• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/39

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

39 Cards in this Set

  • Front
  • Back

timing of congenital HD

weeks 3-8

genetic congenital HD

Trisomies 13, 15, 18, 21, turner syndrome

environmental congenital HD

congenital rubella

fetal right atrium

slight mixing of deoxygenated and oxygenated blood

fetal Inferior vena cava

bring oxygenated blood from the placenta

path of oxygenated blood flow

placenta -> IVC -> foramen ovale -> left atrium -> left ventricle -> aorta -> body

fetal superior vena cava

brings deoxygenated blood from the upper body

path of deoxygenated blood in fetus

upper body -> SVC -> right ventricle -> pulmonary artery -> small amount to lungs, rest through ductus arteriosus -> aorta

Left to right shunts

oxygenated blood moves from L->R = incr. volume in right atrium and ventricle = right sided Hypertrophy = pulmonary HTN = eventually leads to R->L shunting and cyanosis

Atrial septal defects

Left to right shunt, 3 types: secundum (90%), primum (assoc. w/ cleft mitral valve), sinus venosus (connections of right pulmonary veins)

Atrial septal defects shunt

left to right; pulmonary blood flow 2-4 times normal




well tolerated until 30s, <10% develop pulmonary HTN

ASD complications

systolic murmur due to blood flow across pulmonic valve, arrhythmias

Ventricular septal defect

incomplete closure of the ventricular septum, many assoc. w/ other defects (tetralogy)




membranous portion most common (90%)




many spontaneous close over time esp. muscular

symptomatic VSD

size of aortic orifice

VSD shunt

left to right = RV hypertrophy and pulmonary HTN




leads to shunt reversal, cyanosis and death

complications of large VSD

recurrent pneumonia, chronic resp. Sx, exercise intolerance, FTT, endocarditis, murmurs

Atrioventricular septal defect

incomplete fusion of endocardial cushions leads to a low ASD, high VSD, and incomplete formation of mitral and tricuspid valves

partial AV septal defect

primary ASD and cleft anterior mitral leaflet

complete AV septal defect

common AV valve

AV septal defect association

1/3 have Down's syndrome

Patent ductus arteriosus

90% isolated; continuous harsh murmur




left to right shunt (aorta to pulmonary artery)




shunt reversal due to obstructive pulmonary vascular dz

Right to left shunts sx

think cyanosis!!




other sx: clubbing and polycythemia

Right to left shunts

The "T's" = tetralogy of Fallot, transposition, persistent truncus arteriosus, tricuspid atresia

Tetralogy of Fallot

VSD, subpulmonary stenosis, aorta that overrides the VSD, right ventricular hypertrophy

Transposition of Great Vessels

abnormal formation of truncal and aortopulmonary septa, so aorta arises from RV and lies anterior and to right of pulm. artery

35% of transposition patients also have

VSD (stable)

transposition + patent foramen ovale or ductus arteriosus

unstable shunt

transposition presents with

right ventricular hypertrophy

Truncus Arteriosus

failure of separation into aorta and pulmonary artery

Tricuspid atresia cause

unequal division of the AV canal + underdevelopment of the right ventricle




ASD or VSD

Tricuspid atresia

valve doesn't develop, so no link b/t right atrium and right ventricle

defects assoc. with tricuspid atresia

septal defect, hypoplastic or absent RV, enlarged mitral valve and left ventricle, pulmonic stenosis

Total anomalous pulmonary venous connection

no pulmonary veins directly joins the left atrium b/c common pulmonary vein doesn't develop

Total anomalous pulmonary venous connection assoc. defect

ASD or patent foramen ovale

coarctation of aorta

2:1 males, two forms - infantile and adult




50% accompanied by bicuspid aortic valve

infantile coarctation of aorta

hypoplasia of aorta proximal to PDA (worse prognosis)

adult coarctation of aorta

hypoplasia of aorta distal to ductus - more common, less serious

aortic stenosis and atresia

valvular (hypoplastic, dysplastic, abnormal in normal), sub- or supravalvular

Hypoplastic left heart syndrome (HLHS)

underdeveloped left side of the heart




must have a PDA to allow blood to get to systemic circulation pass the narrowed aorta