Renal Flashcards
Proteinuria found on urine dipstick
- what is cause most likely?
- next step?
Most likely transient proteinuria
Reevaluate with repeat urine dipstick testing on 2 separate occasions to r/o persisten proteinuria
Sodium, K, Cl requirement per day?
Na = 3-4 meq/kg/day
K = 2 meq/kg/day
Cl = 1 meq/kg/day
Vesicoureteral reflux
- what is it
- sx
- dx
- tx
Backflow of urine from bladder –> kidney
2/2 incompetence of vesicoureteral junction
Common cause of HTN in kids and can lead to renal scaring
Reflux seen in 50% boys w/ posterior urethral valves
Dx:
- VCUG
- use ISC to grade 1-5
Tx
- can resolve w/ time
- abx ppx (TMP/SMX or nitrofurantoin)
- surgery for grade 4 or 5 reflux or persistent UTI
Acute poststreptococcal glomerulonephritis
- what is it
- sx
- dx
- tx
After group A beta hemolytic strep infections
- throat
- skin
Happen 1-2 wks after strep infection
Hematuria
Edema
HTN
Renal insufficiency
Dx
- RBC casts on UA
- DNase B antigen to test for past group A strep infection
- mild anemia
- decreased C3
- renal bx not needed in classic cases
Tx
- abx sometimes
Alport syndrome
1 hereditary nephritis
X linked dominant
Asymptomatic hematuria + sensorineural hearing loss
Dx
- renal bx showing glomerular sclerosis + thickened basement membrane
- foam cells
Tx
- men more prone to developing ESRD and need transplant - women are ok
Hemolytic uremic syndrome
Usually 2/2 E coli O157:H7
Acute renal failure
MIcroangiopathic hemolytic anemia
Thrombocytopenia
Helmet + burr cells
Coombs -
Tx:
- manage renal failure
- peritoneal dialysis
- steroids not helpful
Vs TTP - ttp usually in young women; also affects CNS
Nephrotic syndrome characteristics
Proteinuria
Hypoalbuminemia
Edema
Hyperlipidemia
HTN common in minimal change disease?
NO
Will have normal C3
Tx minimal change disease
Steroid
Cyclophosphamide (if unresponsive to steroids or recurrs)
Complications of nephrotic syndrome
Infection
Prone to developing spontaneous peritonitis 2/2 strep pneumo
- always give polyvalent pneumococcal vaccine!
Abonrmal lab values in:
- Williams
- DiGeorge
- Beckwith Weidman Syndrome
Williams - hypercalcemia
DiGeorge - hypocalcemia
Beckwith-Weidman Syndrome - hypoglycemia
Type 1 renal tubular acidosis
Distal RTA
Defect in H+ secretion
Acidotic
Hypo K
Inc urinary pH
Usually get nephrolithiasis
Type 2 renal tubular acidosis
Decreased bicarb reabsorption in PCT
Fanconi syndrome is common cause
Type 4 renal tubular acidosis
Defect in Na/K exchange in DCT
Hyper K
Hyper Cl
Acidosis
Common causes in kids:
- obstructive uropathy
- renal dz
- multicystic dysplastic kidneys
Renal tubular acidosis can present as…
growth failure
FTT
Low bicarb level
Increased Cl
Normal anion gap metabolic acidosis