Clinical Glomerular Disease Flashcards
what lab should always be ordered w/ nephritic syndrome
complement- low complement indicates immune complex mediated diseases
4 pulmonary renal syndromes
ANCA
goodpasture
SLE
cryoglobulinemia
4 dermato renal syndromes
ANCA
SLE
IgA vasculitis
cryoglobulinemic
urine protein creatinine ratio is equal to…
x g/g is equivalent to urine protein excretion in 24 hrs
early intervention w/ AKI
ACEi to lower glomerular pressure, protect the kidneys
normal protein excretion
less than 150mg per day
normal protein-creatinine ratio
less than 2, correlates w/ daily excretion
3 kinds of proteinuria
transient, orthostatic, (less than 500 mg/day) and fixed (denotes glomerular disease)
complications of nephrotic syndrome (3)
thrombosis- loss of balance b/w anticoag and procoag, leads to DVT, CVA, etc
infections- loss of Ig
accelerated atherosclerosis- from hyperlipidemia
etiology of most membranous nephropathy
autoAb against phospholipase A2
age dependent causes of hematuria
kids/young adults: mostly glomerular causes
adults above 40- more commonly cancer and kidney stones
clues for glomerular hematuria
brown or tea colored urine
proteinuria
dysmorphic RBCs, RBC casts
extra renal manifestaions
main 2 clinical pres of IgA
episodic hematuria, asymptomatic
pathogenesis of IgA nephropathy
serum IgA has reduced glycosylation at the hinge region, target for other antibodies
define rapidly progressive GN
loss of over half of GFR w/i weeks
acute onset of azotemia, HTN, proteinuria, edema, oliguria
associated w/ crescentic GN