Nephrology Flashcards
tests to get in AKI
U/A
Protein/Cr ratio
Ultrasound
Best: biopsy - NEVER CORRECT
U/A in AKI
casts, hints, never definitive
Protein/Cr ratio in AKI
nephrotic syndrome
Ultrasound in AKI
hydro
what the nitrates in urine means
infection
what leukocyte esterase in urine means
infection
what RBCs in urine mean
hematuria
what no RBC’s but positive blood in urine mean
rhabdo (check myoglobin)
what eosinophils in urine mean
AIN
what RBC casts mean
glomerulonephritis
what WBC casts mean
pyelo
what muddy brown casts mean
ATN
what waxy urine casts mean
CKD
what hyaline casts in urine mean
nothing
post-renal failure path
obstruction: stone, cancer, BPH, neurogenic bladder
post-renal failure pt
abdominal pain and renal failure
distended or palpable bladder
post-renal failure dx
Foley catheter = large residuals
u/s = hydronephrosis
post-renal failure tx
catheter (relieves bladder outlet)
nephrostomy (relieves ureteral obstruction)
ATN path
tubules slough off, die
toxins: contrast, rhabdo
low flow: shock kidney
ATN pt
one of the above pathologies
ATN dx
u/a = waxy brown casts
ATN tx
oliguric phase: dialysis
polyuric phase: IVF
ATN ppx
vigorous hydration, reduce time in contact with toxin
indications for dialysis
AEIOU Acidosis Electrolytes (Na/K) Ingestion (toxins) Overload (CHF, edema) Uremia (pericarditis)
chronic kidney disease - hyperparathyroidism
cinacalcet
ckd - hyperphosphatemia
sevelamer
ckd - HTN
CCB
ACE-I
BB
Clonidine
ckd - vit D
Ca + vit D3
ckd - dialysis
hemodialysis TiW
peritoneal qHS
nephrotic syndrome
HTN
nephrotic range proteinuria
edema
hypercholesterolemia
nephritic syndrome
hematuria
HTN
oliguria
treatment of mild HypoNa
po
treatment of moderate HypoNa
IVF = NS
treatment of severe HypoNa
3% NaCl
treatment of mild hyperNa
po
treatment of moderate hyperNa
IVF = NS
treatment of severe HyperNa
IV = D5W
symptoms of mild hyper/hypoNa
asymptomatic
symptoms of moderate hyper/hypoNa
in between
symptoms of severe hyper/hypoNa
coma
seizures
sodium correction
no faster than 0.25mEq/hr
except if seizing or in a coma
osmotic demyelination syndrome path
rapid correction of sodium
osmotic demyelination syndrome pt
spastic quadriplegic (irreversible)
osmotic demyelination syndrome
central pontine myelinolysis
osmotic demyelination syndrome dx
clinical, sodium rises too fast
osmotic demyelination syndrome tx
none, prevention only
work-up for sodium
serum osm
urine Na
urine Osm
hypertonic serum osm
EtOH, glucose
isotonic serum osm
fats and proteins
hypotonic serum osm
continue
urine Na
surrogate for aldosterone
urine osm
surrogate for ADH
if hypervolemic + sodium dysfunction
give diuresis
if hypovolemic + sodium dysfunction
give fluids
if euvolemic + sodium dysfunction
TSH
cortisol
renal electrolytes
SIADH is dx of exclusion
SIADH path
hypothyroidism - TSH looks like ADH
lung lesions (small cell, pneumonia)
brain lesions
water, but not all, is retained -> decreased tonicity
SIADH pt
hyponatremia
SIADH dx
diagnosis of exclusion
U Na should be high (aldo off)
U osm should be high (ADH on)
SIADH tx
volume restrict
correct underlying disorder
symptomatic hyperCa pt
stones, bones, groans, and moans
symptomatic hyperCa dx
calcium and albumin
symptomatic hyperCa tx
IVF
bisphosphonates
calcitonin adjunct
hyperparathyroidism path
primary: adenoma
secondary: early CKD, physiologic response
tertiary: multiple adenomas from secondary
