Nephrology/Urology Flashcards

(74 cards)

1
Q

Electrolyte requirements

A

Na - 1 mEq/kg
K - 2 mEq/kg
Cl - 3 mEq/kg

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2
Q

Volume of distribution

A

0.6 x wt x 1L/kg

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3
Q

Osmolarity calculation

A

2NA + BUN/2.6 + glucose/18

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4
Q

Electrolyte disturbances in hypernatremic dehydration

A

Hyperglycemia, hypocalcemia

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5
Q

FENa calculation

A

(Una x Pcr)/(Ucr x Pna)

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6
Q

FENa in prerenal AKI

A

< 1%

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7
Q

RAS stimulation

A

decreased renal perfusion

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8
Q

Angiotensin II effects

A

vasoconstriction, renal effects (efferent vasoconstriction, Na reabsorption, aldosterone secretion), ADH secretion

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9
Q

Aldosterone effects

A

Na reabsorption, K secretion

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10
Q

ANP effects

A

vasodilation, renal effects (dilates afferent/constricts efferent, decrease Na reabsorption, decrease RAS)

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11
Q

Diagnosis of nephrotic syndrome

A

Proteinuria (> 40 mg/mg2/hr)
Edema
Elevated cholesterol

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12
Q

False positive for protein on UA

A

pH > 7.5

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13
Q

FSGS diagnosis

A

Nephrotic syndrome NOT responsive to steroids

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14
Q

FSGS prognosis

A

50-70% progress to CKD (30% relapse in transplant)

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15
Q

Nephrotic syndrome causes

A

Primary (90%) - MCD&raquo_space;> FSGS > MPGN

Secondary (10%) - HSP, SLE, HUS

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16
Q

Renal disease with decreased C3

A

PSGN, MPGN, SLE nephritis

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17
Q

Congenital nephrotic syndrome genetics

A

AR

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18
Q

Congenital nephrotic syndrome findings

A

Oligohydramnios, large placenta, presentation < 1 yo, death by E. coli sepsis

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19
Q

MCD age group

A

preschool

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20
Q

Complications of MCD

A

peritonitis (s. pneumo, e. coli), thrombosis

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21
Q

Treatment of refractory MCD

A

cyclophosphamide, cyclosporine

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22
Q

Most common vasculitis in children

A

HSP

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23
Q

HSP pathogenesis

A

IgA deposition

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24
Q

HSP findings

A

Palpable purpura, abdominal pain (intussusception), arthralgia/arthritis, renal dz

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25
HSP diagnosis
clinical (biopsy reserved for atypical cases)
26
Indications for glucocorticoids in HSP
abdominal pain (NOT indicated for renal dz)
27
Recurrence rate of HSP
up to 1/3 (screen with UA every 6 mo)
28
HUS findings
microangiopathic hemolytic anemia, AKI, thrombocytopenia
29
HUS prognosis
5% mortality, 5% complictions
30
Risk factors for development of HUS
antimobility agents, vomiting (if < 5.5 yo), WBC > 13 K
31
ARPKD presentation
Infant - enlarged kidney, pulmonary hypoplasia, highest mortality Children - liver fibrosis, less renal dz
32
Most common cause of congenital hydronephrosis
UPJ obstruction
33
Prophylactic antibiotics in VUR
For patients 2-24 mo
34
Prune belly syndrome eponym
Eagle-Barrett syndrome
35
Prune belly syndrome findings
lack of abd. muscles, cryptorchidism, GU abnormalities
36
RTA type 1
Distal - inability to secrete H+ causes severe acidosis
37
RTA type 2
Proximal - inability to reabsorb HCO3
38
RTA type 4
Deficiency or resistance to aldosterone (decreased K+, mild acidosis
39
Alport genetics
X-linked
40
Alport defect
type IV collagen
41
Alport findings
Glomerulonephritis, hearing loss, ocular abnormalities
42
Cystinosis genetics
AR
43
Cystinosis defect
defect in lysosomal transport
44
Liddle syndrome genetics
AD
45
Liddle syndrome defect
"gain on function" of aldosterone sensitive Na channels --> HTN, hypokalemia, alkalosis
46
Membranous glomerulonephritis association
HBV
47
Diagnosis of metabolic syndrome
3/5 of obesity, HTN, insulin resistance, hyperlipidemia, hyperglycemia
48
Most common cause of severe HTN in childhood
renal artery stenosis
49
Lethal side effect of metformin
lactic acidosis
50
Causes of anion gap acidosis
Methanol, Uremia, DKA, Paraldehyde, Inborn EM, Lactic acidosis, Ethylene glycol, Salicylate
51
Ammonium chloride (acid load) test
Expect acidification (pH < 5.5) of urine (does NOT happen in RTA type 1)
52
Diagnosis of RTA type 2
24-hour urine collection (?Fanconi syndrome)
53
Unilateral cystic kidney
Multicystic dysplastic kidney
54
Multiscystic dysplastic kidney association
VUR (40%)
55
PSGN treatment
symptomatic - ie diuretic if HTN
56
Hypokalemia metabolic acidosis
Bartter syndrome, Gitelman syndrome
57
Bartter syndrome
Hypercalciuria, nephrocalcinosis, polyhydramnios
58
Gitelman syndrome
Hypocalcemia, hypomagnesemia, salt-wasting
59
Most common cause of abdominal mass in a newborn
multicystic dysplastic kidney
60
Management of UPJ obstruction
surgical intervention if decreased ipsilateral function on renal scan
61
2nd most common cause of prenatal hydronephrosis
megaureter
62
Management of hypospadias and unilateral undescended testicle
karyotype - possible mixed gonadal dysgenesis (45 XO, 46 XY)
63
Radiographic evaluation of undescended testicle
unnecessary
64
Age of orchidopexy
6-12 months
65
Rate of foreskin retraction
1 yr - 50%, 5 yr - 90%
66
Balanoposthitis
inflammation of prepuce and glans
67
Paraphimosis
foreskin stuck in retracted position
68
Most common complication of circumcision
meatitis leading to meatal stenosis
69
Hypospadias location
ventral side (underside)
70
Medical management of bladder instability
oxybutynin (SE: dry mouth, facial flushing, constipation)
71
Management of enuresis
bedwetting alarm, desmopressin, imipramine
72
Indication for management of varicocele
ipsilateral testicular hypotrophy
73
Management of torsion of appendix testis
NSAIDs
74
Age range for testicular torsion and torsion of appendix testis
appendix testis - pre-pubertal | testicular torsion - pubertal boys