Nephrology Flashcards
causes of primary renal disease
minimal change disease (MCD): 15-20% focal segmental glom sclerosis (FSGS): 33% membranous: 33% membranoproliferative GN (MPGN): 5% mesangial GN: 3-5%
how to differentiate primary renal disease
renal biopsy
renal biopsy procedure
light microscopy
immunoflorescence
electron microscopy
nephrotic syndrome causes
70% primary**
30% systemic
layers of glomerular capillary
endothelium
basement membrane
podocytes
glomerular disease work up
Hx, PE
lab/serologies
urinalysis**
glomerular disease tx
prednisone cytotoxic: cyclophosphamide (cytoxin), chlorambucil mycophenolate mofetil (MMF) cyclosporine, tacrolimus rituximab ACE-I or ARBs + statins for all
SLE dx criteria
4/11 malar rash discoid rash photosensitivity oral ulcers arthritis serositis renal (proteinuria) neuro heme immuno ANA+
types of SLE and kidney disease
lupus assoc GN (6 variants)
tubulointerstitial nephritis
anti-phos ab syndrome
lupus nephritis class I
normal
mesangial immune deposits but norm light microscopy
lupus nephritis class II
mesangial
mesangial hypercellularity
lupus nephritis class III
focal
lupus nephritis class IV
diffuse
>50% glom w/ endocap or extracap hypercellularity
lupus nephritis class V
membranous
subepi deposits or any membranous
lupus nephritis class VI
sclerosis
>90% glom are sclerosed
causes of transient proteinuria
fever exercise UTI matignant HTN CHF
normal albumin excretion
up to 30 mg/day
normal protein excretion
100 - 150 mg/day
normal protein to creatinine ratio
0.1 - 0.15
glomerular proteinuria detection
dipstick (only one)
mostly albumin
proteins lost in tubular proteinuria
low molecular weight proteins
tubular or overflow proteinuria detection
urine protein electrophor (UPEP) urine immunofixation (UIF) serum studies (SPEP or SIF)
nephrotic syndrome
edema (anasarca) hypoalbuminemia albuminuria hyperlipidemia lipiduria hypercoagulable states
nephrotic syndrome tests
dipstick: high protein, low/no blood
sediment: bland, maybe lipid
polarized: maltese cross
AKI definition
abrupt (w/in 48hr) reduction in kidney fxn
AKI reduction in kidney fxn definition
up serum Cr > 0.3 in 2 weeks
up serum Cr > 50%
down urine:
anuria #s
oliguria #s
100-400 cc/24hr
non-oliguric
> 400cc/24 hr
polyuria #s
> 3000 cc/24hrs
AKI i hospital
50% of hospital ARF is iatrogenic
uremic milieu (gen)
n/v, malaise, altered taste/ sensorium
uremic mileau (CV)
pericardial effusion
tamponade
uremic mileau (pulm)
rales w/ hypervolemia
uremic mileau (abd)
diffuse abd pain and ileus
uremic mileau (neuro)
encephalopathic changes asterixis confusion seizures nerve irritation (hiccups)
ways to reduce renal perfusion
intravascular vol depletion
inadequate cardiac output
systemic vasodilation
renal vasoconstriction
which SLE classes do you treat aggressively
III, IV, V
aggressive tx for SLE kidney issues
Steroids (prednisone) and IV Cytoxan (cyclophosphamide)
Current: cellcept (mycophenolate mofetil) + low dose steroids
Or Rituximad
PSA confounders
infection/prostatitis/UTI
catheterization
ejaculation (48hrs)
medication (down)
low risk prostate Ca
T1c-2a
Gleason 2-6
PSA 0-10
intermediate risk prostate Ca
T2b
G 7
PSA 10.1-20
high risk prostate Ca
T2c
G 8-10
PSA > 20
UTI clues
pyuria
dysuria
GN clues
recent URI
calculus clues
unilat flank pain
radiation
BPH clues
hesitancy
dribbling
hematuria imaging
(after exclusion of glom bleeding) IVP (intravenous pyelogram) renal US (cysts) helical CT scan (stones) biopsy (GN)
nephritic syndrome sx
HTN edema azotemia oliguria coca-cola or tea colored urine
nephritic syndrome dipstick
(+) blood
maybe trace protein