hyperPTH pt
hyperCa
pathologic fracture, decrease density
brown tumors
hyperPTH dx
calcium labs - very increased PTH - increase Ca - decrease PO4 sestamibi scan - primary: single adenoma - tertiary: multiple adenomas
hyperPTH tx
parathyroidectomy
hyperPTH f/u
hypocalcemia post-op - Perioral tingling - Chvostek's sign - Trousseau's sign decrease tertiary hyperPTH with calcimetics - cinacalcet
hyperCa of malignancy path
mets cause bone destruction
increase Ca -> decrease PTH
hyperCa of malignancy pt
malignancy with elevated Ca
hyperCa of malignancy dx
calcium labs
- very increased calcium
- decreased PTH
- increase PO4
- decrease PTH-rp
hyperCa of malignancy tx
tx underlying cancer
hyperCa of malignancy PTH-rp path
squamous cell carcinoma of the lung
increase PTH-rp -> increase Ca -> decrease PTH
hyperCa of malignancy PTH-rp pt
malignancy and elevated calcium
hyperCa of malignancy PTH-rp dx
calcium labs - increase PTH-rp - decrease PTH - decrease PO4 increase Ca
hypervitaminosis D path
granulomatous disease
hypervitaminosis D pt
hypercalcemia, chest lesion (TB, sarcoid)
hypervitaminosis D dx
calcium labs
- increase Ca
- decrease PTH
- increase PO4
- increase 1,25-vitD
hypervitaminosis D tx
treat granulomatous disease
hyperCa of immobilization path
old people in nursing homes
hyperCa of immobilization pt
old person in nursing home
debility, bed-bound, or post-op
hyperCa of immobilization dx
increase Ca
decrease PTH
increase PO4
hyperCa of immobilization tx
mobilization
familial hypercalcemia hypocalciuria path
higher set point of calcium
familial hypercalcemia hypocalciuria pt
asymptomatic
family history of high Ca
familial hypercalcemia hypocalciuria dx
calcium labs - increase Ca (11-12) - normal PTH - normal PO4 urine calcium decrease
familial hypercalcemia hypocalciuria tx
none
vitamin D labs and treatment - 25-VitD (D2)
lab = CKD med = osteoporosis
vitamin D labs and treatment - 1,25 VitD (D3)
lab = granulomatous disease med = ckd
hypoPTH path
iatrogenic (thyroidectomy is an error, PTH is physiologic)
hypoPTH pt
tetany, Chvostek’s sign
perioral tingling, trousseau’s sign
hypoPTH dx
decrease PTH
decrease Ca
neutral PO4
hypoPTH tx
IV calcium
pseudo-hypoPTH hormone path
PTH-insensitivity
pseudo-hypoPTH hormone pt
asymptomatic
pseudo-hypoPTH hormone dx
increase PTH
decrease Ca
increase PO4
vitamin D deficiency path
dairy
sunshine
vitamin D deficiency pt
osteopenia
Dexa scan -2.0
vitamin D deficiency dx
25-VitD
vitamin D deficiency tx
Ca + vit D
Vit D2 (25-VitD) 50000 q Week
bisphosphonates (osteoporosis)
CKD path
kidney’s can’t win because they are dead
CKD pt
frequent monitoring of electrolytes
CKD dx
increase PTH
decrease Ca
decrease Phos
CKD tx
calcimimetics - cinacalcet
phosphate binders - sevelamer
Ca + VitD3
HyperK path
hypoaldo (ACE, ARB, spironolactone) artifact iatrogenic ESRD ingestion + CKD
hyperK pt
asymptomatic
hyperK dx
potassium level
EKG = peaked t-waves, wide QRS
hyperK tx
if EKG changes -> stabilize, temporize, and eliminate
if no EKG changes -> eliminate
treatment of hyperK stabilize
IV calcium - no change in serum K or total K
treatment of hyper K temporize
NaHCO3, D50+insulin
- decrease serum K, no change total K
treatment of hyperK eliminate
kayexalate, diuretics, dialysis
- decrease serum K and total K
hypoK path
GI loss - vomiting or diarrhea renal loss - hyperaldosteronism - diuretics (loops) - large volume infusion
