Paeds RENAL Flashcards

1
Q

How does UTI present in an infant as compared to a child?

A

Infant: fever, vomiting, lethargy, poor feeding, jaundice, septicaemia

Children: dysuria, frequency, abdo pain, lethargy, anorexia, haematuria

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2
Q

How should UTI be investigated?

A

URINE DIP
Nitrite stick test: very specific
Leucocyte esterase: less specific than nitrites
Urine MC+S: diagnostic
Only do imaging if recurrent/ atypical UTI

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3
Q

Recall the different UTI management for different age groups

A

<3m: admit, IV Abx then switch to oral prophylaxis: emergency: book urgent USS

> 3m, upper UTI: consider admission with IV Abx, if not, oral Abx: book USS

> 3m, lower UTI: oral Abx as local guidelines for 3d (eg trimethoprim, nitrofurantoin)

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4
Q

How should recurrent UTI be managed in children?

A

Abx prophylaxis

<6 months: USS urgently + MCUG
>3y: USS within 6w

DMSA scan 4-6m later

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5
Q

By what age should children be dry by day?

A

4 years old

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6
Q

By what age should children be dry by day and night?

A

5 years old

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7
Q

What is ‘primary bedwetting’?

A

Bedwetting that has not previously been resolved

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8
Q

How should primary bedwetting be managed in children <5 years old?

A

Reassure parents: often resolves by 5y

Educate: easy access to toilet at night, bladder emptying before bed, positive reward system

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9
Q

How should primary bedwetting be managed in children >5 years old?

A

Infrequent (<2/ week): watch + see approach

Frequent: 1st line: enuresis alarm, pos reward system (eg encourage child to help change sheets)

2nd line: desmopressin (1st line for short-term control like sleepovers + school trips)

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10
Q

How should enuresis with daytime symptoms be managed?

A

Refer to enuresis clinic, community paediatrician

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11
Q

What causes of secondary bedwetting can be managed in primary care?

A

UTI + constipation

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12
Q

What causes of secondary bedwetting should be managed in secondary care?

A

Diabetes
Psychological
LD
Recurrent UTI

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13
Q

What is phimosis?

A

Inability to retract foreskin as it is too ‘tight’

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14
Q

By what age should phimosis only be present in 10% of children who were born with it?

A

4y (it is physiological at birth)

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15
Q

How should phimosis be managed?

A

If <2: reassure + review in 6m - add personal hygiene promotion

If >2: circumcision or topical steroid creams (depending on severity)

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16
Q

What is the name given to pathological phimosis?

A

Balantis Xerotica Obliterans

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17
Q

What are 5 signs and symptoms of BXO?

A

Haematuria
Painful erections
Recurrent UTI
Weak stream
Swelling

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18
Q

What is paraphimosis?

A

Emergency in which foreskin becomes trapped in the retracted position proximal to swollen glans

Restriction of blood flow to head of penis: penis turns dark purple

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19
Q

How should paraphimosis be managed?

A

1st line: adequate analgesia, attempt to reduce foreskin (gently compresswith saline soaked swab)
2nd line: emergency referral to urologist

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20
Q

What is hypospadias?

A

Wrongly positioned meatus ventrally (if dorsal = epispadias)

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21
Q

What are 4 key features of hypospadias?

A

Ventral foramen
Hooded foreskin
Chordee (ventral curvature)
Foreskin not fused ventrally

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22
Q

How should hypospadias be managed?

A

Repair surgery after 3 month:- no Mx required before that

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23
Q

What is balanoposthitis?

A

Inflamed/ purulent discharge from foreskin

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24
Q

How common is balanoposthitis?

