Congenital Heart Disease Flashcards

1
Q

what two categories are congenital heart diseases divided into?

A

cyanotic and acyanotic

cyanotic means baby turns blue because low oxygen from defect flow

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2
Q

name the six acyanotic lesions

A
atrial septal defect
ventricular septal defect
patent ductus arteriosus
congenital aortic stenosis
pulmonic stenosis
coarctation of the aorta
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3
Q

what is the most common atrial septal defect?

A

ostium secundum

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4
Q

what is another atrial septal defect?

A

patent foramen ovale

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5
Q

what is a risk with an older person with old patent foramen ovale?

A

stroke

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6
Q

what two chambers of the heart enlarge with atrial septal defect?

A

right atrium and right ventricle because of shunt from left to right and abnormally larger volumes in right system

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7
Q

with a ventricular septal defect…what chambers of the heart enlarge and why?

A

all except the right atrium…due to increased volume in right ventricle resulting in increased pressure to the left atrium and left ventricle

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8
Q

name the three signs of heart failure in an infant

A

tachypnea
respiratory distress
difficulty feeding

will often see cyanosis and sweating

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9
Q

with a patent ductus arteriosus…what chambers of the heart get enlarged and why?

A

the left atrium and ventricle because they become overloaded with blood as it passes from aorta and to pulmonary artery

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10
Q

what happens to diastolic systemic perfusion with patent ductus arteriosus

A

decrease because of aorta flowing into pulmonary artery

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11
Q

what is the only congenital heart defect that has a drug treatment?

A

patent ductus arteriosus

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12
Q

what is the drug used to treat patent ductus arteriosus?

A

indomethacin

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13
Q

what is the MOA of indomethacin?

A

it is a prostaglandin synthesis inhibitor and prostaglandins keep the ductus open so if you decrease them the ductus arteiosus will close

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14
Q

define Eisenmenger syndrome…when does it occur?

A

this is when pulmonary tension has been high for so long that it finally reaches a pressure that is greater than the left and the shunt goes back to the left

this is when you have ASD, VSD or PDA

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15
Q

what are the symptoms of eisenmenger syndrome?

A

cyanosis and clubbing

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16
Q

which chamber of the heart is enlarged with aortic stenosis

A

left ventricle

17
Q

which chamber of the heart is enlarged with pulmonic valve stenosis?

A

right ventricle

18
Q

define coarctation of the aorta

A

this is a narrowed aortic lumen

19
Q

what can the aorta rely on for blood flow if severe coarctation?

A

a patent ductus arteriosus

20
Q

which chamber might enlarge in coarcation of the aorta?

A

left ventricle

21
Q

what is the persistent truncus arteriosus?

A

failure of the truncus arteriosus to divide into the pulmonary trunk and the aorta…usually have a VSD too

22
Q

what happens with transposition of the great vessels?

A

aorta linked to RV and pulmonary trunk to LV

get cyclic flow in separate sides of heart so easily leads to cyanotic babies

23
Q

with transposition of the great vessels..what circulation is the baby dependent on?

A

fetal circulation

24
Q

what happens in tricuspid atresia?

A

no tricuspid valve…leads to hypoplastic RV

25
Q

what do you need for survival with tricuspid atresia

A

ASD and VSD

26
Q

name the four issues with tetralogy of fallot

A

VSD
pulmonic stenosis
overriding aorta
RVH

27
Q

explain why tetralogy of fallot leads to cyanosis

A

with VSD, pulmonic stenosis and overriding aorta… you get lots of flow out of the aorta and pretty much none to the lungs

pretty much a right to left shunt

28
Q

what is a tet spell?

A

dyspnea on exertion leads to cyanosis from worsening R to L shunt in tetralogy of fallot

so when baby cries they get bluer

29
Q

what is a total anomalous pulmonary venous return

A

pulmonary veins drain into the wrong locations…specifically the right heart circulation…pretty much creates a cyclical issue in right system

30
Q

name the 5 cyanotic heart defects

A
truncus arteriosus
transposition of great vessels
tricuspid atresia
tetralogy of fallot
total anomalous pulmonary venous return