoms Compresses subclavian A Raynaud's Subclavian steal Reduced venous outflow-\> oedema Can-\> neurological symptoms Compresses lower trunk of brachial plexus, T1 nerve root or stellate ganglion Wasting of intrinsic hand muscles Paraesthesia along medial border of arm
Cervical rib
3550
Cervical rib
3551
Herniation of pharyngeal mucosa through its muscular coat at its weakest point: Killian's dehiscence: between thyroid and cricopharyngeal muscles that form inferior constrictor
Zenker's diverticulum
3552
Killian's dehiscence
Killian's dehiscence (also known as Killian's triangle, Laimer triangle, Laimer-Killian triangle, or Laimer-Haeckermann area) is a triangular area in the wall of the pharynx between the thyropharyngeal and cricopharyngeus of the inferior constrictor of the pharynx
3553
Why is Zenker's diverticulum a misnomer
It is a pseudodiverticulum as it doesn't involve the muscle
3554
Swelling on LHS of neck in posterior triangle Regurgitation and aspiration Halitosis Gurgling sounds Food debris-\> expansion-\> oesophageal compression-\> dysphagia
Zenker's diverticulum/Pharyngeal pouch
3555
Ix in pharyngeal pouch
Barium swallow
3556
Rx in Pharyngeal pouch
Excision and cricopharyngeal myotomy Endoscopic stapling
3557
Congenital multiloculated lymphangioma arising from jugular lymph sac
Cystic hygroma
3558
Infants Lower part of posterior triangle but may extend to axilla Increases in size when child coughs/cries Transilluminates
Cystic hygroma
3559
Cystic hygroma
3560
Rx of cystic hygroma
Excision or hypertonic saline sclerosant May recur
3561
How to differentiate between nipple eczema and Paget's disease of the breast
Pagets disease differs from eczema of the nipple in that it involves the nipple primarily and only latterly spreads to the areolar (the opposite occurs in eczema).
3562
A 25-year-old man from the far east presents with a fever and right upper quadrant pain. As part of his investigations a CT scan shows an ill defined lesion in the right lobe of the liver. A.Haemangioma B.Hepatocellular carcinoma C.Hepatic metastasis D.Polycystic liver disease E.Simple liver cyst F.Hyatid cyst G.Amoebic abscess H.Mesenchymal hamartoma
Amoebic abscesses will tend to present in a similar fashion to other pyogenic liver abscesses. They should be considered in any individual presenting from a region where Entamoeba histiolytica is endemic. Treatment with metronidazole usually produces a marked clinical response.
3563
A 42-year-old lady presents with right upper quadrant pain and a sensation of abdominal fullness. An ultrasound scan demonstrates a 6.5 cm hyperechoic lesion in the right lobe of the liver. Serum AFP is normal. ## Footnote A.Haemangioma B.Hepatocellular carcinoma C.Hepatic metastasis D.Polycystic liver disease E.Simple liver cyst F.Hyatid cyst G.Amoebic abscess H.Mesenchymal hamartoma
A large hyperechoic lesion in the presence of normal AFP is likely to be a haemangioma. An HCC of equivalent size will almost always result in rise in AFP.
3564
90% develop in women in their third to fifth decade Linked to use of oral contraceptive pill Lesions are usually solitary They are usually sharply demarcated from normal liver although they usually lack a fibrous capsule On ultrasound the appearances are of mixed echoity and heterogeneous texture. On CT most lesions are hypodense when imaged prior to administration of IV contrast agents In patients with haemorrhage or symptoms removal of the adenoma may be required
Liver cell adenoma
3565
Most common benign tumours of mesenchymal origin Incidence in autopsy series is 8% Cavernous haemangiomas may be enormous Clinically they are reddish purple hypervascular lesions Lesions are normally separated from normal liver by ring of fibrous tissue On ultrasound they are typically hyperechoic
Haemangioma
3566
Congential and benign, usually present in infants. May compress normal liver
Mecenchymal hamartomas
3567
Liver abscess is the most common extra intestinal manifestation of amoebiasis Between 75 and 90% lesions occur in the right lobe Presenting complaints typically include fever and right upper quadrant pain Ultrasonography will usually show a fluid filled structure with poorly defined boundaries Aspiration yield sterile odourless fluid which has an anchovy paste consistency Treatment is with metronidazole
Amoebic abscess
3568
Biliary sepsis is a major predisposing factor Structures drained by the portal venous system form the second largest source Common symptoms include fever, right upper quadrant pain. Jaundice may be seen in 50% Ultrasound will usually show a fluid filled cavity, hyperechoic walls may be seen in chronic abscesses
Liver abscess
3569
Usually occurs in association with polycystic kidney disease Autosomal dominant disorder Symptoms may occur as a result of capsular stretch
Polycystic liver disease
3570
Rare lesions with malignant potential Usually solitary multiloculated lesions Liver function tests usually normal Ultrasonography typically shows a large anechoic, fluid filled area with irregular margins. Internal echos may result from septa Surgical resection is indicated in all cases
Cystadenoma
3571
Seen in cases of Echinococcus infection Typically an intense fibrotic reaction occurs around sites of infection The cyst has no epithelial lining Cysts are commonly unilocular and may grow to 20cm in size. The cyst wall is thick and has an external laminated hilar membrane and an internal enucleated germinal layer Typically presents with malaise and right upper quadrant pain. Secondary bacterial infection occurs in 10%. Liver function tests are usually abnormal and eosinophilia is present in 33% cases Ultrasound may show septa and hyatid sand or daughter cysts. Percutaneous aspiration is contra indicated Treatment is by sterilisation of the cyst with mebendazole and may be followed by surgical resection. Hypertonic swabs are packed around the cysts during surgery
Hyatid cysts
3572
A 34-year-old lady is admitted with recurrent episodes of non-specific abdominal pain. On each admission all blood investigations are normal, as are her observations. On this admission a CT scan was performed. This demonstrates a 1.5cm nodule in the right adrenal gland. This is associated with a lipid rich core. Urinary VMA is within normal limits. Other hormonal studies are normal.
This is typical for a benign adenoma.Benign adenomas often have a lipid rich core that is readily identifiable on CT scanning. In addition the nodules are often well circumscribed.
3573
Neuroendocrine tumour of the chromaffin cells of the adrenal medulla
Phaeochromocytoma
3574
A 70-year-old patient with prostate cancer is commenced on goserelin therapy. A week after starting treatment, he attends a local emergency department complaining of worsened lower urinary tract symptoms and new onset back pain. Which of the following treatment options may have helped avoid this deterioration? Higher dose goserelin Pretreatment with flutamide Lower dose goserelin Low dose-rate brachytherapy Joint therapy with corticosteroids
During the first stages of treatment, goserelin may cause a transient increase in symptoms of prostatic cancer. This is known as the 'flare effect' and is caused by an initial increase in luteinizing hormone production prior to receptor down-regulation. Flutamide, a synthetic antiandrogen, can be used preemptively to attenuate the tumour flare through its antagonistic effects at androgen receptors. The new onset back pain in this patient is significant and demands further investigation of spinal metastasis.
3575
A 28-year-old man with Crohn's disease has undergone a number of resections. His BMI is currently 18 and his albumin is 18. He feels well but does have a small localised perforation of his small bowel. The gastroenterologists are giving azathioprine. What is the most appropriate advice regarding feeding? Nil by mouth Nil by mouth and continuous intra venous fluids until surgery Enteral feeding Parenteral feeding Nutritional supplements
This man is malnourished, although he is likely to require surgery it is best for him to be nutritionally optimised first. As he may have reduced surface area for absorption and has a localised perforation TPN is likely to be the best feeding modality.
3576
A 72-year-old man has just undergone an emergency repair for a ruptured abdominal aortic aneurysm. Pre operatively he was taking aspirin, clopidogrel and warfarin. Intra operatively he received 5000 units of unfractionated heparin prior to application of the aortic cross clamp. His blood results on admission to the critical care unit are as follows: Full blood count Hb8 g/dl Platelets40 \* 109/l WBC7.1 \* 109/l His fibrin degradation products are measured and found to be markedly elevated. Which of the following accounts for these results? Anastomotic leak Disseminated intravascular coagulation Heparin induced thrombocytopenia Adverse effect of warfarin Adverse effects of antiplatelet agents
The combination of low platelet counts and raised FDP in this setting make DIC the most likely diagnosis.
3577
Prolonged PT Prolonged APTT Prolonged Bleeding time Plt: low
DIC
3578
Stone burden of less than 2cm in aggregate Renal colic
Lithotripsy
3579
Stone burden of less than 2cm in pregnant females Renal colic
Ureteroscopy
3580
Complex renal calculi and staghorn calculi
Percutaneous nephrolithotomy
3581
Ureteric calculi less than 5mm
Manage expectantly
3582
A 19-year-old female presents with severe anal pain and bleeding which typically occurs post defecation. On examination she has a large posteriorly sited fissure in ano. ## Footnote A.Excision and primary closure B.Incision and drainage C.Topical steroids D.Topical diltiazem E.Steroid injections F.Haemorroidectomy G.Manual anal dilation H.Injection with 88% aqueous phenol I.Sphincterotomy
Topical diltiazem Theme from January 2013 Exam Initial therapy should be with pharmacological agents to relax the sphincter and facilitate healing. This is particularly true in females presenting for the first time
3583
A 27-year-old man is involved in a road traffic accident. He is seen in the emergency department with chest pain. Clinical examination is essentially unremarkable and he is discharged. He subsequently is found dead at home. What is the most likely underlying injury? Tracheobronchial tree injury Traumatic aortic disruption Cardiac laceration Diaphragmatic rupture Rupture of the oesophagus
Aortic injuries that do not die at the scene may have a contained haematoma. Clinical signs are subtle and the diagnosis may not be apparent on clinical examination. Without prompt treatment the haematoma usually bursts and the patient dies.
3584
A 24-year-old lady from Western India presents with symptoms of lethargy and dizziness, worse on turning her head. On examination her systolic blood pressure is 176/128. Her pulses are impalpable at all peripheral sites. Auscultation of her chest reveals a systolic heart murmur.
Takayasu's arteritis most commonly affects young Asian females. Pulseless peripheries are a classical finding. The CNS symptoms may be variable.
3585
Large vessel granulomatous vasculitis Results in intimal narrowing Most commonly affects young asian females Patients present with features of mild systemic illness, followed by pulseless phase with symptoms of vascular insufficiency Treatment is with systemic steroids
Takayasu's arteritis
3586
What is used to grade prostate cancer?
Gleason score
3587
A 34-year-old man presents to an emergency surgery with abdominal pain. This started earlier on in the day and is getting progressively worse. The pain is located on his left flank and radiates down into his groin. He has had no similar pain previously and is normally fit and well. Examination reveals a man who is flushed and sweaty but is otherwise unremarkable. What is the most suitable initial management? Oral ciprofloxacin IM diclofenac 75 mg Oral co-amoxiclav and metronidazole IM morphine 5 mg IM diclofenac 75 mg + start bendroflumethiazide to prevent further episodes
Diclofenac
3588
What is recommended as analgesia of choise in renal colic
Diclofenac
3589
How to prevent Ca renal stones?
high fluid intake low animal protein, low salt diet (a low calcium diet has not been shown to be superior to a normocalcaemic diet) thiazides diuretics (increase distal tubular calcium resorption)
3590
How to prevent oxalate stones
cholestyramine reduces urinary oxalate secretion pyridoxine reduces urinary oxalate secretion
3591
How to prevent uric acid stones
allopurinol urinary alkalinization e.g. oral bicarbonate
3592
What is an important consideration re: diclofenac
Increased CV risk, likely to be substituted for other NSADIs e.g. naproxen
3593
A.Interstitial nephritis B.Membranous glomerulonephritis C.Endometriosis D.Placenta percreta E.Adult polycystic kidney disease F.Renal vein thrombosis G.Urinary tract infection A 22 year female who is 24 weeks pregnant presents with frank haematuria. She is sexually active. She has had a previous pregnancy resulting in caesarean section.
Pregnancy and frank haematuria, especially if there is a history of placenta previa or prior caesarean section, should indicate this diagnosis. There is invasive placental implantation into the myometrium, which can rarely extend into the bladder causing severe bleeding.
3594
A 22-year-old woman presents with macroscopic haematuria. She is sexually active. She is known to have renal calculi and had a berry aneurysm clipped.
APKD is associated with liver cysts (70%), berry aneurysms (25%) and pancreatic cysts (10%). Patients may have a renal mass, hypertension, renal calculi and macroscopic haematuria.
3595
A 45-year-old woman presents with haematuria and loin pain. She has a temperature of 37 oC and is found to have a Hb 180 g/l and a creatinine of 156 umol/l. Her urine dipstick shows 3+ blood. Blood and urine cultures are negative.
Renal vein thrombosis is a common feature of renal cell carcinoma as it invades the renal vein. Other features include PUO, left varicocele and paraneoplastic endocrine effects due to erythropoietin factor, renin, ACTH and PTH like substance.
3596
A 56-year-old man presents with episodic facial pain and discomfort whilst eating. He has suffered from halitosis recently and he frequently complains of a dry mouth. He has a smooth swelling underneath his right mandible. What is the most likely underlying diagnosis? Stone impacted in Whartons duct Stone impacted in Stensens duct Benign adenoma of the submandibular gland Adenocarcinoma of the submandibular gland Squamous cell carcinoma of the submandibular gland
The symptoms are typical for sialolithiasis. The stones most commonly form in the submandibular gland and therefore may occlude Whartons duct. Stensens duct drains the parotid gland.
3597
Submandibular tumours
Only 8% of salivary gland tumours affect the sub mandibular gland Of these 50% are malignant (usually adenoid cystic carcinoma) Diagnosis usually involves fine needle aspiration cytology Imaging is with CT and MRI In view of the high prevalence of malignancy, all masses of the submandibular glands should generally be excised.
3598
Mass of submandibular gland, action
Excision 50% are malignant
3599
A 55-year-old lady has undergone a wide local excision and sentinel lymph node biopsy for breast cancer. The histology report shows a completely excised 1.3cm grade 1 invasive ductal carcinoma. The sentinel node contained no evidence of metastatic disease. The tumour is oestrogen receptor negative.
The correct answer is Radiotherapy Radiotherapy is routine following breast conserving surgery. Without irradiation the local recurrence rates are approximately 40%.
3600
An 88-year-old lady presents with a large mass in the upper inner quadrant of her right breast. Investigations confirm an oestrogen receptor positive, invasive ductal carcinoma. She has declined operative treatment.
he correct answer is Endocrine therapy using letrozole Elderly patients may be managed using endocrine therapy alone. Eventually most will escape hormonal control. In post menopausal women oestrogens are produced by the peripheral aromatization of androgens and aromatase inhibitors are therefore the most popular agent in this age group.
3601
A 38-year-old lady has undergone a mastectomy and axillary node clearance for invasive ductal carcinoma. The histology report shows a completely excised 3.5cm lesion which is grade 3. Two of the axillary lymph nodes contain metastatic disease. The tumour is oestrogen receptor negative.
The combination of a grade 3 tumour and axillary nodal metastasis in a young female would attract a recommendation for chemotherapy. Some may also add herceptin (if they are HER 2 positive).
3602
Indications for mastectomy
Multifocal tumour Central tumour Large lesion in small breast DCIS \>4cm
3603
Indications for Wide local excision
Solitary lesion Peripheral tumour Small lesion in large breast DCIS \<4cm
3604
RTx in breast ca
Whole breast RTx recommended in all those with WLE Offered for T3-T4 tumours in women who've had a mastecomty and those with four or more +ve axillary nodes
3605
ER breast cancer therapy in pre and peri-menopasual women
Tamoxifen
3606
ER breast bancer, post menopausal women
Aromatase inhibotrs e.g. anastrozaloe This is because the process of aromatisation accounts for most oestrogen production
3607
CI to trastuzumab in HER2 positive breast Ca
Heart disorders
3608
Issues with PSA
Poor specificity and sensitivity around 33% of men with PSA 4-10 will have prostate cancer. Increases to 0% in PSA10-20 Around 20% with prostate cancer have normal PSA PSA levels increase with age
3609
Causes of raised PSA
BPH Prostatitis and UTI (NICE recommend that PSA test should be postponed for at least 1m) Ejaculation Vigorous exercise Urinary retention Insturmentaiton of the urinary tract (DRE)
3610
A 47-year-old woman presents with loin pain and haematuria. Urine dipstick demonstrates: Blood++++ NitritesPOS Leucocytes+++ Protein++ Urine culture shows a Proteus infection. An x-ray demonstrates a stag-horn calculus in the left renal pelvis. What is the most likely composition of the renal stone? Xanthine Calcium oxalate Struvite Cystine Urate
Stag-horn calculi are composed of struvite and form in alkaline urine (ammonia producing bacteria therefore predispose)
3611
A 67-year-old woman is reviewed 6 months after she had a mastectomy following a diagnosis of breast cancer. Which one of the following tumour markers is most useful in monitoring her disease? ## Footnote CA 125 CD 34 CA 15-3 CA 19-9 CD 117
CA-15-3
3612
A 4-year-old boy is brought to the clinic by his mother who has noticed a small lesion at the external angle of his eye. On examination there is a small cystic structure which has obviously been recently infected. On removal of the scab, there is hair visible within the lesion. What is the most likely diagnosis? Dermoid cyst Desmoid cyst Sebaceous cyst Epidermoid cyst Keratoacanthoma
The lesion is unlikely to be a desmoid cyst as these are seldom located either at this site or in this age group. In addition they do not contain hair. Sebaceous cysts will usually have a punctum and contain a cheesy material. Epidermoid cysts contain keratin plugs.
3613
Progressive dysphagia, may have previous symptoms of GORD or Barretts oesophagus.
Adenocarcinoma of the oesophagus
3614
Longer history of dysphagia, often not progressive. Usually symptoms of GORD. Often lack systemic features seen with malignancy
Peptic stricture
3615
A 42-year-old man presents with a painless lump in the left testicle that he noticed on self examination. Clinically there is a firm nodule in the left testicle, ultrasound appearances show an irregular mass lesion. His serum AFP and HCG levels are both within normal limits. What is the most likely diagnosis? Yolk sack tumour Seminoma Testicular teratoma Epididymo-orchitis Adenomatoid tumour
This mans age, presenting symptoms and normal tumour markers make a seminoma the most likely diagnosis. Epididymo-orchitis does not produce irregular mass lesions which are painless.
3616
What is the commonest type of testicular malgiancny
Seminoma
3617
Testicular tumour \>40 AFP normal HCG elevated in 10% LDH elevated in 10-20%
?Seminoma
3618
20-30y/o at presentation AFP elevated in 70% of cases HCG elevated in up to 40$
Teratoma or other nonseminomatous germ cell tumours
3619
Testicular tumour Sheet like lobular patterns of cells with substantial fibrous component. Fibrous septa contain lymphocytic inclusions and granulomas may be seen.
