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This review summarizes recent advances in risk stratification and targeted therapies for pulmonary arterial hypertension associated with congenital heart disease.
Pulmonary arterial hypertension is a serious complication of adult congenital heart disease associated with systemic-to-pulmonary shunts. Although early shunt closure restricts development of pulmonary arterial hypertension, patients remain at risk even after repair. The development of pulmonary arterial hypertension is associated with a markedly increased morbidity and mortality. It is important to identify patients with a poor prognosis using disease specific markers. Echocardiography and biomarkers arise as practical tools to determine the risk of mortality. Although pulmonary arterial hypertension cannot be cured, four classes of disease-targeting therapies are currently available and several promising therapies are being studied. There is a shift in drug studies towards more clinically relevant endpoints such as time to clinical worsening and morbidity and mortality events.
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Blok et al. (2015) conducted a review in Pulmonary arterial hypertension due to congenital heart disease. Targeted PAH therapies and surgical/percutaneous interventions was evaluated.
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