Urinary System Flashcards

(368 cards)

1
Q

Definition of bacteriuria?

A

o presence of bacteria in the urine. This may be symptomatic or asymptomatic. Asymptomatic bacteriuria should be confirmed by two consecutive urine samples

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2
Q

Definition of UTI?

A

o presence of characteristic symptoms and significant bacteriuria from kidneys to bladder
o >105 (cfu/ml)

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3
Q

Types of UTI?

A

o Lower UTI = infection of the bladder (cystitis)

o Upper UTI = infection of kidney and ureters (acute pyelonephritis)

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4
Q

Classifications of UTI?

A

o Uncomplicated – normal renal tract/function

o Complicated – abnormal renal tract, obstruction, decreased renal function, immunocompromised

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5
Q

Epidemiology of UTIs?

A
  • Incidence is 5% in UK
  • More common in females due to short urethra
  • 40% have genitourinary anomalies
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6
Q

Risk factors of UTIs?

A
o	Women
o	Sexual intercourse
o	Catheter
o	Abnormality of renal tract
o	Antibiotic use
o	Pregnancy
o	Immunocompromise
o	Diabetes Mellitus
o	Spermide
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7
Q

Causative organisms of UTIs?

A

o E. coli in 90% of cases
o Proteus (present under prepuce)
o Klebsiella
o Enterococcus faecalis
o Saprophytic staphylococci (young women)
o Pseudomonas (may indicate structural damage in urinary tract)

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8
Q

Symptoms of lower UTIs?

A
o	Dysuria
o	Frequency
o	Urgency
o	Haematuria
o	Suprapubic discomfort
o	Burning
o	Cloudy urine with offensive smell
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9
Q

Investigations in lower UTI?

A
  • Urine dipstick MSU
    o Leukocytes and nitrites, haematuria and proteinuria
  • Urine M, C&S
    o Male, child under 16, pregnant, very ill
    o May show leukocytes, RBC commonly seen, renal pathology if crystals or granular casts found
  • Renal USS (KUB)
    o If recurrent or complicated
  • Bloods
    o FBC, U&Es, CRP, cultures if unwell
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10
Q

Management of lower UTI - referral?

A
  • Referral to hospital if sepsis suspected
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11
Q

Management of lower UTI - general advice?

A

o Paracetamol for pain
o Hygiene: clean perineum front to back
o Increase fluid intake
o Voiding after intercourse

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12
Q

Management of lower UTI - in non-pregnant women?

A

o Back-up antibiotic or immediate prescription, depending on clinical picture
 Back-up prescription should be used if no improvement in 48 hours of taking antibiotic or worsens

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13
Q

Management of lower UTI - non-pregnant women - antibiotics - first & second choice?

A

First Choice
• Nitrofurantoin (if eGFR>45) 100mg MR BD for 3 days
• Trimethoprim 200mg BD for 3 days

Second Choice (worsening UTI on first choice for >48 hours)
•	Nitrofurantoin (if eGFR>45 and not first choice) 100mg MR BD for 3 days
•	Pivmecillinam 400mg initial dose then 200mg TDS for 3 days
•	Fosfomycin 3g single dose sachet
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14
Q

Management of lower UTI - pregnant women, men and children - investigations?

A

 Midstream urine for M, C & S in pregnant women, men and children <16

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15
Q

Management of lower UTI - antibiotics children <16 years old - under 3 months?

A

• Under 3 months – refer to paediatric specialist

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16
Q

Management of lower UTI - antibiotics children <16 years old - over 3 months?

A

o First Choice
 Nitrofurantoin (if eGFR>45) for 3 days
 Trimethoprim for 3 days

o Second choice
 Nitrofurantoin (if eGFR>45) for 3 days
 Amoxicillin for 3 days
 Cefalexin for 3 days

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17
Q

Management of lower UTI - antibiotics men first choice?

A
o	Nitrofurantoin (if eGFR>45) 100mg MR BD for 7 days
o	Trimethoprim 200mg BD for 7 days

Follow up in 48 hours

If not working consider alternative diagnosis

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18
Q

Management of lower UTI - antibiotics - pregnant women - first & second choice?

A
•	First choice
o	Nitrofurantoin (if eGFR >45) 100mg MR BDS for 7 days

Second choice
o Amoxicillin (only if cultures results available) 500mg TDS for 7 days
o Cefalexin 500mg BDS for 7 days

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19
Q

Management of lower UTI - antibiotics - in asymptomatic bacteriuria?

A

• Nitrofurantoin, amoxicillin or cefalexin

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20
Q

Management of lower UTI - catheterised patients - general management?

A

o Remove catheter or changing as soon as possible if been in place for >7 days
o Obtain urine sample via sampling port

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21
Q

Management of lower UTI - catheterised patients - non-pregnant women and men >16 - antibiotics if lower symptoms?

A

o First choice
 Nitrofurantoin, trimethoprim, amoxicillin (only if cultures available)

o Second choice
 Pivmecillinam

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22
Q

Management of lower UTI - catheterised patients - non-pregnant women and men >16 - antibiotics if upper symptoms?

A

o First choice
 Cefalexin, ciprofloxacin, co-amoxiclav, trimethoprim

o First choice IV
 Co-amoxiclav, cefuroxime, ceftriaxone, gentamicin, amikacin

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23
Q

Management of lower UTI - catheterised patients - pregnant women - antibiotics?

A
  • First choice oral – cefalexin

* First choice IV - cefuroxime

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24
Q

Management of lower UTI - catheterised patients - children <16 - antibiotics?

A

Under 3 months – refer to paediatrics

Over 3 months
o First choice oral
 Trimethoprim, amoxicillin, cefalexin, co-amoxiclav
o First choice IV
 Co-amoxiclav, cefuroxime, ceftriaxone, gentamicin, amikacin

