Cardio, Pulmonary, Endocrine & Renal Flashcards

1
Q

___% of kids have a benign murmur

A

30

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2
Q

Two types of benign murmurs

A

stills murmur and venous hum

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3
Q

Stills murmur

A

SYSTOLIC,

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4
Q

Venous hum

A

best heard in anterior neck, disappears when jugular vein is compressed

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5
Q

Murmurs that are NEVER normal; tx

A

DIASTOLIC, anything >II/VI; get an echo

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6
Q

Dx–Newborn is cyanotic @

birth, O2 does not improve; most common in ____; [NO MURMUR]

A

transposition of great arteries; infants of diabetic mothers

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7
Q

Transposition of great arteries–tx

A

PGE1 to keep PDA patent

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8
Q

Dx–2y/o child who gets cyanotic and hyperpnea while playing, squats down; tx

A

TOF [pulm stenosis, RA hypertrophy, overriding aorta, VSD]; O2 and knees to chest, sx

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9
Q

TOF–murmur type

A

harsh SEM + single S2

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10
Q

Dx–Bipolar woman gives birth to a child w/ holosystolic murmur worse on inspiration

A

Ebstein anomaly

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11
Q

Ebstein anomaly

A

Tricuspid insuficciency 2/2 TV displacement into RV

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12
Q

Ebstein anomaly–arrhythmia

A

Wolff-Parkinson-White

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13
Q

Dx–Cyanosis @ birth with holosystolic murmur, depends on VSD or ASD for life. EKG shows LVH

A

Tricuspid atresia

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14
Q

Tricuspid atresia–tx

A

PGE1 until sx

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15
Q

Dx–Heart defect associated with DiGeorge syndrome. CXR shows ↑pulm blood flow and bi-ventricular hypertrophy

A

Truncus arteriosis

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16
Q

In truncus arteriosis, _____ develops early. Tx w/ sx in first few weeks of life

A

Eisenmenger

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17
Q

Describe Eisenmenger syndrome

A

increased blood flow to lungs instead of body causing extreme pulm HTN–>instead blood goes through shunt from RV to LV and gives O2-poor blood to body

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18
Q

MC congenital heart murmur; describe murmur

A

VSD; harsh holosystolic over LL sternal border, loud P2

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19
Q

If harsh holosystolic over LL sternal border at II/VI in 2mo w/ no sxs, next step

A

continue to monitor [VSD must close by 1-2yrs]

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20
Q

Gold standard test for murmurs

A

echo

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21
Q

VSD–surgery is indicated if____

A

FTT, 6-12mo w/ pHTN, >2yr w/ Qp/Qs >2:1

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22
Q

VSD–is louder murmurs better or worse? why?

A

Better. It means the defect is small. Most often membranous. More likely to spontaneously
close

