Revision 3: Congenital heart disease Flashcards
freq. of congenital heart diseases and most common types
they are common -> 6-8/1000 births
the most common types are VSD, then ASD
Congenital heart defects
acyanotic: ASD, PFO, VSD, PDA (although a PDA can lead to Eisenmerger syndrome, which leads to cyanosis), co-arctation of aorta
cyanotic: tetralogy of Fallot, tricuspid atresia, transposition of great arteries, hypoplastic left heart
Atrial septal defects
gap in intra-atrial wall allows blood through l -> r, ACYANOTIC
most common site is at the foramen ovale -> ostium secundum ASD
- a less common site is the inf. part of the septum -> ositum primum ASD
patent foramen ovale
It is not a true ASD as the flaps are normally kept shut by the high left pressure - ACYANOTIC
however, a venour embolism may be allowed through if even a transient drop in the left-side pressure allows the flaps to open -> paradoxical embolism
Ventricular septal defects
opening in intra ventricular septum, most common in membranous portion, allows blood l -> r, ACYANOTIC
patent ductus arteriosus
In foetuses the DA allows blood to flow from the pulm. artery to the aorta
If this is open in neonates it allows flow the other way, as the pressure is greater in the aorta - (normally) ACYANOTIC
chronic l -> r shunting leads to vascular remodelling in the pulmonary circulation and an inc. in pulm. resistance
-> if pulm.>syst. resistance, leads to r->l shunt, CYANOSIS - Eisenmenger syndrome
co-arctation of the aorta
ACYANOTIC
narrowing of the aortic lumen in the region of the ligamentum arteriosum (formally the DA) -> inc. after-load on l/ventricle -> l/ventricular hypertrophy
vessels carrying blood to head and u/limbs emerge proximally to the co-arctation, so these are not affected, but the rest of the body has a reduced blood supply
In severe cases, may present at birth with cardiac failure
In less severe cases it may even be detected as late as an adult
tetralogy of fallot
CYANOTIC
defect placing outflow portion of i/vent. septum in an anterior and cephalad direction
4 abnormalities: Mainly pulmonary stenosis, r/vent. hypertrophy (as a result of the first), overriding aorta, VSD
high press. in r/side leads to r->l shunt
can present w/ cyan. in infacny but mild cases can present in adulthood
tricuspid atresia
CYANOTIC
lack of development of tricuspid valve, no inlet to r/vent.
complete r->l shunt of all blood returning to r/atrium w/ ASD/PFO and VSD/PDA to allow the blood back to the right side in the ventricles
Transition of great arteries
CYANOTIC
r/vent-> aorta, l/vent.-> pulmonary artery
not compatible w/life after birth, unless a shunt ie PDA a/o ASD allows communication
hypoplastic left heart
CYANOTIC
l/vent. and aorta fail to develop correctly
PFO and ASD are present, blood -> systemic circulation via PDA
lethal w/o surgery