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25
Management of recurrent UTIs - definiton of recurrent?
at least 2 episodes within 6 months, or 3 or more within 12 months
26
Management of recurrent UTIs - when to refer?
 Men >16  People with recurrent upper UTI  People with recurrent lower UTI when underlying cause unknown  Pregnant women
27
Management of recurrent UTIs - general measures?
 Non-pregnant women may wish to try D-mannose or cranberry products  Avoid douching  Wipe from front to back after defaecation  Avoid delay in post-coital urination  Hydration important
28
Management of recurrent UTIs - antibiotic prophylaxis - men and pregnant women?
First choice o Trimethoprim 200mg when exposed to trigger or 100mg at night o Nitrofurantoin 100mg when exposed to trigger or 50mg at night Second choice o Amoxicillin 500mg when exposed to trigger or 250mg at night o Cefalexin 500mg when exposed to trigger or 125mg at night • Review in 6 months
29
Management of recurrent UTIs - antibiotic prophylaxis - non-pregnant women?
* Vaginal oestrogen (estriol cream) for postmenopausal women with recurrent UTI if behavioural and personal hygiene measures are not effective * Can consider single-dose antibiotic prophylaxis or daily antibiotic prophylaxis if needed
30
When to refer lower UTI to specialist - in women?
 Recurrent lower UTI when cause unknown
31
When to refer lower UTI to specialist - in men?
 Ongoing symptoms despite antibiotic treatment  Suspected bladder outlet obstruction, Hx of pyelonephritis, urinary calculi or previous GU surgery  Recurrent episodes of UTI (2 or more in 6 months)
32
Further investigations needed in children with UTI - When to arrange US of UT?
 During acute infection in all children with atypical infection: • Poor urine flow, abdominal/bladder mass, raised creatinine, sepsis, failure to respond to antibiotics within 48 hours, non-E.coli organism  During acute infection if child <6 months with recurrent UTI  Within 6 weeks if child >6 months with recurrent UTI  Within 6 weeks if <6 months with first-time UTI that responds to treatment
33
Further investigations needed in children with UTI - other tests needed and when?
o Dimercaptosuccinic acid scintigraphy (DMSA) carried out within 4-6 months of acute infection if:  All children <3 years with atypical or recurrent UTI  All children >3 years or over with recurrent UTIs
34
Definition of recurrent UTI in children?
* 2 or more UTI with acute pyelonephritis or, * 1 episode of acute pyelonephritis + one or more lower UTI with cystitis or, * 3 or more UTI with cystitis
35
When referred to secondary care for UTI - what further tests can be performed?
o US KUB o CT KUB o Cystoscopy o Urodynamic studies
36
Risk factors for pyelonephritis?
``` o Women o Sexual intercourse o Catheter o Abnormality of renal tract o Antibiotic use o Pregnancy o Immunocompromise o Diabetes Mellitus o Spermide ```
37
Causative organisms of pyelonephritis?
o E. coli in 90% of cases o Proteus (present under prepuce) o Klebsiella o Enterococcus faecalis o Saprophytic staphylococci (young women) o Pseudomonas (may indicate structural damage in urinary tract)
38
Symptoms of acute pyelonephritis?
``` o UTI symptoms (dysuria, frequency, urgency) o Malaise o Fever o Loin pain +/- back pain o Vomiting o Rigors ```
39
Investigations in pyelonephritis?
- Urine dipstick MSU o Leukocytes and nitrites, haematuria and proteinuria - Urine M, C&S o Obtain before starting antibiotics
40
When to refer to hospital - with suspected pyelonephritis?
o Septic signs o Significantly dehydrated or unable to take oral fluids o Pregnant o Structural or functional abnormality of GU tract o Immunosuppression o Diabetes
41
Management of pyelonephritis - general measures?
 Paracetamol for pain  Increase fluid intake  Seek medical advice if worsens or does not improve within 48 hours, or person systemically unwell o Midstream urine sample for M, C & S
42
Management of pyelonephritis - antibiotics - non-pregnant women and men - oral antibiotics?
o Oral cefalexin 500mg BD/TD for 7-10 days o Oral ciprofloxacin 500mg BD for 7 days o If culture results known:  Oral Co-amoxiclav 500/125mg TDS for 7-10 days  Oral trimethoprim 200mg BD for 14 days
43
Management of pyelonephritis - antibiotics - non-pregnant women and men - IV antibiotics?
``` o Ceftriaxone o Cefuroxime o Ciprofloxacin o Gentamicin o Amikacin o Co-amoxiclav (in combination or if culture results known) ```
44
Management of pyelonephritis - antibiotics - pregnant women - oral antibiotics?
o Cefalexin 500mg BD/TD for 7-10 days
45
Management of pyelonephritis - antibiotics - pregnant women - IV antibiotics?
o Cefuroxime 750mg to 1.5g TDS/QDS
46
Management of pyelonephritis - antibiotics - children <16 - oral antibiotics?
• Under 3 months – refer to paediatric specialist Over 3 months  Cefalexin  Co-amoxiclav (only if culture results available and sensitive)
47
Management of pyelonephritis - antibiotics - children <16 - IV antibiotics?
```  Co-amoxiclav (only in combination or if culture result known)  Cefuroxime  Ceftriaxone  Gentamicin  Amikacin ```
48
When to review antibiotics in acute pyelonephritis?
o Review antibiotics at 48 hours if IV and when cultures available
49
Definition of acute urinary retention?
- Inability to voluntarily urinate
50
Mechanism of acute urinary retention?
o Increased resistence to flow o Inappropriate detrusor muscle innervation o Bladder over-distention o Drugs
51
Epidemiology of acute urinary retention?
- Medical emergency, abrupt development of inability to pass urine - Common 0.3% - Men 10x
52
Causes of acute urinary retention - anatomical?
```  BPH (most common)  Urethral strictures  Prostate carcinoma  Prostate haematoma  Urethral stone  Foreign body  Urinary stent occlusion  Constipation  Meatal stenosis ```
53
Causes of acute urinary retention - functional?
```  Neurogenic bladder  MS, Parkinsons, Alzheimer’s, cauda equina syndrome  SCI  CVA  Tumour  Spinal anaesthesia  Alcohol  Pain  UTI  Acute prostatitis (E.coli, proteus) ```
54
Causes of acute urinary retention - drugs?
 Anticholinergics, antihistamines, amphetamines, morphine, hyoscine, TCAs
55
Symptoms of acute urinary retention?
o Severe pain o Unable to pass urine o Previous episodes
56
Signs of acute urinary retention?
Tender, distended bladder – dull to percuss above pubic symphysis
57
Initial investigations of acute urinary retention?
Rule out cauda equina Bladder US scan  Calculates bladder volume DRE of prostate – after catheterisation  Check anal tone, prostatic size, nodules, tenderness and exclude faecal impaction Urinalysis - MSU Bloods – FBC, U&E, glucose
58
Investigations to perform on ward of acute urinary retention?
o Renal US if any renal impairment
59
Immediate management of acute urinary retention?
o Catheterisation immediately  Document post-catheterisation residual volume, type of catheter (14/16G) o Alpha-blocker given before catheter (tamsulosin)
60
Subsequent management of acute urinary retention?
o Treat cause  If BPH – tamsulosin with finasteride as an adjunct can be used o Trial without catheter (TWOC) in men with BPH
61
Follow up of acute urinary retention?
o If secondary to BPH, constipation, UTI with no previous UT symptoms – no follow up o Referral to urology clinic
62
Complications of acute urinary retention?
- UTIs - AKI - Post-retention diuresis, haematuria
63
Physiology of potassium?
- Potassium is mostly intracellular and thus serum potassium is poor indicator of total potassium - Concentrations of H and K tend to vary together - Insulin and catecholamines stimulate K into cells via Na/K/ATPase pump
64
Normal values of potassium?
- Normal values – 3.5-5mmol/L
65
Classifications of hyperkalaemia?
o Mild 5.5-6mmol/L o Moderate 6.1-6.9mmol/L o Severe >7.0mmol/L
66
Causes of hyperkalaemia?
o Spurious – Haemolysed sample o Decreased renal excretion – AKI, CKD, K+ sparing diuretics o Hypoaldosteronism – Addison’s disease, NSAIDs, ACEi o Cell injury – Crush injury, rhabdomyolysis, burns, incompatible blood transfusion o K+ cellular shifts – Metabolic acidosis, suxamethonium
67
Symptoms of hyperkalaemia?
o Muscle weakness/cramps o Paraesthesia o Focal neurological deficits o Fast, irregular pulse with palpitations
68
ECG changes of hyperkalaemia?
o Peaked (tall, tented) T waves o Small, flat P waves o Widening QRS complexes (becomes sinusoidal) o VF
69
When to treat hyperkalaemia immediately?
(>6.5 or >6 with ECG changes needs immediate treatment
70
Management of hyperkalaemia - immediate drug management?
o 10mL 10% calcium gluconate IVI to stabilise cardiac membrane (up to 30ml if no improvement in ECG) o 10U soluble insulin (Actrarapid) in 50mL 50% glucose given over 5-15 minutes o 5mg NEB Salbutamol, repeated once as necessary o Calcium Resonium 15g orally every 6-8 hours (removes K from GI tract)  Co-prescribe with lactulose o Review potassium intake, medications o Contact renal team – may need dialysis if intractable
71
Definition of hypokalaemia?
- Potassium <2.5 needs urgent treatment but any value under 3.5 considered hypokalaemic - Hypokalaemia exacerbates digoxin toxicity
72
Causes of hypokalaemia?
``` o Diuretics o D&V o Cushing’s/Steroids/ACTH o Alkalosis o Conn’s syndrome o Renal tubular failure o Pyloric stenosis o Intestinal fistula ```
73
Symptoms and signs of hypokalaemia?
``` o Muscle weakness o Hypotonia o Hyporeflexia o Cramps o Tetany o Palpitations o Light-headedness o Constipatio ```
74
ECG changes of hypokalaemia?
o Small/Inverted T waves o Prominent U waves (after T wave) o Long PR interval o Depressed ST segments
75
Management of hypokalaemia - mild?
 Oral K+ supplement (Sando K tablets) and U&Es daily
76
Management of hypokalaemia - severe?
 IV potassium (normal max rate if 10mmol/hr but if severe 20mmol/h) and ensure continuous cardiac monitoring
77
Physiology of sodium regulation?
- Sodium controlled by aldosterone on DCT and collecting duct to increase Na reabsorption from urine - Natriuretic peptides ANP, BNP, CNP reduce resorption from DCT and inhibit renin - Derangement can occur with hypervolaemia, euvolaemia, hypovolaemia
78
Normal range of sodium?
- Normal ranges – 135-145mmol/L
79
Causes of hypernatraemia?
o Diabetes insipidus (lack of ADH or renal response) o Fluid loss without replacement – Diarrhoea, vomiting o Osmotic diuretics (mannitol, isosorbide) o Hypertonic saline o Cushing’s syndrome
80
Symptoms and signs of hypernatraemia?
o Lethargy, thirst, weakness, irritability, confusion and coma o Signs of dehydration
81
Blood tests of hypernatraemia?
o High Na, PCV, albumin, urea
82
Management of hypernatraemia?
o Water orally if possible o If hypovolaemia, 0.9% saline to correct o Dextrose 5% IV (1L/6h) guided by urine output and serum Na (check every 2-3 hours)
83
Complications of hypernatraemia?
o Seizures o Cerebral/subdural haemorrhages o Dural sinus thrombosis o Cerebral oedema
84
