Congenital heart disease
Bicuspid aortic valve
- Function well at birth and go undetected
- Eventually develop AS and or AR
Atrial septal defect
- Ostium secundum defects are the most common
- Ostium primum defects are associated with AV valve anomalies
- Secundum ASDs may not present until adulthood
- Left to right shunting may precipitate heart failure
- There may be pulmonary hypertension, cyanosis, arrhythmia, haemoptysis and chest pain
- Signs;
- AF
- Raised JVP
- Fixed split S2
- Pulmonary ejection systolic murmur
- Pulmonary hypertension may cause pulmonary or tricuspid regurgitation
- AF
- Complications
- Reversal of the left to right shunt (Eisenmenger’s complex)
- Paradoxical embolisation
- Reversal of the left to right shunt (Eisenmenger’s complex)
VSD
- Can be congenital (2 in 1000 births) or post-MI
- May present with severe heart failure in infancy or remain asymptomatic until detected in later life
- Signs
- Harsh pansystolic murmur heard over the left sternal edge with a systolic thrill and left parasternal heave
- Larger holes may be associated with pulmonary hypertension
- Harsh pansystolic murmur heard over the left sternal edge with a systolic thrill and left parasternal heave
Coartation of the aorta
- Congenital narrowing of the aorta usually occurring just distal to the origin of the left subclavian artery
- Associated with biscuspid aortic valve and Turner’s syndrome
- Signs
- Radio-femoral delay, weak femoral pulse, raised BP, scapular bruit, systolic murmur best heard over left scapula
- Radio-femoral delay, weak femoral pulse, raised BP, scapular bruit, systolic murmur best heard over left scapula
- Complications
- Heart failure
- Infective endocarditis
- Heart failure
- Tests
- ECG shows rib notching
- ECG shows rib notching