A

Single attacks are common

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25
How should balanthoposthitis be managed?
Warm baths + Abx (broad spec) If recurrent (rare): circumcision
26
What is the mean age for testicular torsion?
16y
27
What is the appendixtestis?
Small remnant of Mullerian duct
28
How does torsion of the appendixtestis present?
Similarly to torsion but evolving over a few days
29
What is the one indication that surgery isn't needed in suspected testicular torsion?
Blue dot seen over superior pole of testes (shows it is torsion of appendixtestis)
30
Recall the signs and symptoms of torsion?
Redness, oedema, N+V Sudden onset pain in testis or abdomen
31
How can torsion and epididymitis be differentiated clinically?
Prehn's sign: lifting testes increases pain in torsion but decreases it in epididymitis Torsion = -ve Prehn's
32
What is the surgical management of testicular torsion?
Exploratory surgery +/- BL orchidopexy +/- orchidectomy +/- fixation of contralateral testes
33
What is the key window of time in which torsion needs to be fixed?
< 6 hours
34
Recall the serum creatinine changes/ measurements for each stage of AKI
Stage 1: increase >26 or 1.5-1.9x reference sCr Stage 2: 2-2.9 x reference sCr Stage 3: >354mmol increase or >3 x the reference sCr
35
Recall the urinary output values for each stage of AKI
Stage 1: <0.5mL/kg/hr, 6-12h Stage 2: <0.5mls/kg/hr, >12h Stage 3: <0.3mL/kg/hr, >24h
36
What is the difference in clinical syndrome produced by proliferative vs non-proliferative glomerulonephritis?
Proliferative: nephritic syndrome Non-proliferative: nephrotic syndrome
37
What are the 3 types of non-proliferative glomerulonephritis?
Focal segmental Membranous glomerulonephritis Minimal change disease
38
What are the 3 types of proliferative glomerulonephritis?
IgA nephropathy Membranoproliferative glomerulonephritis Post-infectious (post strep)
39
What can focal segmental glomerulonephritis be secondary to?
Obesity HIV
40
What can membranous glomerulonephritis be secondary to?
SLE Drugs
41
Which type of glomerulonephritis is most common in children?
Minimal change disease
42
Recall the triad of symptoms seen in IgA nephropathy
Petechiae Abdo pain Nephritic syndrome
43
What are the triad of symptoms in nephrotic syndrome?
Low albumin Peripheral oedema Proteinuria
44
What are the signs and symptoms of nephrotic syndrome?
1st = peri-orbital oedema (often misdiagnosed as allergy) 2nd = other features of oedema (delayed) - eg leg swelling, features of underlying dx
45
What % of nephrotic syndrome is steroid-sensitive?
80-95%
46
How quickly does steroid-sensitive nephrotic syndrome respond to treatment?
<6 weeks
47
How should the nephrotic syndrome be investigated?
Urine tests: dipstick, urea, urine MC+S, urinary sodium FBC, U+Es,ESR, creatinine, albumin Complement (C3,C4) (SLE?) Anti-streptolysin O (recent strep throat) HBV/HCV
48
If podocyte fusion is seen on microscopy, what is this indicative of?
Minimal change disease
49
What are the 3 main complications of nephrotic syndrome?
Risk of thrombosis Risk of infection Hypercholesterolaemia
50
How does the nephrotic syndrome cause hypercholesterolaemia?
Loss of albumin Less oncotic pressure Hepatic cholesterol synthesis
51
What are the 2 most common causes of Acute renal failure in children?
HUS + ATN
52
What is the triad of features that characterises the HUS?
Low RBC Low platelets AKI
53
What is the most common cause of ATN in children?
Organ failure following cardiac surgery
54
Recall the signs and symptoms of acute renal failure in children
Oligo/anuria Oedema (feet, legs, abdo, weight gain) Brown discoularisation of urine Fatigue, lethargy, N+V
55
What is the key treatent for prerenal fialure?
Fluid replacement + circulatory support
56
What is the key treatment for intrinsic renal failure?
High calorie, normal protein feed: to decrease catabolism, uraemia + hyperkalaemia
57
How should postrenal ARF be managed in children?
Assess site of obstruction: relief may be obtained by nephrostomy/ Catheter
58
What is the most important investigation to do in ARF children?
Renal USS
59
What woud be seen on USS In CKD?
Small kidneys
60
What would be seen on USS in AKI?
Large, bright kidneys with loss of cortical medullary differentiation
61
In what age group is minimal change disease most common?
2-4 years old
62
In what age group is focal segmental glomerulonephritis most common?
Older children
63
How does minimal change disease affect renal function?
Renal function will be normal
64
How does FSGN affect renal funcion?
Impairs renal function --> HTN
65
In which age group is membranous nephropathy more common?
Adults
66
What is another name for IgA vasculitis?
Henoch-Shonlein purpura
67
Which vessels does IgA vasculitis affect?
Small vessels
68
What is the usual cause of IgA vasculitis?
Usually preceded by an URTI by 2-3 days
69
What is the pathophysiolgy of IgA vasculitis?
IgA + IgG complex, deposit in organs, activating complement
70
Recall the signs and symptoms of IgA vasculitis?
100% = purpuric rash sparing trunk: looks a bit like HUS 60-80% = arthralgia + periarticular oedema: joint pain + swelling 60% = abdo pain: can cause intussusecption 20-60% = glomerulonephritis (within 3m of onset = 97%) with nephritic syndrome
71
What should be the first investigations ordered in IgA vasculitis?
FBC, clotting screen, urine dip and U+Es Urinalysis to rule out meningococcal sepsis
72
How should IgA vasculitis be managed?
Most cases resolve spontaneously within 4w For joint pain: NSAIDs If scrotal involvement/ severe oedema/ severe abdo pain: oral prednisolone If renal involvement: IV corticosteroids
73
What is another name given to nephroblastoma?
Wilm's tumour
74
In what age group is nephroblastoma most common?
<5 years old
75
Recall 2 common symptoms and signs of nephroblastoma
Asymptomatic abdo mass Painless haematuria
76
Recall 4 less common signs and symptoms of nephroblastoma
Abdo pain Anaemia (from haemorrhage into the mass) Anorexia HTN
77
When is a biopsy indicated in suspected nephroblastoma?
Never: may worsen the condition
78
What investigations should be done in suspected nephroblastoma?
US SCT/MRI
79
How is nephroblastoma managed?
Nephrectomy + chemotherapy (+ neoadjuvant radiotherapy if advanced disease) 80% cure rate