Nephrotic syndrome and acute nephritis Flashcards

1
Q

Presentation of nephrotic syndrome (4)

A

proteinuria

oedema

hypoalbuminaemia (<30)

may also get hyperlipidaemia and thrombophilia

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2
Q

Features of minimal change disease (2)

A

most common cause of nephrotic syndrome in children-often precipitated by respiratory tract infection

90% are steroid-sensitive, 10% steroid-resistant

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3
Q

Mx and prognosis of minimal change disease (5)

A

prednisolone PO for 4wks. Steroid resistant if no remission w/i 4wks.

biopsy if no remission after 8wks

colloid to raise intravascular volume

may need prophylactic Abx (penicillin) and pneumococcal vaccine

1/3 never recur, 1/3 have few relapses, 1/3 have frequent relapses

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4
Q

Steroid-resistant causes of nephrotic syndrome (3)

A

FSGS: HIV, HTN

Mesangiocapillary: HCV

Membranous: HBV, SLE

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5
Q

Factors suggesting congenital nephrotic syndrome

A

placenta >25% baby’s wt.

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6
Q

Presentation of acute nephritis (4)

A

volume overload

decreased UO

HTN>encephalopathy>seizures

haematuria and proteinuria

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7
Q

Causes of nephritis (5)

A

post-strep GN

IgA nephropathy

vasculitis: HSP, polyarteritis nodosa, SLE, Wegener’s, microscopic polyangitis

anti-GBM disease-Goodpasture’s

familial nephritis

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8
Q

Features and Dx of post-strep GN

A

presents 2-3 wks after strep sore throat

Dx w. ASOT

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9
Q

Rx of Post-Strep GN (4)

A

salt restriction

furosemide

penicillin

CCBs if needed to control BP

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10
Q

Presentation of IgA nephropathy

A

presents 2-3d after URTI

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11
Q

Familial nephritic syndromes and their features (4)

A

Alport’s:

  • X-linked
  • ESRF w. sensorineural deafness and ocular defects
  • female carriers may have haematuria

benign familial haematuria:
-asymptomatic haematuria w. no hearing loss

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