Renal Flashcards

1
Q

Proteinuria found on urine dipstick

  • what is cause most likely?
  • next step?
A

Most likely transient proteinuria

Reevaluate with repeat urine dipstick testing on 2 separate occasions to r/o persisten proteinuria

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2
Q

Sodium, K, Cl requirement per day?

A

Na = 3-4 meq/kg/day

K = 2 meq/kg/day

Cl = 1 meq/kg/day

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3
Q

Vesicoureteral reflux

  • what is it
  • sx
  • dx
  • tx
A

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
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4
Q

Acute poststreptococcal glomerulonephritis

  • what is it
  • sx
  • dx
  • tx
A

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

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5
Q

Alport syndrome

A

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

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6
Q

Hemolytic uremic syndrome

A

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

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7
Q

Nephrotic syndrome characteristics

A

Proteinuria
Hypoalbuminemia
Edema
Hyperlipidemia

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8
Q

HTN common in minimal change disease?

A

NO

Will have normal C3

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9
Q

Tx minimal change disease

A

Steroid

Cyclophosphamide (if unresponsive to steroids or recurrs)

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10
Q

Complications of nephrotic syndrome

A

Infection

Prone to developing spontaneous peritonitis 2/2 strep pneumo
- always give polyvalent pneumococcal vaccine!

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11
Q

Abonrmal lab values in:

  • Williams
  • DiGeorge
  • Beckwith Weidman Syndrome
A

Williams - hypercalcemia

DiGeorge - hypocalcemia

Beckwith-Weidman Syndrome - hypoglycemia

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12
Q

Type 1 renal tubular acidosis

A

Distal RTA

Defect in H+ secretion

Acidotic
Hypo K
Inc urinary pH

Usually get nephrolithiasis

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13
Q

Type 2 renal tubular acidosis

A

Decreased bicarb reabsorption in PCT

Fanconi syndrome is common cause

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14
Q

Type 4 renal tubular acidosis

A

Defect in Na/K exchange in DCT

Hyper K
Hyper Cl
Acidosis

Common causes in kids:

  • obstructive uropathy
  • renal dz
  • multicystic dysplastic kidneys
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15
Q

Renal tubular acidosis can present as…

A

growth failure
FTT

Low bicarb level
Increased Cl

Normal anion gap metabolic acidosis

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16
Q

Indications for renal and bladder ultrasound

A

Infants and children < 24 mo with first febrile UTI

Recurrent febrile UTIs in kids of any age

UTI in child of any age w/ family hx of renal or urologic disease, HTN, or poor growth

Children who d not respond to appropriate abx treatment

17
Q

Indications for voiding cystourethrogram

A

Hydronephrosis on renal and bladder US

Evidence of renal scarring on renal and bladder US

Evidence of high-grade vesioureteral reflux on renal and bladder US

Evidence of obstructive uropathy on renal and bladder US

Atypical or complex clinical presentation

Recurrence of febrile UTI

Children with 1st febrile UTI and FHxs of renal or urologic dz, poor growth and hypertension

Children w/ 1st febrile UTI with a non-E coli organism

18
Q

When giving IV boluses, what do you use?

A

ONLY use isotonic solutions

  • 0.9% saline
  • lactated Ringer’s
19
Q

1 cause of urinary tract obstruction in newborn boys

A

Posterior urethral valves

Will cause oligohydramnios –> potter sequence

20
Q

Causes of secondary enuresis

A

Psychological stress

UTI (dysuria, hesitancy, urgency, ab pain)

DM (polyuria, polydipsia, polyphagia, wt loss)

Diabetes insipidus (polyuria, polydipsia)

OSA (snoring, dry mouth, fatigue, irritability)

21
Q

Minimal change disease

  • LM
  • EM
A

LM = nothing

Immunofluorescence = nothing

EM = diffuse efacement of foot processes of podocytes

22
Q

Renal vein thrombosis

A

Seen more often in infants that are dehydrated, had birth depression, have polycythemia, ir were born to diabetic mothers

presents with oliguria + hematuria + palpable kidney

Confirm with renal US with renal V doppler studies

23
Q

Result of coombs test in HUS

A

NO positive

24
Q

Tx HUS

A

Fluid and electolyte management

- DO NOT use antibiotics

25
Q

Prehn sign

A

pain relief upon elevation of testicle

26
Q

Idiopathic hypercalciuria

A

Recurrent gross hematuria
persistent microscopic hematuria

Complaints of dysuria
Ab pain w/o initial stone formation

27
Q

Why is there elevated LDL in nephrotic syndrome?

A

Inc generalized protein synthesis in live

Decrease in lipid metabolism 2/2 reduced plasma lipoprotein lipase levels

28
Q

Tx edema in pts with nephrotic syndrome

A

albumin infusions + diuretic

29
Q

Bartter syndrome

A

AR condition

HYPO K
HYPER Ca
Alkalosis
HYPER aldo
HYPERreniemia

BP normal

Usually present 6-12 mo

  • FTT
  • constipation
  • weakness
  • vomiting
  • polyuria + polydipsia

Tx:

  • prevent dehydration
  • nutritional support
  • return K level to normal