Usually picked up through antenatal scans or newborn examinations
Atrial septal defects (ASDs) are the most likely congenital heart defect to be found in adulthood. They carry a significant mortality, with 50% of patients being dead at 50 years.
Pathophysiology
- Caused by defects in the formation of the atrial septum in utero (weeks 4,5) - leading to the formation of a shunt = blood flows from L to R atrium due to higher pressure in L side
- As blood continues to flow to lungs - patient DOES NOT become cyanotic, however increased flow to right side of heart = overload and right sided strain causing right sided heart failure and pulmonary hypertension
- Eventually this leads to Eisenmenger syndrome - where pulmonary pressure>systemic pressure reversing the shunt from right to left across the ASD
- blood bypasses the lungs and patient becomes CYANOTIC
Types of ASDs:
- ostium secundum (70% of ASDs) - septum secondum doesnt close (hole in the wall)
- ostium primum - septum primum doesnt close (atrioventricular septal defect)
- patent foramen ovale - not strictly classified as an ASD
PC
May be asymptomatic in childhood and present later with:
- dyspnoea
- heart failure
- stroke
On examination:
- ejection systolic murmur, loudest at upper left sternal border
- a fixed split second heart sound - hear the closure of the aortic and pulmonary valves at slightly different times (takes longer for R ventricle to empty)