Causes of hyponatraemia - if dehydrated?
 High urine Na – Addison’s disease, renal failure, diuretic excess, osmolar diuresis  Low urine Na – Diarrhoea, vomiting, burns, small bowel obstruction, CF
85
Causes of hyponatraemia - if not dehydrated?
 Oedematous – Nephrotic syndrome, cardiac failure, liver failure, renal failure  Not oedematous – SIADH, water overload, hypothyroidism, glucocorticoid insufficiency
86
Symptoms of hyponatraemia?
Anorexia, nausea, malaise, headache, irritability, confusion, weakness and seizures
87
Management of hyponatraemia - acute (<24 hours)?
Assess volume status Urine osmolarity  <100 - primary polydipsia or low solute intake  >100 and urine sodium >30 & hypovolaemic - vomiting, Addison's, diuretics, salt wasting  >100 and urine sodium >30 & euvolaemic - SIADH, secondary adrenal insufficiency, hypothyroid, diuretics  >100 and urine sodium <30 - heart failure, liver failure, nephrotic syndrome, D&V Mild  If hypervolaemic - fluid restriction  If hypovolaemic - 0.9% saline IV slowly • Rapid change can lead to central pontine myelinolysis Na <120mmol/L associated with risk of cerebral herniation  In emergency consider hypertonic saline (1.8/3%)
88
Management of hyponatraemia - chronic?
 Slowly increase Na <10mmol/L per day  Treat cause  May need hypertonic saline
89
Definition of hyponatraemia?
Mild hyponatraemia — serum sodium 130–135 mmol/L. Moderate hyponatraemia — serum sodium 125–129 mmol/L. Severe hyponatraemia — serum sodium less than 125 mmol/L.
90
Classes of hyponatraemia?
Acute — hyponatraemia duration for less than 48 hours. Chronic — hyponatraemia duration for 48 hours or more
91
Complications of hyponatraemia?
Life-threatening if severe and/or of acute onset Swelling of brain cells, cerebral oedema and raised intracranial pressure can lead to seizures, coma, or cardio-respiratory arrest Increased mortality and longer hospital admission Chronic hyponatraemia can cause falls, gait disturbances, concentration and cognitive deficits
92
Definition of CKD?
- Abnormal kidney function or structure present for >3 months or eGFR <60
93
Normal functions of kidney?
Excretory –  inorganic substances (e.g. potassium, phosphate)  organic (urea, creatinine)  clinically “uraemic toxicity” Homeostasis – fluid balance, blood pressure, acid-base Endocrine – erythropoietin, bone metabolism
94
Epidemiology of CKD?
- Over 70% due to DM, hypertension - Prevalence increases with age - 8.5% Stage 3-5 CKD
95
Causes of CKD - intrinsic?
o Hypertension o DM (Type 2 most common) o Glomerulonephritis o Renal artery stenosis
96
Causes of CKD - nephrotoxic?
o NSAIDs, Lithium, Ciclosporin, Tacrolimus, Aminoglycosides, Mesalazine
97
Causes of CKD - obstructive?
o Bladder voiding dysfunction o Urinary diversion surgery o Recurrent urinary stones
98
Causes of CKD - multi-system disease?
o SLE, vasculitis, myeloma, polycystic kidney disease, Alport’s syndrome
99
Symptoms of CKD?
- Asymptomatic at first - Anaemia – Low EPO – Pallor, SOB - Renal osteodystrophy – osteomalacia, bone pain - Epistaxis/bruising - Uraemic symptoms - Anorexia/nausea/vomiting - Restless legs, weakness, pruritus and bone pain
100
Signs of CKD?
- Pallor, uraemic tinge, purpura, increased BP, signs of fluid overload, ballotable kidneys
101
When to test people for CKD?
Test people with risk factors for CKD: o Diabetes, hypertension, AKI, CVD, SLE, structural renal tract disease, recurrent calculi, BPH o Family history of CKD stage 5 o Taking nephrotoxic drugs (ciclosporin, tacrolimus, lithium, NSAIDs) Test people with incidental findings: o Proteinuria or persistent haematuria (2/3 with 1+) after exclusion of UTI o eGFR of <60
102
What tests to perform in people suspecting CKD?
- Serum creatinine (eGFR) - Early Morning Urine – Albumin Creatinine Ratio (ACR) - Urine dipstick for haematuria
103
Specific advice for testing eGFR in CKD?
o No meat in 12 hours before, caution if extreme muscle mass o Confirm result if <60 with test 2 weeks later o If stable but same, repeat 3 months
104
Specific advice for testing EMU ACR in CKD?
- Early Morning Urine – Albumin Creatinine Ratio (ACR) o Repeat if 3-70mg/mmol within 3 months, no need if >70 o >3 is clinically proteinuria
105
Specific advice for testing urine dipstick in CKD?
o Significant haematuria if 1+ or more, exclude UTI by sending MSU
106
Specific advice for testing renal USS in CKD?
o If accelerated progression of CKD, visible or persistent invisible haematuria, symptoms of UT obstruction, FHx of PKD and >20 years, eGFR <30
107
Other tests to find cause of CKD?
- Bloods (low Hb, Ca, high PO4 and ALP and PTH, glucose, U&Es) - Urine – ACR, dipstick - USS to check kidneys size and anatomy - Renal biopsy if rapid decline and cause unclear - Immunology – Goodpasture’s syndrome, IgA nephropathy
108
Diagnosis of CKD can be made when?
- EGFR <60 and/or ACR >3 after 3 months - If repeat eGFR 45-59 and urine ACR <3 and no proteinuria: o Use eGFRcystatinC test  Hypothyroidism elevates, hyperthyroidism reduces
109
Classification of CKD stages?
- Stage 1 - >90 No impairment - Stage 2 – 89-60 Slight - Stage 3A – 59-45 Moderate - Stage 3B – 44-30 Severe - Stage 4 – 29-15 Severe - Stage 5 - <15 Renal Failure - ACR classified in each stage as A1 - <3, A2 – 3-30, A3 - >30
110
When to refer CKD to nephrologist?
- eGFR <30 - ACR >70mg/mmol - ACR >30mg/mmol with haematuria - Decrease by >25% in year or decrease GFR >15ml/min/1.73 in year - Poorly controlled BP on 4 antihypertensives - Suspected genetic causes or renal artery stenosis
111
Monitoring of CKD?
- Annual eGFR and ACR if no CKD and risk factors - eGFR, ACR (stage 1-3a annually, stage 3b-4 biannually, stage 5 quarterly) - FBC (Stage 3b, 4, 5) - Serum calcium, phosphate, vitamin D and PTH in (stage 4, 5)
112
Management of CKD - self-management?
- Stop smoking - Regular exercise and healthy body weight - Eat healthy diet – low sodium, Vit D analogues and Ca supplements - Avoid NSAIDs, nephrotoxics - Manage and minimise risk factors
113
Management of CKD - antihypertensives?
o If hypertensive and ACR <30 – follow guidelines o If hypertension and ACR >30 – ACEi/ARB o If ACR >70 and normotensive OR CKD and diabetic – ACEi/ARB (aim <130/80)
114
Management of CKD -aim of antihypertensives?
Aim <140/90 in hypertensive + CKD + ACR <70 Aim <130/80 in ACR>70 + normotensive or CKD + diabetes
115
Management of CKD -monitoring of antihypertensives?
 Measure serum potassium and eGFR before ACEi, 1-2 weeks later and at any dose change (before starting K<5, otherwise don’t start ACE/ARB, stop if K>6 after 1-2 weeks)  If eGFR decreased by >25% then repeat test 1-2 weeks – if <25% then continue and repeat test in 1-2 weeks, if >25% investigate causes and stop drug
116
Management of CKD - statin therapy?
- Atorvastatin 20mg daily (if eGFR <60 and ACR >3) o Baseline lipids, CK, LFTs o Can increase dose if not >40% reduction in non-HDL cholesterol and eGFR >30 in 3 months o Repeat lipids at 3 months
117
Management of CKD -antiplatelets and anticoagulants?
- Antiplatelets o Secondary prevention only - Anticoagulant o Secondary prevention of CVD – Apixaban used if eGFR 30-50 and non-valvular AF and 1 of: Hx of TIA/stroke, >75, HTN, DM, HF
118
Management of CKD - complications - anaemia?
o Check Hb in people with eGFR <45 o Offer iron tablet if deficient – if Hb level not reached within 3 months, offer IV therapy o If on dialysis – offer IV iron first o EPO may be needed
119
Management of CKD - complications - bone complications?
o Measure serum Ca, phosphate, PTH and Vit D when eGFR <30  If needed – cholecalciferol o Bisphosphonates for prevention of osteoporosis when eGFR >30, if indicated only
120
Management of CKD - complications - bicarbonate level?
- Oral sodium bicarbonate | o eGFR<30 or sodium bicarbonate <20
121
Definition of deterioration of CKD?
- Decrease by >25% or 15ml/min/1.73 in year - Repeat eGFR 3x over 90 days - Refer to nephrologist as before
122
When to discuss RRT in CKD?
- Discuss when eGFR <20 - Dialysis started when impact of symptoms of uraemia on daily living, biochemical measures or uncontrollable fluid overload or at eGFR around 5-7 if no symptoms
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Options of RRT in CKD?
- Haemodialysis o Diffusion solutes between blood and dialysis fluid – access via fistula inserted 6 months before start - Peritoneal dialysis o Diffusion solutes between blood in peritoneal capillaries and dialysis fluid in peritoneal cavity o Continuous ambulatory peritoneal dialysis (4x a day) o Automated PD (several exchanges per night) - Kidney transplant o From deceased donor or live donor o Lifelong immunosuppression o Must be medically fit for surgery
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Prognosis of CKD?
- CKD progresses to End-stage KD in 2% of people | - 20x more likely to die of CVD then to progress to End-stage KD
125
Complications of CKD?
- Renal replacement therapy - CVD and events - Renal anaemia, bone disease (low Ca, high PO4 and PTH) - Malnutrition - Neuropathy - Lipid abnormalities
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Definition of AKI?
- Rapid reduction in kidney function over hours to days, as measured by serum urea and creatinine – leading to failure to maintain fluid, electrolyte and acid-base homeostasis
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Epidemiology of AKI?
- Occurs in 18% of hospital patients
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Risk factors of AKI?
- Age>75 - CKD - Cardiac failure - PVD - Liver failure - Diabetes - Drugs - Sepsis - Poor fluid intake
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Causes of AKI - pre-renal?
Most common o Renal hypoperfusion due to hypotension (hypovolaemia, D&V, sepsis), renal artery stenosis +/- ACEi o Reduced cardiac output (cardiac and liver failure)
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Causes of AKI -intrinsic?
10-50% ``` o Acute tubular necrosis  Due to drugs, aminoglycosides, radiological contrast, rhabdomyolysis o Glomerulonephritis o Vasculitis, thrombosis o Interstitial nephritis, lymphoma ```
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Causes of AKI - post-renal?
10-25% Urinary tract obstruction  Luminal – stones, clots  Mural – malignancy, BPH, strictures  Extrinsic compression – malignancy, retroperitoneal fibrosis
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Symptoms and signs of AKI?
- May be none - Fatigue, malaise, rash - Joint pains, nausea and vomiting - Chest pain, palpitations, SOB, fluid overload - Oliguria, hypo/hypertension
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When to measure U&Es to identify AKI?
 CKD, HF, liver disease, Hx of AKI, oliguria (<0.5ml/kg/hour), hypovolaemic, NSAIDs, ACEi/ARBs, diuretics, urinary obstruction, sepsis, severe diarrhoea, nephritis, hypotension, >65
134
When to detect AKI in hosptial patients?
