1
Q
What are some risk factors for a UTI in children?
A
- <1
- Female (if neonate then male)
- Caucasian
- Voiding dysfunction
- Vesicoureteral reflex (VUR) (33%)
- Sexual abuse
- Spinal abnormalities
- Constipation
- Immunosuppression
2
Q
How may a UTI present in babies and younger children?
A
- Fever
- Vomiting
- Lethargy
- Irritability
- Vomiting
- Poor feeding
- Urinary frequency
- Offensive smelling urine
3
Q
Once children are old enough to verbalise, what are some symptoms they may have if they have a UTI?
A
- Increased frequency
- Painful urination
- Changes in continence
- Abdominal pain (suprapubic)
- Loin tenderness
- Fever
- Haematuria
- Cloudy urine
- Offensive smelling urine
4
Q
When should you consider pyelonephritis over cystitis in children?
A
- Temp of 38oC or higher and bacteriuria
- Temp lower than 38oC with loin pain/tenderness and bacteriuria
If no systemic symptoms but bacteriuria present then cystitis should be considered
5
Q
If a child has urinary symptoms, what examinations should you do on them?
A
6
Q
What are some differentials for a UTI in children?
A
- Vulvovaginitis
- Kawasaki disease
- Voiding dysfunction
- Threadworms
- Consider abuse if recurrent but no underlying cause
7
Q
What investigations should be done if you suspect a child to have a UTI?
A
- Clean Catch Urine Sample for Urine Dipstick
- MC+S MSU: if temp over 38 or leucocytes and nitrates positive on dipstick
- Arrange imaging
8
Q
How do you describe to a parent how to get a clean-catch sample?
A
- Clean genitals with water
- Tap suprapubic area with two fingers 1 hour after feed
- Avoid first stream of urine
9
Q
What are the different types of imaging used in investigating UTIs in children and what all they show us?
A
- Abdominal US: look for reflux but low sensitivity
- DMSA (Dimercaptosuccinic Acid) Scan: Assess for damage after recurrent UTIs 4-6 months after infection. Inject radioactive material and a gamma camera to see how much is taken up by kidney. Patches indicate areas of scarring
- Micturating Cystourethrogram (MCUG): Used to diagnose VUR. Catheterise the child and inject contrast into bladder and take a series of X-Rays to see if contrast is refluxing back into ureters. Given prophylactic abx for 3 days before
10
Q
What is the definition of the following:
- Recurrent UTI in children
- Atypical UTI in children
A
Atypical UTI features:
- Poor urine flow
- Abdominal or bladder mass
- Raised creatinine
- Sepsis
- Failure to respond to treatment within 48 hours
- Non-E.Coli organism
Definition of recurrent UTI:
- 2 or more episodes of upper UTI (pyelonephritis)
- 1 episode of upper UTI and 1 episode of lower UTI
- 3 episodes of lower UTI
11
Q
When should children be offered an US for a UTI and at what time frame?
A
<6 months: within 6 weeks
Recurrent UTI: within 6 weeks
Atypical UTI: during illness
If just normal UTI and over 6 months no US needed
12
Q
When should children be offered a DMSA for a UTI and at what time frame?
A
Needs to be minimum 4 months since infection as pyelonephritis changes can look like scarring
Do for any atypical or recurrent UTIs in children up to 3.
If over 3 only do if atypical UTI
13
Q
When should children be offered an MCUG for a UTI and at what time frame?
A
Only in under 6 months if recurrent/atypical UTI
Should also be considered in those with FHx of VUR, poor urinary flow or abnormal dilatation of ureter on US
14
Q
What is the gold standard for diagnosing VUR and how is this managed if diagnosed?
A
MCUG
Causes scarring due to reflux and predisposes to further UTIs
Usually give prophylactic antibiotics or ureteric reimplantation surgery if grade 4/5 VUR
Investigate siblings as genetic component
15
Q
How are lower UTIs (cystitis) treated in children?
A
Under 3 months: immediate referral to paediatrics for IV antibiotics (Ceftriaxone) and investigations for sepsis
Over 3 months: PO Nitrofurantoin for 3 days, if not improved within 48 hours reassess so safety net to parent. Use Cephalexin if cannot swallow
16
Q
How are upper UTIs (pyelonephritis) treated in children?