Seminoma
3620
Testicular tumour Heterogenous texture with occasional ectopic tissue such as hair
Teratoma
3621
RFs for testciular cancer
Cryptorchidism Infertility FHx Klinfelter's Mumps orchtitis
3622
Key features to identify in cervical lymphadenopathy
Consistency Number Fixation Symmetry Tenderness Face and scalp for infection or neoplasm Chest exam: infection or neoplasm Breast examinatoin Formal full ENT examination Rest of RES
3623
Hx in cervical lymphadenoapthy
Symptoms form the lumps e.g. EtOH induced pain General symptoms e.g. fever, malaise, weight loss Systemic disease: PMH, previous operations Social Hx: Ethnic origin, HIV RFs
3624
Causes of cervical lymphadenopathy LIST
Lymphoma and leukaemia infection Sarcoid Tumours
3625
Infective causes of cervical lymphadenopathy
Bacterial Tonsilitis, dental abscess TB Bartonella henselae Viral: EBV HIV Protozoal Toxoplasmosis
3626
Ix in cervical lymphadenopathy
FBC, ESR, film (atypical lymhpocytes0 TFTs, serum ACE Monospot test, HIV test Radiological: US CT scan Path FNAC Excision biopsy
3627
Features of hypertrophic scars
Scar confined to wound margins Across flexor surfaces and skin creases Appear soon after injury and regress spontaneously Ang age: commonly 8-20y M=F All races
3628
Hypertrophic scar
3629
Features of keloid scar
Scar extends beyond wound margins Earlobes, chin, neck, shoulder, chest Appear months after injury and continue to grow Puberty to 30y F\>M Black and hispanic
3630
Keloid scar
3631
Wound associations of hypertrophic and keloid scars
Infection Trauma Burns Tension Certain body areas
3632
Mx of hypertrophic and keloid scars
Mechanical-pressure therapy Topical silicone gel sheets Intralesional steroid and LA injections Revision of scar with closure by direct suturing
3633
Embryology of the thyroid
Migrates from its origin at the foramen caecum at the base of the tonuge Passes behind the hyoid bone Lies anterior to 3rd and 4th tracheal rings in the pretracheal fascia Leaves behind the thyroglossal cyst which atrophies Ectopic thyroid tissue can be found anywhere aloing this descent
3634
Congenital thyroid lesions
Lingual thyroid Thyroglossal cyst Ectopic thyroid tissue
3635
DDx Diffuse goitre
Simple colloid goitre: endemic iodine deficiency, sporadic: autoimmune, hereditary, goitrogens e.g. sulphonylureas Grave's Thyroditis: Hashimoto's De Quervain's, Subacute lymphocytic
3636
Ddx multinodular goitre
Multinodular colloid goitre (commonest) Multiple cysts Multiple adenomas
3637
Ddx in solitary thyroid nodule
Dominant nodule in multinodular goitre Adenoma: hot or cold Cyst Malignancy
3638
Ix in thyroid lumps
TFTs FBC, Ca, LFTs, eSR Antibodies: anti-TPO, TSH Ix: CXR High resolution US Radionucleotide Tc or I scan Histology or cytology (FNAC can't distinguish adneoma vs follicular Ca). Biopsy Laryngoscopy: Important pre-op to assess vocal cords
3639
Indications for thyroid sx: 5Ms
Mechanical obstruction Malignancy Marred beauty Medical Rx failure Mediastinal extension
3640
History in salivary gland lesions
Swellling/pain related to food: calculi Malaise, fever, mumps Dry eyes/mouth: Sjogrens (Sicca, Mickulicz)
3641
Causes of whole salivary gland enlargement
Parotitis Sjogrens Sarcoid Amyloid ALL CLD Anorexia or bulimia
3642
Causes of localised salivary gland enlargement
Tumours Stones
3643
Viral causes of acute parotitis
Mumps, Coxsackie A, HIV
3644
Bacterial causes of acute parotitis
Staph aureus Associated with calculi and poor oral hygiene
3645
Features of salivary gland calculi
Recurrent unilateral swelling and pain Worse on eating Red, tender, swollen gland (80%) submandibular
3646
Ix in ? salivary gland calculi
Plain XR or sialography
3647
Rx in salivary gland calculi
Gland excision
3648
What is the classic sign of salivary gland neoplasm
Deflection of ear outwards
3649
Salivary gland neoplasm with CNVII palsy=
Malignancy
3650
Demographics of salivary gland lesions
80% in parotid (80% superficial) 80% are pleomorphic adneomas
3651
How can salivary gland neoplasms be classified
Benign 1st: pleomorphic adneoma 2nd: adenolymphoma (Warthin's) Malignant (CN7 palsy and fast growing) 1st: Mucoepidermoid 2nd: Adenoid cystic
3652
Ix in salivary gland neoplasms
ENT exam US +/- CT FNAC
3653
Features of pleiomorphic adenoma
Commonest salivary gland neoplasm (80%) Presentation: 90% in parotid Occur in middle age F\>M Benign and slow growing Histo: different tissue types Rx: superficial parotidectomy
3654
Warthin's tumour
Benign soft cystic tumour Older men Rx: enucleation
3655
Features of adenoid cystic carcinoma
One of the commonest malignant salivary tumours Highly malignant and often incurable Rapid growth Hard, fixed mass Pain Facial palsy
3656
Sx in salivary gland tumours
Superificial or radical parotidectomy Facia lata face lift for facial palsy
3657
Cx of salivary gland sx
Facial palsy Salivary fistula Frey's syndrome
3658
Frey's syndrome
Gustatory sweating Redness and sweating skin over parotid area Occurs in relation to food (inc. thinking) Auriculotemporal branch of CNV3 carrries sympathetic fibres to sweat glands over parotid area and parasympathetic fibres to the parotid Reinervation of divided sympathetic nerves by fibres from the secretomotory branch or auriculotemporal branch of CN V3
3659
Epidemiology of breast cancer
Affects 1/10 women 20,000 cases per year in the UK Commonest cause of cancer death in females 15-54 Second commonest caues of cancer deaths overall
3660
How can the aetiology/risk factors in breast Ca be categorised?
Familial Oestrogen exposure Other factors
3661
FHx in breast Ca
10% Ca breast is familial One first degree relative = 2x risk 5% assodiated with BRCA mutations BRCA1-\> 80% breast, 40% ovarian BRCA2- 80% bresat
3662
Oestrogen exposure in breast ca
Early menarche, late menopause HRT, OCP First child \>35y/o Obesity
3663
Other factors in breast Ca risk
Proliferative breast disease with atypia Previous Ca breast Increased age (v. rare \<30) Breast feeding is protective
3664
What is commonest breast malignancy?
Invasive ductal carcinoma
3665
Features of DCIS/LCIS
Non-inavsive pre-malignant condition Microcalcificaiton on mammography 10x increased risk of invasive Ca
3666
Non-invasive pre-malignant condition Microcalcification on mammography 10x increased risk of invasive Ca
DCIS/LCIS
3667
Features of invasive ductal carcinoma, NST/NOS
Commonest (70%) of cancers Feels hard (scirrhous)
3668
20% of breast cancers are this histological subtype
Invasive lobular
3669
This type of breast malignancy affects younger patients and may feel soft
Medullary
3670
This type of breast cancer occurs in the elderly
Colloid/mucinous
3671
Breast cancer Pain Erythema Swelling Peau d'orange
Inflammatory breast ca
3672
This type of breast cancer is a stromal tumour presenting as a large, non-tender mobile lump
Phyllodes tumour
3673
Spread of breast cancer
Direct extension-\> muscle and or skin Lymph-\> p'eau d'oange and arm oedema Blood: Bones- bone pain, #, raised Ca Lungs: dyspnoea, pleural effusion Liver- abdo pain, hepatic impairment Brain: headache, seizures
3674
Inflammatory breast cancer with peau d'orange
3675
Features of the breast cancer screening programme
50-70y/o women. Every 3 years. Being extended as a trial to some women aged 47-73
3676
Impact of the breast cancer screening programme
Reduce breast Ca deaths by 25% 10% false negative rate
3677
Presentation of breast Ca
Lump: commonest presentation Usually painless 50% in UOQ +/- axillary nodes Skin changes: Paget's disease of skin: persistent eczema Peau d'orange Nipple: Discharge Inversion Mets: Pathological #s SOB Abdo pain Seizures May present through screening
3678
Triple assessment of any breast lump
Hx and clinical examination Radiology \<35y: US \>35y: US + mammography Pathology Solid lump- core biopsy Cystic lump: FNAC (18g needle) Reassure if clear fluid Send cytology if bloody fluid Core biopsy residual mass Core biospy if +ve cytology
3679
Additional Ix in ?breast ca
Bloods: FBC, LFTs, ESR, bone profile Imaging: help staging CXR Liver USS CT scan Breast MRI Bone scan and PET/CT May need wire-guided excision biopsy
3680
Clinical staging of breast Ca
Stage 1: Confined to breast, mobile, no LNs Stage 2: Stage 1 and nodes in ipsilateral axilla Stage 3: Stage 2 + fixation to muscle but not chest wall. LNs matted and fixed and large skin involvement Stage 4: Complete fixation to chest wall + mets
3681
TNM staging in breast cancer
Tis (no palpable tumour): CIS T1 \<2cm: no skin fixation T2: 2-5cm, skin fixation T3: 5-10cm, ulceration + pectoral fixation T4: \>10cm, chest wall extension, skin involved N1: mobile nodes N2: fixed nodes
3682
Principles of Breast Ca management
Manage in MDT with individual approach Oncologist Breast sx Breastcare nures Radiologist Histopathologist Try to enroll in a trial Factors: age, fitness, wishes, clinical stage 1-2: surgical 3-4: palliation
3683
Aims of sx in breast cancer
To gain local control
3684
What are the two surgical options in breast cancer
WLE- conservation surgery Mastectomy- removal of whole breast
3685
WLE + LN biopsy
3686
Mastectomy
3687
WLE vs mastectomy
Same survival but WLE has increased recurrence rates
3688
Rationale for sentinal node biopsy
SN= first node that a section of breast drains to If clinically -ve axillary LNs, no need for further dissection if SN is clear
3689
Procedure in SN biopsy
Blue dye/ radiocolloid injected into tumour Visual inspection/gamma probe at surgery to ID SN SN removed and sent for frozen section If node +ve-\> axillary clearance or RTx
3690
Evidence of SNB vs axillary clearance
2 RCTs compared No differences in overall or disease-free surivival Reduced morbidity with SNB alone: lymphoedema Pain numbness
3691
What are the other axillary options for clinically negative axilla
Axillary sampling: Removal of lower nodes. Clearance or DXT if +ve Axillary clearance: Can be done to various levels
3692
?Axillary clearance
3693
Sx complications of breast cancer treatment
Haematoma, seroma Frozen shoulder LTN palsy Lymphoedema
3694
What can be used for prognosis in breast cancer?
Nottingham Prognostic Index
3695
Features of Nottingham prognostic index
Predicts survival and risk of relapse Guides appropriate adjuvant systemic therapy 0.2 x tumour size + histo grade + nodal status
3696
What is used to grade breast tumours histologically?
Bloom-Richardson system
3697
What are the systemic Rx used in breast cancer management?
RTx CTx Endocrine therapy
3698
Indications for RTx in breast ca
Post-WLE: reduces local recurrence Post-mastecomty: only if high risk of local recurrence. Large, poorly differentiated, node +ve Axillary: node +ve disease Palliation: bone pain
3699
Indications for CTx in breast cancer
Pre-menopasual Node High grade Recurrent tumours
3700
CTx in breast Ca 6 x FEC
5-FU Epirubicin Cyclophosphamide
3701
Trastuzumab
Anti-Her2
3702
Trastuzumab SE
Cardiac toxicity
3703
|ndications for endocrine therapy in breast Ca
Used in ER or PR +ve disease: reduces recurrence, increases survival 5y of adjuvant therapy
3704
Tamoxifen MOA
SERM antagonist @ breast Agonist at uterus
3705
Se of tamoxifen
Menopausal symptoms Endometrial Ca
3706
Anastrazole MOA
Aromatse inhibitor-\> reduced oestrogen Better cf. tamoxifen if post-men (ATAC trial)
3707
Se of anastrazole
Menopausal symptoms
3708
Alternative endocrine rx to tamoxifen and anastrazole
If pre-menopausal and ER +ve may consider ovarian ablation or GnRH anlogues
3709
Rx in treating advanced breast Ca
Tamoxifen if ER +ve Chemo for relapse Her 2 +ve tumours may respond to trastuzumab Supportive Bone pain: DXT, bisphosphonates, analgeisa Brain: occassional surgery, DXT, steroids, AEDs Lymphoedema: decongestion, compression
3710
Features of breast reconstruction following mastectomy
Offered either at 1o sx or delayed procedure Implants: silastic or saline inflatable
3711
What are the myocutaneous flaps used in breast reconstruction
Latissimus dorsi myocutaneous flap (LDMF) Transverse recturs abdominis myocutaneous flap (TRAM)
3712
Features of lat dorsi myocutaneous flap
Pedicled flap: skin, fat, muscle and blood supply Supplied by thoracodorsal A via subscapular A Usually used with an implant
3713
Features of transverse rectus abdominis myocutaneous flap
Gold standard Pedicled (inf. epigastric A) or free: attached to internal thoracic artery No implant necessary and combined tummy tuck Risk of abdominal hernia
3714
CI to transverse rectus abdominis myocutaneous flap
Poor circulation: smokers, obese, PVD, DM
3715
Lat dorsi myocutaneous flap Usually used with implant
3716
Transverse rectus abdominis myocutaneous flap
3717
Congenital breast disease
Amastia: complete absence of breast and nipple Hypoplasia more common, some asymmetry normal Accessory nipples: can occur anywhere along the milk line. Present in 1%
3718
Gynaecomastia
Occurs in 30% of boys at puberty Hormone secreting tumours e.g. sex-cord testicular CLD: hypogonadism and reduced E2 metabolism Drugs: sprionolactone, digoxin, cimetidine
3719
\<35 Breat pain Pre-menstrual Relieved by menstruation Commonly in UOQ bilaterally
Cyclical mastalgia
3720
Breast pain \>45y Severe lancing breast pain (often left) May be associated with back pain
Non-cyclical mastalgia
3721
Mx of mastalgia
Conservative: Reassurance, better fitting bra Medical: Topical diclofenac Evening primrose oil 2nd line: Danazol (anti-gonadotrophin) is licesnsed for severe pain
3722
What are the inflammatory breast lesions
Acute mastitis Fat necrosis Duct ectasia (dilatation) Periductal mastitis
3723
What are the benign epithelial breast lesions
Benign mammary dysplasia Cystic disease Ductal papilloma
3724
What are the stromal breast diseases
Fibroadenoma Phyllodes tumour
3725
Lactating Painful, red breast May-\> abscess (lump near nipple)
Acute mastitis
3726
Rx in acute mastitis
Fluclox alone in early stages Fluclox and I+D if abscess
3727
Breast lesion Associated with previous trauma Painless, palpable, non-mobile mass May calcify simulating Cancer
Fat necrosis
3728
Rx in breast fat necrosis
Analgesia No F/U necessary
3729
Post-menopausal (50-80y) Slit-like nipple Often bilateral +/- peri-areolar mass Thick white/green discahrge May be calcified on mammography
Duct ectasia
3730
Smoker 30y/o Painful, erythematous, sub-areolar mass Associated with inverted nipple +/- purulent discharge May-\> abscess or discharging fistula
Periductal mastitis
3731
Rx in duct ectasia
Need to distinguish from Ca Surgical duct excision if mass present or discharge troublesome Close f/u
3732
Rx in peri-ductal mastitis
Broad-spectrum abx
3733
30-50y/o Pre-menstural breast nodularity and pain often in upper outer quadrant Tender, lumpy bumpy breasts ANDI
Benign mammary dysplasia Aberration of normal development and involution: Fibroadenosis Cyst formation Epitheliosis Papillomatosis
3734
Peri-menopausal Distinct, fluctuant round breast mass Often painful
Cystic disease
3735
40-50y/o Boody breast discharge (common cause) not often palpable
Duct papilloma
3736
Rx in benign mammary dysplasia
Triple assessment Reassurance Analgesia Good bra +/- Evening primrose oil Danazol
3737
Rx in cystic breast disease
Aspiration: green-brown fluid Persistence or blood-\> triple assessment
3738
Rx in duct papilloma
Triple assessment Excise due to incresaed risk of Ca
3739
\<35y/o Rare post-menopause Commonest benign breast tumour
Fibroadenoma
3740
Painless, mobile, rubbery breast mass. Often multiple and bilateral Popcorn calcification
Fibroadenoma
3741
\>50y/o Large, fast growing breast mass Mobile, non-tender Epithelial and connective tissue elements
Pnyllodes tumour
3742
Rx in phyllodes tumour
WLE
3743
Presents as microcalcification on mammogram Rarely associated with symptoms e.g. lump, discharge, eczematous change
DCIS
3744
Ca risk in DCIS
1%/y (10x risk) in ipsilateral breast
3745
Rx in DCIS
WLE + RTx Extensive or multifocal: mastectomy + reconstruction + SNB
3746
Unilatreral scaly, erythematous, itchy breast skin Persistent +/- palpable mass
Paget's
3747
Incidental biopsy finding (no calcification) Often bilateral (20-40%) Young women breast lesion
LCIS
3748
Ca risk in LCIS
x10 in both breasts
3749
Rx in LCIS
Bilateral prophylactic mastectomy or close watching with mammographic screening
3750
Rx in paget's disease of breast
usually underlying invasive or DCIS breast cancer Mastectomy + radio +/- CTx
3751
Level 1 evidence
Evidence obtained from systematic review of all relevant randomised controlled trials
3752
Level II evidence
Evidence derived from at least one properly designed randomised controlled trial
3753
Level III evidence
Evidence derived from well designed pseudo-randomised controlled trials (e.g. alternate allocation) or historical controls
3754
Level IV evidence
Evidence derived from case series or case reports
3755
Level V evidence
Panel or expert opinion
3756
A 45-year-old lady recovering from a mastectomy and axillary node clearance notices that sensation in her armpit is impaired A.Intercostobrachial B.Median C.Axillary D.Radial E.Ulnar F.Musculocutaneous G.Brachial plexus upper cord H.Brachial plexus lower cord
The intercostobrachial nerves are frequently injured during axillary dissection. These nerves traverse the axilla and supply cutaneous sensation.
3757
An 8-year-old boy falls onto an outstretched hand and sustains a supracondylar fracture. In addition to a weak radial pulse the child is noted to have loss of pronation of the affected hand. A.Intercostobrachial B.Median C.Axillary D.Radial E.Ulnar F.Musculocutaneous G.Brachial plexus upper cord H.Brachial plexus lower cord
This is a common injury in children. In this case the angulation and displacement have resulted in median nerve injury.
3758
A 24-year-old man falls sustaining an inversion injury to his ankle. On examination he is tender over the lateral malleolus only. On x-ray there is a fibular fracture that is distal to the syndesmosis. ## Footnote A.Surgical fixation B.Below knee amputation C.Aircast boot D.Application of full leg plaster cast to include midfoot E.Application of below knee plaster cast to include the midfoot F.Application of external fixation device G.Application of compression bandage and physiotherapy.
Application of below knee plaster cast to include the midfoot Theme from 2008 Exam These distal injuries are generally managed conservatively. Conservative management will involve a below knee cast, this will need to extend to the midfoot. It can be substituted for an aircast boot once radiological union is achieved.
3759
An 86-year-old lady stumbles and falls whilst opening her front door. On examination her ankle is swollen with both medial and lateral tenderness. X rays demonstrate a fibular fracture at the level of the syndesmosis. ## Footnote A.Surgical fixation B.Below knee amputation C.Aircast boot D.Application of full leg plaster cast to include midfoot E.Application of below knee plaster cast to include the midfoot F.Application of external fixation device G.Application of compression bandage and physiotherapy.
Although, this is a potentially unstable injury operative fixation in this age group generally gives poor results owing to poor quality bone. A below knee cast should be applied in the first instance. If this fails to provide adequate control it can be extended above the knee.
