nephrotic syndrome Flashcards

1
Q

what is the most common cause of AKI in children?

what is it caused by?

what is the most common age for H.U.S?

A
  • haemolytic uraemic syndrome
  • E.coli 157
  • 6 months to 5 years
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2
Q

how will a child with H.U.S present?

A
  • profuse diarrhoea, turning bloody 1 to 3 days later
  • fever
  • abdo pain
  • vomiting
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3
Q

what investigations would you do for H.U.S?

A
  • FBC: haemolysis, anaemia and thrombocytopenia
  • Renal function and electrolytes: rise in urea and creatinine
  • LDH: is high
  • CRP
  • clotting screen
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4
Q

what is the management of H.U.S?

A
  • notifiable disease!

- supportive: fluid and electrolytes, antihypertensives, dialysis

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5
Q

what are the complications of H.U.S?

A
  • intestinal strictures and perforations
  • intussusception and rectal prolapse
  • pancreatitis
  • seizures
  • AKI
  • haematuria
  • hypertension
  • proteinuria
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6
Q

what is the criteria for nephrotic syndrome?

A
  • proteinuria (>3-3.5 g/24 hours)
  • hypoalbuminaemia <25g/L
  • peripheral oedema
  • severe hyperlipidaemia (total cholesterol often >10 mol/L)

all due to increased capillary wall permeability in glomerulus allowing protein to leak into urine

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7
Q

what is the age of onset for nephrotic syndrome?

what is most common cause?

A
  • <6 years (M2:1F)

- minimal change glomerulonephritis

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8
Q

what are the causes of primary glomerular disease?

A
  • minimal change (78%) glomerular disease
  • FSGS (8%)
  • membranous glomerular disease
  • membranoproliferative glomerulonephritis
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9
Q

what are the broad causes of secondary glomerular disease?

A
  • infection
  • vascular disease
  • metabolic (DM/ amyloidosis)
  • inherited disease: alports, sickle cell
  • malignancy
  • nephrotoxic drugs
  • pregnancy (pre-eclampsia)
  • transplant rejection
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10
Q

how may nephrotic syndrome patients present?

A
  • following viral URTI
  • oedema: puffy pale face, swollen lips, periorbital oedema
  • frothy urine
  • leukonychia, xanthelasma
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11
Q

what investigations would you do in the urine?

what blood investigations?

A
  • urinalysis and protein +++
  • microscopy
  • protein: creatinine ratio
  • serum albumin
  • U+Es (
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12
Q

how can nephrotic syndrome be managed?

A
  • admit to hospital
  • fluid restriction
  • diuretics
  • low salt diet
  • corticosteroids (2-3 months)
  • prophylactic penicillin
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13
Q

what is the prognosis of nephrotic syndrome?

A
  • relapses common in 75%

- HSP carries a worse prognosis and may result in renal failure

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14
Q

what potential complications are there of nephrotic syndrome?

A
  • increased risk of infection and thrombosis due to loss of antithrombin, plasminogen and Ig
  • AKI and CKD
  • pulmonary oedema
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