A
Under 3 months: Immediate referral to paediatrics for IV antibiotics (Ceftriaxone) and septic screen
Over 3 months: PO Cefalexin or Co-Amoxiclav for 10 days. Consider referral to paediatrics if poor fluid intake, cannot take oral antibiotics or is deteriorating
17
Q
What advice can be given to parents to prevent UTIs in their children in the future?
A
- Treat and prevent constipation
- Clean the perineum from front to back
- Avoid nylon underwear and bubble baths
- Encourage fluid intake and double micturition
- Consider prophylaxis if recurrent UTIs
18
Q
What are the complications of UTIs in children?
A
- Renal scarring
- Hydronephrosis
- Chronic renal failure
- Hypertension
19
Q
Vulvovaginitis is common in girls aged 3-10 before puberty. What are some causes of this?
A
- Wet nappies
- Use of chemicals or soaps in cleaning the area
- Tight clothing that traps moisture or sweat in the area
- Poor toilet hygiene
- Constipation
- Threadworms
- Pressure on the area, for example horse riding
- Heavily chlorinated pools
20
Q
How may vulvovaginitis present in young girls?
A
Often have positive leucocytes on dipstick and negative nitrites so misdiagnosed as UTI
- Soreness
- Itching
- Erythema around the labia
- Vaginal discharge
- Dysuria
21
Q
How can vulvovaginitis be managed in young girls?
A
Do not treat as UTI or Thrush!!!
- Avoid washing with soap and chemicals
- Good toilet hygiene, wipe from front to back
- Keep the area dry
- Emollients, such as sudacrem
- Loose cotton clothing
- Treating constipation and worms where applicable
- Avoiding activities that exacerbate the problem
In severe cases may recommend oestrogen cream to improve symptoms
22
Q
What is an AKI and the causes of this in children?
A
Acute rapid decline in renal function leading to a rise in creatinine and/or oliguria/anuria. Pre-renal, Renal and Post-renal causes
- Nephroxicity (NSAIDs, aminoglycosides, vancomycin, aciclovir, and contrast nephropathy)
- Sepsis
- Gastroenteritis causing diarrhoea/dehydration
- Glomerulonephritis
- Haemolytic uraemic syndrome (HUS)
23
Q
What are the different stages of AKI in children and how may it present?
A
Uses pRIFLE or AKIN criteria
Always consider if child has haematuria, oedema or oliguria
24
Q
What investigations should be done for a suspected AKI?
A
- Detailed history and examination (e.g drugs)
- Urine dipstick testing and MSU and consider nephritic screen
- U+Es
- Creatinine
- Calcium, phosphate, bicarbonate, chloride
- LFTs (inc. albumin)
- Glucose
- FBC
- ECG
- Abdominal US: look for obstruction of above show no cause
- Renal biopsy
25
What are the serious complications of an AKI in a child?
* Hyperkalaemia
* Metabolic acidosis - kidneys cant remove the acids in food and also cant prosuce as much bicarbonate
* Pulmonary Oedema
Need dialysis for these!!!!!
26
What might you see on MSU for AKI caused by GN?
* Red cell casts
* Proteinuria
27
How is an AKI in children managed?
* **Remove any cause** e.g NSAIDs
* **Refer to paediatric nephrology** team to treat underlying cause
* **Initial fluid management** depending on cause of AKI. Start fluid chart
* **Monitor BP**
* **Monitor weight daily** (aim for 0.5% loss/day)
* **Monitor ECG** (give no K+ in fluids)
* **If fluid overload consider haemodialysis**
28
What is haemolytic uraemia syndrome and what is it caused by?
***Thrombosis*** within ***small blood vessels*** throughout the body
Triggered by a bacterial toxin called ***shiga toxin*** produced by ***e.coli 0157*** or ***Shigella***
Use of antibiotics and anti-motility medications such as loperamide to treat gastroenteritis caused by these pathogens increases the risk of developing HUS
29
What is the classic triad in HUS?
* ***Haemolytic anaemia***: caused by red blood cells being destroyed
* ***AKI***
* ***Thrombocytopenia***: low platelet count
30
How may HUS present?
Preceded by blood diarrhoea around 5 days before
* Reduced urine output
* **Haematuria or dark brown urine**
* Abdominal pain
* Lethargy and irritability
* Confusion
* Oedema
* Hypertension
* **Bruising**
31
How is HUS managed in children?