3760
Maisonneuve fracture
Weber classification Related to the level of the fibular fracture. Type A is below the syndesmosis Type B fractures start at the level of the tibial plafond and may extend proximally to involve the syndesmosis Type C is above the syndesmosis which may itself be damaged A subtype known as a Maisonneuve fracture may occur with spiral fibular fracture that leads to disruption of the syndesmosis with widening of the ankle joint, surgery is required.
3761
A 56-year-old man presents with symptoms of nasal pain, anosmia and rhinorrhea. He has been well until recently and has worked as a wood carver for many years. A.Ethmoid sinus cancer B.Maxillary sinus cancer C.Ethmoid adenoma D.Maxillary adenoma E.Ethmoidal fracture F.Nasal polyps G.Sphenoid osteoma H.Ethmoidal sinusitis I.Maxillary sinusitis
Theme from September 2012 Exam Theme from September 2013 Exam Nasopharyngeal cancer is strongly associated with wood work. Most cases require an occupational exposure of greater than 10 years and are adenocarcinomas on histology. Most cases are ethmoidal in origin
3762
With what products is the risk of TRALI greatest?
Plasma components
3763
Def: massive haemorrhage
Loss of one blood volume in 24h or loss of 50% of circulating blood volume in 3 hours. Bloods loss of 150ml is also included
3764
Normal adult blood volume
7% of total adult bodweight 5 litres
3765
Cx of massive haemorrhage
Hypothermia Hypocalcaemia Hyperkalaemia Delayed TRs TRALI Coaglopathy
3766
Hypothermia in massive blood transfusion
Blood is refrigerated Hypothermic blood impairs homeostasis Shifts Bohr curve to the left
3767
Hypocalcaemia in massive blood transfusion
Both FFP and plt contain citrate anticoagulant, this may chelate calcium
3768
Hyperkalaemia following massive blood transfusion
Plasma of red cells stored for 4-5w contains 5-10mmol K+
3769
What is the leading cause of transfusion related death?
TRALI
3770
What causes lung injury in TRALI
Occurs as a result of leucocyte antibodies in transfused plasma Aggregation and degranulation of leucocytes in lung tissue accounts for lung injury
3771
Coagulopathy following massive blood transfusion
Anticipate once circulating blood transfused 1 blood volume usually drops plt to \<100 1 bv will both dilute and not replace clotting factors Fibrinogen concentration halves per 0.75 blood volume tranfused
3772
A 70-year-old female is admitted with a history of passing brown coloured urine and abdominal distension. Clinically she has features of large bowel obstruction with central abdominal tenderness. She is maximally tender in the left iliac fossa. There is no evidence of haemodynamic instability. What is the most appropriate investigation? Cystogram Abdominal X-ray of the kidney, ureters and bladder Computerised tomogram of the abdomen and pelvis Flexible sigmoidoscopy Barium enema
This lady is most likely to have a colovesical fistula complicating diverticular disease of the sigmoid colon. In addition she may also have developed a diverticular stricture resulting in large bowel obstruction. A locally advanced tumour of the sigmoid colon may produce a similar clinical picture. The best investigation of this acute surgical patient is an abdominal CT scan, this will demonstrate the site of the disease and also supply regional information such as organ involvement and other local complications such as a pericolic abscess. A barium enema would require formal bowel preparation and this is contra indicated where large bowel obstruction is suspected. A flexible sigmoidoscopy is unlikely to be helpful and the air insufflated at the time of endoscopy may make the colonic distension worse. A cystogram would provide only very limited information.
3773
What can be used to describe perforations of the colon due to diverticulitis?
Hinchey classificaiton
3774
Post-splenectomy blood film features
Howell- Jolly bodies Pappenheimer bodies Target cells Irregular contracted erythrocytes
3775
A 20-year-old lady is referred to the vascular clinic. She has been feeling generally unwell for the past six weeks. She works as a typist and has noticed increasing pain in her forearms whilst working. On examination she has absent upper limb pulses. Her ESR is measured and mildly elevated. ## Footnote A.Wegeners granulomatosis B.Polyarteritis nodosa C.Giant cell arteritis D.Takayasu's arteritis E.Buergers disease
Takayasus arteritis may be divided into acute systemic phases and the chronic pulseless phase. In the latter part of the disease process the patient may complain of symptoms such as upper limb claudication. In the later stages of the condition the vessels will typically show changes of intimal proliferation, together with band fibrosis of the intima and media.
3776
Inflammatory, obliterative arteritis affecting aorta and branches Females\> Males Symptoms may include upper limb claudication Clinical findings include diminished or absent pulses ESR often affected during the acute phase
Takyasu's arteritis
3777
Segmental thrombotic occlusions of the small and medium sized lower limb vessels Commonest in young male smokers Proximal pulses usually present, but pedal pulses are lost An acuter hypercellular occlusive thrombus is often present Tortuous corkscrew shaped collateral vessels may be seen on angiography
Buergers disease
3778
Systemic granulomatous arteritis that usually affects large and medium sized vessels Females \> Males Temporal arteritis is commonest type Granulomatous lesions may be seen on biopsy (although up to 50% are normal)
Giant cell arteritis
3779
Systemic necrotising vasculitis affecting small and medium sized muscular arteries Most common in populations with high prevalence of hepatitis B Renal disease is seen in 70% cases Angiography may show saccular or fusiform aneurysms and arterial stenoses
Polyarteritis nodosa
3780
Predominantly affects small and medium sized arteries Systemic necrotising granulomatous vasculitis Cutaneous vascular lesions may be seen (ulceration, nodules and purpura) Sinus imaging may show mucosal thickening and air fluid levels
Wegeners granulomatosis
3781
What are the classical features of a Colles #?
FOOSH 1. Transverse fracture of the radius 2. 1 inch proximal to the radio-carpal joint 3. Dorsal displacement and angulation Colles' fracture (dinner fork deformity)
3782
Volar angulation of distal radius fragment (Garden spade deformity) Caused by falling backwards onto the palm of an outstretched hand or falling with wrists flexed
Smith's fracture (reverse Colles' fracture)
3783
Intra-articular fracture of the first carpometacarpal joint Impact on flexed metacarpal, caused by fist fights X-ray: triangular fragment at ulnar base of metacarpal
Bennet's fracture
3784
Bennet's Fracture
3785
Dislocation of the proximal radioulnar joint in association with an ulna fracture Fall on outstretched hand with forced pronation Needs prompt diagnosis to avoid disability
Monteggia's fracture
3786
Radial shaft fracture with associated dislocation of the distal radioulnar joint Direct blow
Galeazzi fracture
3787
Bimalleolar ankle fracture Forced foot eversion
Pott's fracture
3788
Distal radius fracture (Colles'/Smith's) with associated radiocarpal dislocation Fall onto extended and pronated wrist Submit answer
Barton's fracture
3789
What BP is required to generate a palpable femoral pulse?
\>65mmHg
3790
Mg homeostasis
Magnesium is required for both PTH secretion and its action on target tissues. Hypomagnesaemia may both cause hypocalcaemia and render patients unresponsive to treatment with calcium and vitamin D supplementation. Magnesium is the fourth most abundant cation in the body. The body contains 1000mmol, with half contained in bone and the remainder in muscle, soft tissues and extracellular fluid. There is no one specific hormonal control of magnesium and various hormones including PTH and aldosterone affect the renal handling of magnesium. Magnesium and calcium interact at a cellular level also and as a result decreased magnesium will tend to affect the permeability of cellular membranes to calcium, resulting in hyperexcitability. Submit answer
3791
A.Fissure in ano B.Intersphincteric abscess C.Haemorroidal disease D.Proctitis E.Solitary rectal ulcer syndrome F.Rectal cancer G.Anal cancer An 18-year-old man with a previous history of constipation presents with bright red rectal bleeding and diarrhoea. He has suffered episodes of faecal incontinence, which have occurred randomly throughout the day and night.
Nocturnal diarrhoea and incontinence are typical of inflammatory bowel disease.
3792
A.Fissure in ano B.Intersphincteric abscess C.Haemorroidal disease D.Proctitis E.Solitary rectal ulcer syndrome F.Rectal cancer G.Anal cancer A 56-year-old man presents with episodes of pruritus ani and bright red rectal bleeding. On examination there is a mass in the ano rectal region and biopsies confirm squamous cell cancer.
These are features of anal cancer. Anal cancers arise from the cutaneous epithelium and are therefore typically squamous cell. They are usually sensitive to chemoradiotherapy.
3793
A 19-year-old man presents with bright red rectal bleeding. He has a longstanding history of irritable bowel syndrome. At flexible sigmoidoscopy a lesion is biopsied and reported as showing 'fibromuscular obliteration'. A.Fissure in ano B.Intersphincteric abscess C.Haemorroidal disease D.Proctitis E.Solitary rectal ulcer syndrome F.Rectal cancer G.Anal cancer
This is the typical presentation of SRUS. These patients require careful diagnostic work up to elicit the underlying cause of their altered bowel habit. The histological appearances of solitary rectal ulcers are characteristic and extensive collagenous deposits are often seen. This is usually termed fibromuscular obliteration.
3794
A 42-year-old teacher is admitted with a fall. An x-ray confirms a fracture of the surgical neck of the humerus. Which nerve is at risk? A.Median nerve B.Ulnar nerve C.Radial nerve D.Posterior interosseous nerve E.Anterior interosseous nerve F.Musculocutaneous nerve G.Axillary nerve H.Brachial Trunks C5-6 I.Brachial trunks C6-7 J.Brachial Trunks C8-T1
Axillary nerve The Axillary nerve winds around the bone at the neck of the humerus. The axillary nerve is also at risk during shoulder dislocation.
3795
A 32-year-old window cleaner is admitted after falling off the roof. He reports that he had slipped off the top of the roof and was able to cling onto the gutter for a few seconds. The patient has Horner's syndrome. A.Median nerve B.Ulnar nerve C.Radial nerve D.Posterior interosseous nerve E.Anterior interosseous nerve F.Musculocutaneous nerve G.Axillary nerve H.Brachial Trunks C5-6 I.Brachial trunks C6-7 J.Brachial Trunks C8-T1
The patient has a Klumpke's paralysis involving brachial trunks C8-T1. Classically there is weakness of the hand intrinsic muscles. Involvement of T1 may cause a Horner's syndrome. It occurs as a result of traction injuries or during delivery.
3796
A 32-year-old rugby player is hit hard on the shoulder during a rough tackle. Clinically his arm is hanging loose on the side. It is pronated and medially rotated. ## Footnote A.Median nerve B.Ulnar nerve C.Radial nerve D.Posterior interosseous nerve E.Anterior interosseous nerve F.Musculocutaneous nerve G.Axillary nerve H.Brachial Trunks C5-6 I.Brachial trunks C6-7 J.Brachial Trunks C8-T1
The patient has an Erb's palsy involving brachial trunks C5-6.
3797
A 30-year-old women is involved in a road traffic accident. She is a passenger in a car involved in a head on collision with another vehicle. Her car is travelling at 60mph. She has been haemodynamically stable throughout with only minimal tachycardia. On examination she has marked abdominal tenderness and a large amount of intra abdominal fluid on CT scan ## Footnote A.Tension pneumothorax B.Haemopericardium C.Haemothorax D.Aortic transection E.Ruptured spleen F.Duodeno-jejunal flexure disruption G.Aorto iliac disruption H.Recto-sigmoid junction disruption
This is another site of sudden deceleration injury. Given the large amount of free fluid, if it were blood, then a greater degree of haemodynamic instability would be expected.
3798
A 30-year-old women is involved in a road traffic accident. She is a passenger in a car involved in a head on collision with another vehicle. Her car is travelling at 60mph. She has been haemodynamically stable throughout with only minimal tachycardia. On examination she has marked abdominal tenderness and a large amount of intra abdominal fluid on CT scan ## Footnote A.Tension pneumothorax B.Haemopericardium C.Haemothorax D.Aortic transection E.Ruptured spleen F.Duodeno-jejunal flexure disruption G.Aorto iliac disruption H.Recto-sigmoid junction disruption
Duodeno-jejunal flexure disruption. This is another site of sudden deceleration injury. Given the large amount of free fluid, if it were blood, then a greater degree of haemodynamic instability would be expected.
3799
Acanthosis nigricans involving the mucous membranes
Brown to black, poorly defined, velvety hyperpigmentation of the skin. Usually found in body folds such as the posterior and lateral folds of the neck, the axilla, groin, umbilicus, forehead, and other areas. The most common cause of acanthosis nigricans is insulin resistance, which leads to increased circulating insulin levels. Insulin spillover into the skin results in its abnormal increase in growth (hyperplasia of the skin). In the context of a malignant disease, acanthosis nigricans is a paraneoplastic syndrome and is then commonly referred to as acanthosis nigricans maligna. Involvement of mucous membranes is rare and suggests a coexisting malignant condition
3800
A.Giardia Infection B.Cryptosporidium infection C.Clonorchis sinensis infection D.Ancyclostoma duodenale infection E.Ascaris lumbricoides infection F.Echinococcus granulosus infection G.Enterobius vermicularis infection A 6-year-old boy presents with symptoms of recurrent pruritus ani. On examination there is evidence of a small worm like structure protruding from the anus.
nfection with enterobius is extremely common. Pruritus is the main symptom, as there is a lack of tissue invasion it is rare for individuals to have any signs of systemic sepsis.
3801
A 25-year-old man returns from a backpacking holiday in India. He presents with symptoms of coughing and also of episodic abdominal discomfort. Peri anal examination is normal. Stool microscopy demonstrates both worms and eggs within the faeces. A.Giardia Infection B.Cryptosporidium infection C.Clonorchis sinensis infection D.Ancyclostoma duodenale infection E.Ascaris lumbricoides infection F.Echinococcus granulosus infection G.Enterobius vermicularis infection
Infection with Ascaris lumbricoides usually occurs after individuals have visited places like sub Saharan Africa or the far east. Unlike ancyclostoma duodenale infection there is usually evidence of both worms and eggs in the stool. The absence of pruritus makes enterobius less likely. The presence of coughing may be due to the migration of the larva through the lungs.
3802
Hookworms that anchor in proximal small bowel Most infections are asymptomatic although may cause iron deficiency anaemia Larvae may be found in stools left at ambient temperature, otherwise infection is difficult to diagnose Infection occurs as a result of cutaneous penetration, migrates to lungs, coughed up and then swallowed Treatment is with mebendazole
Ancylostoma duodenale
3803
Due to organism Enterobius vermicularis Common cause of pruritus ani Diagnosis usually made by placing scotch tape at the anus, this will trap eggs that can then be viewed microscopically Treatment is with mebendazole
Enterobiasis
3804
Due to infection with roundworm Ascaris lumbricoides Infections begin in gut following ingestion, then penetrate duodenal wall to migrate to lungs, coughed up and swallowed, cycle begins again Diagnosis is made by identification of worm or eggs within faeces Treatment is with mebendazole
Ascariasis
3805
Due to infection with Strongyloides stercoralis Rare in west Organism is a nematode living in duodenum of host Initial infection is via skin penetration. They then migrate to lungs and are coughed up and swallowed. Then mature in small bowel are excreted and cycle begins again An auto infective cycle is also recognised where larvae will penetrate colonic wall Individuals may be asymptomatic, although they may also have respiratory disease and skin lesions Diagnosis is usually made by stool microscopy In the UK mebendazole is used for treatment
Strongyloidiasis
3806
Protozoal infection Organisms produce cysts which are excreted and thereby cause new infections Symptoms consist of diarrhoea and cramping abdominal pains. Symptoms are worse in immunosuppressed people Cysts may be identified in stools Treatment is with metronidazole
Cryptosporidium
3807
Diarrhoeal infection caused by protozoa Infections occur as a result of ingestion of cysts Symptoms are usually gastrointestinal with abdominal pain, bloating and passage of soft or loose stools Diagnosis is by serology or stool microscopy First line treatment is with metronidazole
Giardiasis
3808
Classification of causes of urinary tract obstruction
Luminal Mural Extramural
3809
Luminal causes of urinary tract obstruction
Stones Blood clots Sloughed papilla
3810
Mural causes of urinary tract obstruction
Congenital/acquired stricture Tumour: renal, ureteric, bladder Neuromuscular dysfunction
3811
Extramural causes of urinary tract obstruction
Prostatic enlargement Abdo/pelvic mass/tumour Retroperitoneal fibrosis
3812
Presentation of acute upper urinary tract obstruction
Loin pain-\> groin
3813
Presentation of acute lower urinary tract obstruction
Bladder outflow obstruction precedes severe suprapubic pain with distended palpable bladder
3814
Presentation of chronic upper urinary tract obstruction
Flank pain Renal pain (may be polyuric)
3815
Presentation of chronic lower urinary tract obstruction
Frequency, hesitancy, poor stream, terminal dribbling, overflow incontinence Distended, palpable bladder +/- large prostate PR
3816
Ix of urinary tract obstruction
Bloods: FBC, U+E Urine: dip, MC+S Imaging: USS- hydronephrosis/hydrouretur Anterograde/retrograde ureterograms (allow therapeutic drainage) Radionucleotide imaging: renal function CT/MRI
3817
Mx of upper urinary tract obstruction
Nephrostomy Ureteric stent
3818
Mx of lower urinary tract obstruction
Urethral or suprapubic catheter- may be a large post-obstructive diuresis
3819
Cx of ureteric stents
Common: Infection Haematuria Trigonal irritation Encrustation Rare: Obstruction Ureteric rupture Stent migration
3820
Causes of urethral stricture
Trauma: instrumentation, pelvic fractures Infection e.g. gonorrhoea CTx Balanatitis xerotica obliterans
3821
Presentation of urethral stricture
Voiding difficulty Hesitancy Strangury Poor stream Terminal dribbling Pis en deux
3822
Pis en deux
Urinary urgency shortly after voiding
3823
Examination in urethral stricture
PR: exclude prostatic cause Palpate urethra through penis Examine meatus
3824
Ix of urethral stricture
Urodynamcs: reduced peak flow, increased micturition time Urethroscopy and cystoscopy Retrograde urethrogram
3825
Mx of urethral stricture
Internal urethrotomy Dilatation Stent
3826
Pathogenesis of obstructive uropathy
Acute retention on a chronic background may go unnoticed for days due to lack of pain Se Cr may be up to 1500uM Renal function should return to normal over days although some background impairment may remain
3827
Cx of obstructive uropathy
Hyperkalaemia Metabolic acidosis Post-obstructive diuresis Na and HCO3 losing nephropathy Infection
3828
Post-obstructive diuresis
Kidneys produce a lot of urine in the acute phase after relief of obstruction Must keep up with losses to avoid dehydration
3829
Na and HCO3 losing nephropathy post obstruction
Diuresis-\> loss of Na and HCO3 May require replacement with 1.26% NaHCO3
3830
Classification of causes of urinary retention
Obstructive Neurological Myogenic
3831
Mechanical causes of urinary retention
BPH Urethral stricture Clots, stones Constipation
3832
Dynamic causes of obstructive urinary retention
Increased smooth muscle tone (alpha adrenergic) Post-op pain Drugs
3833
Neurological causes of urinary retention
Interruption of sensory or motor innervation pelvic sx, ms, dm, spinal injury/compression
3834
Myogenic causes of urinary retention
Over-distension of the bladder Post-anaesthesia High EtOH intake
3835
Suprapubic tenderness Palpable bladder: dull to percussion, can't get beneath it Large prostate on PR (check anal tone and sacral sensation) \<1l drained on catheterisation
Acute urinary retention
3836
Ix in acute urinary retention
Blood: FBC, U+E, PSA (prior to PR) Urine: dip, MC+S Imaging: US- bladder volume, hydropnephrosis Pelvic XR
3837
Mx of acute urinary retention
Conservative: analgesia, privacy, walking, running water or hot bath Catheterise: Use correct catheter (e.g. 3 way if clots) +/- STAT gent cover Hourly UO + replace: post-obstruction diuresis Tamsulosin: redcued risk of recatheterisation after retention TWOC after 24-72h: can be d/c and have OPD f/U. More likely to be successful if predisposing factor and lower residual volume
3838
TURP in acute urinary retention
Failed TWOC Impaired renal function Elective
3839
How can chronic urinary retention be classified?
