Peds Cardio X3 Flashcards

1
Q

Cardiac disease in infants SX

A

FTT

Tachypnea with feeding/activity

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2
Q

Cadiac disease in older children sx

A

palpitations, chest pain
dizzines/syncope
exercise intolerance,
unexplained hypertension

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3
Q

what will hepatomegaly and Ascities indiicate

A

R sided heart failure

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4
Q

Clubbing of fingers/toes associated with?

A

appears after age 1

with cyanotic congenital heart disease

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5
Q

Echocardiogram

A

Gold standard
Ultrasound of the heart
1. Transthorasic echo (more common)
2. Transesophageal echo

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6
Q

EKG

A

evaluates electrical activity and cardiac postition

-evolves with age

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7
Q

CXR

A

exaluates

  • position of heart/size/shape
  • position of abdominal viscera
  • pulmonary vasculature
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8
Q

Cardiac Catherization

A

fluroscopy when a wire is threaded up to the heart

  • radioopaque dye injecednto evaluate anatomy
  • samples and measure pressure
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9
Q

Innocent Murmurs characteristics

A
  • no FH
  • -<= 2grade 2
  • short systolic duration
  • minimal radiation
  • soft intensity
  • musical or vibratory quality
  • normal pulse
  • normal pulse ox,CXR, EKG
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10
Q

Still murmur

A

-most common innocent murmur
musical/vibratory
-short high pitched
- loudest supine, dimishes/disappears with inspiration or sitting

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11
Q

Pulmonary flow murmur

A

most common in older children and alsults >3

  • sof SEM
  • louder supine
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12
Q

venoud hum

A
2 and up 
continuous musical hum 
-hear at R/L USB 
*louder in diastole**
-disappears with turning head or placing shild in supine
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13
Q

Acyanotic congenital heart disease

A

Vesntral septal defect
atrial septal defect
patent ductus arteriosis
coartication of aorta

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14
Q

Cyanotic conegital heart disease

A
  • tetrlogy of Fallot
  • transposition of the great arteries
  • tricuspid ateriosus
  • total anomalous pulmonry venoud return

-hypoplastic left heart syndrome

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15
Q

when should the ductus arteriosus close?

A

14 days

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16
Q

Vesntricular septal defect (VSD)

A
  • most common congenital heart defet

- associated trisomy 21 and tetralogy of fallot

17
Q

VSD presentation

A

Small VSD may be aymptomatic
Larger: FTT, poor growth, dyspnea, frequent respiratory infections
PE: tachycardia, tachypnea, hepatomegaly
**blowing harsh holosystolic murmur LLSB

18
Q

VSD dx

A

Echo: locates
EKG: LVH
CXR: cardiomegaly, increased pulmonary vascular markings

19
Q

VSD Managment

A

wait and see> esp with asymptomatic
Med: tx CHF (diuretic Ace inhibitor
Surgical: septal occlusion via caterization
* prefereec surgical closure via median sternotomy

20
Q

Atrial Septal defect ASD classifies

A
Ostium secundum (most common)> oftenisolated 
Ostium primum> often associaye with other anomolies
21
Q

ASD presentation

A

CHF, recurrent resp infections FTT
-fixed widely split s2 at pulmonary area
@ULSB
-surgical patch if larger than 6mm

22
Q

Eisenmenger syndrome

A

if you have a PDA for a log time and the shunt can reverse at high pulomary pressures casuing cyanosis

23
Q

Tx of PDA

A

Monitor
Keep open : IV prostagladin E1
Close it up : IV indomethacin (prostagandin inhibit)
Surgery if nonresponders

24
Q

Coarctation of the Aorta

A

Narrowing of the aortic arch in the proximaldecending aorta near takeoff of the left subclavian artery

25
Q

What is female coarctation of the aorta associated with

A

Turner syndrome

26
Q

Coarctation of the aorta

A
Echo  
CXR
-figure 3 sign 
-inferior rib notching 
Tx: surgery
27
Q

Teralogy of fallot

A
Righ ventricular hypertrophy 
ventricular septal defect 
overiding aorta
RV outflow obstruction 
**most common cyanotic CHD
28
Q

Tetralogy of fallot presentation

A

“Test spells”

  • begins 4-6 mo
  • sunden onset or worsening of cyanosis
  • alterations of consciousness (irratable to syncope )
  • often occuring with crying or feeding or exercise
  • toddlers may squat to relieve dyspnea
29
Q

tetralogy of fallot

A
Pe: harsh systolic ejection ULSB 
echo-DX
CXR: boot shaped heart > upturned apex 
Tx: oxygen knees to chest 
surgery by age 1
30
Q

Tranpostion of the great arteries

A

second most common
-no murmur becuase no holes in heart
Presentation: profoundly cyanotic neonate “ blue baby

31
Q

What do you need to keep open in transposition of great arteries

A

keep ASD open or PFO!!

so you can get some mixing of blood

32
Q

Tx: of transposition of vessels

A

-balloon atrial septostomy to improve intraatrial communication
-prostaglandin E1 administration -keep ductus art open
-Surgery 4-7 days
arterial switch operation

33
Q

Tricuspid Atresia

A

absence of a tricuspid valve - must occur with other defects at the sme time becuase we need to keep blood goign

34
Q

Tricuspid atresia pres

A

centra cyanosis at birth, single heart sound
FTT tachpnea axhaustion during feeding
Tx: prostaglandin E1 to maintain PDA > surgery

35
Q

Truncus Arteriorsis

A

aorta and PA fail to separate
**VSD is always present
Sx: poor feeding lethary respiratory distress. narrow s2 spil at LLSB

36
Q

Total ANomalous Pulmonary venoud return

A

pulmonary veins drain into venoud system
*need some kind of R to Left shunt for oxygenation
Sx: varies depedning on location of venous connection
Tx: surgery