Nephrotic syndrome: Flashcards

1
Q

What is the classic triad of nephrotic syndrome?

A
  • Proteinuria
  • Hypoalbuminaemia
  • Oedema (ascites/SOB)
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2
Q

Why are the features of the triad present?

A

Due to massive loss of protein from the kidneys (idopathic causes or 2ndry such as HSP). This causes low albumin which in turn reduces the oncotic pressure in the blood causing oedema.

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3
Q

What other feature is often present in nephrotic syndrome and why?

A

Hyperlipidaemia - due to ^ lipoprotein production to compensate for protein loss.

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4
Q

What is then an increased risk of during nephrotic syndrome?

A

Thombosis (due to reduced anticoagulation factors and ^ clotting factors) & ^ risk of infection

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5
Q

How is nephrotic syndrome confirmed?

A

Clinical features and confirmed proteinuria (24hr urine protein collection)

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6
Q

What is nephrotic syndrome typically caused by?

A

Minimal change disease (85-90%)

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7
Q

What is the treatment for nephrotic syndrome?

A

6 week course of steroids (prednisolone)

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8
Q

What is the prognosis of nephrotic syndrome?

A

> 60% will go on to relapse; a minority will go on to develop renal failure

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9
Q

What observations are typically performed in those with nephrotic syndrome?

A
  • Daily weight
  • U+Es
  • Strict fluid input-output
  • Diuretics if required
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10
Q

What are the two main types of nephrotic syndrome?

A

Steroid sensitive (90%)

Steroid resistant - no response after 4 weeks (10%) - investigate with biopsy

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11
Q

How do you describe a big and small non-blanching rash?

A

Petechial - <5mm

Purpuric - 5-9mm

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12
Q

Give some differentials for a non-blanching rash:

A
  • Infection: meningococcal septicaemia
  • Bleeding disorders: ITP, acute leukaemia, HUS
  • Vasculitis: HSP
  • Mechanical/trauma: recurrent coughing/vomiting; non-accidental injury
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13
Q

What is the typical aetiology of someone with HSP?

A

3-10 years old. Recent Hx of URTI

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14
Q

What is HSP classed at?

A

IgA vasculitis

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15
Q

What are the 4 classical features of HSP?

A
  • Rash (purpuric)
  • Joints affected (arthritis)
  • Abdo pain
  • Haematuria

OR

H - Haematuria
S - Skin (purpuric rash)
P - Pain (abdo and joints)

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16
Q

What GI pathology is often associated with HSP?

A

Intussuseption

17
Q

What is the treatment of HSP?

A

Symptomatic - 75% resolve spontaneously. Take home with calpol. Call and follow up - BP monitoring, urine dip

18
Q

What marker can be raised in HSP?

A

IgA

19
Q

What is Idiopathic thrombocytopaenic purpura typically caused by?

A

Antiplatelet antibodies. These are produced roughly 1-2 weeks after viral URTI.

20
Q

What FBC findings are likely to be seen in ITP?

A
  • Normal Hb
  • Normal WCC
  • Low platelet count
21
Q

How is ITP managed?

A

Usually resolves spontaneously. Advised to avoid contact sports as 1 in 300 develop intracranial haemorrhage/splenic problems

22
Q

What sign/symptoms is seen in ITP?

A

Non-blanching petechiae and superficial bruising in a well child.