High pressure Low pressure
3840
Features of high pressure chronic urinary retention
High detrusor pressure @ end of micturition Typically bladder outflow obstruction-\> bilateral hydronpehrosis and impaired renal function
3841
Features of low pressure chronic urinary retention
Low detrusor pressure @ end of micturition Large volume retention with very compliant bladder Kidney able to excrete urine No hydronephrosis therefore normal renal function
3842
Insidiuous presentation as bladder capacity increases Typically painless Overflow incontinence/ nocturnal enuresis Acute on chronic picture possible Lower abdo mass UTI Renal failure
?Chronic urinary retention
3843
Mx of high pressure urinary retention
Catheterise if: renal impairment, pain, infection Hourly UO and replace post-obstruction diuresis Consider TURP before TWOC
3844
Mx of low pressure chronic urinary retention
Avoid catheterisation if possible due to risk of introducing infection Early TURP: often do poorly due to poor detrusor function. Need CISC or permanent catheter
3845
Advantages of suprapubic catheterisation
Reduceed UTIs Reduced stricture formation TWOC w/o catheter removal Pt preference: increased comfort Maintain sexual function
3846
Disadvantages of suprapubic catheterisation
More complex: need skills Serious cx can occur
3847
CI to suprapubic catheterisation
Known or suspected bladder carcinoma Undiagnosed haematuria Previous lower abdominal surgery: adhesions of small bowel to abdominal wall
3848
Features of CISC
Clean intermittent self-catheterisation Alternative to indwelling catheter in AUR and CUR Also useful in pts who fail to void after TURP
3849
Causes of false haematuria
Beetroot Rifampicin Porphyria PV bleed
3850
How can the causes of true haematuria be classified
General Renal Uretur Bladder Prostate Urethra
3851
General causes of true haematuria
HSP Bleeding diathesis
3852
Renal causes of true haematuria
Infarct Trauma inc. stones Infection Neoplasm GN Polycystic kidneys
3853
Uretur causes of true haematuria
Stone Tumour
3854
Bladder causes of true haematuria
Infection Stones Tumour Exercise
3855
Prostate causes of true haematuria
BPH Prostatitis Tumour
3856
Urethral causes of true haematuria
Infection Stones Trauma Tumour
3857
Haematuria at beginning of stream
Urethral
3858
Haematuria throughout stream
Renal/systemic, bladder
3859
Haematuria at end of stream
Bladder stone Schistosomiasis
3860
Clinical features to determine in haematuria
Timing Painful or painless Obstructive symptoms Systemic symptoms
3861
Ix in haematuria
Bloods: FBC, U+E. clotting Urine: dip, MC+S, cytology Imaging: Renal US IVU Flexible cystoscopy and biopsy CT/MRI Renal angiography
3862
Aetiology of peri-aorititis
Idiopathic retroperitoneal fibrosis Inflammatory AAAs Perianeurysmal RPF RPF 2o to malignancy e.g. lymphoma
3863
Idiopathic retroperitoneal fibrosis pathophysiology
Autoimmune vasculitis Fibrinoid necrosis of vasa vasorum Affects aorta and small/medium sized retroperitoneal vessels Ureters are embedded in dense, fibrous tissue-\> bilateral obstruction
3864
Associations of idiopathic retroperitoneal fibrosis
Drugs: beta blockers, bromocriptine, methysergide, methyldopa AI disease: thyroiditis, SLE, ANCA+ vasculitis Smoking Asbestos
3865
Middle aged male Vague loin, back or abdo pain Raised BP Chronic urinary tract obstruction
?Para-aortitis
3866
Ix in idiopathic retroperitoneal fibrosis
Blood: raised U and Cr, raised ESR/CRP, reduced Hb US: bialteral hydronephrosis + medial ureteric deviation CT/MRI: peri-aortic mass Biopsy to exclude cancer
3867
Rx in peri-aortitis
Relieve obstruction: retrograde stent placement Ureterolysis: dissection of uretur from retroperitoneal tissue +/- immunosuppression
3868
Epidemiology of urolithiasis
Lifetime incidence: 15% Young men: peak age 20-40y. Sex M\>F 3:1
3869
Pathophysiology of urolithiasis
Increased concentration of urinary solute Reduced urine volume Urinary stasis
3870
What are the common anatomical sites of urolithiasis
Pelviureteric junction Crossing the iliac vessels at the pelvic brim Under the vas or uterine artery Vesicoureteric junction
3871
What is the most common type of renal stone?
Calcium oxalate
3872
Struvite stones associated with
Proteus infection (staghorn calculi)
3873
Types of renal stone
Calcium oxalate: 75% Struvite: 15% Urate: 5% (radiolucent) Cystine: 1% (faint)
3874
Factors associated with urolithiasis
Dehydration Hypercalcaemia: 1o HPT, immobilisation Increased oxalate excretion: tea, strawberries UTIs Hyperuricaemia: gout Urinary tract abnromalities e.g. bladder diverticulae Drugs: frusemide, thiazides
3875
Ureteric colic=
Severe loin pain radiating to the groin Associated with n/v Patient cannot lie still
3876
Severe loin pain radiating to goin Bladder irritability: frequency, dysuria, haematuria Strangury: painful urinary tenesmus Suprapubic pain radiating to tip of penis or in labia Pain and haematuria worse at the end of micturition Other possible features: UTI Haematuria Sterile pyruira Anuria Examination: usually no loin tenderness Haematuria
?Urolithiasis
3877
Ix in urolithiasis
Urine: dip- haematuria. MC+S Blood: FBC, U+E, Ca, PO4, urate Imaging: KUB XR USS- hydronephrosis CT KUB: gold standard IVU Functional scans
3878
CT KUB stone visualisation
99% of stones visualised
3879
Featuers of IVU
600x radiation dose of KUB IV contrast injected and control, immediate and serial films taken until taken at level of obstruction Abnormal findings: Failure of flow to the bladder Standing column of contrast Clubbing of the calcyces Delayed, dense nephrogran- no flow from kidney
3880
CI to IVU
Contrast allergy Severe asthma Meformin Pregnancy
3881
Different types of functional kidney scan
DMSA: dimeracptosuriccinic acid DTPA: diethylenetriamene penta-acetic acid MAG-3
3882
Prevention of renal stones
Drink plenty Treat UTI rapidly Reduce oxalate intake: chocolate, tea, strawberries
3883
Initial Rx in urolithiasis
Analgesia: diclofenac 75mg PO/IM or 100mg PR Opioids if NSAIDs CI e.g. pethidine Fluids: IV if unable to tolerate PO Abx if infection e.g. cefuroxime 1.5mg IV TDS
3884
Conservative Mx of renal stones
\<5mm in lower 1/3 of uretur 90-95% pass spontaneously Can discharge patient with analgesia Sieve urine to collect stone for OPD analysis
3885
Indications for medical expulsive therapy in urolithiasis
Stone 5-10mm Stone expected to pass
3886
Drugs used in medical expulsive therapy in urolithiasis
CCB or alpha antag: nifedipine or tamsulosin +/- pred Most pass within 48h, 80% within 30d
3887
Indications for active stone removal in urolithiasis
Low likelihood of spontaneous passage e.g. \>10mm Pesistent obstuciton Renal insufficeincy Infection
3888
What are the options for active stone removal in urolithiasis
Extracorporeal shockwave lithotripsy Ureterorenoscopy + Dormier basket removal Percutaneous nephrolithotomy Lap or Open surgery
3889
What determines options for stone removal
Location and size of stone
3890
Stone in renal pelvis \>20mm Option
PNL or URS 2nd line: SWL
3891
Stone in renal pelvis \<20mm
SWL 2nd line: URS, PNL
3892
Stone in proximal uretur \>10mm
URS or SWL
3893
Stone in proximal uretur \<10mm
SWL
3894
Stone in distal uretur \>10mm
URS 2nd line: SWL
3895
Stone in distal uretur \<10mm
URS or SWL
3896
Indications for extracorporeal shockwave lithotripsy
Stones \<20mm in kidney or proximal uretur
3897
SE of SWL
Renal injury may-\> raised BP
3898
CI to SWL
Pregnancy AAA Bleeding diathesis
3899
indications for ureterorenoscopy and dormier basket removal
Stone \>10mm in distal uretur or if SWL failed Stone \>20mm in renal pelvis
3900
Indications for percutaneous nephrolithotomy
Stone \>20mm in renal pelvis e.g. staghorn calculus: do DMSA first
3901
Febrile with renal obstruction
Surgical emergency Percutaneous nephrostomy or ureteric stent IVAbx: cefurime, 1.5g IV TDS
3902
Epidemiology of RCC
90% of renal cancer 55y/o Sex: M\>F 2:1
3903
RFs for RCC
Obesity Smoking HTN Dialysis (15% of patients develop RCC) 4% heritable e.g. VHL syndrome
3904
Pathology of renal cell carcinoma
Adenocarcinoma from proximal renal tubular epithleium Subtypes: Clear cell (glycogen): 70-80% Papillary: 15% Chromophobe: 5% Collecting duct 1%
3905
Most common presentation of RCC
50% incidental finding
3906
Triad in renal cell carcinoma
Haematuria, loin pain, loin mass
3907
50% incidental finding Triad: haematuria, loin pain, loin mass Systemic: anorexia, malaise, weight loss, PUO Clot retention invasion of L renal vein-\> varicocele Cannonball mets-\> SOB
RCC
3908
What are the paraneoplastic features of RCC
EPO-\> polycythaemia PTHrP-\> hypercalcaemia Renin-\> HTN ACTH-\> Cushing's syndrome Amyloidosis Deranged LFTs
3909
Spread of RCC
Direct: renal vein Lymphatic Haematogenous: bone, liver and lung
3910
Ix in RCC
Blood: polycythaemia, ESR, U+E, ALP, Ca Urine: dip, cytology Imaging: CXR- cannonball mets US: mass IVU: filling defect CT/MRI
3911
Robson staging of RCC
Confined to kidney Involves perinephric fat but not Garota's fascia Spread into renal vein Spread to adjacent/distant organs
3912
Mx of RCC
Medical: reserved for patients with poor px Temsirolimus (mTOR inhibitor) Surgical: Radical nephrectomy Consider partial if small tumour or 1 kidney
3913
Epidemiology of TCC
2nd commonest renal cancer 50-80y M\>F: 4:1
3914
RFs for TCC Renal
Smoking Amine exposure (rubber industry) Cyclophosphamide
3915
Pathology of TCC
Highly malignant Locations: bladder (50%), uretur, renal pelvis
3916
Presentation of TCC
Painless haematuria Frequency, urgency, dysuria Urinary tract obstruction
3917
Ix in TCC renal
Urine cytology CT/MRI IVU: pelviceal filling defect
3918
Mx of renal TCC
Nephouretectomy Regular f/up: 50% develop bladder tumours
3919
Childhood tumour of primitive renal tubules and mesenchymal cells May be associated with Chr 11 mutation May be associated with WAGR syndrome
Nephroblastoma
3920
WAGR syndrome
Wilms Aniridia GU abnormaltities Retardation
3921
2-5y/o 5-10% bilateral Abdominal mass that doesn't cross the midline haematuria Abdo pain HTN
?Wilm's
3922
Benign neoplasms of kidney
Cysts: very common Renal papillary adenomas Oncocytoma: eosinophilic cells with numerous mitochondria Angiomyolipoma: seen in tubeorus sclersosis
3923
Additional malignant renal neoplasms
SCC associated with chronic infected staghorn calculi
3924
NB re: renal benign tumours
Commonly require nephrectomy to exclude malignancy
3925
Epidemiology of bladder tumours
1:5000/y M\>F 4:1
3926
Pathology of bladder tumours
TCC account for 90% SCCs: associated with schistosomiasis Adenocarcinoma
3927
Natural hx of bladder tumours
Low-grade: 80% Non-invasive, generally not life-threatening High recurrence rate High grade: 20% Invasive and life-threatening High recurrence rates
3928
RFs for bladder tumours
Smoking Amine exposure (rubber industry) Previous renal TCC Chronic cystitis Schistosomiasis (SCC) Urechral remnants (adenocarcinomas): embryological remnants of communication between umbilicus and bladder Pelvic irradiation
3929
Painless haematuria Voiding irritability: dysuria, frequency, urgency Recurrent UTIs Retention and obstructive renal failure Anaemia Palpable bladder mass Palpable liver
?bladder tumour
3930
TNM staging of Bladder tumours
80% confined to mucosa 20% penetrate muscle (increased moratlity) Tis: carcinoma in situ, not fetlt at EUA Ta: confined to epithelium, not felt at EUA T1: tumour in lamina propria: not felt T2: superficial muscle involved: rubbery thickness T3: deep muscle involved: mobile mass T4: invasion of prostate, uterus, vag: fixed mass
3931
Spread of bladder tumours
Local-\> pelvic structures Lymph-\> iliac and para-aortic nodes Haem-\> bones, liver and lungs
3932
Histological classification of bladder tumours
Grade 1: well differentiated Grade 2: intermediate Grade 3: poorly differentiated
3933
Ix in bladder tumours
Urine: dip (sterile pyuria), cytology IVU: filling defects Cystoscopy with biopsy- diagnostic Bimanual EUA helps to assess spread CT/MRI helps stage
3934
Mx of bladder tumours
Depends on histological grade and the presence of dissemination
3935
Mx of bladder cancer: Tis, Ta, T1
80% of all patients diathermy via transurethral cystoscopy/TURBT Intravesicular chemo: mitomycin C Intravesicular immunotherapy: BCG
3936
Mx of bladder cancer: T2, T3 (invasive)
Radical cystectomy with ileal conduit is gold standard RTx: worse 5ys but preserves bladder: salvage cystectomy can be performed Adjuvant chemo: M-VAC Neoadjuvant chemo may have a role
3937
Mx of bladder cancer: T4
Palliate CT/RTx Long-term catheterisation Urinary diversions
3938
Cx of bladder cancer treatment
Massive haemorrhage Cystectomy-\> sexual and urinary malfunction
3939
F/U of bladder TCC
Up to 70% of bladder tumours recur, therefore intensive F/U is required Hx, ex and regular cystoscopy High risk tumours: every 3m for 2y then ever 6m Low risk: @9m then yearly
3940
Px in bladder cancer
Depends on age and stage Non invasive: 95% 5ys T2: 40-50% T3: 25% T4 \<1y
3941
Epidemiology of BPH
70% @60y 90% @80y
3942
Pathophysiology of BPH
Benign nodular or diffuse hyperplasia of stromal and epithelial cells Affects inner (transitional) layer of prostate (cf. Ca)-\> urethral compression DHT produced from testosteroe in stromal cells by 5-a reductase enzyme DHT-induced GFs-\> raised stromal cells and reduced epithelial cell death
3943
Presentation of BPH categorisation
Storage symptoms: nocturia, frequency, urgency, overflow incontinence Voiding symptoms: hesitancy, straining, poor stream/flow + terminal dribbling, strangury, incomplete emptying Bladder stones: 2o to stasis UTI: 2o to satasis
3944
Examination in BPH
PR: smoothly enlarged prostate Definable median sulcus Bladder not usually palpable unless acute-on-chronic obstruction
3945
Ix in BPH
Bloods: U+E, PSA Urine: dip, MC+S Imaging: transrectal US +/- biopsy Urodynamics: pressure/flow cystometry Voiding diary
3946
Conservative Mx of BPH
Reduce caffeine, EtOH Double voiding Bladder training: hold on-\> increase time between boiding
3947
Medical mx of BPH
Useful in mild disease while awaiting TURp 1st line: alpha blockers: tamsulosin, doxazosin 2nd line: 5alpha reductase inhibitors: finasterid
3948
Use of alpha blockers in BPH
Tamsulosin, doxazosin Relax prostate smooth muscle SE: drowsiness, reduced BP, depression, ED, weight gain, extra-pyramidal signs
3949
Use of 5 alpha reductase inhibitors in BPH
Finasteride Inhibit conversion of testosterone to DHT Preferred if significantly enlarged prostate SE: secreted in semen, ED
3950
Indications for surgical mx of BPH
`Symptoms affect QoL Cx of BPH
3951
What are the surgical options for BPH
TURP TUIP Transurethral electrovaporisation of prostate Laser prostatectomy Open retropubic prostatectomy
3952
Features of TURP
Cystoscopic resection of lateral and middle lobes \<14% become impotent
3953
TUIP
Transurethral incision of prostate (TUIP) less destrction than TURP so less risk to sexual function Similar benefits if small prostate (\<30g)
3954
Features of laser prostatectomy
Reduced ED and retrograde ejaculation Similar efficacy as TURP
3955
Use of open retropubic prostatectomy
Used for very large prostates \>100g
3956
What are the immediate cx of TURP
TUR syndrome: absorption of large quantity of fluids-\> hyponatraemia Haemorrhage
3957
What are the early cx of TURP
Haemorrhage Infection Clot retention: requires bladder irrigation
3958
What are the late cx of TURP
Retrograde ejaculation: common ED: 10% Incontinence: 10% Urethral stricture Recurrence
3959
What is the epidemiology of prostate cancer
Commonest male cancer 3rd commonest cause of male cancer death 80% of men \>80y Increased in blacks
3960
Pathology of prostate cancer
Adenocarcinoma Peripheral zone of prostate
3961
Usually asymptomatic Urinary: nocturia, frequency, hesitancy, poor stream, terminal dribbling, obstruction Systemic: weight loss, fatigue Mets: bone pain
Prostate Ca
3962
Examination findings in prostate ca
Hard irregular prostate on PR Loss of midline sulcus
3963
Spread of prostate cancer
Local: seminal vesicles, bladder, rectum lymph: para-aortic nodes Haemo: sclerotic bony lesions
3964
Ix in prostate cancer
Bloods: PSA, U+E, acid and ALP, Ca Imaging: XR chest and spine transrectal US + biopsy Bone scan Staging MRI: contrast enhancing magnetic nanoparticles increases detection of affected nodes
3965
Features of PSA
Proteloytic enzyme used in liquefaction of ejaculate Not specific for prostate Ca: increases with age, PR, TURP and prostatitis \>4ngml: 40-90% sensitivie, 60-90% specific. Only 1 in 3 will have cancer Normal in 30% of small cancers
3966
What can be used to grade prostate cancer
Gleason Grade Score 2 worst affected areas Sum is inversely proportional to px
3967
TNM staging of prostate Ca
Tis: carcinoma in situ T1: incidental finding on TURP or raised PSA T2: intracapsular tumour with deformation of prostate T3: extraprostatic extension T4: fixed to pelvis + invading neighbouring structures N1-4: 1 or more LNs involved M1: distant mets e.g. spine
3968
Prognostic factors in prostate cancer
Help determine whether to pursue radical Rx Age Pre-Rx PSA tumour stage Tumour grade
3969
Issues with mx of prostate cancer
Difficult to know which tumours are indolent and will not lead to mortality before something else Radical therapy associated with significant morbidity
3970
Conservative mx of prostate cancer
Close monitoring with DRE and PSA
3971
Radical mx of prostate ca
Radical prostatectomy (+ gosrelin if node +ve) Performed laparoscopically with robot Only improves survival vs active monitoring if \<75y Brachytherapy: implantation of palladium seeds
3972
SEs of radical therapy for prostate cancer
ED, urinary incontinence, death
3973
Use of radical prostatectomy in prostate cancer
Performed laparoscopically Only improves survival vs active monitoring if \<75y
3974
Medical mx of prostate cancer
Used for metastatic or node +ve diseae LHRH analgoues e.g. gosrelin: inhibits pituitay gonadotrophins-\> reduce testosterone Anti-andrognes: e.g. cyporterone actetate, flutamide
3975
Symptomatic mx of prostate cancer
TURP for obstruction Analgesia RTx for bone mets/cord compression
3976
PSA and screening
Population based screening not recommended in UK PSA not an accurate tumour marker ERSPC trial showed small mortality benefit, PLCO trial showed no benefit Must balance mortality benefit with harm caused by over diagnosis and over treatment of indolent cancers
3977
Aetiology of prostatitis
S. faecalis E. coli Chlamydia
3978
Usually \>35y UTI/dysuria Pain: low backache, pain on ejaculation Haematospermia Fever and rigors Retention Malaise Pyrexial Swollen/boggy/tender prostate Examine testes to exclude epididymo-orchitits
