Eisenmenger Syndrome
Eisenmenger syndrome occurs as a result of a chronic process in which an uncorrected left-to-right shunt leads to increased pulmonary blood flow, causing pathological remodelling of the pulmonary vasculature and finally, pulmonary hypertension. It consists of the triad:
- Congenital structural defect causing initial left-to-right shunt
- Subsequent pulmonary hypertension causing shunt reversal from right-to-left
- Cyanosis
Clinical manifestations include clubbing, raised JVP, central cyanosis, right parasternal heave and loud P2. Complications of Eisenmenger syndrome include:
- RV dilatation and dysfunction
- Cyanotic heart disease- erythrocytosis; bleeding
- Intrapulmonary haemorrhage / haemoptysis
- Pulmonary artery aneurysm
- Pulmonary thrombosis
- Stroke/TIA – Paradoxical embolism
- Brain abscess
- Arrhythmias
- Sudden cardiac death
- Infective endocarditis
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