 Rise in serum creatinine >26 within 48 hours  50% or greater rise in serum creatinine within 7 days  Fall in urine output to <0.5ml/kg/hour for >6 hours in adults and >8 hours in children  25% or greater fall in eGFR in children and young people within 7 days
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KDIGO staging of AKI - Stage 1?
* Rise in creatinine >26umol/L in 48h OR >1.5-1.9x baseline (best figure in last 3 months) * Urine output <0.5ml/kg/h for >6 consecutive hours
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KDIGO staging of AKI - Stage 2?
* Increase in creatinine 2-2.9x baseline | * Urine output <0.5ml/kg/h for >12h
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KDIGO staging of AKI - Stage 3?
* Increase in creatinine >3x baseline OR >354umol/L OR commenced on RRT * Urine output <0.3ml/kg/h for >24h OR anuria for >12h
138
Tests to identify cause of AKI?
Bloods • FBC, U&E, LFTs, Ca, Phosphate • Cultures if signs of infection Urinalysis • Test for blood, protein, leucocytes, nitrites and glucose as soon as suspected • If haematuria and proteinuria and no obvious cause/UTI/trauma – think acute nephritis Ultrasound • Do not offer if cause of AKI identified • If pyonephrosis suspected – US within 6 hours • If no cause of AKI found – urgent US within 24 hours
139
Management of AKI - if urinary obstruction suspected/identified?
Refer immediately when one or more of following is present:  Pyonephrosis  Obstructed solitary kidney  Bilateral upper urinary tract obstruction  Complications of AKI caused by urological obstruction Nephrostomy or stenting performed within 12 hours of diagnosis if needed
140
Management of AKI -investigations to perform?
o ABG/VBG o ECG o Catheterisation and urine output
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Management of AKI - initial management - STOP AKI?
Sepsis  Complete sepsis 6 if sepsis suspected Toxins  Stop/avoid nephrotoxics (Gentamicin, NSAIDs, ACE/ARBs, diuretics, contrast) Optimise BP  If low BP – fluid bolus (0.9% saline 500ml IV 15-20 minutes) Assess volume status  BP, JVP, skin turgor, fluid balance sheet, weight  IV fluids • If low BP – fluid bolus (0.9% saline 500ml IV 15-20 minutes) • IV fluids maintenance if not hypovolaemic ``` Prevent Harm  Treat complications • Hyperkalaemia • Pulmonary oedema • Acidosis • Pericarditis  Review all medications  Identify cause ``` Refer to renal team early for opinion
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Management of AKI - monitoring?
o Check pulse, BP, JVP, urine output hourly o CVP line if on HDU/ICU o Daily U&Es, fluid balance chart and daily weight
143
Management of AKI - when to discuss with nephrology?
```  Specialist treatment needed (vasculitis, glomerulonephritis, nephritis, myeloma)  AKI with no clear cause  Inadequate response to treatment  Complications associated  Stage 3 AKI  Renal transplant  CKD Stage 4/5 ```
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Management of AKI -indications for RRT?
o Refractory pulmonary oedema o Persistent hyperkalaemia o Severe metabolic acidosis (7.15) o Ureamic complications (pericarditis, encephalopathy) o Drug overdose – Barbituates, lithium, alcohol, salicylates, theophylline
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Options for RRT in AKI?
Haemodialysis  Blood passed over semi-permeable membrane against dialysis fluid flowing in opposite direction Hemofiltration  Water is cleared across dialysis membrane using positive pressure to drag small and larger size solutes into waste by convection Peritoneal Dialysis  Uses peritoneum as semi-permeable membrane and allows solutes to diffuse slowly  Can be performed continuously and at home so allows more freedom
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Follow up after AKI?
o Monitor U&Es for 2-3 years after AKI
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Complications of AKI?
- Hyperkalaemia - Metabolic acidosis - Volume overload - Uraemia - CKD
148
Symptoms in urinary incontinence?
Stress - leakage of urine on sneezing, coughing, exercise, rising from sitting or lifting Urge - urgency and failure to reach toilet, frequency and nocturia possible Other symptoms to ask: Frequency during day/night, dysuria, haematuria,, dribbling of urine after leaving toilet, feeling incomplete bladder emptying
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Gynaecological history important in urinary incontinence?
``` Uterus or not Pre/Postmenopausal Problems with intercourse How many babies - delivery method Smear tests up to date ```
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PMH important in urinary incontinence?
``` Uterus or not Pre/Postmenopausal Problems with intercourse How many babies - delivery method Smear tests up to date ```
151
DH important in urinary incontinence?
Diuretics Laxatives Medications for urinary symptoms in past
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SH for urinary incontinence?
``` Caffeine intake Carbonated drinks Alcohol Smoking Ketamine Occupation - heavy lifting? ```
153
Examination performed in incontinence?
``` History including obstetric, sexual and functional status BMI and Urine dipstick & MSU Abdominal and pelvic examination Cough - any leakage? Assess for prolapse Assess for vaginal atrophy VE Smear ```
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Investigations in urinary incontinence?
- Urinalysis and MSU microscopy (culture and sensitivity) o Exclude UTI - OGTT if diabetes suspected - Frequency/volume chart o Should be filled in for 72h and give idea off fluid intake and voiding problems
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When should a cystoscopy be performed in urinary incontinence?
o Used to visualise urinary tract | o Indicated if recurrent UTI, haematuria, bladder pain, suspected fistula, tumour
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What are the specialist tests performed for urinary incontinence?How do they work?
Urodynamics o Uroflowmetry Ability of bladder to store and void urine Patient voids in private onto commode with urinary flow meter, measuring voided volume over time and plotting graph o Cystometry Invasive and involves measuring pressure and volume in bladder during filling and voiding Bladder filled with saline and intravesical & vaginal/rectal probe measure differences in pressure to give detrusor pressure Patient first desire to void, strong desire to void and cough Diagnoses stress incontinence
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Initial management of stress urinary incontinence?
``` Lifestyle interventions • Weight reduction if BMI >30 • Smoking cessation • Reduce caffeine and fizzy drinks • Treatment of chronic cough and constipation ``` Pelvic floor muscle training • For at least 3 months • Exercises continued long-term. • 8-12 slow maximal contractions sustained for 6-8 seconds each, 3x per day Follow up 3 months
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Follow up management of stress urinary incontinence?
Urodynamics MDT Meeting Duloxetine • SNRI enhances urethral striated sphincter activity via a centrally mediated pathway. • Dose-dependent decreases in frequency of incontinence episodes Transvaginal tape
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Pharmacological management of stress urinary incontinence?
Duloxetine • SNRI enhances urethral striated sphincter activity via a centrally mediated pathway. • Dose-dependent decreases in frequency of incontinence episodes
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Surgical management of stress urinary incontinence ? When considered and what types?
Considered when other measures failed Transvaginal Tape • Polypropylene mesh tape placed under mid-urethra via small vaginal incision • Risks – bladder injury, voiding difficulty, tape erosion Periuretheral injections • Bulking agents, better for older, frail or young women
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Initial management of urge urinary incontinence?
Lifestyle advice • Weight reduction if BMI >30, smoking cessation, reduce caffeine and fizzy drinks, treatment chronic cough and constipation Pelvic floor muscle training • 3 months, exercises continued long-term, 8-12 slow maximal contractions sustained for 6-8 seconds each, 3x per day Bladder diary (>3 days) - idea of fluid intake and bladder voiding problems Bladder drills • Ability to suppress urinary urge and extend the intervals between voiding Anticholinergics - Oxybutynin (+/- vaginal oestrogen if vaginal atrophy) Follow up 3 months
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Describe properties of initial pharmacological management of urge urinary incontinence? SE? CI? When is botox used?
Anticholinergic (antimuscarinic) agents (oxybutynin) • Block the sympathetic nerves thereby relaxing the detrusor muscle • Side effects = dry mouth (up to 30%), constipation, nausea, dyspepsia, flatulence, blurred vision, dizziness, insomnia, palpitation, arrhythmias. • Contraindications = acute (narrow angle) glaucoma, myaesthenia gravis, urinary retention or outflow obstruction, severe UC, GI obstruction. Oestrogens • In women with vaginal atrophy, intravaginal oestrogens may be tried Botulinum Toxin A • Blocks neuromuscular transmission – causing the muscle to become weak. • Used in follow up and injected cystoscopically into the detrusor, usually under local anaesthetic.
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Follow up management of urge urinary incontinence?
Try 2nd anticholinergic (tolterodine) Urodynamic study (increased detrusor pressure upon voiding) MDT meeting Cystoscopy & Botox (botulinum toxin A) Nerve stimulation - percutaneous posterior nerve/percutaneous sacral nerve Augmentation cystoplasty - if small bladder Urinary diversion
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Management of overflow incontinence?
o Treat with catheter • Can cause urinary retention in 5-20% of cases, in which intermittent self catherterisation may be required. o Surgical  Reserved as last resort for debilitating symptoms, failed therapies  Bladder distension, sacral neuromodulation, detrusor myomectomy have limited efficacy
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How common is urogenital prolapse?
* Occurs in 40-60% of parous women | * Most common reason postmenopausal women have hysterectomy
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Definition of urogenital prolapse?
o Weakness of supporting structures (levator ani muscles and endopelvic fascia) allows the pelvic organs to protrude within the vagina o Can be bladder, urethra, rectum, and bowel
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Risk factors of urogenital prolapse?
``` o Increasing age o Vaginal delivery o Increasing parity o Obesity o FHx of prolapse o Constipation/Chronic cough ```
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Types of urogenital prolapse?