***Medical emergency*** and has a 10% mortality so refer to paediatric nephrologist.
**_Self limiting and supportive management:_**
* Urgent referral to the paediatric renal unit for ***renal dialysis*** if required
* Antihypertensives if required
* Careful maintenance of fluid balance
* Blood transfusions if required
32
What is nephrotic syndrome characterised by and what is the pathophysiology of this?
Glomerular basement membrane is damaged allowing proteins through. In children usually due to podocyte foot processes being fused together
* **Hypoalbuminaemia (\<25g/L)**
* **Proteinuria** (\>3+ protein on urine dipstick or \>200mg/mmol)
* **Oedema**
* **Hypercholesterolaemia/Hyperlipidaemia**
33
What are some of the causes of nephrotic syndrome?
* **Minimal change disease:** MOST COMMON!!! 90% of cases in children. Usually affects 2 to 5 year olds
* **Secondary to intrinsic kidney disease**
* **Secondary to systemic disease**
34
How may nephrotic syndrome present and what are some differentials for this presentation?
* **Frothy urine**
* **Oedema** (starts periorbital then generalised)
* **Pallor**
* **Ascites**
* **Anorexia**
**Differentials:** heart failure, anaphylaxis, malnutrition (Kwashiorkor)
35
What are some atypical features of nephrotic syndrome that would warrant a renal biopsy?
* Poor renal function
* Haematuria
* Hypertension
36
What investigations should you do to confirm a diagnosis of nephrotic syndrome (minimal change disease cause)?
**_Baseline_**
* **Urine dip and MSU:** small molecular weight proteins and hyaline casts
* **Urinary protein:creatinine ratio**
* **U+Es:** usually normal
* **FBC**
* **Bone profile and Serum albumin**
* **VZIG:** check for immunity as will be starting steroids
**_Additional_**
Complement levels, Anti-streptolysin O Titre (ASOT) and autoimmune ANA, ANCA, anti-dsDNA.
37
How is nephrotic syndrome managed?
**-High dose steroids:** Prednisolone for 4 weeks then weaned off over 8 weeks. Take renal biopsy first and ***give gastric protection***
**-VZIG and Pneumococcal vaccine**
**-Low salt diet** (low Na): avoid more oedema
**-Diuretics and Fluid restrict:** to treat oedema
**-Albumin infusions** may be required in severe hypoalbuminaemia
**-Antibiotic prophylaxis:** immunoglobulins leak through membrane so at higher risk of infection, give penicillin
38
What are the different types of minimal change disease based off of how they respond to treatment?
**Steroid Sensitive Nephrotic Syndrome:** 80% of children are this type and 80% of those children will have a relapse but remit
**Steroid Dependent:** difficult to wean off steroids
**Steroid Resistant:** Do not respond to steroids, need ACEi and immunosuppressants like cyclophosphamide, tacrolimus
39
What are the complications of nephrotic syndrome?
* **Intravascular hypotension:** only give diuretics if symptomatic oedema to prevent this complication
* **Spontaneous pneumococcal peritonitis:** give vaccine and penicillin
* **Infection:** loss of Ig's and steroids
* **Relapse of minimal change disease**
* **VTE:** proteins that normally prevent blood clotting are lost in the kidneys, and because the liver responds to low albumin by producing pro-thrombotic proteins
40
What is nephritic syndrome characterised by and the pathophysiology of this?
Inflammation within the nephrons of the kidney
* **Haematuria**
* **Oliguria**
* **Hypertension**
41
What investigations should you do for nephritic syndrome?
* **MSU:** may have red cell casts
* **FBC**
* **U&E** (creatinine, K, bicarbonate, calcium, phosphate and al- bumin),
* **Complement** (low C3, normal c4)
* **Anti Streptolysin O Titre**
* **Throat swabs**
* **ANA, Anti-dsDNA** if SLE or vasculitis
* **Renal US**
42
What are the main causes of nephritic syndrome in children and some other causes?
* **Post Streptococcal Glomeruonephritis**
* **IgA Nephropathy** (Berger's)
**Others:** autoimmune like SLE and ANCA
43
How does post-streptococcal GN present and what is the pathophysiology of this?
Occurs **7-21 days** after B-haemolytic strep infection e.g **tonsillitis or impetigo** by Strep Pyogenes
**Immune complexes** made up of streptococcal antigens, antibodies and complement proteins get stuck in the glomeruli of the kidney and cause inflammation and AKI
44
What investigations should you do for PSGN?
