Nephrotic syndrome and acute nephritis Flashcards
Presentation of nephrotic syndrome (4)
proteinuria
oedema
hypoalbuminaemia (<30)
may also get hyperlipidaemia and thrombophilia
Features of minimal change disease (2)
most common cause of nephrotic syndrome in children-often precipitated by respiratory tract infection
90% are steroid-sensitive, 10% steroid-resistant
Mx and prognosis of minimal change disease (5)
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
Steroid-resistant causes of nephrotic syndrome (3)
FSGS: HIV, HTN
Mesangiocapillary: HCV
Membranous: HBV, SLE
Factors suggesting congenital nephrotic syndrome
placenta >25% baby’s wt.
Presentation of acute nephritis (4)
volume overload
decreased UO
HTN>encephalopathy>seizures
haematuria and proteinuria
Causes of nephritis (5)
post-strep GN
IgA nephropathy
vasculitis: HSP, polyarteritis nodosa, SLE, Wegener’s, microscopic polyangitis
anti-GBM disease-Goodpasture’s
familial nephritis
Features and Dx of post-strep GN
presents 2-3 wks after strep sore throat
Dx w. ASOT
Rx of Post-Strep GN (4)
salt restriction
furosemide
penicillin
CCBs if needed to control BP
Presentation of IgA nephropathy
presents 2-3d after URTI
Familial nephritic syndromes and their features (4)
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