hypoK pt
weakness, paralysis, loss of reflexes
or
asymptomatic
hypoK dx
potassium level
EKG = U waves
hypoK tx
replete K PO > IV 10mEq increase serum K by 0.1mEq 10mEq/hr by PIV 20mEq/hr by central line
kidney stones pt
hematuria
colicky flank pain that radiates to groin
no fever or leukocytosis
kidney stones dx
1st: U/A
best: non-contrast CT
other: U/s if pregnant, KUB if tracking disease
kidney stones tx
If < 5mm: IVF + analgesia
if < 7mm: MET (CCB, α blocker)
if <1.5cm: lithotripsy (proximal), ureteroscopy (distal)
if >1.5cm: surgery
sepsis: nephrostomy (proximal), stent (distal)
kidney stones f/u
strain and analyze stone
24hr urine for Ca, PO4, urate, oxalate
calcium oxalate stone radio
opaque
calcium oxalate stone risk
increase Ca
- vit D, PTH
increase oxalate
- decrease red meat, increase fruits & vegetables, increase vitC
Mg ammonium phosphate (struvite) stone radio
opaque
struvite stone risk
pH increase (alkalotic urine) proteus -> urea splitting
uric acid stone radio
lucent
uric acid stone risk
gout, tumor lysis
- allopurinol (before)
- rasburicase (after)
cystine stone radio
lucent
cystine stone risk
genetic disorder
simple cyst pt
incidental - another test
small, no loculations, no septations
simple cyst tx
none
complex cyst pt
flank mass peel pain hematuria \+ loculations + septations
complex cyst dx
CT scan or u/s (pregnant)
biopsy (only if suspicion of cancer is low)
complex cyst tx
resection
renal cell carcinoma pt
flank mass, flank pain, hematuria
cancer (decrease Hgb)
paraneoplastic (increase Hgb, EPO)
hematogenous spread of mets
renal cell carcinoma dx
CT scan or U/s (pregnant)
renal cell carcinoma tx
nephrectomy (excisional biopsy)
AD polycystic kidney disease path
adults, autosomal dominant
ADPKD pt
cysts -> flank mass
infection -> pyelo
bleed -> hematuria
ADPKD dx
CT scan or U/s (pregnant)
biopsy
ADPKD tx
supportive -> dialysis or transplant
ADPKD f/u
pancreases -> pancreatitis
liver -> hepatitis
brain = SAH
- MRI, CTA
AR polycystic kidney disease path
autosomal recessive
entire kidney replaced by cysts
ARPKD pt
renal failure day 1 of life
flank mass
anuric
ARPKD dx
u/s
biopsy = radially oriented cysts
ARPKD tx
supportive -> death
transplant
respiratory acidosis path
hypoventilation
respiratory acidosis pt
opiates -> pinpoint pupils, track marks
Asthma/COPD -> wheezing
OSA -> fat, daytime somnolence
respiratory acidosis dx
decrease pH, increase pCO2
respiratory acidosis tx
no next step
respiratory alkalosis path
hyperventilation
respiratory alkalosis pt
pain, anxiety
hypoxemia
fast RR
respiratory alkalosis dx
increase pH, decrease pCO2
respiratory alkalosis tx
no next step
metabolic alkalosis path
hyperaldosteronism
metabolic alkalosis pt
volume deplete (diuresis, dehydration, NG tube suction, emesis) other (chloride non-responsive)
metabolic alkalosis dx
increase pH, increase pCO2
metabolic alkalosis tx
urine chloride
- UCL < 10 -> fluids
- UCL >10
- -HTN: RAS, Conn’s
- -no HTN: Bartter, Gitelman
metabolic acidosis path
gap vs. nonGap
metabolic acidosis pt
noncontributory
metabolic acidosis dx
decrease pH, decrease pCO2
metabolic acidosis tx
AG >12 -> + anion gap
- MUDPILES: Methanol, Uremia, DKA, Propylene glycol, Iron/isoniazid, Lactic acid, Ethanol, Salicylates
AG <12 -> no anion gap
- urine AG: + -> renal tubular; negative -> diarrhea