step 2 Flashcards
(91 cards)
underlying defect in type I, II, IV renal tubular acidosis
type I - defective H secretion
type II - defective bicarbonate reabsorption
type III - aldosterone deficiency or resistance
serum K in renal tubular acidosis
type I and II = low
type III = high
urinary PH in renal tubular acidosis
type I and II = < 5.5
type III = variable
treatment of renal tubular acidosis
type I: K bicarbonate
type II: treat underlying cause, K bicarbonate
type II: depends on eitology, may reuqire mineralocorticoid supplementation, Na bicarbonate or K wasting diuretics
causes of type I renal tubular acidosis
amphotericin B
hypercalciuria
autoimmune
ifosamide (cyclophosphamide analogue)
causes of type II renal tubular acidosis
aminoglycosides
acetazolamide
cisplatin
ifosfamide (cyclophosphamide analogue)
multiple myeloma
amyloidosis
all other causes fanconi syndrome
what metabolic derrangement does renal tubular acidosis cause
non-anion gap metabolic acidosis
fractional excretion of Na and urinary Na in pre renal vs intra-renal AKI
pre renal < 1% FEN (urine Na < 20)
intra-renal >2% FEN (urine Na > 40)
pre-renal or intra-renal AKI with urine osmolality > 500
pre renal
intra renal would be < 350
NOTE: pre renal does have fen < 1% and urinary Na < 20 as the kidney is retaining Na and water causing highly concentrated urine with low Na)
when is erythropoetin stimulating agents reommended for patients with CKD
Hg < 10 g/dL
when should a statin be started in patients with CKD
patients 50 or older with CKD should start a statin
patients 18-49 with CKD plus history of CVD, diabetes or stroke should also start a statin
management of rhabdomyolysis
IV saline
bicarbonate
ECG (to rule out hyperkalaemia
what diuretics should be avoided in a patient with sulpha allergy
acetazolamide
loop diuretics
thiazide like diuretics
renal impairment presenting 2 weeks post infection with low C3
post infectious glomerulonephritis
renal impairment presenting at the time of illness with normal C3
IgA nephropathy
what organs does the following conditions affect;
- granulomatosis with polyangitis
granulomatosis with polyangitis = kidney + lungs + sinus
chug-strauss syndrome = kidney + asthma
microscopic polyangitis = kidney + lung
cut off for nephrotic syndrome on protein:creatinine ratio
2
patient presents with palpable purpura, arthralgia, haematuria, peripheral oedema and low C3
mixed cryoglobinuria
will likely have history of hep C
vaccination against what is required for patients with nephrotic syndrome and why
23-polyvalent pneumococcal vaccine due to loss of immunoglobulins in the urine
glomerulonephritis with positive antihospholipase A2 receptor antibodies
membranous glomerulopathy
investigations for diagnosis of minimal change disease
clinical diagnosis
renal biopsy required for treatment resistance or if > 12 years old
treatment for renal amyloidosis
prednisolone and melphalan (chemo)
gold standard for diagnosis of renal stones
nonconstract abdominal CT
what type of kidney stones are radio-lucent
non-visible stones = uric acid
RF: gout, high purine turnover i.e. cancer