BRS Renal Flashcards

1
Q

Total body fluid requirements =

A

maintenance fluid needs +
prior loss +
ongoing losses

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2
Q

Two types of fluid losses

A

sensible (urine, etc. measurable)

insensible (sweat, skin etc…not measurable)

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3
Q

Maintenance fluid requirements for children

A
1500 mL/m^2/day 
or.....
100ml/kg/day for first 10 kg 
50ml/kg/day for second 10 kg 
20 ml/kg/day for any additional 10 kg
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4
Q

How much should maintenance fluids be increased during fever?

A

12% for every degree increase in temp above 38

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5
Q

Normal sodium range + relevance to dehydration

A

130-150
above= hypernatremic dehydration, correct over 48 hours
below/equal= hypo/isonatremic, correct over 24 hours

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6
Q

Three severities of dehydration

A

3-5%: mild
7-10%: moderate
12%+: severe

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7
Q

Typical bolus amount

A

20ml/kg normal saline for all dehydrated patients What

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8
Q

Composition of oral rehydration salts

A

glucose + electrolytes

coupled cotransport mechanism

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9
Q

Define microscopic hematuria (#)

A

more than 6 RBCs per HPF

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10
Q

Cause of false negative urine dipsticks

A

vitamin C

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11
Q

Shape of RBCs from upper vs lower urinary tract

A

upper: dysmorphic, blebs in membrane
lower: normal biconcave discs

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12
Q

Three hematologic causes of hematuria

A

sickle cell
thrombocytopenia
thrombosis

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13
Q

Four glomerular diseases leading to hematuria

A
  • bergers
  • HSP
  • PSGN
  • Alports
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14
Q

Proteinuria level considered pathologic

A

more than 100mg/m^2/day

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15
Q

What causes incorrect measures of protein in urine

A

high concentration = false +

low concentration = false -

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16
Q

Typical test for urine protein in children + normal levels

A

TP/CR
6-24 months, less than 0.5 normal
2+ years, less than 0.2 normal

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17
Q

Dipstick + for blood but no RBS on U/A… cause?

A

hemoglobinuria, myoglobinuria

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18
Q

Orthostatic proteinuria, protein is excreted when?

A

when upright but not supine

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19
Q

Cause of glomerular proteinuria

A

increased permeability of the glomerular capillaries

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20
Q

Cause of tubular proteinuria

A

decreased reabsorption due to injury

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21
Q

Marker for tubular vs glomerular proteinuria

A

tubular: B(two)macroglobulin
glomerular: microalbumin

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22
Q

Two types of glomerulonephritis

A

primary vs secondary

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23
Q

Signs of acute nephritic syndrome

A
  • gross hematuria
  • hypertension
  • fluid overload
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24
Q