o Can occur in anterior, middle or posterior compartments of pelvis
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Anterior types of urogenital prolapse?
```  Cystocele • Prolapse of bladder into the vagina  Urethrocele • Prolapse of urethra into the vagina, associated with USI  Cysto-urethrocele when both (MC) ```
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Middle types of of urogenital prolapse?
 Uterine prolapse • Descent of uterus into vagina • Baden-Walker Graded  Vaginal vault prolapse • Descent of vaginal vault post-hysterectomy, associated cystocele, rectocele and enterocele common  Enterocele • Herniation of pouch of Douglas into vagina • Pouch usually contains loops of small bowel
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Posterior types of urogenital prolapse?
 Rectocele | • Prolapse of rectum into vagina
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POPQ staging of urogenital prolapse?
o 0 = No prolapse o 1 = >1cm above hymen o 2 = At level of hymen o 3 = >1cm below hymen but protrudes <2cm total length of vagina o 4 = Complete eversion of vagina (complete procidentia)
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General symptoms of urogenital prolapse?
- Dragging sensation discomfort, and heaviness within the pelvis.  Usually worse at the end of the day or when standing up. - Feeling of ‘a lump coming down’ - Dyspareunia or difficulty in inserting tampons. - Discomfort and backache.
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Cysto-urethrocele symptoms of urogenital prolapse?
- Urinary urgency and frequency. - Incontinence - Incomplete bladder emptying o Urinary retention or reduced flow where the urethra kinked
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Rectocele symptoms of urogenital prolapse?
- Constipation | - Difficulty with defecation (may digitally reduce it to defecate).
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Other symptoms of urogenital prolapse?
* Symptoms tend to become worse with prolonged standing and towards the end of the day. * Grade 3 or 4 prolapse, there may be mucosal ulceration and lichenification, resulting in vaginal bleeding and discharge. * Symptoms can affect quality of life, causing social, psychological, occupational or sexual limitations to a woman’s lifestyle.
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Examinations performed in urogenital prolapse?
• Examine patient in both standing and left lateral position o Ask woman to strain and observe • Bimanual examination (exclude pelvic masses) • Sims speculum examination o Inspect anterior and posterior walls, ask to strain
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Investigations of urogenital prolapse?
* USS to exclude pelvic or abdominal masses. * Urodynamics are required if urinary incontinence is present * Assess fitness for surgery – ECG, CXR, FBC, U&Es
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Prevention of urogenital prolapse? | Conservative management of urogenital prolapse?
Prevention - Reduction of prolonged labour, trauma caused by instrumental delivery - Encouraging persistence with post-natal pelvic floor exercises. General Advice - Weight reduction - Avoid heavy lifting - Treatment of chronic constipation and cough (including smoking cessation) - Pelvic floor muscle exercises
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Further management of urogenital prolapse - Intravaginal (pessary) devices? When used? What is it? Instructions?
- Conservative line of therapy for women who decline surgery, who are unfit for surgery, or for whom surgery is contraindicated. o Artificial pelvic floor placed in the vagina to stay behind the symphysis pubic and in front of the sacrum. o Sexually active women can use ring pessaries, either have sex with it in place or take it out and replace after o They should be changed 6 monthly and if post-menopausal, topical oestrogen may be given to decrease risk of vaginal erosion.
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Types of pessary and when used?
Ring pessary = most commonly used o Placed between the posterior aspect of the symphysis pubis and posterior fornix of the vagina. Shelf pessary = used when a correctly sized ring pessary will not sit in the vagina and/or where the perineum is deficient Others: Hodge pessary, cube and doughnut pessaries (very rarely used).
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Indications for surgical management of urogenital prolapse?
- Failure of conservative treatment - Voiding or defaecation problems - Recurrent prolapse after surgery - Ulceration - Irreducible prolapse - Preference
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Surgical management of anterior compartment of urogenital prolapse?
• Anterior colporrhaphy (anterior repair) | - Appropriate for repair of a cysto-urethrocele.
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Surgical management of posterior compartment of urogenital prolapse?
``` Posterior colporrhaphy (posterior repair) - Appropriate for correction of a rectocele and deficient perineum ```
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Surgical management of uterovaginal (apical) compartment of urogenital prolapse?
* Vaginal hysterectomy (most common) * Sacrohysteropexy - Preserve the uterus. - Attaches the prolapsed uterus to the sacrum
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Surgical management of vaginal vault of urogenital prolapse?
• Sacrospinous ligament fixation | - Suturing vaginal vault to sacrospinous ligaments using a vaginal approach.
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Surgical management of recurrent compartment of urogenital prolapse?
* ~1/3 of prolapse surgery is for recurrent prolapse. * Vaginal epithelium may be scarred and atrophic (makes surgery harder and gives increased risk of damage to bladder and bowel)
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Surgical management of recurrent compartment of urogenital prolapse?
* ~1/3 of prolapse surgery is for recurrent prolapse. * Vaginal epithelium may be scarred and atrophic (makes surgery harder and gives increased risk of damage to bladder and bowel)
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Definition of nephrotic syndrome?
``` - Clinical syndrome defined as: o Proteinuria (>3.5g/24h (ACR>250)) o Oedema o Hypoalbuminemia (<30g/L) ``` - It is caused by injury to podocyte which increase permeability of serum protein through the damaged basement membrane in the renal glomerulus
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Classes of nephrotic syndrome?
- Classified as steroid sensitive, steroid resistant or steroid dependent
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Aetiology of nephrotic syndrome - primary?
Minimal change disease – 85% in children • Idiopathic, NSAIDs, Hodgkin’s lymphoma • Biopsy – normal under light microscopy • Steroids usual course of treatment Focal segmental glomerulonephritis (FSGN) – most common in adults • Segmental areas of mesangial collapse and sclerosis • Due idiopathic, HIV, SCD, Alport’s, obesity, reflux nephropathy Membranous nephropathy – common in older adults • Due to – malignancy, hepatitis B, gold, penicillamine, NSAIDs, thyroid, SLE • Thickened GBM Membranoproliferative glomerulonephritis
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Aetiology of nephrotic syndrome - secondary?
 Infection – HIV, HepB/C, syphilis, malaria  SLE, HSP, Lupus  Diabetes – MC secondary cause  Alport’s syndrome  Malignancies  Toxins (snake bites, bee stings) and heavy metals
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Symptoms and signs of nephrotic syndrome?
- Periorbital oedema, leg/ankle oedema, ascites and breathlessness - Oliguria - Proteinuria, oedema, hypoalbuminemia - Dyslipidaemia, abnormalities in coagulation/fibrinolysis, reduced renal function
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Investigations of nephrotic syndrome?
Urine dipstick o Check for protein & microscopic haematuria Urine MSU o Microscopy, culture and sensitivities to exclude UTI  Red cell casts, protein electrophoresis Urine ACR Bloods o FBC, CRP, ESR, U&E’s (creatinine, low albumin) o Complement levels o Autoimmune screen – ANA, ANCA, anti-DNA, anti-GBM, complement) o Syphilis/HepB/C screen CXR and renal USS Renal biopsy
195
Management of nephrotic syndrome - general advice?
- Sodium and fluid restriction - High-dose loop diuretics (furosemide) - Daily weight & U&Es - Pneumococcal and influenza vaccination
196
Management of nephrotic syndrome - minimal change disease
Steroid-sensitive nephrotic syndrome  Oral prednisolone for 4 weeks then wean over 4 months • If steroid toxicity, use cyclophosphamide Steroid-resistant nephrotic syndrome  Management of oedema with diuretics, salt restriction and ACE inhibitors (enalapril)
197
Management of nephrotic syndrome - focal segmental glomerulonephritis?
o Corticosteroids | o Cyclophosphamide if steroid-resistant
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Management of nephrotic syndrome - membranous nephropathy?
o Secondary – treat cause | o ACEi and diuretics
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Management of nephrotic syndrome - mesangiocapillary GN?
o ACEi | o Steroids and cyclophosphamide if rapid deterioration
200
Complications of nephrotic syndrome ?
- Susceptible to infections - Risk of VTE – urinary excretion of antithrombin 3 - Hyperlipidaemia - AKI/CKD
201
Pathology of bladder cancer?
o Calyces, renal pelvis, ureter, bladder and urethras lined by transitional epithelium o 50% in bladder
202
Spread of bladder cancer?
o Local – pelvic structures o Lymph – iliac and para-aortic nodes o Bloods – liver and lungs
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Epidemiology of bladder cancer?
- Men > Women | - Age >40
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Cell types of bladder cancer?
o 90% transitional cell carcinoma | o Rare – adenocarcinoma, SCC (from schistosomiasis)
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Aetiology of bladder cancer?
``` o Cigarette smoking o Aromatic amines (rubber industry) o Chronic cystitis o Drugs – cyclophosphamide o Schistosomiasis (SCC) ```
206
Symptoms of bladder cancer?
``` o Painless haematuria o UTI symptoms without bacteriuria o Pain o Voiding irritability o If in ureters, pelvis – flank pain due to obstruction ```
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When to refer on 2 week pathway of bladder cancer?
Over 45 with: • Unexplained visible haematuria without UTI OR • Visible haematuria persisting or recurring after treatment of UTI Over 60 with unexplained non-visible haematuria and either: • Dysuria OR • Raised WCC
208
When to refer non-urgently of bladder cancer?
o Non-urgent referral in over 60 with recurrent or persistent UTIs
