期刊
CHEST
卷 126, 期 1, 页码 14S-34S出版社
ELSEVIER SCIENCE BV
DOI: 10.1378/chest.126.1_suppl.14S
关键词
catheterization; chronic thromboembolic pulmonary hypertension; Doppler echocardiography; HIV; idiopathic pulmonary arterial hypertension; genetics; method; pulmonary arterial hypertension; scleroderma
Pulmonary arterial hypertension (PAH) occurs as an idiopathic process or as a component of a variety of disease processes, including chronic thromhoembolic disease, connective tissue diseases, congenital heart disease, and exposure to exogenous factors including appetite suppressants or infectious agents such as HIV. This article reviews evidence for screening in susceptible patient groups and the approach to diagnosing PAH when it is suspected, and provides specific recommendations for applying this evidence to clinical practice.
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