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23
Q

Dx–Loud S1 w/ fixed and split S2. Older child w/ exercise intolerance

A

ASD

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24
Q

Dx–Most common defect in Down Syndrome baby

A

Endocardial cushion defect

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25
Endocardial cushion defect--describe murmur
Fixed & split S2 + SEM w/ diastolic rumble
26
Endocardial cushion defect----tx
sx before pHTN at 6-12mo [at risk for early Eisenmengers]
27
Dx--Continuous machine-like murmur w/ bounding pulses and wide pulse pressure
PDA
28
PDA--associated pathologies
prematurity, congenital rubella syndrome
29
PDA--tx
if not closed by 1wk, give indomethacin or sx
30
Dx--Most common defect in Turner’s baby
Coarctation of aorta
31
Dx--Decreased femoral pulses, “reverse 3 sign”, “notching” @ inf rib border 2/2 incr collateral
Coarctation of aorta
32
Dx--15yo athlete w/ occasional palpations, angina, dizziness. Last week, fainted during baseball game
Hypertrophic CM
33
Hypertrophic CM--murmur type; better with ____ preload, ___ w/ valsalva/standing/exercise
SEM; increased; louder
34
Hypertrophic CM--tx
ß-blockers or CCB, alcohol ablation or surgical myotomy
35
Hypertrophic CM--restrictions
no sports/heavy exercise!
36
Why can't you use diuretics or digitalis in Hypertrophic CM?
Dig--glycosides contraindicated except in pts a/ uncontrolled afib; Diuretics--potential adverse effect on the LV outflow gradient and ventricular volume
37
Dx--7yo w/ vague chest pain, pain in different joints over the past few days, and a rash. ESR is elevated. EKG shows prolongation of the PR interval
Acute rheumatic fever
38
Acute rheumatic fever--Tx
oral PCN (or erythromycin) for 10 days then prophylactically until 20yo
39
Acute rheumatic fever--cardiac complications
mitral stenosis (M > aorta > tricuspid)
40
CF--signs at birth; dx and tx
meconium ileus (dilated loops), "ground glass", +/- rectal prolapse from chronic diarrhea; gastrograffin enema
41
Early childhood, expect CF when see ____
FTT (
42
CF--genetics and inheritance
AR, mut chr7, CFTR protein
43
CF--dx
sweat test [>60mEq/L chloride]
44
CF--tx (A) thick resp secretions (B) pneumonia (C) pancreatic insuff (D) electrolyte loss thru skin
(A) DNAse (mucolytic), albuterol/saline nebs (B) piperacillin + tobramycin or ceftazidime (C) enz replace w/ meals + ADEK supplement (D) fluid replacement
45
CF--MC type pneumonia
pseudomonas or b. cepacia
46
Asthma tx--pt has sxs twice a week and PFTs are normal
albuterol only
47
Asthma tx--pt has sxs 4x a week, night cough 2x a month and | PFTs are normal
albuterol + inhaled CS
48
Asthma tx--pt has sxs daily, night cough 2x a week and FEV1 is 60-80%
albuterol + inhaled CS + long-acting ß-ag (salmeterol)
49
Asthma tx--pt has sxs daily, night cough 4x a week and FEV1 is
Albuterol + inhaled CS + salmeterol + montelukast and oral steroids
50
Asthma exacerbation--tx w/ _____.
albuterol and PO/IV steroids
51
Asthma exacerbation--watch __ and ___. PCO2 should be ____
peak flow rates; blood gas; low [if normalizing PCO2, means impending resp failure--must INTUBATE]
52
Asthma can cause severe complications during this case _____
allergic bronchopulmonary aspergillus [hyper-reactivity of immune system]
53
Type 1 DM--sxs when present to ER in DKA; labs--__ Na/Cl, ___HCO3, __ glucose
emesis, wt loss, polyphagia, polydipsia, polyuria; low; low/nl; high
54
Child w/ DKA--next best steps
Start insulin drip + IVF, monitor BGL and anion gap, start K, bridge w/ glargine once tolerating PO
55
Type 1 DM--pathophys
T-cell destruction of islet cells in pancreas, insulin autoAb, glutamic acid decarboxylase autoAb
56
Diagnostic criteria for DM?
fasting glc >125 (x2) OR 2hr OGTT (75g) >200, random glc >200 + sxs
57
Kid peeing blood--best first test
UA
58
Kid peeing blood--dysmorphic RBCs or RBC casts
glomerular source
59
Kid peeing blood--1-2 days after runny nose, sore throat and cough
Berger's Dz (IgA nephropathy) = MCC
60
Nephritic syndrome
proteinuria (
61
Kid peeing blood--1-2 wks after sore throat of skin infx
Post-strep GN
62
Post-strep glomerulonephritis characteristics
smoky/cola urine, best 1st test is ASO titer. Subepithelial IgG humps
63
Hematuria + hemoptysis
Goodpasture syndrome (Abs to collagen IV)
64
Hematuria + deafness
Alport syndrome (XLR mut in collagen IV)
65
Dx--Flank pain radiating to groin + hematuria
kidney stone
66
Kidney stone--best test
CT
67
Kidney stone--MC type; tx
calcium oxalate; HCTZ
68
Kidney stone--kid w/ family hx stones--MC type
cysteine (can't resorb certain AA)
69
Kidney stone--chronic indwelling foley and alkaline pee--MC type
struvite = Mg/Al/PO4
70
What pathogens cause struvite kidney stones?
proteus, staph, pseudomonas, klebsiella
71
Kidney stone--leukemia being tx w/ chemo--MC type
uric acid [tx by alkalinizing urine + hydration]
72
Kidney stone--s/p bowel resection for volvulus--MC type
pure oxylate stone (CA not reabsorbed by gut and so pooped out)
73
Kidney stone--tx of stones
will pass, hydrate
74
Kidney stone--tx of stones >2cm
open or endoscopic sx
75
Kidney stone--tx stones 5mm-2cm
extracorporal shock wave lithotropsy
76
Kid peeing protein--best first test
repeat in 2 wks then quantify w/ 24hr urine
77
Kid peeing protein--MC
minimal change disease (fusion foot processes)
78
Minimal change disease--tx; MC complication
prednisone 4-6wks; infection (make sure immunized for pneumo and varicella)
79
Nephrotic syndrome
>3.5g protein/24hrs, hypoalbuminemia, edema, hyperlipidemia (fatty/waxy casts)
80
Kid peeing protein--random cause
orthostatic =MC in school-aged kids; normal while supine
81
Dx--nephrotic pt suddenly w/ flank pain
renal vein thrombosis (EMERGENCY), 2/2 peeing out ATIII, protein C/S; do CT/US!!