renal shiz Flashcards

(41 cards)

1
Q

nephrotic syndrome associated with:

  • African American or Hispanic
  • obesity
  • HIV
  • heroin use
A

Focal segmental glomerulosclerosis

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2
Q

nephrotic syndrome associated with:

  • adenocarcinoma (solid tumors of breast, lung)
  • NSAIDS
  • Hep B
  • SLE
A

Membranous nephropathy

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3
Q

nephrotic syndrome associated with:

  • Hep B and C
  • lipdystrophy
A

Membranoproliferative glomerulonephritis

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4
Q

nephrotic syndrome associated with

  • NSAIDs
  • lymphoma
  • children
A

Minimal change disease

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5
Q

nephrotic syndrome associated with

-URI

A

IgA nephropathy

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6
Q

dysmorphic red cells

A

glomerulonephritis

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7
Q

red cell casts

A

glomerulonephritis

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8
Q

white cell casts

A

pyleonephritis

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9
Q

eosinophil casts

A

Acute (allergic) interstitial nephritis (except won’t show up with NSAIDs)

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10
Q

hyaline casts

A

dehydration (normal Tamm-horsfall protein)

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11
Q

broad waxy casts

A

chronic renal disease

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12
Q

granular “muddy brown” casts

A

ATN (collections of dead tubular cells)

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13
Q

sudden rise in Cr and BUN

A

Acute Kidney Injury
usually symptomatic but may have N+V, malaise
shortness of breath, edema, and fluid overload
very severe: confusion, arrhythmia from hyperkalemia, pleurtic chest pain from PERICARDITIS

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14
Q

hypoperfusion of kidney
BUN rises more than Cr
BUN:Cr >20:1
urine Na 500mOsm

A

Pre-renal

hypotension systolic

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15
Q

obstruction of urinary system

BUN: Cr >20:1

A

Post-renal
must block BOTH ureters for Cr rise
prostate hypertrophy, stone in ureter, cervica cancer, urethral sricture, neurogenic/atonic bladder, retroperitoneal fibrosis (bleomycin)
usually reversible

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16
Q

BUN:Cr ~10:1
high amount of sodium in urine >20 mEq
high FeNA >1%
low urine osmol

A

Intrinsic renal disease
acute interstiail nephritis (ofte penicillin)
USUALLY Acute Tubular Necrosis (ATN) due to toxins or ischemia
rhabdomyalsis/hemoglobinuria
contrast and NSAIDs
crystals like hyperuricemia, hypercalcemia, hyperoxaluria
Bence-jones proteins from multiple myeloma
post strep infection
Tumor lysis syndrome–>hyperuricemia

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17
Q

urine osmol of >500mOsm

A

high osmol=more concentrated
usually in hypovolemic state
more ADH–>concentrates
(but still expect low urine Na+ becuase aldosterone is preserving to keep up intravasc volume)

18
Q

urine osmol 300mOsm

A

relatively dilute

often in intrinsic renal damage because damage causes loss of ability to concentrate

19
Q

Acute Tubular Necrosis

A
toxins cause sloughing of tubular cells-->lose Na+ into urine and have dilute urine because cannot concentrate
Tx: reverse underlying cause
-HYDRATE and correct electrolyte abnormalities
-dialysis when:
1. fluid overload
2.encephalopathy
3.pericarditis
4. metabolic acidosis
5. hyperkalemia
20
Q

prevention of contrast induced nephropathy

A

1-2 L normal saline before and during angiography

21
Q

prevent renal failure from tumor lysis syndrome

A

allopurinol, hydration, rasburicase

22
Q

cardiac cath after chest pain–> AKI!, purple lesions on fingers/toes, ocular problems, livedo reticularis
PLUS eosinophils in urine and high in blood

A

atheroemboli all over including to kidney causing AKI

can biopsy skin purple lesions and find cholesterol

no treatment

23
Q

drug causes of acute interstitial nephritis

also cause drug rashes, Stevens-Johnson, TEN, hemolysis!

DO Hansel and Wright stain for eosinophils!!!!!!!!!!!!!!!!!!