* Ask about history of tonsillitis
* **Throat swab**
* **Anti-streptolysin O Antibody Titres** (ASOT)
* **U+Es:** raised urea and creatinine
* **Complement:** low C3
* **Urinalysis**
45
What is the management for PSGN?
* **Antihypertensives**
* **Diuretics** e.g Furosemide
46
How does IgA nephropathy present and what is the pathophysiology of this?
* Related to [Henoch-Schonlein Purpura](http://zerotofinals.com/paediatrics/rheumatology/hsp/)
* **Days** after URTI, UTI or gastroenteritis
* **IgA deposits** in the nephrons of the kidney causes inflammation
* **Normal complement**
* **Renal biopsy** will show IgA deposits and glomerular mesangial proliferation
It usually presents in teenagers or young adults
47
How is IgA nephropathy treated?
* ***Supportive treatment*** of the renal failure
* ***Immunosuppressant*** such as steroids and cyclophosphamide to slow progression of the disease
48
How do you work out eGFR in children?
49
What are the causes of CKD in children?
**-Congenital –** Renal dysplasia, obstructive uropathies like PUV, VUR
**-Hereditary** – ARPKD, ADPKD, hereditary nephritis like Alport syndrome
**-Glomerulonephritis –** FSGS, MPGN, lupus nephritis, congenital nephrotic syndrome, ANCA vasculitis
**-Tumours/Vascular –** Wilms tumour, renal venous thrombosis, renal artery stenosis
**-Infection –** Hemoltic uraemic syndrome
**-AKI leading to CKD**
50
What are the stages of CKD?
51
How may a child present with CKD?
* Weakness
* Tiredness
* Headache
* Hypertension
* Hypertensive retinopathy
* Anaemia
* Failure to thrive
52
What are the complications of chronic renal disease in children? (important)
* Failure to grow/thrive
* Intellectual disability
* Tendency to bleed
* Hyperuricaemia
* Renal osteodystrophy
* Anaemia
* Metabolic acidosis with low sodium and increased potassium
* CVD due to HTN and hyperlipidaemia
53
How is poor growth managed in CKD for children?
* Get a dietician’s help
* Extra calories, especially if vomiting
* Provide protein at a level of 2.5g/kg/24h
* Reduce K+ in diet
* NG tube feeding
* ***Growth hormone therapy*** combined with optimal dialysis
54
What is renal osteodystrophy and how is it managed?
* Poor mineralization due to renal failure, causing poor growth, muscle weakness, slipped epiphyses, bone pain, and bone deformity
* If glomerular filtration falls to \<25% of normal, compensatory mechanisms to enhance phosphate excretion fail causing **hyperphosphataemia** and **hypocalcaemia**, so **PTH rises**, which **enhances bone resorption** to release Ca2+ in an attempt to correct hypocalcaemia. Also, the failing kidneys cannot convert enough 25-hydroxycholecalciferol to active 1,25-dihydroxycholecalciferol, **so GI calcium absorption falls**, so worsening hypocalcaemia
* Use **phosphate binders,** eg calcium carbonate taken just before food
* If Ca2+ is low despite correcting serum phosphate, give **calcitriol**
55
How is anaemia managed in children with CKD?
damaged kidneys produce less erythropoietin (EPO), a hormone that signals the bone marrow to make red blood cells, leading to a deficiency in red blood cell production and resulting in anemia
Typical Hb is 60–90g/L
* SC EPO, if on haemodialysis given IV
* Do not transfuse, as this suppresses erythropoietin production
* Iron and Folic Acid supplementation
56
What are some important things to monitor when a child has CKD?
* Always look at growth and nutrition
* Educate family about the function of the kidneys
57
What type of polycystic kidney disease presents in children rather than adults and how does it present?
***Autosomal recessive polycystic kidney disease*** (***ARPKD***) usually picked up on antenatal ultrasound scans
**_Features_**
* ***Cystic enlargement*** of the ***renal collecting ducts***
* ***Oligohydramnios*** on antenatal scans leading to pulmonary hypoplasia and Potter syndrome
* ***Congenital liver fibrosis***
Pulmonary hypoplasia present with difficult breathing after birth and Potter syndrome has dysmorphic features
58
What is the management of ARPKD?
***Renal dialysis*** within the first few days of life Most patients develop ***end stage renal failure*** before reaching adulthood.
The prognosis is poor, around 1/3 will die in the neonatal period. Around 1/3 will survive to adulthood.
59
What is **Multicystic Dysplastic Kidney** and how does it differ to ARPKD?
