Urology Flashcards

1
Q

Investigation for nephrotic syndrome***

A

> Blood

  • FBC: Hb, WCC and Hct
  • BUSE/ Cr
  • LFT: hypoalbuminemia <25g/L
  • Serum complement level: decrease C3, 4 in SLE
  • Serum ASOT and anti-DNAse B: exclude PSGN

> Urine

  • Urine dipstick: proteinuria
  • 24 hour urine collection
  • UFEME + C&S

> Renal biopsy (Main indication = steroid resistant nephrotic syndrome)

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2
Q

4 classical features of nephrotic syndrome

A
  • Edema
  • Proteinuria: 24-h urine protein >40 mg/m2/hr or spot urine protein:creatinine index of >200mg/mmol
  • Hypoalbuminemia <25g/L
  • Hypercholesterolemia
  • Only require both proteinuria and hypoalbuminemia for diagnosis
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3
Q

Etiology of nephrotic syndrome

A

> Primary - Most common >90% in <10 y/o

  • Minimal change disease (<5 y/o) - 80-90%
  • Primary focal glomerulosclerosis
  • Congenital (family hx of Alport syndrome)
  • Primary idiopathic nephrotic syndrome

> Secondary

  • Autoimmune ds (eg: HSP, SLE)
  • Diabetic nephropathy
  • Amyloidosis
  • PSGN
  • Chronic infection (eg: Hep B, C, HIV)
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4
Q

Management algo of nephrotic syndrome***

A
  1. Initial ep
    - Prednisolone 60mg/m2/day for 4 weeks
    - If response -> 40mg/m2/alternate day for 4 weeks, then taper over 4 weeks and stop
    - If no response -> renal biopsy
  2. Relapse
    - Prednisolone 60mg/m2/day till remission
    - 40mg/m2/alternate day for 4 weeks then stop
  3. Frequent relapse
    - Reinduce as (2) + low dose alternate day Prednisolone for 6 months
  4. Relapse while on Pred
    - Treat as (3) if not steroid toxic
    - Consider cyclophosphamide if steroid toxic
  5. Relapse post cyclophosphamide
    - As for (2) and (3) if not steroid toxic
    - Refer specialist for steroid sparring agents
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5
Q

General management for nephrotic syndrome***

A
  • Penicillin V is recommended at diagnosis and during relapse to prevent infection
  • Careful assessment of the hemodynamic status
  • Human albumin can be used at symptomatic grossly edematous states with IV frusemide to produce diuresis
  • Fluid restriction not recommended except chronic edematous
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6
Q

Complication of nephrotic syndrome**

A
  • Hypovolemia
  • Thrombosis
  • Infection
  • Hypercholesterolemia
  • Renal failure
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7
Q

Management for nephritic syndrome***

A
  • Penicillin V for 10 days: to eliminate B-hemolytic strep
  • Fluid restriction: to control edema and circulatory overload
  • Diuretics (eg: Frusemide): for pulmonary edema
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8
Q

Complication of nephritis syndrome and how to manage

***

A

> Hypertensive encephalopathy
- Anti-HPT to reduce mean arterial pressure by approx 25% over the first 24 hour

> Pulmonary edema

  • O2 support if necessary
  • IV Frusemide, fluid restriction
  • Consider dialysis if no response to diuretics

> Acute renal failure
- Treat cause and complication?

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9
Q

Pathophysiology of IgA nephropathy

A
  • (Onset within 24 hours after URTI)
  • Immune complexes deposit into glomerulus from circulation, leading to inflammation and proliferation of cells in glomerulus
  • Inflammatory process damages capillary walls, leading to abnormal permeability to RBC or proteins
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10
Q

ECG changes in hyperkalemia

A
  • Tall, tented T waves
  • Prolonged PR interval
  • Widened QRS complexes
  • VF or asystole

(Peads protocol)

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11
Q

Description of impetigo*

A
  • Non-bullous impetigo (most common form)
  • Begins as papules -> vesicles surrounded by erythema -> pustules -> enlarge and rapidly break down to form thick, adherent crusts with characteristic golden appearance
  • Seen in group A strep (eg: strep. pyogenes) and S. aureus infection
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12
Q

Investigation for nephritic syndrome***

A
  • Urinalyses and culture: hematuria, proteinuria, RBC cast, pyuria
  • Bacteriological and serological evidence: raised ASOT, anti-DNAse B, throat/ skin swab
  • Renal function test: blood urea, electrolyte and serum creatinine
  • FBC: anemia, leukocytosis
  • Complement level: C3 low, C4 normal
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13
Q

Nephrotic vs Nephritic syndrome*

A

> Nephrotic syndrome

  • Frothy urine, edema, xanthelasma
  • Urinalysis: proteinuria (++++), frothy appearance

> Nephritic syndrome

  • Hematuria, uremic symptoms
  • Urinalysis: hematuria, proteinuria (mild), red cell casts
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14
Q

Pathogenesis of PSGN

A
  • Deposition of circulating immune complex induced by GAS in glomerular
  • Trigger complement activation and inflammation in the glomerular
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15
Q

Definition for hypertension in children

A
  • Auscultatory-confirmed BP reading >= 95th percentiles on 3 different occasion (oscillometric tend to give higher BP reading)
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16
Q

Definition of nephrotic symptoms

  • Remission
  • Relapse
  • Frequent relapse
  • Steroid-resistant
  • Steroid dependent
A

> Remission
- Urine dipstick is trace or nil for 2 consecutive days within 28 days

> Relapse

  • Urine albumin excretion >40mg/m2/hour OR
  • Urine dipsticks of ≥2+ for 3 consecutive days

> Frequent relapse

  • ≥2 relapses within 6 months of initial diagnosis OR
  • ≥4 relapses within any 12 month period

> Steroid-resistant
- Failure to achieve remission despite 4 weeks treatment with prednisolone at 60mg/m2/day

> Steroid dependence

  • ≥2 consecutive relapse occurring during steroid taper OR
  • Within 14 days of the cessation of steroids