A
eosinophils attack tubular cells
penicillins/cephalosporins
sulfa drugs and diuretics
phenytoin
rifampin
quinolones
allopurinol
proton pump inhibitors

other: SLE, Sjogren, sarcoidosis

24
Q

papillary necrosis

A

sudden onset of flank pain
fever
hamturia
in patient with sickle cell, DM, obstruction, or chronic pyelo AND taking NSAIDs

will look like pyelo

best test= CT showing loss of papillae

no treatment

25
lung and kidney (hematuria, red cell casts, protienuria) problems only NO upper respiratory
Goodpasture dx: antiglomerular basement membrane antibodies biopsy kidney or lung (kidney-linear deposits) tx: plasmapheresis, steroids
26
Asian with gross hematuria 1-2 days after URI
``` IgA nephropathy/Berger disease increased IgA in 50% kidney biopsy no tx some resolve, some progress to ESRD ```
27
``` glomerulonephritis 1-2 WEEKS after strep throat r impetigo cola colored urine LOW COMPLEMENT levels periorbital edema HTN oluguria ```
post-strep golmerulonephritis dx: antistreptolysin O titers (ASO titers) antiDNAse antibody LOW COMPLEMENT LEVELs tx: antibiotics as needed, diuretic if fluid overload
28
hearing loss visual disturbances PLUS glomerulonephritis
Alport syndrome type IV collagen defect no tx
29
glomerulonephritis fever malaise myalgias all organs BUT NOT LUNGS, skin-GI pain, stroke in young person, gangrene, livedo reticularis Hep B
``` Polyarteritis Nodosa anemia ESR and CRP elevated angiography of area with suspected problem-renal, mesenteric check for Hep B tx: prednisone ```
30
Lupus and the kidney
most likely to have membranous glomerulonephritis or glomerulosclerosis biopsy!!!!! tx: glucorticoids
31
large kidneys on sonogram | history of rheumatoid arthritis, cancer, Crohns, chronic infection
Amyloidosis biopsy fat pad green birefringence wit Congo red stain treat underlying disease
32
nephrotic sydnrome
protienuria >3.5 g/24 hours edema hyperlipidemia thrombosis (URINARY LOSS OF PROTEIN C
33
metabolic acidosis with normal anion gap (between 6-12)
Renal Tubular Acidosis diarrhea Na+ - (Cl- + HCO3-)= anion gap due to hyperchloremic in each
34
high urine pH above 5.5 plus hyperchloremic and nonanion gap metabolic acidosis hypokalemic nephrolithiasis
Type I-distal tubule damaged and therefore bicarb not made and acd not excreted-->alkaline urine test by giving ammonium chloride-->should cause decrease in urine pH as able to excrete acid again (BUT will not happen in distal RTA damage secondary to SLE, Sjogren, amphotericin Tx; give more bicarb high urine pH could also be due to infection with proteus and staghorn calculus
35
intially high urine pH then gradually becomes acidic nonanion gap metabolic acidosis, hyperchloremic hypokalemic
``` bicarb reabsorbed at proximal tubule normally proximal RTA (type II) damage due to amyloid, myeloma, Fanconi, acetazolamide, heavy metals ``` deplete bicarb until urine acidic (osteomalacia test: give bicarb and see if able to resabsorb-->type II if urine becomes alkaline tx: deplete volume with thiazide diuretic to increase bicarb reabsorption
36
persistently high urine sodium in spite of sodium depleted diet hyPERkalemic urine pH
Type IV RTA-hyporeninemia, hypoaldo decreased amount or effect of aldosterone-->hyperkalemia, hyponatremia, retain hydrogen ions tx: fludrocortisone to replace aldosterone
37
urine anion gap
urine sodium minus urine chloride distinguish between diarrhea and RTA as cause of NONANION GAP METABOLIC ACIDOSIS RTA= positive urine anion gap diarrhea=negative urine anion gap
38
Elevated anion gap metabolic acidosis | Na+ - (Cl- + HCO3-) = greater than 12
``` lactate in hypotension/hypoperfusion ketoacids in DKA/starvation oxalic acid in ethylene glycol OD formic acid in methanol OD uremia in renal failure salicylates in aspirin OD ```
39
increased serum pH slight increase in pCO2 increased bicarb
metabolic alkalosis-always with resp compensation increasing pCO2
40
stones with gout or tumor lysis
uric acid stones- require CT due to not visualized on x-ray
41
hypertensive crisis!!
htn w/ end organ damage tx: labetalol or nitroprusside