Signs of acute nephrotic syndrome

A
  • heavy proteinuria
  • hypercholesterolemia
  • edema
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25
Labs for glomerulonephritis (6)
- U/A - TP/CR - blood chem - complement levels - antibodies (DNAB, ASO) - IgA
26
How long after GAS infection does PSGN onset?
8-14 days
27
PSGN assc labs
- low complement | - ASO+ 90%, ADB + for all
28
When is renal biopsy indicated for PSGN
within 8 weeks if kidney function isn't normalized
29
Most common acute glomerulonephritis worldwide? chronic?
acute: PSGN chronic: IgA Nephropathy (Bergers)
30
Recurrent bouts of gross hematuria assc with URI: | cause
IgA Nephropathy (Bergers)
31
Histo findings assc with PSGN + Bergers
mesangial cell proliferation + increased mesangial cell matrix for both + IgA deposition in Bergers
32
Prognosis PSGN vs Bergers
PSGN- usually full recovery | Bergers- 20-40% ESRD
33
In addition to purpura, abdominal pain, what signs are assc with HSP ?
- arthritis | - hematuria
34
What type of disease is HSP?
IgA mediated vasculitis
35
When is renal biopsy indicated for HSP?
heavy or nephrotic range proteinuria
36
Histo findings assc with MPGN
- lobular mesangial hypercellularity | - thickening of GBM
37
Prognosis MPGN
almost all = ESRD
38
Labs assc with MPGN
75% have low complement
39
Most common cause nephrotic syndrome in US adults?
Membranous Nephropathy | =heavy proteinuria --> renal insufficiency
40
Definition of nephropathy
heavy proteinuria greater than 50mg/kg/day
41
In addition to proteinuria, what labs are assc with nephropathy?
- hypoalbuminemia - hypercholesterolemia - edema
42
Most common cause primary nephropathy
minimal change disease
43
Two systemic diseases that cause nephrotic syndrome
SLE | HSP
44
Physiologic cause of nephrotic syndrome
loss of normal charge and size glomerular barrier
45
When does edema occur in nephrotic syndrome?
following URI
46
Two risks assc with nephrotic syndrome?
thrombosis infection with encapsulated bacteria (COD in 5%)
47
CBC changes assc with nephrotic syndrome?
- elevated hematocrit | - hemoconcentration
48
Nephrotic syndrome: | biopsy?
only if creatinine clearance is impaired/ corticosteroids don't work
49
Treatment of widespread edema in nephrotic syndrome
25% albumin IV no added salt in diet steroids
50
Cause of ESRD in NS
FSGS
51
Abx treatment for HUS?
NO! | and... abx treatment of hermorrhagic colitis= ^^ risk HUS
52
E coli strain responsible for HUS ?
0157:H7
53
Key to pathogenesis in HUS
injury to endothelial cells by shiga toxin
54
Causes of death in HUS
toxic megacolon | CNS infarctions
55
Poor prognostic signs in HUS
high WBC count | prolonged oliguria
56
Alports: inheritance pattern defect
XD | type 4 collagen in basement membrane
57
Three manifestations of alports
cant see cant pee cant hear high C
58
Most common cause of a renal mass in the newborn
multicystic renal dysplasia
59
Adult vs infantile polycystic kidney diseases
ARPKD (infantile) | ADPKD (adult)
60
Two organ systems effected by ARPKD in addition to renal:
pulmonary hypoplasia | liver involvement= constant (portal HTN, cirrhosis)
61
Prognosis of ARPKD/ ADPKD:
most = severe HTN + renal insufficiency and require transplant
62
# Define: - normal HTN - significant HTN - severe HTN - malignant TN
- normal 90-95th %ile - significant 95th%ile+ - severe above 99th%ile - malignant: end organ damage
63
Most hypertension in childhood is _____ HTN
secondary
64
Three secondary causes of HTN in newborn
- renal artery embolus/ stenosis - coarctation - renal disease
65
2 most common causes of HTN in kids 1-10
coarctation | renal disease
66
2 most common causes of HTN in adolescents
renal disease | essential
67
Consequences of chronic HTN in kids
growth retardation | poor school performance
68
Initial evaluation of HTN in peds
- CBC/BMP/UA/BUNCr/renin | - CXR/RUS
69
Signs of RTA
- calculi - weakness/ myalgias - FTT - vomiting
70
Drug that may cause acquired RTA
amphotericin
71
Classic electrolyte presentation of RTA
hypercholermic acidosis + normal serum anion gap
72
How to calculate urine anion gap
Na+K-Cl
73
``` hypokalemia hypophosphatemia aminoaciduria +RTA =suggestive of ```
Fanconis
74
Defect assc with: | Type 1 vs Type 2 RTA
Type 1= distal= failure to excrete H+ | Type 2= proximal= failure to absorb bicarb
75
Type III RTA defect
variant of type I but = proximal bicarb wasting in babies
76
Hallmark of Type IV RTA
transient acidosis + hyperkalemia
77
Treatment of all RTAs
oral alkali
78
Treatment of Type IV RTA
oral alkali + furosemide
79
Which type RTA is assc with: Fanconis amphotericin/nephrotic syndromes obstructive uropathy aldo def
- Fanconis= type II - amp/nephrotic syndromes (acquire)= Type I - obstructive/aldo def= Type IV
80
Type RTA assc with stones
Type I
81
Define oliguria
less than one ml/kg/hr
82
Renal failure management
-restore volume -electrolyte intake to match losses -protein restriction +/-dialysis
83
Disease that manifests SECONDARY TO renal failure
renal osteodystrophy
84
BUN/Cr and FeNa in prerenal ARF
^^^ BUNCR move than 20 | low FeNa less than 1
85
Renal Tubular ARF assc FeNa + marker
high B2 microglobuin | FENA above 1
86
ARF due to glomerular damage causes ____ and _____
hematuria and proteinuria
87
Interstitial nephritis marker
eosinophilia/uria
88
post renal ARF findings
renal dilation on US
89
Vascular related ARF findings
decreased renal blood flow on nuclear renal scan
90
Two types of ureteral obstruction
ureteropelvic | ureterovesical
91
Cause of bladder outlet obstruction in males
posterior urethral valve obstruction
92
Absence of rectus muscles + bladder outlet obstruction + cryptorchidism=
prune belly syndrome
93
Most common newborn abdominal mass
multicystic dysplastic kidney +atretic ureter
94
Most common anomaly assc with UTIs + inheritance pattern
vesicoureteral reflux =AD
95
How to Dx VUR
voiding cystourethrogram
96
Px treatment of VUR
low dose abx to prevent UTI until it is outgrown
97
Grade 1-2 VUR
1: reflux into distal ureter only 2: reflux into pelvis without dilation
98
Grade 3-5 VUR
3: into calyces + dilation 4: into calyxes + dilation + clubbing 5: gross dilation of entire collecting system + tortuosity of ureters
99
Workup for any kid with renal stones
rule out metabolic disorders
100
What UTI type is assc with stones
proteus
101
Three common stone components
calcium oxalate uric acid
102
When are UTIs most common in boys?
more common in boys before 6 months | girls after 6 months
103
Most common pathogenesis of UTI
ascending infection
104
Sign of pyelo
fever + systemic illness
105
gold standard dx of UTI
more than 10k colones on catherized sample any bacteria on suprapubic sample more than 50k colonies on clean catch
106
When is imaging needed in case of UTI ?
pyelo recurrent UTI all males girls younger than 4 with cystitis
107
Two options of treatment for empiric uti
TMP-SMX | cephalexin
108
Neonate UTI treatment
amp & gent
109
How to prevent renal scarring in infants
3 months px antibiotics after pyelo episode