Only one of the kidneys is made up of many cysts while the other kidney is normal
Normally diagnosed on ***antenatal ultrasound scans***.
Cystic kidney will atrophy and disappear before 5 years of age.
60
How is multi cystic dysplastic kidney managed?
* No treatment
* Follow up renal ultrasound scans
* Prophylactic abx for UTI
**Complications:** UTIs, hypertension and CKD
61
What is a Wilm's tumour and how may it present?
Nephroblastoma (undifferentiated mesodermal tumour) usually occurring in under 5's
**Child under the age of 5 with:**
* Painless palpable abdominal mass
* Abdominal pain
* Haematuria
* Lethargy
* Fever
* Hypertension
* Weight loss
62
How is a Wilm's tumour diagnosed and managed?
**_Ix_**
* Initial: US
* CT or MRI for staging
* Biopsy
**_Mx_**
* ***Surgical excision*** of the tumour and ***nephrectomy***
* ***Adjuvant chemotherapy***
* ***Adjuvant radiotherapy***
**_Prognosis_**
Early stage tumours have 90% chance of cure
63
What is a posterior urethral valve and how is it diagnosed?
* Affects male fetuses
* Folds of bladder mucosa block proximal urethra, causing outflow obstruction and hydronephrosis
* Usually diagnosed antenatally with oligohydramnios and renal tract dilatation or postnatally with absent or feeble voiding
* Do **MCUG** and **US** then **catheterise** and do an **ablation**
64
What are some risk factors for undescended testes ad some risks of this condition?
**_Risk Factors_**
* Family history of undescended testes
* Low birth weight
* Small for gestational age
* Prematurity
* Maternal smoking during pregnancy
**_Risks_**
* Testicular torsion
* Testicular cancer
* Infertility
65
How is cryptorchidism managed?
absent testicle due to undescended
* Watchful waiting
* If they have not descended by 6 months should be seen by paediatric urologist
* ***Orchidopexy*** between 6 and 12 months of age to prevent 5 fold risk of cancer
66
What are retractile testes?
* May mistake for undescended testes
* Normal in boys that have not reached puberty for the testes to move out of the scrotum and into the inguinal canal when it is cold or the cremasteric reflex is activated
67
What is hypospadias and the complications of this?
* Urethral meatus displaced to the ventral side of the penis. 90% at bottom of glans
* Epispadias is where the meatus is displaced to the dorsal side
**Complications:** Cordee, Difficulty directing urination, Sexual dysfunction, Cosmetic concerns
68
How is hypospadias managed?
Referral to a paediatric urologist for ongoing management
* Warn parents not to circumcise until urologist says it is ok as need it for repair
* Mild cases may not require any treatment
* Surgery is usually performed after 3 – 4 months of age
* Surgery aims to correct the position of the meatus and straighten the penis
69
What are the two types of nocturnal enuresis (inability to control urination)?
Nocturnal Enuresis is normal up to age 5!!!!
* **Primary nocturnal enuresis:** never achieved urinary continence overnight
* **Secondary nocturnal enuresis:** have previously achieved urinary continence overnight for at least 6 months
70
What are some causes of primary nocturnal enuresis?
* Variation on normal development
* Family history of delayed dry nights
Other causes of primary nocturnal enuresis include:
* Overactive bladder
* Fluid intake prior to bedtime
* Psychological distress
* Secondary causes such as chronic constipation, UTI, learning disability or cerebral palsy
71
How is primary nocturnal eneuresis investigated and managed?
If FHx then just give reassurance, no further investigations needed
**_Ix_**
* 2 week diary of toileting, fluid intake and bedwetting episodes
* Look for psychological causes
**_Mx_**
* **Reassure if children under 5** that likely to resolve without treatment
* **Lifestyle changes:** reduced fluid intake in evenings, pass urine before bed and ensure easy access to toilet
* **Encouragement and positive reinforcemen**t: avoid blame or shame
* **Treat any underlying causes:** e.g constipation
* **Enuresis alarms**
* **Pharmacological treatment**
72
What are some causes of secondary nocturnal enuresis?
* UTI
* Constipation
* Type 1 diabetes
* New psychosocial problems (e.g. stress in family or school life)
* Maltreatment
Always think about ***abuse*** and ***safeguarding***
73
How is secondary nocturnal enuresis managed?
* Treating the underlying cause e.g UTI or constipation
* Enuresis alarm
* Investigate for abuse
74
What is diurnal enuresis?