Prostatitis
3979
Ix in prostatitis
Blood: FBC, U+E, CRP Urine dip: MC+S
3980
Rx in prostatitis
Fluoroquinolone for 4 w Analgesia e.g. levofloxacin 500mg/d for 28d
3981
Features of male urinary incontinence
Usually caused by prostatic enlargement Urge incontinence or dribbling may result from partial retention Retention may lead to overflow (palpable bladder after voiding) TURP and pelvic surgery may weaken external urethral sphincter
3982
Urinary incontinence in women
Stress: Leakage from incompetent sphincter when raiesd IAP Loss of small amounts of urine when coughing Pelvic floor weakness Urge/OAB can't hold urine May have precipitatnt Dx: urodynamic studies
3983
Mx of urinary incontinence
Check PR: faecal impaction Palpable bladder after voiding: retention with overflow DM CNS: MS, parkinson's, stroke, spinal trauma Diuretics Stress: Pelvic floor exercises Ring pessary Duloxetine Surgery: tension free vaginal tape Urge: Bladder training Weight loss Anti-AChM: tolterodine, imipramine
3984
Epidemiology of undescended testes
3% at birth 1% at 1y Unilateral 4x commoner cf. bilateral: should have genetic testing if bilateral Commoner in prems: incidence up to 30%
3985
Normal descent of testes
Testes remain in abdomen (retroperitoneal) until 7m Gubernaculum connects inferior pole of testis to scrotum Testes descend through inguinal canal to scrotum with an out-pouching of peritoneum: processus vaginalis
3986
Def: cryptorchidism
Complete absence of testis from scrotum Anorchism= absence of both testes
3987
Def: retractile testis
Normal development but excessive cremasteric reflex Testicle often found at external inguinal ring Will descend, no Rx required
3988
Def: maldescended testis
Found anywhere along normal path of descent Testis and scrotum are usually under-developed Often associated with patent processus vaginalis
3989
Def: ectopic testis
Found outside line of descent Usually in superior inguinal pouch (anterior to external oblique aponeurosis) Abdominal, perineal, penile, femoral triangle
3990
Cx of undescended testes
Infertility 10x risk of malignancy (remains after surgery) Increased risk of trauma Increased risk of torsion Associated with hernias (90%) or UT abnormalities
3991
Reasons for intervening in undescended testes
Restores potential for spermatogensis Make ca surveillance easier
3992
Surgical mx of undescended testes
Orchidopexy by Dartos Pouch Procedure Perform before 2y Mobilisation of testis and cord Removal of patent processus testicle brought through a hole made in the dartos muscle to lie in a subcutaneous pouch Dartos prevents retraction
3993
Hormonal mx of undescended testis
Beta-HCG may be tried if testis is in inguinal canal
3994
Aetiology of testicular torsion
Usually 2o to some exertion or minor trauma Occurs because testicles don't have a large bare area to attach to scrotal wall: Tunica vaginalis invests whole of testicle Free hanging clapper-bell testicle can twist on its mesentry
3995
Usually 10-25y/o Sudden onset severe pain in one testis May have lower abdo pain (testis supplied by T10) Associated with n+v May be hx of previous testicular pain
?Testicular torsion
3996
Inflammation of one testis: hot, swollen, extremely tender Testis rides high and lie transversely
Testicular torsion
3997
Ddx in ?testicular torsion
Epididymo-orchtiis: older patient, UTI symptoms, more gardual onset Torted Hydatid of Morgagni: remnant of mullerian duct, younger patient, less pain. Tiny ble dot visible on scrotum tumour Trauma Strangulated hernia Appendicitis
3998
Ix in torsion
Doppler US may demonstrate absence of flow must not delay surgical exploration
3999
Mx of ?torsion
Surgical emergency: 4-6h window from onset of pain to salvage testis Inform senior NBM IV access: analgesia, bloods: FBC, U+E, G+S, clotting Sx: consent for possible orchidectomy, bilateral orchidopexy: suture testes to scrotum if no torsion found and epidydiom-orchtitis dx- take fluid for bacteriology and rx with abx
4000
Groin/scrotal lump: Can't get above
Inguinoscrotal hernia
4001
Groin/scrotal lump: Separate, cystic
Epididymal cyst
4002
Groin/scrotal lump: separate, solid
Varicocele Sperm granuloma Epidydimitis
4003
Groin/scrotal lump: Testicular, cystic
hydrocele
4004
Groin/scrotal lump: testicular, solid
Tumour Orchitis haematocele
4005
Develop in adulthood Contiain clear or milky fluid Lie above and behind testis Remove if symptomatic
Epididymal cyst
4006
Feel like bag of worms in scrotum may be visible dilated veins reduced size on lying down Patient may complain of dull ache May lead to oligospermia-\> reduced fertility
Varicocele (dilated veins of pampiniform plexus)
4007
Pathology of testicular varicocele
1o: left side commoner, drain into LRV 2o: left renal tumour has tracked down renal vein-\> testicular vein obstruction
4008
Mx of testicular varicocele
Conservative: scrotal support Surgical: clipping the testicular vein (open or lap)
4009
Painful lump of extravasated sperm after vasectomy
Sperm granuloma
4010
Collection of serous fluid within tunica vaginalis Can be primary: associated with patent processus vaginalis, commoner, larger, tense, younger men Can be secondary: tumour, trauma, infection, smaller, less tense
Hydrocele
4011
Ix in testicular hydrocele
US testicle to exclude tumour
4012
Mx of testicular hydrocele
May resolve spontaneously: surgery- Lord's repair: plication of the sac Jaboulay's repair: eversion of the sac Aspiration: usually recur so not 1st line Send fluid for cytology and MC+S
4013
Blood in tunica vaginalis Hx of trauma May need drainage or incision
haematocele
4014
Aetiology of epididymo-orchitis
STI: chlamydia, gonorrhoea Ascending UTI: E. Coli Mumps
4015
Sudden onset tender testicular swelling Dysuria Sweats, fever Tender, red, warm swollen testis and epidydimitis Prehn's sign positive Secondary hydrocele urethral discharge
Epididymo-orchitis
4016
Prehn's sign
Positive Prehn's sign indicates there is pain relief with lifting the affected testicle, which points towards epididymitis
4017
Ix in epididymo-orchitis
Blood: FBC, CRP Urine: dip, MC+S (first catch) Urethral swab and STI screen US: may be needed to exclude abscess
4018
Cx of epididymo orchitis
May-\> infertility
4019
Mx of epididymo-orchitis
Bed rest Analgesia Scrotal support Abx: doxy or cipro Drain abscess if present
4020
Epidemiology of testicular tumours
Commonest male malignancies from 15-44y Whites \> blacks 5:1
4021
Painless testicular lump- often noticed after trauma Haematospermia 2o hydrocele Mets: SOB from lung mets Abdo mass: para-aortic lymphadenopathy Hormones: gynaecomastia, virilisation Contralateral tumour in 5%
Testicular tumours
4022
RFs for testicular tumours
Undescended testis: 10% occur in this group Infant hernia Infertility
4023
How can the different types of testicular tumour be classified?
Germ Cell Sex-cord Stromal lymphoma/leukaemia
4024
What classification of testicular tumour is the most common?
Germ cell (95%)
4025
What are the subtypes of germ cell testicular tumours
Pure Seminomas (40%) Non-seminomas (inc. mixed): (60%) Mixed Teratoma Yolk sac Choriocarcinoma
4026
Commonest single subtype of testicular tumour 30-40 Raised beta HCG in 15% Raised ALP in some Very radiosensitive
Seminoma
4027
Commonest NSGCT
Mixed
4028
Testicular tumour Arise from all 3 germ layers Common and benign in children Rare and malignant in adults: 15-30y Secrete beta HCG and or AFP Chemosensitive
Teratoma
4029
Teratoma: secretes Two
Beta HCG and or AFP
4030
Commonest testicular tumour in children
Yolk sac
4031
Testicular tumour Raised +++ BetaHCG
Choriocarcinoma
4032
What are the sex cord stromal subclassifications of testicular tumours
Leydig cell Sertoli cell Both mostly benign
4033
Leydig cell tumours may secrete
Androgens or oestrogens
4034
Sertoli cell tumours may secrete
Oestrogens
4035
What is the commonest malignant testicular mass \>60y
NHL
4036
What is the commonest malignant testicular mass \<5
ALL
4037
What can be used to stage testicular tumours?
Royal Marsden Staging
4038
Royal Marsden Staging of Testicular tumours
1. Disease only in testis 2. Para-aortic nodes involved (below diaphragm) 3. Supra and infra-diaphragmatic LNs involved 4. Extra-lymphatic spread: lungs, liver
4039
Ix in testicular tumours
Tuour markers: useful for monitoring Raised AFP and hCG in 90% of teratomes Raised hCG in 15% of seminomas Normal AFP in pure seminomas Scrotum US Staging: CXR, CT NB: percutaneous needle biopsy should not be performed due to risk of seeding along the needle tract
4040
Mx of testicular tumours: both testes involved
Semen can be cryopreserved
4041
Mx of stage 1-2 seminoma
Inguinal orchidectomy + RTx Groin incision allows cord clamping to prevent seeding
4042
Mx of stage 3-4 seminoma
Inguinal orchidectomy + RTx + chemo (BEP) Bleomycin, etoposide, cisPlatin
4043
Mx of stage 1 testicular non-seminoma
Inguinal orchidecctomy and surveillance
4044
Mx of stage 2 non-seminoma
Orchidectomy + chemo + para-aortic LN dissection
4045
Mx of stage 3 non-seminomatous testicular tumour
Orchidectomy + chemo
4046
F/U in testicular tumours
Typically within 18-24m Repeat CT scanning and tumour markers
4047
Px in testicular tumours
Stage 1: 98% 5ys Stage 2: 85% Stage 4: 60%
4048
Def: balanatitis
Acute inflammation of foreskin and glans
4049
Cause of balantitis
Strep, staph, candida
4050
RFs of balantitis
DM Young children with tight foreskin
4051
Rx of balantitis
Hygiene advice Abx Circumcision
4052
Phimosis
Foreskin occludes the meatus
4053
Child Recurrent balantitis and ballooning
Phimosis
4054
mx of childhood phimosis
Gentle retraction Steroid creams Circumcision
4055
Adult presentation of phimosis
Dyspareunia, infection
4056
Mx of adult phimosis
Circumcision
4057
Balantitis xerotica obliterans
Thickening of foreskin and glans-\> phimosis + meatal narrowing
4058
Pathology of paraphimosis
Tight foreskin is retracted and becomes irreplaceable Reduced venous return-\> oedema and swelling of the glans Can rarely lead to ischaemia
4059
Causes of paraphimosis
Catheterisation, masturbation, intercourse
4060
Mx of paraphimosis
Manual reduction: use ice and lignocaine jelly May require glans aspiration or dorsal slit
4061
Hypospadia
Developmental abnormality of the position of the urethral opening Opens on ventral surface of penis
4062
Epispadia
Developmental abnormality of the position of the urethral opening Opens on the dorsal surface
4063
Epidemiology of penile cancer
1:100,000/y in UK commoner in far east and africa
4064
Aetiology of penile cancer
V. rare if circumcised RFs: HPV, chronic irritation
4065
Pathology of penile cancer
Erythroplasia of Querat-\> Penile CIS SCC
4066
Chronic fungating penile ulcer Bloody/purulent discharge Inguinal nodes in 50% at presentation
Penile cancer
4067
Mx of penile cancer
Medical: early growths with no urethral invovlement: DXT and iridium wires Surgical: Amputation required if urethral involvement LN dissection
4068
A 24-year-old man presents with localised spinal pain over 2 months which is worsened on movement. He is known to be an IVDU. He has no history suggestive of tuberculosis. The pain is now excruciating at rest and not improving with analgesia. He has a temperature of 39 oC.
In an IVDU with back pain and pyrexia have a high suspicion for osteomylelitis. The most likely organism is staph aureus and the cervical spine is the most common region affected. TB tends to affect the thoracic spine and in other causes of osteomyelitis the lumbar spine is affected.
4069
A 56-year-old lady has undergone a Hartman's procedure for diverticulitis. 6 months post operatively she complains of painless passage of blood stained mucous per rectum.
Rectal diversion may result in proctitis.
4070
Bright red rectal bleeding Painful bleeding that occurs post defecation in small volumes. Usually antecedent features of constipation Muco-epithelial defect usually in the midline posteriorly (anterior fissures more likely to be due to underlying disease)
Fissure in ano
4071
Bright red or mixed blood Bleeding that is accompanied by other symptoms such as altered bowel habit, malaise, history of fissures (especially anterior) and abscesses. Perineal inspection may show fissures or fistulae. Proctoscopy may demonstrate indurated mucosa and possibly strictures. Skip lesions may be noted at colonoscopy.
Crohns disease
4072
Bright red bleeding often mixed with stool Diarrhoea, weight loss, nocturnal incontinence, passage of mucous PR. Proctitis is the most marked finding. Peri anal disease is usually absent. Colonoscopy will show continuous mucosal lesion.
Ulcerative colitis
4073
Bright red blood mixed volumes Alteration of bowel habit. Tenesmus may be present. Symptoms of metastatic disease. Usually obvious mucosal abnormality. Lesion may be fixed or mobile depending upon disease extent. Surrounding mucosa often normal, although polyps may be present.
Rectal cancer
4074
A 35-year-old woman has undergone a wide local excision. The histology shows an invasive lobular carcinoma present at 3 of the resection margins. Cavity shavings taken at the original operation are also involved. Sentinel node biopsy was negative.
This patient has an extensive disease process and lobular cancers are notorious for being multifocal. In this case a mastectomy is the safest next step.
4075
A 28-year-old female presents with a painless lump in the upper outer quadrant of her left breast. Imaging using ultrasound is indeterminate (U3). Two core biopsies have now been performed and both show normal breast tissue (B1
The imaging and biopsy results are not concordant. At this stage an excision biopsy is the safest option
4076
A cyclist loses control and falls off the side of a road landing on the bicycle handlebars. CT scanning shows a large amount of retroperitoneal air.
Retroperitoneal air is more likely with a duodenal injury. As it is largely retroperitoneal. A handlebar type injury is the commonest cause and the pancreas should be carefully inspected as it too may be injured. It would be unusual for the ileum to be injured in this type of scenario as it is mobile.
4077
Retroperitoneal air is more likely with a duodenal injury. As it is largely retroperitoneal. A handlebar type injury is the commonest cause and the pancreas should be carefully inspected as it too may be injured. It would be unusual for the ileum to be injured in this type of scenario as it is mobile.
1. Small bowel injury is the most common type of injury in this scenario. The enteric contents will tend to result in a large amount of intra abdominal fluid.
4078
Unusual injuries. In blunt trauma most injuries occur within 4cm of the carina. Features suggesting this injury include haemoptysis and surgical emphysema. These injuries have a very large air leak and may have tension pneumothorax.
Tracheobronchial tree injury
4079
Post-trauma Usually cardiac arrhythmias, often overlying sternal fracture. Perform echocardiography to exclude pericardial effusions and tamponade. Risk of arrhythmias falls after 24 hours
Cardiac contusion
4080
Typically, these patients have a viral prodrome followed by anaemia, often with haemoglobin concentrations falling below 5.0 g/dL and reticulocytosis.
Transient aplastic crisis in SCD following parvovirus B19 infection
4081
A 44-year-old man attends for counselling with regards to a vasectomy. Which one of the following statements is true regarding vasectomy? Vasectomy is effective immediately Female sterilisation is more effective Two negative semen samples should be obtained at 2 and 4 weeks before other contraceptive methods are stopped Chronic testicular pain is seen in more than 5% of patients Sexual intercourse should be avoided for one month to reduce the chance of a sperm granuloma
Chronic testicular pain is seen in more than 5% of patients
4082
Features of male sterilisation
Failure rate: 1/2000 Simple operation, can be done under LA, go home after a couple of hours Doesn't work immediately. Requires semen analysis 2 weeks following procedure before a man can hvae unprotected sex
4083
Cx of vasectomy
Bruising Haematoma Infection Sperm ganuloma Chronic testicular pain (affects 5-30% of men)
4084
Female sterilisation features
1/200 fail Usually done laparoscopically under GA Day case Many different techniques
4085
Cx of female sterilisation
Increased risk of ectopic if sterilisation fails General Cx of GA/lap
4086
Wallace's rule of 9s for burns
head + neck = 9% Each arm= 9% Each anterior part of leg= 9% Each posterior part of leg= 9% Ant chest= 9% Post chest= 9% Ant abdo and post abdo= 9% each
4087
What is the most accurate method for assessing the extent of a burn
Lund and Browder chart
4088
How to calculate fluid replacement in burns?
Parkland formula: volume= total body surface area of the burn x weight (kg) x 4 Half of the fluid is administered in the first 8h
4089
A 53-year-old woman presents with a bloody nipple discharge. On mammography there is calcification behind the nipple areolar complex. A core biopsy shows background benign change, but cells that show comedo necrosis which have not breached the basement membrane.
Comedo necrosis is a feature of high nuclear grade ductal carcinoma in situ. It is has a high risk of being associated with foci of invasion.
4090
A 74-year-old woman presents with a breast lump. On examination is has a soft consistency. The lump is removed and sliced apart. Macroscopically there is a grey, gelatinous surface
Mucinous carcinomas comprise 2-3% of all breast cancers. They are one of the special type of carcinomas. These have a better prognosis that tumours of Non Special Type (NST) and axillary nodal disease is rare in this group
4091
A 74-year-old woman presents with an erythematous rash originating in the nipple. It is spreading to the surrounding areolar area and the associated normal tissue.
Paget's is associated with DCIS or invasive carcinoma.Unlike eczema of the nipple which predominantly affects the areolar region, Pagets will usually affect the nipple first and then spread to the areolar area. Diagnosis is made by punch biopsy.
4092
A 28-year-old Indian woman, who is 18 weeks pregnant, presents with increasing shortness of breath, chest pain and coughing clear sputum. She is apyrexial, blood pressure is 140/80 mmHg, heart rate 130 bpm and saturations 94% on 15L oxygen. On examination there is a mid diastolic murmur, there are bibasal crepitations and mild pedal oedema. She suddenly deteriorates and has a respiratory arrest. Her chest x-ray shows a whiteout of both of her lungs.