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Diagnostic investigations performed in secondary care of bladder cancer?
US KUB Cystoscopy with biopsy If invasive – CT/MRI Transurethral Resection of bladder tumour • With photodynamic diagnosis, narrow-band imaging, cytology or urinary biomarker test • Obtain detrusor muscle • Record size and number of tumours • Offer single dose of intravesical mitomycin C
210
Staging investigations of bladder cancer?
TURBT within 6 weeks if no detrusor muscle CT scan • If diagnosed with muscle-invasive or high-risk and being assessed for radical treatment CT urography CT thorax PET scan – if indeterminate findings on CT or high risk of metastatic disease
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Management of bladder cancer - general advice?
o Clinical nurse specialist – support | o Smoking cessation
212
Management of bladder cancer - non-muscle invasive - risk classification?
o Risk Classification – determined on size, number, histology, type, grade, stage
213
Management of bladder cancer - non-muscle invasive - low risk?
White-light guided TURBT o With photodynamic diagnosis, narrow-band imaging, cytology or urinary biomarker test o Obtain detrusor muscle o Record size and number of tumours o Offer single dose of intravesical mitomycin C o TURBT within 6 weeks if no detrusor muscle Follow-Up o Cystoscopy at 3 months and 12 months after diagnosis o Discharge if no recurrence
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Management of bladder cancer - non-muscle invasive - medium risk?
6 doses of intravesical mitomycin C o If recurs, specialist MDT Follow Up o Cystoscopy follow up at 3, 9 and 18 months and annually after
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Management of bladder cancer - non-muscle invasive - high risk?
TURBT before 6 weeks – if 1st TURBT shows high risk Intravesical BCG or o Induction and maintenance Radical cystectomy o Urinary stoma or urinary diversion (unless cognitive impairment, impaired renal function or bowel disease) ``` Follow Up o Cystoscopy every 3 months for 2 years, every 6 months for 2 years and then annually o CT every 6 months for 2 years o Annually  Measure eGFR  US of KUB  B12 and folate level  Urethral washing for cytology ```
216
Management of bladder cancer - muscle invasive?
Neoadjuvant Chemotherapy – cisplatin then:  Radical Cystectomy OR • Urinary stoma or urinary diversion (unless cognitive impairment, impaired renal function or bowel disease) • Adjuvant chemotherapy - cisplatin  Radiotherapy with Radiosensitiser • Mitomycin in combo with 5-FU • Over 6.5 or 4 weeks ``` Follow up  Cystoscopy every 3 months for 2 years, every 6 months for 2 years and then annually  CT every 6 months for 2 years  Annually • Measure eGFR • US of KUB • B12 and folate level • Urethral washing for cytology ```
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Management of bladder cancer - locally advance or metastatic cancer?
Chemotherapy  MVAC with G-CSF (if ECOG 0,1 and GFR >60) • Carboplatin with gemcitabine (if ECOG 2 or GFR<60) • Pembrolizumab if cisplatin unsuitable  Gemcitabine with MVAC and G-CSF
218
Management of bladder cancer - symptoms management?
Bladder (haematuria, dysuria, frequency, nocturia) • Radiotherapy Loin Pain or Renal Failure • Percutaneous nephrostomy or retrograde stenting Bleeding • Radiotherapy or embolization Pelvic Pain • Radiotherapy • Nerve block • Palliative chemotherapy
219
Type of prostate cancer?
- Malignant tumour of the prostate o >95% are adenocarcinomas, developing in glandular tissue in posterior or peripheral parts of prostate - BPH more common in centre of gland
220
Spread of prostate cancer?
- Spread may be local (seminal vesicles, bladder, rectum), via lymph or haematogenous (sclerotic bony lesions)
221
Epidemiology of prostate cancer?
- Commonest cancer in males - 1 in 8 men will get prostate cancer in lives - Older men - >50% occur after 75 years
222
Risk factors of prostate cancer?
``` o Genetics  BRCAII & pTEN genes o Radiation exposure o Diet o Anabolic Steroids (due to increased testosterone) o Age o African/Afro-Caribbean o Family History ```
223
Symptoms of prostate cancer?
``` o Asymptomatic o Poor stream o Nocturia o Terminal dribbling o Polyuria o Metastatic symptoms  Weight loss, anaemia, lower back pain, MSCC ```
224
Signs of prostate cancer?
o Rectal Examination  Enlarged, hard, craggy gland  Loss of median sulcus
225
Investigations in primary care of prostate cancer?
Prostate Specific Antigen (PSA) increased • Test in men with: o Lower UT symptoms o Erectile dysfunction o Visible haematuria • Better prognosis if picked up, may be high or low falsely • 75% of men with abnormal PSA do not have cancer • Most men who have abnormal test will have biopsy which is invasive Digital Rectal Examination  After PSA
226
Investigations in secondary care in suspected prostate cancer?
```  Transrectal USS and biopsy  If curative intent: • MRI  If metastatic concerns: • Radiolabelled technetium bone scan ```
227
Staging of prostate cancer?
 TMN
228
Grading of prostate cancer?
 Gleason grading 2-5 and then added together, scored on basis of histological patterns 2-10 • Low risk – GS<7, T1/2, PSA<10 • Moderate risk – GS=7, T2, PSA 10-20 • High risk – GS>7, PSA>20
229
When to refer for 2-week appointment of prostate cancer?
o DRE – prostate feels malignant | o PSA raised
230
2-week referral assessment of prostate cancer?
o Urology clinic appointment o Imaging MRI/USS/X-rays o Trans-rectal Biopsy – 10 cores  Rectal discomfort, blood in urine or semen, 3% risk of sepsis
231
Management of prostate cancer - observational?
 Asymptomatic prostate cancer confined to prostate, particularly in elderly and where other conditions limit length of survival
232
Management of prostate cancer - surgery?
Radical Prostatectomy with curative intent • T2 or less • Perineal or retroperineal routes • May have temporary or lasting impotence and incontinence Palliative surgery • Used to relieve prostatic symptoms or urinary obstruction
233
Management of prostate cancer - radiotherapy?
Performed by external beam irradiation, interstitial implantation of radioisotopes or both Radical radiotherapy • Can be used in T1/T2 tumours or to control locally advanced tumours Adjuvant radiotherapy • Following radical surgery if concerns about residual disease Palliative used to palliate primary tumour or treat complications Side Effects: Dysuria, rectal bleeding, diarrhoea, impotence, incontinence
234
Management of prostate cancer - brachytherapy?
 TRUS used and used in fit men with no-comorbidity
235
Management of prostate cancer - hormonal?
Treating advanced disease or in conjunction with radiotherapy for localised disease LHRH agonists (leuprorelin, goserelin) • Reduces level of testosterone • Given monthly or 3-monthly via SC/IM depots • Medical castration causes increased CVD, osteoporosis Gonadotrophin-releasing hormone antagonist (degarelix) • Castrate levels of testosterone within 3 days • Monthly SC injection Oestrogen Therapy • Inhibit LHRH, rarely used Anti-Androgens (bicalutamide) • Slows progression and survival benefit combined with LHRH
236
Management of prostate cancer - chemotherapy?
 Used in castrate-refractory metastatic disease
237
Follow up of prostate cancer?
Watchful waiting followed up in primary care according to MDT outcome  PSA measured once a year Radical treatment  PSA 6 weeks after treatment, 6 monthly for 2 years, then yearly
238
Definition of urinary tract obstruction?
o Impaired urinary flow which results in proximal distention of urinary tract depending on location:  Urethra – bladder dilation, secondary hypertrophy and diverticulae formation  Ureter – megaureter and hydronephrosis
239
Points most susceptible to urinary tract obstruction?
 Pelvi-ureteric junction  Where ureters cross pelvic brim, at level of iliac vessels  Vesico-ureteric junction
240
definition of hydronephrosis?
o Urine-filled dilation of renal pelvis and calyces due to obstruction o Increased pressure being transmitted to kidney, leading to infection, stones and decreasing renal function
241
Epidemiology of urinary tract obstruction?
- In older men, BPH - 1 in 100 foetuses have hydronephrosis on US - Women – pelvic tumours, prolapse or pregnancy
242
Causes of urinary tract obstruction - within lumen?
 Blood clot  Calculi  Sloughed papillae  Tumour of renal pelvis or ureter
243
Causes of urinary tract obstruction - within wall?
```  Ureteric, urethral strictur  Congenital megaureter  Bladder neck obstruction  Congenital urethral valves  Pinhole meatus  Neurogenic bladder  SCI or MS ```
244
Causes of urinary tract obstruction - pressure from outside?
```  PUJ compression  Tumours  BPH  Retroperitoneal fibrosis • Present with dull abdominal pain, or complications of that • 50% hypertension • Anaemia, raised ESR/CRP  Pancreatitis  Crohn’s Disease  Phimosis ```
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Symptoms of acute upper urinary tract obstruction?
o Flank pain  Dull, sharp or colicky, varies in severity  Unable to lie still  Radiates to iliac fossa, inguinal area, testis or labium  Provoked by alcohol, diuretics or high fluid intake o Nausea & Vomiting o Loin tenderness, enlarged kidney o Anuria – bilateral
246
Symptoms of chronic upper urinary tract obstruction?
o Flank or abdominal pain o Chronic kidney disease o Polyuria
247
Symptoms of acute lower urinary tract obstruction?
``` o Severe suprapubic pain o Distended bladder – abdominal distention, suprapubic dullness on percussion o Urine hesitancy o Narrow/Weak urine stream o Terminal dribbling o Incomplete bladder emptying ```
248
Symptoms of chronic lower urinary tract obstruction?
``` o Urine hesitancy o Narrow/Weak urine stream o Terminal dribbling o Incomplete bladder emptying o May have signs of UTI o Distended bladder ```
249
Investigations in urinary tract obstruction?
DRE ``` Blood Tests o FBC – anaemia, infection o U&Es o If stones – serum calcium, phosphate and urate levels o If prostate enlarged - Serum PSA ``` Urinalysis – dipstick and M,C&S Blood cultures if signs of sepsis
250
Imaging in urinary tract obstruction?
US KUB  If abnormal – CT KUB or XR KUB  If suspected calculi – non-contrast helical CT  If renal pathology – contrast CT Renal scintigraphy – shows function and excretion Retrograde urethrography – demonstrates structural abnormalities Nephrostography Urodynamic studies
251
Urological emergencies requiring urgent treatment in urinary tract obstruction?
``` o Complete UT obstruction o Any obstruction in single kidney o Obstruction with fever/infection o CKD o Suspicion of neurological dysfunction o Uncontrolled pain ```
252
Management of urinary tract obstruction - general management?
``` o Analgesia o Hydration o Relieve blockage  Acute lower – catheter  Acute upper – nephrostomy or ureteric stent ```
253
Management of urinary tract obstruction - PUJ obstruction?