When a child is dry at night but not during the day
* Psychosocial problems
* UTI
* Constipation
* Stress and Urge
75
What advice do you need to give parents with an enuresis alarm?
it detects some mositure and then the child knows they need to get out of bed and go to the toilet
Need to use for at least 3 months/prolonged period for them to start to make a difference
76
What pharmacological treatment is available for enuresis and when may this be used?
**Desmopressin (analogue of ADH):** Taken at bedtime especially at sleepovers. Reduces volume of urine made by kidneys
**Oxybutinin:** anticholinergic medication that reduces the contractility of the bladder
**Imipramine:** TCA that relaxes bladder and lightens sleep
77
If a child has haematuria what differentials are you considering?
* Glomerulonephritis (e.g PSGN)
* Nephritic syndrome
* Alport syndrome
* UTI
* Trauma
* Wilm's tumour
* Obstructing stone
78
B, D, E
Need bone profile because albumin comes under this
79
A, C and D
Need antibiotics in form of Penicillin V for all oedematous patents to prevent infection with Pneumococcal
80
B and D
81
How can you tell the difference between glomerular and non-glomerular haematuria in children?
**_Glomerular_**
**Raised BP:** due to decreased filtration
**Rusty colour**
**Red cell casts**
82
What are some clues for the cause of a childs GN?
**Henoch-Schonlein purpura is painful.** It is an IgA autoimmune vasculitis precipitated by infections and vaccinations
83
**Bleeding tendency:** Increase in urea results in abnormal platelet adhesion and aggregation
**Hyperuricaemia:** decreased urinary excretion
**Intellectual impairment:** Neurological findings can range from seizures and severe intellectual disability to subtle deficits resulting in poor school performance.
84
What is important in the care of children that have glomerulonephritis?
Need follow up as at risk of developing CKD
85
CHECK TUTORIALS ON NOTABILITY AND ADD THE NOTES DURING EXAM REVISION!!!!!!!
86
What should parents be doing once their child is discharged with minimal change disease?
* **Urine dipstick for albumin:** if +++ on 3 consecutive days this is a relapse and needs steroids
87
What could abdominal pain in nephrotic syndrome be?
* UTI
* Mesenteric vein thrombosis
If any thrombosis suspected give LMWH
88
What are the different medications given to treat minimal change disease?
* Steroids
* PPI
* Penicillin prophylaxis
* Clindamycin to cover Group A strep
* Diuretics
* Vaccines
* Cyclophosphamide, Tacrolimus, Ciclosporin if above not working
89
How is VUR managed?
* Watch and wait as may resolve as continence develops
* Antibiotic prophylaxis
* Surgery if grade 4/5
90
What is the biggest complication of nephrotic syndrome?
Intravascular Shock
Give IV albumin
91
How does PUV present?
* Poor wee stream
* Eneuresis
* UTI
92
what gender is the posterior urethra seen in
boys
Boys are more likely to develop posterior urethral valves (PUVs) than girls because this condition arises from a developmental anomaly that occurs specifically in the male urethra during early fetal development,
however posterior urethral valve is not normal and can cause difficulties in boys emptying their bladder, can cause UTI
Y4 Paediatrics SA
flashcards
Decks in class (32)
# Cards
-
1 - History Taking and Communications with the Child33
-
2 - Examination and Practical Procedures57
-
3 - Genetics63
-
4 - Neonatology93
-
5 - Surveillance and Development61
-
6 - Community Paediatrics 195
-
7 - Safeguarding34
-
8 - Respiratory 175
-
9 - Respiratory 296
-
10 - Cardiology92
-
11 - ENT76
-
12 - Endocrinology77
-
13 - Puberty58
-
14 - Allergy and Immunology75
-
15 - Dermatology68
-
16 - Nephrology92
-
17 - Haematology86
-
19 - Orthopaedics67
-
18 - Oncology55
-
20 - Rheumatology45
-
21 - Neurology 160
-
22- Neurology 250
-
23 - Gastroenterology85
-
24 - Paediatric Surgery69
-
25 - Paediatric Surgery 251
-
26 - Infectious Diseases 199
-
27 - Infectious Diseases 280
-
28 - Recognition and Management of the Sick Child19
-
29 - Emergency Paediatrics 174
-
30 - Emergency Paediatrics 261
-
31 - Prescribing for Children29
-
questions176