Mitral stenosis is the commonest cause of cardiac abnormality occurring in pregnant women. Mitral stenosis is becoming less common in the UK population, however should be considered in women from countries were there is a higher incidence of rheumatic heart disease. Mitral stenosis causes a mid diastolic murmur which may be difficult to auscultate unless the patient is placed into the left lateral position. These patients are at risk of atrial fibrillation (up to 40%), which can also contribute to rapid decompensation. Physiological changes in pregnancy may cause an otherwise asymptomatic patient to suddenly deteriorate. Balloon valvuloplasty is the treatment of choice.
4093
A 28-year-old woman, who is 30 weeks pregnant, presents with sudden onset chest pain associated with loss of consciousness. Her blood pressure is 170/90 mmHg, saturations on 15L oxygen 93%, heart rate 120 bpm and she is apyrexial. On examination there is an early diastolic murmur, occasional bibasal creptitations and mild peal oedema. An ECG shows ST elevation in leads II, III and aVF.
Aortic dissection is associated with the 3rd trimester of pregnancy, connective tissue disorders (Marfan's, Ehlers- Danlos) and bicuspid valve. Patients may complain of a tearing chest pain or syncope. Clinically they may be hypertensive. The right coronary artery may become involved in the dissection, causing myocardial infarct in up to 2% cases (hence ST elevation in the inferior leads). An aortic regurgitant murmur may be auscultated.
4094
A 73-year-old lifelong heavy smoker presents to the vascular clinic with symptoms of foot ulceration and rest pain. On examination her foot has areas of gangrene and pulses are impalpable.
0.3 This is critical limb ischaemia. Values of 0.3 are typical in this setting and urgent further imaging is needed. Debridement of necrosis prior to improving arterial inflow carries a high risk of limb loss.
4095
A 63-year-old man presents with a claudication distance of 15 yards. He is a lifelong heavy smoker. On examination his foot is hyperaemic and there is a small ulcer at the tip of his great toe.
0.5 Hyperaemia may occur in association with severe vascular disease and is referred to surgically as a "sunset foot". ABPI is usually higher than 0.3, but seldom greater than 0.5. Especially when associated with hyperaemic changes and ulceration. Urgent further imaging and risk factor modification is needed.
4096
A 77-year-old morbidly obese man with type 2 diabetes presents with leg pain at rest. His symptoms are worst at night and sometimes improve during the day. He has no areas of ulceration.
\>1.2 Type 2 diabetes may have vessel calcification. This will result in abnormally high ABPI readings. Pain of this nature in diabetics is usually neuropathic and if a duplex scan is normal then treatment with an agent such as duloxetine is sometimes helpful.
4097
A 38-year-old lady presents with symptoms of obstructed defecation that date back to the birth of her second child by use of ventouse. She passes mucous and suffers from pelvic pain. Digital rectal examination and barium enema are normal.
Rectal intussceception Rectal intussceception (internal rectal prolapse) typically presents with symptoms of obstructed defecation. The pathology is best demonstrated by a defecating procotogram rather than barium enema.
4098
Triad of features in TUR syndrome
Hyponatraemia: dilutional Fluid overload Glycine toxicity Mx: fluid restriction and the treatment of cx associated with the hyponatraemia
4099
A 4-year-old presents with sudden onset of dysphagia. He undergoes an upper GI endoscopy and a large bolus of food is identified in the mid oesophagus. He has no significant history, other than a tracheo-oesophageal fistula repair soon after birth.
The correct answer is Benign oesophageal stricture Children with tracheo-oesophageal fistulas will commonly develop oesophageal strictures following repair. These may require regular dilations throughout childhood.
4100
CVP reading that excludes pulmoanry oedema?
CVP 18mmHg
4101
Stages of ARDS
Early: exudative phase of injury with associated oedema Late stage: repair and consists of fibroproliferative changes Subsequent scarring may rseult in poor lung function
4102
Features of lung recruitment manoeuvres
Transient increases in transpulmonary pressure designed to open up collapsed airless alveoli Primarily used in ARDS Multiple methods have been described 40cmH20 for 40-60 seconds 3 consecutive sighs/min with a plateau pressure of 45cmH2O 2 minutes of peak pressure of 50cmH2O and PEEP above upper inflection point (obese/trauma patients may require \>60-70cmH2O) long slow increase in inspiratory pressure up to 40 cmH2O (RAMP) stepped increase in pressure (e.g. Staircase Recruitment Manoeuvre) Proning can also be considered a recruitment manoeuvre, and other recruitment manoeuvres are more more effective in the prone position
4103
A 34-year-old man is suffering from septic shock and receives and infusion of Dextran 70. Which of the following complications may potentially ensue? Anaphylaxis Vomiting Acute hepatic failure Digital necrosis Deep vein thrombosis
Dextran 40 and 70 have higher incidence of anaphylaxis than either gelatins or starches. Dextrans are branched polysaccharide molecules. Dextran 40 and 70 are available. The higher molecular weight dextran 70 may persist for up to 8 hours. They inhibit platelet aggregation and leucocyte plugging in the microcirculation. Thereby improving flow through the microcirculation, primarily of use in sepsis. Unlike many other intravenous fluids Dextrans are a recognised cause of anaphylaxis.
4104
A 63-year-old lady undergoes an axillary clearance for breast cancer. She makes steady progress. However, 8 weeks post operatively she still suffers from severe shoulder pain. On examination she has reduced active movements in all planes and loss of passive external rotation.
Adhesive capsulitis Frozen shoulder passes through an initial painful stage followed by a period of joint stiffness. With physiotherapy the problem will usually resolve although it may take up to 2 years to do so.
4105
A 78-year-old man complains of a long history of shoulder pain and more recently weakness. On examination active attempts at abduction are impaired. Passive movements are normal.
Rotator cuff tear Rotator cuff tears are common in elderly people and may occur following minor trauma or as a result of long standing impingement. Tears greater than 2cm should generally be repaired surgically.
4106
A 28-year-old man complains of pain and weakness in the shoulder. He has recently been unwell with glandular fever from which he is fully recovered. On examination there is some evidence of muscle wasting and a degree of winging of the scapula. Power during active movements is impaired.
Parsonage - Turner syndrome This is a peripheral neuropathy that may complicate viral illnesses and usually resolves spontaneously.
4107
Please select the source of innervation for the region described. Each option may be used once, more than once or not at all. ## Footnote 22. The skin on the palmar aspect of the thumb 23. The nail bed of the index finger 24. The skin overlying the medial aspect of the palm
Median median Ulnar
4108
A 38-year-old man is playing football when he slips over during a tackle. His knee is painful immediately following the fall. Several hours later he notices that the knee has become swollen. Following a course of non steroidal anti inflammatory drugs and rest the situation improves. However, complains of recurrent pain. On assessment in clinic you notice that it is impossible to fully extend the knee, although the patient is able to do so when asked.
he correct answer is Torn meniscus Theme from September 2012 Exam Twisting sporting injuries followed by delayed onset of knee swelling and locking are strongly suggestive of a menisceal tear. Arthroscopic menisectomy is the usual treatment.
4109
A 28-year-old professional footballer is admitted to the emergency department. During a tackle he is twisted with his knee flexed. He hears a loud crack and his knee rapidly becomes swollen.
The correct answer is Anterior cruciate ligament rupture This is common in footballers as the football boot studs stick to the ground and high twisting force is applied to a flexed knee. Rapid joint swelling also supports the diagnosis.
4110
A 65-year-old diabetic female presents with a painless ulcer at the medial malleolus, it has been present for the past 16 years. On examination she has evidence of truncal varicosities and a brownish discolouration of the skin overlying the affected area.
Venous insufficiency Venous ulcers are usually associated with features of venous insufficiency. These include haemosiderin deposition and varicose veins. Neuropathic ulcers will tend to present at sites of pressure, which is not typically at the medial malleolus.
4111
A 71-year-old man presents with a painful lower calf ulcer, mild pitting oedema and an ABPI of 0.3.
Chronic obliterative arterial disease Painful ulcers associated with a low ABPI are usually arterial in nature. The question does not indicate that features of chronic venous insufficiency are present. Patients may have mild pitting oedema as many vascular patients will also have ischaemic heart disease and elevated right heart pressures. The absence of more compelling signs of venous insufficiency makes a mixed ulcer less likely.
4112
A 28-year-old female presents with a small nodule located on the back of her neck. It is excised for cosmetic reasons and the histology report states that the lesion consists of a sebum filled lesion surrounded by the outer root sheath of a hair follicle.
Pilar cyst Pilar cysts may contain foul smelling cheesy material and are surrounded by the outer part of a hair follicle. Because of their histological appearances they are more correctly termed pilar cysts than sebaceous cysts.
4113
A 40-year-old lady trips and falls through a glass door and sustains a severe laceration to her left arm. Amongst her injuries it is noticed that she has lost the ability to adduct the fingers of her left hand.
Ulnar nerve The interossei are supplied by the ulnar nerve.
4114
What is used to give Px in breast Ca?
Nottingham Prognostic Index
4115
How is NPI calulated
Tumour size x 0.2 + LN score + grade score
4116
A 19-year-old sportswoman presents with knee pain which is worse on walking down the stairs and when sitting still. On examination there is wasting of the quadriceps and pseudolocking of the knee.
Chondromalacia patellae A teenage girl with knee pain on walking down the stairs is characteristic for chondromalacia patellae (anterior knee pain). Most cases are managed with physiotherapy.
4117
A tall 18-year-old male athlete is admitted to the emergency room after being hit in the knee by a hockey stick. On examination his knee is tense and swollen. X-ray shows no fractures.
Dislocated patella A patella dislocation is a common cause of haemarthrosis and many will spontaneously reduce when the leg is straightened. In the chronic setting physiotherapy is used to strengthen the quadriceps muscles.
4118
An athletic 15-year-old boy presents with knee pain of 3 weeks duration. It is worst during activity and settles with rest. On examination there is tenderness overlying the tibial tuberosity and an associated swelling at this site.
Osgood Schlatters disease Athletic boys and girls may develop this condition in their teenage years. It is caused by multiple micro fractures at the point of insertion of the tendon into the tibial tuberosity. Most cases settle with physiotherapy and rest.
4119
Hx and Ex in carpal tunnel syndrome
Pain/pins and needles in thumb, index, middle finger e.g. at night Patient flicks hand to obtain relief Weakness of thumb abduction Wasting of thenar eminence Tinel's sign: tapping causes paraesthesia) Phalen's sign
4120
Causes of carpal tunnel syndrome MEDIAN TRAP
Myxoedema Edema premnestrually DM Idiopathic Acromegaly Neoplasm Trauma Rheumatoid arthritis Amyloidoisis Pregnancy
4121
A 72-year-old man is diagnosed with prostate cancer and goserelin (Zoladex) is prescribed. Which one of the following is it most important to co-prescribe for the first three weeks of treatment? Tamoxifen Lansoprazole Allopurinol Cyproterone acetate Tamsulosin
Anti-androgen treatment such as cyproterone acetate should be co-prescribed when starting gonadorelin analogues due to the risk of tumour flare. This phenomenon is secondary to initial stimulation of luteinising hormone release by the pituitary gland resulting in increased testosterone levels. The BNF advises starting cyproterone acetate 3 days before the gonadorelin analogue.
4122
Compartments of the lower limb
Anterior Peroneal compartment Superficial posterior compartment Deep posterior compartment
4123
Muscles in the anterior compartment of the lower limb
Tibialis anterior EDL Peroneus tertius EHL
4124
Innervation of the anterior compartment of the lower limb
Deep pernoeal nerve
4125
Innervation of the peroneal compartment of the lower limb
Superficial peroneal nerve
4126
Innervation of the psoterior compartment of the lower limb
Tibial nerve
4127
Muscles in the peroneal compartment of the lower limb
Peroneus longus Peroneus brevis
4128
Muscles in the superficial posterior compartment of the lower limb
Gastrocnemius Soleus
4129
Muscles in the deep posterior compartment of the lower limb
FDL FHL Tibialis posterior
4130
Action of tibialis anterior
Dorsiflexis ankle Inverts foot
4131
Action of EDL
Extends lateral 4 toes, dorsiflexes ankle joint
4132
Action of peroneus tertius
Dorsiflexes ankle, everts foot
4133
Action of EHL
Dorsiflexes ankle joint, extends big toe
4134
Action of peronues longus
Everts foot, assits in plantar flexion
4135
Action of peroneus brevis
Plantar flexes the ankle joint
4136
Action of gastrocnemius
Plantar flexes the foot, may also flex the knee
4137
Action of soleus
Plantar flexor
4138
Action of FDL
Flexes lateral four toes
4139
Action of FHL
Flexes the great toe
4140
Action of tibialis posterior
Plantar flexor, inverts the foot
4141
A 73-year-old male presents with a collapse and is brought to the emergency department. On examination he has a cold, painful left hand and forearm.
Sudden arterial embolus will affect the axillary artery in up to 30% cases. Because of the acute nature of the condition there is no time for the development of a collateral circulation so the limb is usually pale and painful. Emboli occur usually occur as a result of atrial fibrillation. Fast atrial fibrillation can cause syncope and an acute embolus.
4142
A 52-year-old lady presents with an episode of nipple discharge. It is usually clear in nature. On examination the discharge is seen to originate from a single duct and although it appears clear, when the discharge is tested with a labstix it is shown to contain blood. Imaging and examination shows no obvious mass lesion.
The correct answer is Intraductal papilloma Intraductal papilloma usually cause single duct discharge. The fluid is often clear, although it may be blood stained. If the fluid is tested with a labstix (little point in routine practice) then it will usually contain small amounts of blood. A microdocechtomy may be performed.
4143
RFs for TCC bladder
Smoking Exposure to aniline dyes int he printing and textile industry Rubber manufacture Cyclophosphamide
4144
RFs for SCC bladder
Schistosomiasis BCG treatment Smoking
4145
A 20-year-old complains of severe pain and swelling of the scrotum after a cystoscopy. He had mumps as a child. The testis is tender. The urine dipstick is positive for leucocytes.
Epididymo-orchitis: acute pain and swelling after urological intervention. To differentiate from testicular torsion there is usually pyrexia and positive urine dipstick.
4146
An 8-year-old presents with scrotal swelling. He has just recovered from an acute viral illness with swelling of the parotid glands. On examination both testes are tender and slightly swollen.
Orchitis Orchitis may be associated with mumps viral infections.
4147
There is decreased secretion of which one of the following hormones in response to major surgery: Insulin Cortisol Renin Anti diuretic hormone Prolactin
Endocrine parameters reduced in stress response: ## Footnote Insulin Testosterone Oestrogen
4148
Hormones increased by stress response
GH Cortisol Renin ACTH Aldosterone Prolactin ADH Glucagon
4149
An 18-year-old female presents with 3 nodules in the right lobe of the thyroid. Clinically she is euthyroid and there is associated cervical lymphadenopathy. She has no family history of thyroid disease.
Papillary carcinoma Papillary thyroid cancer is the most common type of thyroid cancer and are the more common in females (M:F=1:3). Papillary tumours are more likely to develop lymphatic spread than follicular tumours.
4150
A 10-year-old boy undergoes a delayed open reduction and fixation of a significantly displaced supracondylar fracture. On the ward he complains of significant forearm pain and paraesthesia of the hand. Radial pulse is normal.
Fasciotomy The delay is the significant factor here. These injuries often have neurovascular compromise and inactivity now places him at risk of developing complications. In compartment syndrome the loss of arterial pulsation occurs late.
4151
A 28-year-old man falls onto an outstretched hand. On examination there is tenderness of the anatomical snuffbox. However, forearm and hand x-rays are normal.
Discharge home with futura splint and fracture clinic appointment This could well be a scaphoid fracture and should be temporarily immobilised pending further review. A futura splint will immobilise better than an arm sling for this problem.
4152
What can be used to classify open #s?
Gustilo and Anderson Classification System
4153
Components of Gustilo and Anderson
Grade 1: Low energy wound \<1cm Grade 2: \>1cm wound with moderate soft tissue damage Grade 3: High energy wound \>1cm with extensive soft tissue damage A: adeqate soft tissue coverage B: inadequate soft tissue coverage C: associated arterial injury
4154
A 43-year-old man has been troubled with dysphagia for many years. He is known to have achalasia and has had numerous dilatations. Over the past 6 weeks his dysphagia has worsened. At endoscopy a friable mass is noted in the oesophagus.
Squamous cell carcinoma The risk of squamous cell carcinoma of the oesophagus is increased in people with achalasia. The condition often presents late and has a poor prognosis.
4155
A Schatzki ring or Schatzki–Gary ring
is a narrowing of the lower esophagus that can cause difficulty swallowing (dysphagia). The narrowing is caused by a ring of mucosal tissue (which lines the esophagus) or muscular tissue.[1] A Schatzki ring is a specific type of "esophageal ring", and Schatzki rings are further subdivided into those above the esophagus/stomach junction (A rings),[2] and those found at the squamocolumnar junction in the lower esophagus (B rings).[3] Patients with Schatzki rings can develop intermittent difficulty swallowing or, more seriously, a completely blocked esophagus. The ring is named after the German-American physician Richard Schatzki.
4156
What are the critera for brain stem death testing
Deep coma of known aetiology. Reversible causes excluded No sedation Normal electrolytes
4157
Testing for brain death
Fixed pupils which do not respond to sharp changes in intensity of incident light No corneal reflex Absent VOR (no eye movements following the slow injection of at least 50ml of ice-cold water in each ear in turn- caloric test) No response to supraorbital pressure No cough reflex to bronchial stimulat or gagging response to pharyngeal stimulation No observed repiratory effort in response to disconnection of the ventilator for ~5 minutes,
4158
A 56-year-old man undergoes a difficult colonoscopy for assessment of a caecal cancer. 48 hours after the procedure he is admitted with septicaemia. His abdomen is soft and non tender. Blood cultures grow gram positive cocci.
Streptococcus bovis Streptococcus bovis septicaemia is associated with carcinoma of the colon. It also can also cause endocarditis.
4159
An 8-year-old child presents with enlarged tonsils that meet in the midline and are covered with a white film that bleeds when you attempt to remove it. He is pyrexial but otherwise well.
Acute bacterial tonsillitis Theme from April 2012 Exam In acute tonsillitis the tonsils will often meet in the midline and may be covered with a membrane. Individuals who are systemically well are unlikely to have diptheria.
4160
A 10-year-old child presents with enlarged tonsils that meet in the midline. Oropharyngeal examination confirms this finding and you also notice peticheal haemorrhages affecting the oropharynx. On systemic examination he is noted to have splenomegaly.
A combination of pharyngitis and tonsillitis is often seen in glandular fever. Antibiotics containing penicillin may produce a rash when given in this situation, leading to a mistaken label of allergy.
4161
A 62-year-old man is admitted with dull lower back pain and abdominal discomfort. On examination he is hypertensive and a lower abdominal fullness is elicited on examination. An abdominal ultrasound demonstrates hydronephrosis and intravenous urography demonstrated medially displaced ureters. A CT scan shows a periaortic mass
Retroperitoneal fibrosis Retroperitoneal fibrosis is an uncommon condition and its aetiology is poorly understood. In a significant proportion the ureters are displaced medially. In most retroperitoneal malignancies they are displaced laterally. Hypertension is another common finding. A CT scan will often show a para-aortic mass
4162
A 32-year-old man is admitted with a distended tense abdomen. He previously underwent a difficult appendicectomy 1 year previously and was discharged. At laparotomy the abdomen is filled with a gelatinous substance.