o Pyeloplasty – open, laparoscopic or robot-assisted o Endopyelotomy – full-thickness incision through stenosis and leaving stent o Ureteroscopic endoureterotomy – strictures
254
Management of urinary tract obstruction - malignancy?
o Treat cause | o Percutaneous nephrostomy to relieve obstruction
255
Management of urinary tract obstruction - idiopathic retroperitoneal fibrosis?
o Ureterolysis or stent placement o Corticosteroids and/or axathioprine, tamoxifen o Biopsy to exclude malignancy
256
Management of urinary tract obstruction - BPH?
o Acute retention – catheterisation o Mild symptoms – reduce fluid intake, avoid caffeine and alcoholic drinks o Medical treatment – alpha blockers (tamsulosin, alfuzosin, doxazosin, terazosin) & 5-alpha reductase inhibitors (finasteride) o Surgical treatment – Transurethral resection of the prostate
257
Complications of urinary tract obstruction?
``` o Infection o Extravasation o Fistula formation o CKD o Pain ```
258
Epidemiology of renal carcinoma?
- Mostly males | - Mean age 55
259
Types of renal carcinoma?
o 90% are renal cell carcinoma (Grawitz tumour) |  Arise from proximal tubular epithelium – highly vascular with large cells with clear cytoplasm (clear cell carcinoma)
260
Risk factors of renal carcinoma?
``` o Smoking o Males o Older age o Obesity o FHx o Von Hippal Lindau – bilateral RCC common ```
261
Spread of renal carcinoma?
o Direct – renal vein o Lymph o Haematogenous – bone, liver, lung
262
Symptoms of renal carcinoma?
``` o Asymptomatic o Haematuria o Loin pain o UTI o Mass in flank o Anorexia, malaise, weight loss ```
263
Signs of renal carcinoma?
o Anaemia, PCV, high calcium
264
Investigations to perform if suspected of renal carcinoma?
``` - Bloods o FBC – elevated RBC, reduced Hb o LDH raised o High Ca o U&Es ``` - Urinalysis o Haematuria o Proteinuria
265
When to refer for 2 week appointment of renal carcinoma?
- Refer for 2-week appointment if >45 and have: o Unexplained visible haematuria without UTI OR o Visible haematuria that persists or recurs after treatment of UTI
266
Diagnostic investigations of renal carcinoma?
o US KUB o CT scan o Biopsy
267
Management of renal carcinoma - risk assessment?
``` o <1 year to systemic therapy o Performance status o Hb low o Calcium high o Neutrophils high o Platelets high ```
268
Management of renal carcinoma - screening in VHL?
o Annual abdominal US at 11 years | o CT every year after 20
269
Management of renal carcinoma - Stage 1/2?
``` o Surgical Procedures  Laparoscopic cryotherapy  Percutaneous cryotherapy  Percutaneous radiofrequency ablation  Laparoscopic partial nephrectomy  Laparoscopic nephrectomy ``` o Not fit for surgery  Surveillance
270
Management of renal carcinoma - Advanced or metastatic cancer?
o First-Line  Nivolumab + Ipilimumab  Cabozantinib  Tivozanib o Second-Line  Lenvatinib + everolimus  Cabozantinib  Everolimus
271
Definition of renal stones/colic?
- Deposition of stones/blood clots within the urinary tract causing spasmodic pain - Commonly deposited in pelvoureteric junction, pelvic brim, vesicoureteral junction
272
Types of renal stones/colic?
o Calcium Oxalate (65%) o Struvite (15%) o Urate (5%) o Mixed
273
Pathology of renal stones/colic?
o Pressure necrosis causes direct damage to renal parenchyma
274
Epidemiology of renal stones/colic?
- Lifetime risk 10% - Higher prevalence in Middle East - Most occur in upper UT - Male 2x and peak age 20-40 years
275
Aetiology of renal stones/colic?
o Dehydration o Calcium stones – hypercalcaemia (primary, increased Vit D, sarcoidosis), renal disease (PKD tubular acidosis, medullary sponge kidney), hyperoxaluria o Urate stones – diet, increased uric acid, gout o Struvate stones – UTI, recurrent (staghorn calculi)
276
Symptoms of renal stones/colic?
Pain  Dull loin ache (renal pelvis stones), severe colicky pain often sudden onset  Radiating from loin to groin  Bladder stones cause suprapubic pain and perineal ache Haematuria often frank If obstructed then may have dysuria, inability to void
277
Signs of renal stones/colic?
o Restless, sweaty, pale, nauseated | o Fever, loin tenderness, palpable kidneys
278
Investigations of renal stones/colic?
- Bloods – FBC, U&E, Ca, PO4, urate, glucose - Urinalysis - Urine M, C&S if infection
279
Immediate admission when in renal stones/colic?
o Sepsis o CKD, solitary kidney, bilateral obstructing stones o Dehydrated and cannot take oral fluids due to N&V
280
Diagnostic imaging of renal stones/colic?
``` o Urgent (within 24 hours) non-contrast helical CT scan in adults o Urgent USS in children, or pregnant women ```
281
Tests to find cause of renal stones/colic?
o Serum Ca and urate, 24-hour calcium urine, phosphate, oxalate, urate
282
Management of renal stones/colic - initial management?
o Analgesia  Diclofenac 75mg IM repeated after 30 mins  If NSAIDS CI or not sufficient – give IV paracetamol  Opioids used if both NSAIDs and paracetamol not sufficient o Antiemetic if opioid o High fluid intake/IV fluids
283
Management of renal stones/colic - watchful waiting?
- Watchful Waiting for asymptomatic renal stones | o Stone <5mm OR stone >5mm and person wishes for watchful waiting
284
Management of renal stones/colic - when to refer to urology?
- Refer to urology if >5mm stones
285
Management of renal stones/colic - medical treatment?
o Medical expulsion if <10mm |  Give alpha-blocker – tamsulosin, alfuzosin
286
Management of renal stones/colic - surgical treatment - when?
• Offer within 48 hours if pain is ongoing and not tolerated OR stone unlikely to pass Pre-treatment stenting • Only considered in children having shockwave lithotripsy for renal staghorn stones
287
Management of renal stones/colic - surgical treatment of renal - what - if stone <10mm?
o Shockwave Lithotripsy o Ureteroscopy extraction if SWL CI, previous failed SWL o If SWL and URS failed – consider percutaneous nephrolithotomy
288
Management of renal stones/colic - surgical treatment of renal - what - if stone 10-20mm?
o Ureteroscopy or Shockwave lithotripsy | o IF SWL and URS failed – percutaneous nephrolithotomy
289
Management of renal stones/colic - surgical treatment of renal - what - if stone >20mm?
• Renal Stone >20mm, including staghorn stones o Percutaneous nephrolithotomy o URS if PCNL not an option
290
Management of renal stones/colic - surgical treatment of ureteric - if stone <10mm?
o Shockwave Lithotripsy | o Ureteroscopy if stones not cleared within 4 weeks of SWL, SWL CI or previous course failed
291
Management of renal stones/colic - surgical treatment of ureteric - if stone 10-20mm?
o Ureteroscopy extraction | o Percutaneous nephrolithotomy if URS failed
292
Ongoing management in renal colic/stones?
 Stone analysis |  Serum calcium
293
General advice in renal colic/stones?
```  Avoid rhubarb, spinach  High fluid intake 2.5-3L/day  Add fresh lemon juice to water  Avoid carbonated drinks  Restrict sodium intake to <6g/day  Maintain normal calcium intake  Medications for recurrent stones • Calcium Oxalate – potassium citrate + thiazide (after restricting sodium to <6d/day) ```
294
Type of polycystic kidney disease - autosomal dominant?
o 85% mutations in PKD1 (c16), 15% have PKD2 (c4) with slower course, PKD3 also described o Mutations in polycystin 1/2/3 which regulate tubular and vascular development in kidneys and other organs
295
Type of polycystic kidney disease - autosomal recessive?
o Chromosome 6 encoding fibrocystin | o Less common than ADPKD
296
Epidemiology of polycystic kidney disease?
- AD – 1 in 1000 individuals, 10% of people on dialysis
297
Symptoms of autosomal dominant polycystic kidney disease?
 Loin pain  Hypertension  Haematuria
298
Signs of autosomal dominant polycystic kidney disease?
```  Renal enlargement with cysts  Haematuria  Cyst infection  Renal calculi  Hypertension  Progressive renal failure ```
299
Extra-renal signs of autosomal dominant polycystic kidney disease?
```  Liver cysts  Subarachnoid haemorrhage (SAH)  Mitral valve prolapse  Ovarian cysts  Diverticular disease ```
300
Symptoms of autosomal recessive polycystic kidney disease - category 1 - perinatal?
 Large abdomen, renal enlargement  Severe renal impairment in utero – oligohydramnios and pulmonary hypoplasia  75% result in death within a week of birth
301
Symptoms of autosomal recessive polycystic kidney disease - category 2 - neonate?
 Palpable kidneys at birth and kidney disease progresses  Liver involvement  Usually causes death within few months
302
Symptoms of autosomal recessive polycystic kidney disease - category 3 - infancy?
 Enlarged kidneys, hepatosplenomegaly |  Develop ESKD
303
Symptoms of autosomal recessive polycystic kidney disease - category 4 - childhood?
 Marked liver disease  <10% develop ESKD  Renal enlargement and hepatosplenomegaly  Mortality is lowest in this category
304
Investigations in autosomal dominant polycystic kidney disease - screening for people with family affected?
Abdominal USS Diagnosis when FHx &: <30 - at least 2 unilateral or bilateral cysts 30 to 59 - 2 cysts in each kidney >60 - 4 cysts in each kidney
305
Investigations in autosomal dominant polycystic kidney disease - other investigations?
Bloods • FBC (high Hb) • U&E • Bone profile Imaging • USS & CT
306
Investigations in autosomal dominant polycystic kidney disease - screening for SAH?
 MR angiography |  1st degree relatives with SAH + ADPKD
307
Investigations for autosomal recessive polycystic kidney disease?
o USS in perinatal period o CT and MRI in older children o Genetic Testing if one diagnosed case in family
308
Management of polycystic kidney disease - general advice?
o Advise against contact sport o Avoid smoking o Maintain healthy diet and BMI o Regular exercise
309
Management of polycystic kidney disease - monitoring?
Annual o BP o U&E o USS
310
Management of polycystic kidney disease - BP?
o Target BP <130/80 | o Use ACEi/ARBs
311
Management of polycystic kidney disease - drug treatment?
Tolvaptan o Slow progression of cysts development and renal insufficiency if CKD stage 2/3 at start of treatment and evidence of rapidly progressing disease
312
Management of polycystic kidney disease - in end-stage renal failure?
Dialysis or transplant
313
Prognosis of polycystic kidney disease?
o 50% will be in ESRD requiring dialysis or transplant by age of 60 in PKD1 and 75 in PKD2
314
Definition of polycystic ovary disease?
o Hyperandrogenism, oligomenorrhoea and polycystic ovaries on US without other causes of polycystic ovaries
315
Epidemiology of polycystic ovary disease?
- Prevalence = 10% of women at childbearing age. | - Responsible for ~80% of anovulatory subfertility.
316
Pathogenesis of polycystic ovary disease?
