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- W759273360 abstract "Numerous conditions lead to a sustained increase in pulmonary arterial pressure. Pulmonary hypertension is defined as an elevation of mean pulmonary arterial pressure to 25 mmHg or greater. Currently, the pulmonary hypertensive diseases are organized into five groups that include (1) pulmonary arterial hypertension, (2) pulmonary hypertension owing to left-sided heart disease, (3) pulmonary hypertension owing to chronic lung disease, (4) chronic thromboembolic pulmonary hypertension, and (5) miscellaneous causes. Group 2 and 3 represent the most common causes of pulmonary hypertension. Group 1 (PAH) is exceedingly rare but normally progresses to severe pulmonary hypertension and right ventricular failure. PAH is seen more frequently in patients with connective tissue disease, HIV infection, portal hypertension, congenital cardiac shunts, and those who have used amphetamine-like drugs. This chapter provides an in-depth description of the various pulmonary hypertensive diseases and an overview of their epidemiology, including demographics, risk factors, and distinguishing characteristics." @default.
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- W759273360 date "2015-01-01" @default.
- W759273360 modified "2023-09-26" @default.
- W759273360 title "Epidemiology and Disease Classification of Pulmonary Hypertension" @default.
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- W759273360 doi "https://doi.org/10.1007/978-1-4939-2636-7_2" @default.
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