Pseudomyxoma peritonei Pseudomyxoma is classically associated with mucin production and the appendix is the commonest source. Pseudomyxoma peritoneii- Curative treatment is peritonectomy (Sugarbaker procedure) and heated intra peritoneal chemotherapy.
4163
A 73-year-old man develops disseminated intravascular coagulation following an abdominal aortic aneurysm repair. He receives an infusion of cryoprecipitate. What is the major constituent of this infusion? Factor VIII Factor IX Protein C Protein S Factor V
Cryoprecipitate Blood product made from plasma Usually transfused as 6 unit pool Indications include massive haemorrhage and uncontrolled bleeding due to haemophilia Composition AgentQuantity Factor VIII100IU Fibrinogen250mg von Willebrand factorVariable Factor XIIIVariable
4164
A 42-year-old lady who has systemic lupus erythematosus presents to the clinic with a 5 day history of a painful purple lesion on her index finger. On examination she has a tender red lesion on the index finger.
Oslers nodes Osler nodes are normally described as tender, purple/red raised lesions with a pale centre. These lesions occur as a result of immune complex deposition. These occur most often in association with endocarditis. However, other causes include SLE, gonorrhoea, typhoid and haemolytic anaemia.
4165
An 85-year-old man presents with a cough and haemoptysis. He has a modest smoking history of 15 pack years. He is found to have a tumour located in the right main bronchus, with no evidence of metastatic disease. He decides no undergo any treatment and he remains well for a further 12 months before developing symptomatic metastasis.
Squamous cell carcinoma Squamous cell carcinomas are reported to be more slow growing and are typically centrally located. Small cell carcinomas are usually centrally located. However, small cell carcinomas would seldom be associated with a survival of a year without treatment.
4166
A female infant is born by cesarean section at 38 weeks gestation for foetal distress. The attending paediatricians notice that she has a single palmar crease and an anti mongoloid slant to her eyes. Soon after the birth the mother tries to feed the child who has a projectile vomit about 10 minutes after feeding. On examination she has a soft, non distended abdomen.
Duodenal atresia Proximally sited atresia will produce high volume vomits which may or may not be bile stained. Abdominal distension is characteristically absent. Whilst under resuscitated children may be a little dehydrated they are seldom severely ill. The presence of Trisomy 21 (palmar and eye signs) increases the likelihood of duodenal atresia.
4167
A 34-year-old women trips over and falls into a bonfire whilst intoxicated at a party. She suffers burns to her arms, torso and face. These are calculated to be 25% body surface area. She is otherwise stable. The burns to the torso are superficial, her left forearm has a full thickness burn and the burns to her face are superficial. There is no airway compromise. She has received 1000ml of intravenous Hartman's solution, with a further 1000ml prescribed to run over 4 hours.
The correct answer is Transfer to regional burn centre once stabilised This women has been resuscitated and requires transfer for specialist management
4168
A 20-year-old man is trapped in a warehouse fire. He has sustained 60% burns to his torso and limbs. The limb burns are partial thickness but the torso burns are full thickness. He was intubated by paramedics at the scene and is receiving intravenous fluids. His ventilation pressure requirements are rising.
Escharotomy He requires an escharotomy as this will be contributing to impaired ventilation
4169
A 68-year-old man is on the colorectal ward following resection of an extremely large adenocarcinoma in his descending colon. During the operation he had a left hemicolectomy. As the tumour was invading surrounding structures, two loops of small bowel had to be excised along with a partial cystectomy. Now five days after the procedure he is managing well, with pain well controlled. His catheter has drained 2000ml in the last 24 hours. The abdominal surgical drain is still producing 200-300 ml of clear yellow fluid per day and you are concerned that his bladder wall repair following the partial cystectomy may be leaking urine. Which investigation should you order to offer the most definitive result to assess whether the bladder suture line has healed? Cystoscopy CT Ultrasound of the kidneys, ureters and bladder X-ray of the kidneys, ureters and bladder Cystogram
A cystogram involves passing radiopaque dye into the bladder, then performing radiographs to assess the course of the bladder contents. This provides evidence of whether there is any radiopaque fluid that has escaped the bladder and is free in the abdominal cavity.
4170
A 56-year-old man is involved in a road traffic accident. He is found to have a pelvic fracture. He reports that he has some lower abdominal pain. He has peritonism in the lower abdomen. The nursing staff report that he has not passed any urine. A CT scan shows evidence of free fluid.
Bladder rupture A pelvic fracture and lower abdominal peritonism should raise suspicions of bladder rupture (especially as this man cannot pass urine).
4171
A 52-year-old man falls off his bike. He is found to have a pelvic fracture. On examination he is found to have perineal oedema and on PR the prostate is not palpable. A urine dipstick shows blood.
Membranous urethral rupture A pelvic fracture and highly displaced prostate should indicate a diagnosis of membranous urethral rupture.
4172
How to differentiate between bulbar and membranous urethral ruputre
Bulbar rupture: Most common Straddle type injury e.g. bicycles Triad signs: urinary retention, perineal haematoma, blood at the meatus Membarnous rupture: Can be extra or intraperitoneal Commonly due to pelvic fracture Penile or perineal oedema/haematoma PR: prostate displaced upwards (beware coexisiting retroperitoneal haematomas as they make examination difficult)
4173
4175
With which of the following blood products is iatrogenic septicaemia with a gram positive organism most likely? Cryoprecipitate Platelets Packed red cells Factor VIII concentrate Factor IX concentrate
Platelets are stored at room temperature and must be used soon after collection. This places them at increased risk of culturing gram positive organisms. Iatrogenic infection with gram negative organisms is more likely with packed red cells as these are stored at 4 degrees. Infections with blood products of this nature are both rare.
4176
A 23-year-old rugby player falls directly onto his shoulder. There is pain and swelling of the shoulder joint. The clavicle is prominent and there appears to be a step deformity.
Acromioclavicular dislocation Acromioclavicular joint (ACJ) dislocation normally occurs secondary to direct injury to the superior aspect of the acromion. Loss of shoulder contour and prominent clavicle are key features. Note; rotator cuff tears rarely occur in the second decade.
4177
A 22-year-old man falls over and presents to casualty. A shoulder x-ray is performed, the radiologist comments that a Hill-Sachs lesion is present.
Glenohumeral dislocation A Hill-Sachs lesion is when the cartilage surface of the humerus is in contact with the rim of the glenoid. About 50% of anterior glenohumeral dislocations are associated with this lesion.
4178
Mondor's diease of the breast
Mondor's disease (also known as "Mondor's syndrome of superficial thrombophlebitis"[1]) is a rare condition which involves thrombophlebitis of the superficial veins of the breast and anterior chest wall. It sometimes occurs in the arm or penis.[2] In axilla, this condition is known as axillary web syndrome.[3] Patients with this disease often have abrupt onset of superficial pain, with possible swelling and redness of a limited area of their anterior chest wall or breast. There is usually a lump present, which may be somewhat linear and tender. Because of the possibility of the lump being from another cause, patients are often referred for mammogram and/or breast ultrasound.[4]
4179
Features of Pb poisoning
abdominal pain peripheral neuropathy (mainly motor) fatigue constipation blue lines on gum margin (only 20% of adult patients, very rare in children)
4180
A 28-year-old man undergoes a ileocaecal resection and end ileostomy for Crohn's disease. One year later he presents with a deep painful ulcer at his stoma site.
Pyoderma gangrenosum Associated with inflammatory bowel disease/RA Can occur at stoma sites Erythematous nodules or pustules which ulcerate Submit answer
4181
Triad of symptoms in fat embolism
Respiratory Neurological Petechial rash (tends to occur after the first 2 symptoms)
4182
A 35-year-old male presents with haematuria. He is found to have bilateral masses in the flanks. He has a history of epilepsy and learning disability.
Angiomyolipoma This patient has tuberous sclerosis. This is associated with angiomyolipoma, which is present in 60-80% patients. It is a benign lesion.
4183
A 73-year-old lady is undergoing chemotherapy for treatment of acute leukaemia. She develops symptoms of renal colic. Her urine tests positive for blood. A KUB x-ray shows no evidence of stones.
Uric acid Chemotherapy and cell death can increase uric acid levels. In this acute setting the uric acid stones are unlikely to be coated with calcium and will therefore be radiolucent.
4184
A 16-year-old boy presents with renal colic. His parents both have a similar history of the condition. His urine tests positive for blood. A KUB style x-ray shows a relatively radiodense stone in the region of the mid ureter.
Cystine Cystine stones are associated with an inherited metabolic disorder.
4185
Associated with chronic straining and constipation. Histology shows mucosal thickening, lamina propria replaced with collagen and smooth muscle (fibromuscular obliteration) Submit answer
Solitary rectal ulcer
4186
A 32-year-old man is involved in a house fire and sustains extensive partial thickness burns to his torso and thigh. Two weeks post operatively he develops oedema of both lower legs. The most likely cause of this is: Iliofemoral deep vein thrombosis Venous obstruction due to scarring Hypoalbuminaemia Excessive administration of intravenous fluids None of the above
Loss of plasma proteins is the most common cause of oedema developing in this time frame.
4187
Features of pulmoanry artery occlusion pressure monitoring
Indirect measure of left atrial pressure and thus filling pressure of the left heart. When combined with measurements of SVR and CO it is possible to accurately classify the potential cause of shock
4188
How to calculate SVR
Derived from aortic pressure, RAP and CO SVR= 80(mean aortic pressure-mean right atrial pressure)/CO
4189
Normal PAOP
8-12mmHg
4190
Low PAOP
\<5: hypovolaemia
4191
Low PAOP with pulmonary oedema
\<5= ARDS
4192
High PAOP
\>18: suggestive of overload e.g. cardiogenic pulmonary oedema
4193
A 2 month old baby presents with jaundice. He has an elevated conjugated bilirubin level. Diagnosis is confirmed by cholangiography during surgery.
Roux-en-Y portojejunostomy This child has biliary atresia. The aim is to avoid liver transplantation (however, most will come to transplant in time).
4194
Which one of the following is not a risk factor for the development of calcium oxalate and calcium phosphate renal stones? Bendroflumethiazide Aminophylline Acetazolamide Furosemide Prednisolone
Bendroflumethiazide may help prevent the formation of calcium based renal stones. It may however theoretically increase the risk of urate based stones
4195
What is the Mackler Triad for Boerhaave syndrome
Vomiting Thoracic pain Subcutaneous emphysema Commonly presents in middle aged men with a background of alcohol abuse
4196
A 52-year-old male presents with tearing central chest pain. On examination he has an aortic regurgitation murmur. An ECG shows ST elevation in leads II, III and aVF.
Proximal aortic dissection An inferior myocardial infarction and AR murmur should raise suspicions of an ascending aorta dissection rather than an inferior myocardial infarction alone. Also the history is more suggestive of a dissection. Other features may include pericardial effusion, carotid dissection and absent subclavian pulse.
4197
A 60-year-old male is admitted to A&E with a fall. He lives with his wife and still works as a restaurant manager. He has a past history of benign prostatic hypertrophy and is currently taking tamsulosin. He is otherwise fit and healthy. On examination there is right hip tenderness on movement in all directions. A hip x-ray confirms an intertrochanteric fracture.
ynamic hip screw The blood supply to the femoral head may be intact and the fracture should heal with compression type devices such as gamma nails or dynamic hip screws. The latter device being the most commonly performed therapeutic intervention.
4198
An 86-year-old retired pharmacist is admitted to A&E following a fall. She complains of right hip pain. She is known to have hypertension and is currently on bendrofluazide. She lives alone and mobilises with a Zimmer frame. Her right leg is shortened and externally rotated. A hip x-ray confirms a displaced intracapsular fracture.
Hemiarthroplasty Hemiarthroplasty is offered to older, less mobile individuals compared to fracture reduction and fixation in younger patients.
4199
A 74-year-old male is admitted to A&E with a fall. He is known to have rheumatoid arthritis and is on methotrexate and paracetamol. He lives alone in a bungalow and enjoys playing golf. He is independent with his ADLs. He complains of left groin pain, therefore has a hip x-ray which confirms a displaced intracapsular fracture.
Total hip replacement This patient has pre-existing joint disease, good level of activity and a relatively high life expectancy, therefore THR is preferable to hemiarthroplasty.
4200
Base excess
Calculated figure wich provides an estimate of the metabolic componenet of acid-base balance Defined as the amount of H+ ions that would be required to return the pH of the blood to 7.35 if the pCO2 were adjusted to normal BE \>+3: metabolic alkalsois BE \< -3= metabolic acidosis
4201
A 2 week old baby is referred to the surgical team by the paediatricians. They are concerned because the child has a painful area of macerated tissue at the site of the umbilicus. On examination a clear- yellowish fluid is seen to be draining from the umbilicus when the baby cries.
Persistent urachus A patent urachus will present with umbilical urinary discharge. The skin may become macerated if not properly cared for. The discharge is most likely to be present when intra-abdominal pressure is raised. It is associated with posterior urethral valves.
4202
A premature neonate is born by emergency cesarean section at 29 weeks gestation. He initially seems to be progressing well. However, the team are concerned because he becomes systemically septic and on examination has a swollen and erythematous umbilicus.
Omphalitis Infection from omphalitis may spread rapidly and cause severe sepsis especially in immunologically compromised, premature neonates.
4203
A baby boy is born by elective cesarean section at 39 weeks gestation. He initially seems to progress well and is discharged from hospital the following day. The parents bring the child to the clinic at 10 days of age and are concerned at the presence of a profuse and foul smelling discharge at the site of the umbilicus. On examination the umbilicus has some prominent granulation tissue. When the baby cries a small trickle of brownish fluid is seen to pass from the umbilicus.
Persistent vitello-intestinal duct A persistent vitello-intestinal duct may allow the persistent and ongoing discharge of small bowel content from the umbilicus. This fluid may be very irritant to the surrounding skin.
4204
A 63-year-old man presents with a locally unresectable gastrointestinal stromal tumour. Biopsies confirm that it is KIT positive.
Imatinib Imatinib is licensed for treatment of GIST in the United Kingdom for this situation. The guidance from the National Institute of Clinical evidence is that patients be reviewed at 12 weeks after initiating therapy.
4205
A 28-year-old man undergoes an ileocaecal resection to treat terminal ileal Crohns disease. Post operatively he attends the clinic and complains of diarrhoea. His CRP is within normal limits and small bowel enteroclysis shows no focal changes. Which of the following interventions is most likely to be beneficial? 5 ASA drugs Azathioprine Pulsed methylprednisolone Infliximab Oral cholestyramine
Malabsorption of bile salts is a common cause of diarrhoea following ileal resection. A normal small bowel study and CRP effectively excludes active Crohns disease and therefore immunomodulator drugs are not appropriate.
4206
A 78-year-old man is referred to the clinic by his general practitioner. For many years he noticed a smooth swelling approximately 5cm anterior to the tragus of his right ear. Apart from being a heavy smoker he has no co-morbidities. What is the most likely diagnosis? ## Footnote Pleomorphic adenoma Liposarcoma Warthins tumour Adenocarcinoma None of the above
Warthins tumours are most common in elderly smokers. They have a relatively benign and indolent course. They are usually well circumscribed as illustrated below:
4207
An 18 month old boy is brought to the emergency room by his parents. He was found in bed with a nappy filled with dark red blood. He is haemodynamically unstable and requires a blood transfusion. Prior to this episode he was well with no prior medical history. What is the most likely cause? ## Footnote Necrotising enterocolitis Anal fissure Oesophageal varices Meckels diverticulum Crohns disease
Meckels diverticulum is the number one cause of painless massive GI bleeding requiring a transfusion in children between the ages of 1 and 2 years.
4208
Margins of excision related to Breslow thickness 0-1mm thick
1cm
4209
Margins of excision related to Breslow thickness 1-2mm thick
1-2cm depending on site and pathological features
4210
Margins of excision related to Breslow thickness 2-4mm thick
2-3cm depending on site and pathological features
4211
Margins of excision related to Breslow thickness \>4mm thick
3cm
4212
A 23-year-old man suffers a road traffic accident and is due for emergency surgery. Which anaesthetic agent carries the greatest risk of adrenal suppression in the peri-operative period? ## Footnote Ketamine Etomidate Sevoflurane Desflurane Propofol
Although etomidate is widely used in emergency settings due to its favourable haemodynamic profile and cerebroprotective effects, it is associated with depressed corticosteroid synthesis by inhibition of 11-beta-hydroxylase. Adrenal suppression can increase mortality, especially in the post-operative recovery period.
4213
intravenous anaesthetic agent barbiturate: enhance effects of GABA (less specific than benzodiazepines) risk of severe vasospasm → tissue necrosis if accidentally injected into vein
Thiopentone
4214
intravenous anaesthetic agent mode of action unknown rapidly metabolised therefore fast recovery adverse effects: pain on injection site, cardiovascular and respiratory depressant can be used as an infusion
Proprofol
4215
intravenous anaesthetic agent similar to thiopentone but with less cardiovascular and respiratory depression adverse effects: adrenocortical suppression, excitatory effects during induction and recovery Submit answer
Etomidate
4216
A 56-year-old man presents with an adenocarcinoma of the mid oesophagus. Staging investigations show no metastatic disease and he is otherwise fit.
McKeown oesophagectomy He requires a total (3 stage oesophagectomy). This is also called a McKeown oesophagectomy. Ivor Lewis type resections are concluded in the mid third of the oesophagus and would not adequately treat this disease
4217
A 43-year-old man with an adenocarcinoma of the distal oesophagus. His staging investigations are negative for metastatic disease.
Ivor Lewis oesophagectomy This requires an Ivor Lewis oesophagectomy with resection of the distal oesophagus and an intrathoracic anastomosis
4218
A 43-year-old lady presents with severe chest pain. Investigations demonstrate a dissecting aneurysm of the ascending aorta which originates at the aortic valve. What is the optimal long term treatment? Endovascular stent Medical therapy with beta blockers Medical therapy with ACE inhibitors Sutured aortic repair Aortic root replacement
Proximal aortic dissections are generally managed with surgical aortic root replacement. The proximal origin of the dissection together with chest pain (which may occur in all types of aortic dissection) raises concerns about the possibility of coronary ostial involvement (which precludes stenting). There is no role for attempted suture repair in this situation.
4219
A 48-year-old lady presents with discomfort in the right breast. On examination she has a discrete soft fluctuant area in the upper outer quadrant of her right breast. A mammogram is performed and a "halo sign" is seen by the radiologist.
Breast cyst Lesions such as breast cysts compress the underlying fat and produce a radiolucent area (halo sign). If symptomatic these cysts should be aspirated.
4220
A 55-year-old lady presents with discomfort in the right breast. On clinical examination a small lesion is identified and clinical appearances suggest fibroadenoma. Imaging confirms the presence of a fibroadenoma alone. A core biopsy is taken, this confirms the presence of the fibroadenoma. However, the pathologist notices that a small area of lobular carcinoma in situ is also present in the biopsy. What is the best management? Whole breast irradiation Simple mastectomy Mastectomy and sentinal lymph node biopsy Wide local excision and sentinel lymph node biopsy Breast MRI scan
Lobular carcinoma in situ has a low association with invasive malignancy. It is seldom associated with microcalcification and therefore MRI is the best tool for determining disease extent. Resection of in situ disease is not generally recommended and most surgeons would simply pursue a policy of close clinical and radiological follow up.
4221
An 80-year-old woman has a hip fracture. Her calcium is normal. She has never been given a diagnosis of osteoporosis.
