Nephro Flashcards
4 big causes of AIN
PPI
Nsaids
Sjogren
Sarcoid
still have AKI 5 days after cardiac cath, also skin rash
Atheroembolic dz, can have livedo reticularis and peripheral emboli. supportive care, maybe statin and consider stop anticoag
differentiate IgA nephropathy and Post-infectious GN
Both are related to immune complex. Both can happen post-infection.
IgA: will happen w/in 2-3 days. Complement will be NORMAL. its the most common primary GN. Systemic form is HSP (palpable pupura, GI, joints, kidney). Bx = glomerular IgA deposits.
PSGN: latent period, usually 7-10 days but up to 6 weeks. Complement is LOW. Cola-colored urine. Check ASO, anti-DNase for strep.
most common glomerulonephritis
IgA nephropathy (usually a few days after URI (strep pharyngitis)
Causes of glomerulonephritis with low complement
SIP in all the CoMPlements
SLE Infective Endocarditis Postinfection Cryoglobulinemia MembranoProliferative
Note: even though IgA nephropathy (most common GN) and HSP are immune complex mediated, it will not have low complement, HA
vasculitis with low C4
Cryoglobulinemia
tx for lupus nephritis
MMF (mycophenolate mofentil) is the main one. Can also use Cyclophosphamide. Will do this with steroids.
GN with low complement level and Hep C
either Membranoproliferative GN or Cryoglobulinemia-assocated GN
Who gets membranoproliferative GN?
Mainly Hep B and Hep C, also SLE
mononeuritis multiplex plus GN
Microscopic polyangitis
p-anca//anti-MPO. may have palpable purpura and pulmonary hemorrhage. its a vasculitis
associations with minimal change disease
nsaid use Hodgkin disease (so young patient with bulky LN)
black person or HIV or obese with nephrotic syndrome
FSGS
caucasian with nephrotic syndrome
membranous
patient with cancer and nephrotic
membranous (note: hodgkin associated with minimal change disease)
flank pain, hematuria and nephrotic syndrome
suspect renal vein thrombosis/renal infarction with membranous nephropathy. will have high LDH
nephrotic syndrome with low complement
MPGN
trace protein on dipstick but lots of protein on urine protein/cr ratio
multiple myeloma. light chains are not picked up on dipstick, only albumin
most common stone
calcium oxalate
association with calcium phosphate stone
distal RTA
biggest meds for stones
triamterene, indinavir, absorbic acid (vitamin C –> oxalate)
how to reduce hypercalciuria (and thus calcium stones)
- reduce animal protein
- reduce Sodium
- reduce sucrose and fructose
drugs:
- thiazides to reduce calcium in the urine
T/F: You should reduce dietary calcium to reduce kidney stone formation
FALSE. actually when you reduce calcium intake, then this allows oxalate to be free and will actually make more stones.
so you want good calcium in the diet, don’t recommend supplements though
tx for uric acid stone
get urine pH above 6, by giving potassium citrate (alkalinize the urine a bit, acidic pH is a risk factor for uric acid stone)
citrate is also a stone inhibitor
can then do allopurinol if reeeallly needed
2 meds to remember for renal stones
-if hypercalciuria, give thiazides
if uric acid stones or low citrate, give potassium citrate
diet is the big thing though