- Excess androgens o Hypersecretion of LH (increased frequency and amplitude of LH pulses). o LH stimulates androgen secretion from ovarian thecal cells - Androgens are steroid hormones (e.g. testosterone) that stimulates or controls the development and maintenance of male characteristics o Increased androgens in the ovary disrupt folliculogenesis lead to excess small ovarian follicles (hence the cysts) and irregular/absent ovulation. o  peripheral androgens cause hirsutism (acne/body hair). - Insulin resistance leads to hyperinsulinemia: o Reduced sex hormone binding globulin (SHBG) in liver so increased free testosterone o Increased androgen production
317
Aetiology of polycystic ovary disease?
* Unknown | * Genetic (there is familial clustering of PCOS)
318
Symptoms of polycystic ovary disease?
o Asymptomatic o Oligomenorrhoea (irregular periods, <9 per year) or amenorrhoea (no periods) o Signs of hyperaldosteronism: acne, hirsutism, alopecia. o Obesity o Psychological: mood swings, depression, anxiety o Sub/infertility o Recurrent miscarriage
319
Signs of polycystic ovary disease?
o Male-pattern baldness, alopecia o Obesity (usually central) o Acanthosis nigricans (areas of increased velvety skin pigmentation which occur in the axillae and other flexures) o Clitoromegaly, increased muscle mass, deep voice - severe
320
Investigations of polycystic ovary disease - bloods?
```  Total testosterone (normal or slightly raised)  Free testosterone (may be raised if >5nmol/L – exclude androgen-secreting tumours and CAH – 17-hydroxyprogesterone)  SHBG (normal or low in PCOS)  LH (elevated)  FSH (normal)  TFTs  Prolactin • To exclude a prolactinoma ```
321
Investigations of polycystic ovary disease - imaging and screening?
o USS o Screen for diabetes (OGTT) and abnormal lipids o BMI
322
What is the Rotterdam criteria for diagnosing polycystic ovary disease?
Requires the presence of 2 out of 3 of: • Polycystic ovaries on US (12 or more follicles or ovarian volume >10 on USS) • Oligo-ovulation or anovulation • Clinical/biochemical features of hyperandrogenism (Acne, excess body hair, alopecia OR raised serum testosterone)
323
Management of PCOS - general advice?
``` o Weight loss o Diet o Exercise o Stop smoking o Sleep apnoea advice ```
324
Management of PCOS - women not planning pregnancy - improving insulin resistance?
 Metformin (not licensed so risks and benefits weighed up)
325
Management of PCOS - women not planning pregnancy - hormonal control?
 COCP cyclical  IUS  If not taking pill (norethisterone 5mg TDS PO for 10 days)
326
Management of PCOS - women not planning pregnancy - hirsutism control?
```  Co-cyprindol 2mg/d  Waxing, shaving  Eflornithine facial cream  Spironolactone • Avoid in pregnancy, teratogenic ```
327
Management of PCOS - women presenting with subfertility and wishing to conceive?
Clomifene citrate  Induces ovulation  Use for <6 cycles  Need US monitoring Metformin added on Laparoscopic Ovarian Drilling  Needlepoint diathermy in 4 places per ovary to reduce steroid production  When clomifene not working
328
Complications of PCOS?
* Infertility * Endometrial hyperplasia and cancer * CVD risk * T2DM – screening offered if obese, FHx, >40 * GDM – screen in pregnancy 24-28 weeks
329
Definition of urethral stricture?
- Narrowing of urethra due to scar tissue developing in tissues - Men common
330
Causes of urethral stricture?
o Iatrogenic (catheter, endoscope, prostatectomy, TURP) o BPH o Trauma (pelvic fracture, straddle injury) o Infection (UTIs, gonorrhoea, chlamydia) o Congenital o Cancer (rare)
331
Symptoms and signs of urethral stricture?
- Reduced urine flow - Straining to pass urine - Spraying of urine or double stream - Incomplete bladder emptying - UTIs - Reduced force of ejaculation
332
Investigations of urethral stricture?
- Post-void bladder US - Urine flow tests - Retrograde urethrogram (antegrade cystourethrogram if suprapubic catheter in place)
333
Management of urethral stricture?
- Dilating and stretching - Stenting (work best for short strictures) - Internal urethrotomy (endoscopic) - Urethroplasty
334
Definition of vesicoureteric reflux?
- Reflux of urine from bladder into ureter - Usually due to primary maturation abnormality of vesicoureteral junction which leads to impairment of normal pinch-cock action of VUJ in micturition - Can be unilateral or bilateral
335
Epidemiology of vesicoureteric reflux?
Females common - 25% of children <6 with first-time URI have VUR and 25% have significant VUR - 1-3% prevalence in general population - Most common cause of chronic pyelonephritis
336
Associated conditions of vesicoureteric reflux?
o Congenital obstructive posterior urethral membrane (COPUM) o Bulbar urethral obstruction (Cobb collar) o Ureteral partial obstruction o Duplex collecting system
337
Symptoms of vesicoureteric reflux?
``` - Recurrent UTIs o Dysuria o Frequency o Offensive smelling urine o Abdominal pain o Fever ```
338
Investigations of vesicoureteric reflux?
- US KUB | - Micturating cysto-urethrogram (MCUG)
339
What is MCUG and how is it graded in vesicoureteric reflux?
Micturating cysto-urethrogram (MCUG) o Bladder catheterised, then filled with dye and x-ray o Graded:  1 – limited to ureters  2 – renal pelvis  3 – mild dilatation of ureter and pelvicalyceal system  4 – tortuous ureter with moderate dilatations, blunt fornices  5 - severe dilatation of ureter and pelvicalyceal system, loss of fornices
340
Further testing of vesicoureteric reflux?
- Mercapto acetyl tri-glycine reflux test (MAG3) o Injection of special dye is given and pictures taken when passing urine - Dimercapto succinic acid (DMSA) to assess kidneys
341
Management of vesicoureteric reflux - general measures?
o Ensure good fluid intake o Pass urine regularly (women after sexual intercourse) o Avoid constipation
342
Management of vesicoureteric reflux - medication?
o Low-dose prophylactic antibiotics at night |  Trimethoprim/Nitrofurantoin/Amoxcillin
343
Management of vesicoureteric reflux - surgery?
o Cystoscopy and injection of Deflux | o Open/Keyhole ureteric re-implantation
344
Complications of vesicoureteric reflux?
- Renal scarring - Recurrent UTIs - Acute pyelonephritis
345
Definition of glomerulonephritis?
- Increased glomerular cellularity restricts glomerular blood flow and therefore filtration is decreased - Leads to: o Decreased urine output and volume overload o Hypertension o Oedema o Haematuria and proteinuria
346
Epidemiology of glomerulonephritis?
- Peak age 7 years
347
Aetiology of nephritic syndrome - primary causes?
IgA Nephropathy o Visible haematuria o Most common glomerulonephritis Mesangiocapillary glomerulonephritis o Episodes of macroscopic haematuria, commonly associated with URTIs
348
Aetiology of nephritic syndrome - secondary causes?
Post-infectious (streptococcal most common, staph aureus) o Usually presents 7-21 days to streptococcal throat infection o Cola-coloured urine o High anti-DNAse Vasculitis (HSP, SLE, Wegeners granulomatosis) o HSP is vasculitis disease, see HSP o SLE mainly affect adolescent girls and presents with multiple antibodies and haematuria/proteinuria SLE Goodpasture syndrome o Anti-GBM positive o Auto-antibodies to type 1 collagen – renal and lung disease
349
Aetiology of nephrotic syndrome - primary causes?
Minimal change disease – 85% in children o Idiopathic, NSAIDs, Hodgkin’s lymphoma o Biopsy – normal under light microscopy o Steroids usual course of treatment Focal segmental glomerulonephritis (FSGN) – most common in adults o Segmental areas of mesangial collapse and sclerosis o Due idiopathic, HIV, SCD, Alport’s, obesity, reflux nephropathy Membranous nephropathy – common in older adults o Due to – malignancy, hepatitis B, gold, penicillamine, NSAIDs, thyroid, SLE o Thickened GBM Membranoproliferative glomerulonephritis
350
Aetiology of nephrotic syndrome - secondary causes?
* Infection – HIV, HepB/C, syphilis, malaria * SLE, HSP, Lupus * Diabetes – MC secondary cause * Alport’s syndrome * Malignancies * Toxins (snake bites, bee stings) and heavy metals
351
Symptoms of nephritic syndrome?
o Haematuria, raised BP, oliguria, reduced EGFR
352
Symptoms of nephrotic syndrome?
o Proteinuria, oedema, hypoalbuminaemia
353
Symptoms of uraemia?
o Malaise, anorexia, fever
354
Investigations in glomerulonephritis - what bloods to do to find cause??
o FBC, CRP, U&Es (creatinine, K, bicarbonate, calcium, phosphate, albumin) o Complement (low C3, normal C4) o ANA and anti-DNA antibodies (SLE suspected), Anti-GBM (Goodpastures), ANCA (if vasculitis suspected – Wegeners, polyangiitis) o Blood cultures o Glucose o Viral Serology (HepB/HepC)
355
Investigations in glomerulonephritis - other investigations?
Mid-stream urine M, C & S o Count RBCs, WBCs, hyaline, granular casts, red cell casts means glomerular bleeding in post-infectious glomerulonephritis o Urine culture and specific gravity Urine dipstick Urine PCR Renal US Renal biopsy
356
Management of glomerulonephritis?
Early referral to nephrologist Supportive treatment o Attention to fluid balance o Keep BP <130/80 or <125/75 if proteinuria >1g/d  ACEi/ARB – useful as reduce proteinuria and preserve renal function o Treat Oedema  Loop diuretics Nitroprusside for encephalopathy HSP and IgA nephropathy require long term follow-up SLE needs immunosupression
357
What is normal daily urine protein excretion in a day?
- Average daily urine protein excretion in adults is 80mg/day - Normal <150mg/day
358
Definition of orthostatic proteinuria?
o Normal urinary protein excretion during night but increased excretion during the day, associated with activity and upright posture o Due to increased renal dynamics o Mostly albumin
359
Epidemiology of orthostatic proteinuria?
- Most common in children and young adults, males more | - 22% of school males
360
Symptoms of orthostatic proteinuria?
- Transient symptoms – recent strenuous exercise
361
Other causes of proteinuria?
o Physical Exercise, fever, pregnancy, UTI, Nephrotic syndrome, renal tubular disease, CKD o Nutcracker Phenomenon – compression of left renal vein between aorta and superior mesenteric artery
362
Investigations of orthostatic proteinuria?
- Urinalysis - Bloods - Urine ACR/PCR EMU (first-void) & random sample in day - 24-hour urine collection
363
Investigations of orthostatic proteinuria -urinalysis findings?
o Positive protein dipstick during day o Negative EMU protein sample o Exclude UTI, diabetes
364
Investigations of orthostatic proteinuria -bloods findings?
o U&Es normal | o Glucose normal
365
Investigations of orthostatic proteinuria -urine ACR/PCR findings?
o Absence of proteinuria in morning sample and presence in daytime confirms orthostatic proteinuria
366
Investigations of orthostatic proteinuria -24-hour urine collection findings?
Protein, creatinine clearance – split into day and night collections
367
Investigations of orthostatic proteinuria -diagnosing nutcracker phenomenon?
o US KUB normal | o CT
368
Management of orthostatic proteinuria?
- Rule out other causes – may require referral to nephrologist - No specific treatment – may persist but no clinical significance