Risedronate and calcium supplements The osteoporosis guidelines state if a postmenopausal woman has a fracture she should be put on bisphosphonates (there is no need for a DEXA scan).
4222
A 60-year-old man presents with recurrent renal stones. He is found to have a calcium of 2.72 (elevated) and a PTH of 12 (elevated).
Exploration and parathyroidectomy This patient has primary hyperparathyroidism and nephrolithiasis, which is an indication for parathyroidectomy.
4223
An 82-year-old woman from a nursing home is admitted to the orthopaedic ward with a hip fracture. She is acutely confused and agitated. Her Calcium is 2.95 (elevated).
Intravenous fluid (0.9% N.Saline) This patient needs rehydration due to hypercalcaemia. An intravenous bisphosphonate is indicated if the Ca is above 3.
4224
A 49-year-old woman presents with a tender lump around the areola associated with a green nipple discharge.
Mammary duct ectasia
4225
A 16-year-old boy is hit by a car and sustains a blow to the right side of his head. He is initially conscious but on arrival in the emergency department is comatose. On examination his right pupil is fixed and dilated. The neurosurgeons plan immediate surgery. What type of initial approach should be made? Left parieto-temporal craniotomy Right parieto-temporal craniotomy Posterior fossa craniotomy Left parieto-temporal burr holes None of the above
A unilateral dilated pupil is a classic sign of transtentorial herniation. The medial aspect of the temporal lobe (uncus) herniates across the tentorium and causes pressure on the ipsilateral oculomotor nerve, interrupting parasympathetic input to the eye and resulting in a dilated pupil. In addition the brainstem is compressed. As the ipsilateral oculomotor nerve is being compressed, craniotomy (rather than Burr Holes) should be made on the ipsilateral side.
4226
Risk factors for developing TURP syndrome?
Surgical time \>1hr Height of bag \>70cm Resected \>60h Large blood loss Perforation Large amount of fluid used Poorly controlled CHF
4227
A 3-month old infant presents with recurrent abdominal pain, colicky in nature and intestinal obstruction. Imaging results reveal a right sided midline defect where there is herniation of the transverse colon into the thoracic cavity. What is the most likely diagnosis? Bochdalek hernia Umbilical hernia Para umbilical hernia Femoral hernia Morgagni hernia
The right sided midline defect is referring to herniation through the foramen of Morgagni, 60% of Morgagni hernias contain transverse colon whereas Bochdalek hernias tend to be left sided, containing stomach.
4228
A 26-year-old man presents to the emergency department with a swelling over his left elbow after a fall on an outstretched hand. On examination, he has tenderness over the proximal part of his forearm, and has severely restricted supination and pronation movements.
Fracture of the radial head is common in young adults. It is usually caused by a fall on the outstretched hand. On examination, there is marked local tenderness over the head of the radius, impaired movements at the elbow, and a sharp pain at the lateral side of the elbow at the extremes of rotation (pronation and supination).
4229
A 56-year-old lady presents with a painful swelling over the lower end of the forearm following a fall. Imaging reveals a distal radial fracture with disruption of the distal radio-ulnar joint.
Galeazzi fractures occur after a fall on the hand with a rotational force superimposed on it. On examination, there is bruising, swelling and tenderness over the lower end of the forearm. X- Rays reveal a displaced fracture of the radius and a prominent ulnar head due to dislocation of the inferior radio-ulnar joint.
4230
A 3 day old neonate is developing increasing problems with feeding. On examination she has a pan systolic murmur and her forearms have not developed properly.
Oesophageal atresia This child has VACTERL, which is a combination of Vertebral, Ano-rectal, Cardiac, Tracheo-oesophageal, Renal and Radial limb anomalies. Half of babies with oesophageal atresia will have VACTERL.
4231
A 63-year-old man is admitted with severe right sided loin pain to the Emergency Department. A urine dipstick shows blood +++, leucocytes +, protein +. An abdominal radiograph is therefore ordered which shows a stag-horn calculus in the right renal pelvis. What are stag-horn calculi normally composed of? ## Footnote Xanthine Magnesium ammonium phosphate Calcium oxalate Uric acid Magnesium calcium phosphate
Magnesium ammonium phosphate
4232
Relations of the cavernous sinus
Medial: pituitary fossa, Sphenoid sinus Lateral: temporal lobe
4233
Contents of the cavernous sinus
Lateral wall from top to bottom Oculomotor nerve Trochlear nerve V1 V2 Contents of the sinus: from medial to lateral Internal carotid artery and sympathetic plexus Abducens nerve
4234
pain, opthalmoplegia, proptosis, trigeminal nerve lesion (opthalmic branch) and Horner's syndrome.
Cavernous sinus syndrome
4235
A 38-year-old women undergoes a gastric bypass procedure. Post operatively she attends the clinic and complains that following a meal she develops vertigo and develops crampy abdominal pain. What is the most likely underlying explanation? Insulin resistance Irritable bowel syndrome Biliary colic Dumping syndrome Enterogastric reflux
Dumping syndrome, which can be divided into early and late, may occur following gastric surgery. It occurs as a result of a hyperosmolar load rapidly entering the proximal jejunum. Osmosis drags water into the lumen, this results in lumen distension (pain) and then diarrhoea. Excessive insulin release also occurs and results in hypoglycaemic symptoms.
4236
A 15 year-old boy presents to the out-patient clinic with tiredness, recurrent throat and chest infections, and gradual loss of vision. Multiple x-rays show brittle bones with no differentiation between the cortex and the medulla.
Osteopetrosis is an autosomal recessive condition. It is commonest in young adults. They may present with symptoms of anaemia or thrombocytopaenia due to decreased marrow space. Radiology reveals a lack of differentiation between the cortex and the medulla described as marble bone. These bones are very dense and brittle.
4237
A 5-year-old boy presents with a painful limp. The symptoms have been present for 8 weeks. Two hip x-rays have been performed and appear normal.
Perthes' disease should be suspected in boys over 4 years old presenting with a limp. Early disease can be missed on x-ray. MRI is increasingly replacing bone scans as the second line investigation of choice
4238
A 70-year-old coal miner presents with 3 weeks of haematuria and bruising. He is normally fit and well. He is on no medications. His results reveal: Hb 9.0 WCC 11 Pl 255 PT 16 (normal) APTT 58 (increased) Thrombin time 20 (normal).
Acquired haemophilia Factor 8 acquired disorder. The elderly, pregnancy, malignancy and autoimmune conditions are associated with acquired haemophilia. Prolonged APTT is key to the diagnosis. Management involves steroids.
4239
Epiphysitis of the vertebral joints is the main pathological process Predominantly affects adolescents Symptoms include back pain and stiffness X-ray changes include epiphyseal plate disturbance and anterior wedging Clinical features include progressive kyphosis (at least 3 vertebrae must be involved) Minor cases may be managed with physiotherapy and analgesia, more severe cases may require bracing or surgical stabilisation
Scheuermann's disease
4240
Consists of curvature of the spine in the coronal plane Divisible into structural and non structural, the latter being commonest in adolescent females who develop minor postural changes only. Postural scoliosis will typically disappear on manoeuvres such as bending forwards Structural scoliosis affects \> 1 vertebral body and is divisible into idiopathic, congential and neuromuscular in origin. It is not correctable by alterations in posture Within structural scoliosis, idiopathic is the most common type Severe, or progressive structural disease is often managed surgically with bilateral rod stabilisation of the spine
Scoliosis
4241
Congenital or acquired deficiency of the pars interarticularis of the neural arch of a particular vertebral body, usually affects L4/ L5 May be asymptomatic and affects up to 5% of the population Spondylolysis is the commonest cause of spondylolisthesis in children Asymptomatic cases do not require treatment
Spondylolysis
4242
This occurs when one vertebra is displaced relative to its immediate inferior vertebral body May occur as a result of stress fracture or spondylolysis Traumatic cases may show the classic "Scotty Dog" appearance on plain films Treatment depends upon the extent of deformity and associated neurological symptoms, minor cases may be actively monitored. Individuals with radicular symptoms or signs will usually require spinal decompression and stabilisation
Spondylolisthesis
4243
An 18-year-old student is involved in a car crash, with another car crashing into the side of the car. A chest x-ray shows an indistinct left hemidiaphragm.
Diaphragmatic rupture A lateral blunt injury during a road traffic accident is a common cause of diaphragmatic rupture. Diagnosis is usually evident on chest x-ray. CXR changes include non visible diaphragm, bowel loops in the hemithorax and displacement of the mediastinum. In most cases direct surgical repair is the best option.
4244
A 19-year-old student falls from a 2nd floor window. He is persistently hypotensive despite fluid resuscitation. A chest x-ray shows depression of the left main bronchus and deviation of the trachea to the right. Lung markers can be seen in the peripheries of both thoraces.
Aorta rupture He has a deceleration injury, with persistent hypotension (contained haematoma). This should indicate aorta rupture. Widened mediastinum may not always be present on a chest x-ray. A CT angiogram will provide clearer evidence of the extent of injury. The presence of persistent hypotension, from a early stage is more consistent with haematoma than a tension pneumothorax in which it occurs as a final periarrest phenomena.
4245
Intra-articular fracture of the first carpometacarpal joint Impact on flexed metacarpal, caused by fist fights X-ray: triangular fragment at ulnar base of metacarpal
Bennett's fracture
4246
A patient is recovering from a Sistrunk's procedure, what lesion was treated with this operation?
Thyroglossal cyst This is the procedure for excision of the cyst and its associated track. Excision must be complete and thus a small segment of the hyoid bone is removed to gain access to the upper part of the cyst tract.
4247
A patient presents with a facial nerve palsy. This occurred following repeat excision of a facial lump. The histology report remarks on the biphasic appearance of the lesion and mucinous connective tissue.
Pleomorphic adenoma of the parotid The histological features are as described with a classic biphasic (mixed stromal and epithelial elements), although benign local recurrence can complicate incomplete excision. As this is a benign lesion direct extension into the facial nerve is unlikely to occur. Facial nerve injury can happen during repeat parotid surgery.
4248
A 56-year-old man is admitted with passage of a large volume of blood per rectum. On examination he is tachycardic, his abdomen is soft, although he has marked dilated veins on his abdominal wall. Proctoscopy reveals large dilated veins with stigmata of recent haemorrhage.
IV terlipressin Rectal varices are a recognised complication of portal hypertension. In the first instance they can be managed with medical therapy to lower pressure in the portal venous system. TIPSS may be considered. Whilst band ligation is an option, attempting to inject these in same way as haemorroids would carry a high risk of precipitating further haemorrhage.
4249
A 73-year-old lady is admitted with dark red PR bleeding. She undergoes an OGD which is normal. Digital rectal examination shows blood but no masses. She becomes tachycardic and BP is 95/40.
Angiography of mesenteric artery This women is actively bleeding and mesenteric angiography may localise the bleeding. Colonoscopy in this situation is seldom helpful or successful.
4250
A 68-year-old man with ulcerative colitis is admitted with an exacerbation. You are called to see him because he is having brisk PR bleeding. He has been on Intravenous hydrocortisone for 5 days. The gastroenterologists have done an OGD to exclude a duodenal ulcer, this was normal.
A 68-year-old man with ulcerative colitis is admitted with an exacerbation. You are called to see him because he is having brisk PR bleeding. He has been on Intravenous hydrocortisone for 5 days. The gastroenterologists have done an OGD to exclude a duodenal ulcer, this was normal.
4251
Mutation of PTEN gene on chromosome 10q22, dominant Macrocephaly Multiple intestinal hamartomas Multiple trichilemmomas 89% risk of cancer at any site 16% risk of colorectal cancer
Cowden disease
4252
Biallelic mutation of mut Y human homologue (MYH) on chromosome 1p, recessive Multiple colonic polyps Later onset right sided cancers more common than in FAP 100% cancer risk by age 60
MYH associated polyposis
4253
A 30-year-old woman presents with pain and swelling of the left shoulder. There is a large radiolucent lesion in the head of the humerus extending to the subchondral plate.
Giant cell tumour Giant cell tumours on x-ray have a 'soap bubble' appearance. They present as pain or pathological fractures. They commonly metastasize to the lungs.
4254
A 72-year-old woman has a lumbar vertebral crush fracture. She has hypocalcaemia and a low urinary calcium.
Osteomalacia Hypocalcemia and low urinary calcium are biochemical features of osteomalacia.
4255
A 16-year-old boy presents with severe groin pain after kicking a football. Imaging confirms a pelvic fracture. A previous pelvic x-ray performed 2 weeks ago shows a lytic lesion with 'onion type' periosteal reaction.
A Ewings sarcoma is most common in males between 10-20 years. It can occur in girls. A lytic lesion with a lamellated or onion type periosteal reaction is a classical finding on x-rays. Most patients present with metastatic disease with a 5 year prognosis between 5-10%.
4256
A 22-year-old man suffers 20% partial and full thickness burns in a house fire. There is an associated inhalational injury. It is decided to administer intravenous fluids to replace fluid losses. Which of the intravenous fluids listed below should be used for initial resuscitation? Dextran 40 5% Dextrose Fresh frozen plasma Hartmans solution Blood
In most units a crystalloid such as Hartmans (Ringers lactate) is administered initially. Controversy does remain and some units do prefer colloid. Should this leak in the interstial tissues this may increase the risk of oedema.
4257
Indications for fluid resus in burns
: \>15% total body area burns in adults (\>10% children) The main aim of resuscitation is to prevent the burn deepening Most fluid is lost 24h after injury First 8-12h fluid shifts from intravascular to interstitial fluid compartments Therefore circulatory volume can be compromised. However fluid resuscitation causes more fluid into the interstitial compartment especially colloid (therefore avoided in first 8-24h) Protein loss occurs
4258
Fluid resuscitation formula in burns
Parkland formula (crystalloid only) Total fluid requirement in 24h= 4ml x total burn surface area x bodyweight (kg) 1/2 in first 8 hours. Aim for urine output of 0.5-1ml/kg/hr in adults (increase rate of fluid to achieve this) Starting point of resus is time of injury
4259
Fluid management in burns after 24h
Colloid infusion is begun at a rate of 0.5ml x total burn surface area x bodyweight Maintenance crystalloid is continued at rate of 1.5ml x total burn SA x weight Colloids used include albumin and FFP Antioxidants may be used to minimise inflammatory cascade High tension electrical injuries and inhalational injuries require more fluid.
4260
A 17-year-old male is admitted with lower abdominal discomfort. He has been suffering from intermittent right iliac fossa pain for the past few months. His past medical history includes a negative colonoscopy and gastroscopy for iron deficiency anaemia. The pain is worse after meals. Inflammatory markers are normal.
Meckels diverticulum This scenario should raise suspicion for Meckels as these may contain ectopic gastric mucosa which may secrete acid with subsequent bleeding and ulceration
4261
Undisplaced intracapsular fracture Nil comorbidities
Internal fixation, especially if young
4262
Undisplaced intracapsular fracture Major illness or advanced organ specific disease
Hemiarthroplasty
4263
Displaced intracapsular fracture No comorbidities \<70y/o
Internal fixation if possible Hip aryhoplasty if not
4264
Displaced intracapsular fracture No comorbidities \>70 years old
THR
4265
Displaced intracapasular fracture Major comorbidities/immobile
Hemiarthroplasty
4266
Extracapsular fracture (non special type)
Dynamic hip screw
4267
Extracapsular fracture (reverse oblique, transverse or subtronchateric)
Intramedulllary device
4268
A 72-year-old retired teacher is admitted to A&E with a fall and hip pain. He is normally fit and well. He lives with his son in a detached, 2 storey house. A hip x-ray confirms an extracapsular fracture.
Dynamic hip screw Extracapsular fractures should be treated surgically. Since the blood supply to the femoral head is not compromised joint replacement is not usually warranted
4269
A 72-year-old retired teacher is admitted to A&E with a fall and hip pain. He is normally fit and well. He lives with his son in a detached, 2 storey house. A hip x-ray confirms an subtrochanteric fracture.
Intramedullary device Intramedullary device is normally recommended for reverse oblique, transverse or subtrochanteric fractures.
4270
An 86-year-old retired pharmacist is admitted to A&E following a fall. She complains of right hip pain. She is known to have hypertension and is currently on bendrofluazide. She lives alone and does not mobilise. Her right leg is shortened and externally rotated. A hip x-ray confirms a displaced intracapsular fracture.
Hemiarthroplasty non cemented prosthesis This patient warrants a hemiarthroplasty due to reduced mobility and older age. The anterolateral approach is recommended in the SIGN guidelines. In this case most surgeons would not use a cemented prosthesis.
4271
Theme: Muscle relaxants A.Atracurium B.Suxamethonium C.Pancuronium D.Vecuronium E.Curare An agent that is degraded by hydrolysis and may produce histamine release. An agent which should be avoided in a 23-year-old man with burns and bilateral tibial fractures after being trapped in a car accident for 2 hours An agent with a half life of less than 10 minutes.
Atracurium Atracurium is degraded by a process of ester hydrolysis. This uses non specific plasma esterases. Suxamethonium Suxamethonium may induce hyperkalaemia as it induces generalised muscular contractions. In patients with likely extensive tissue necrosis this may be sufficient to produce cardiac arrest. Suxamethonium Suxamethonium is extremely rapidly metabolised, acetylcholinesterases degrade the drug within minutes. In patients who lack this enzyme the drug may last far longer.
4272
Laryngocoele
Air filled sac that communicates with the larynx Can be congenital or acquired (e.g. due to high pressure- COPD) If it is limited to the paraglottic space it presents with stridor and hoarseness. If it protrudes through the thyrohyoid membrane it presents as a reducible lump in the anterior triangle of the neck which recurs with coughing, sneezing, etc.
4273
What is a fistula? What is the exception
Abnormal connection between two epithelial surfaces. AV fistula which is a connection between two endothelial surfaces
4274
Hernia through the triangle bounded by external oblique, lat dorsi and iliac crest?
Petit hernia (lumbar hernia)
4275
Hernia passing through a traingle bounded by 12th rib, sacrospinalis muscle medially and interanl oblique laterally
Grynfelt hernia
4276
Radiographic triad in splenic injury
Elevated left hemidiaphragm Left lower lobe atelectasis Left pleural effusion
4277
Describe the levles of foot amputaiton
4278
Primary lesions giving rise to painful arc?
Incomplete tear of supraspinatus Chronic supraspinatus tendonitis Subacromial bursitis Crack fracture of the greater tuberosity
4279
Differentiating between supraspinatus tendonitis and impingement syndrome
Full can test against resistance- weakness +/- supraspinatus lesion or tear dependent on degree of weakness Empty can test force, assess for weakness or pain impingement= painful arc
4280
Components of Whipple's Procedure 4 things removed 3 anastomoses
Pancreatic head, common bile duct and gallbladder, distal stomach and some of the duodenum. 3 anastomoses: hepato-jejnostomy, pancreatic jejunostomy and a gastrojejunostomy
4281
Schwart test
Saphena varix will demonstrate a fluid thrill when the greater saphenous vein is tapped distally
4282
Anatomy of Kocher's incision
3-5cm below the costal margin Anterior rectus sheath exposed and divided along the line of excision exposing the rectus muscles which may then be divdided, taking care to enure haemostasis when branches of the superior epigastric vessels are sacrificed. Incision is extended through the lateral abdominal wall muscles which are split to allow better access. 8th and 9th intercostal nerves lie between the IO and transversus muscles. 8th nerve often sacrificed. Incision is deepened through the posterior rectus sheath and peritoneum.