Pulmonary arterial hypertension (PAH) is a type of pulmonary hypertension (PH) that fundamentally affects the pulmonary vasculature. (1) Pulmonary hypertension may be defined as a resting mean pulmonary artery pressure of 25 mm Hg or above as measured by right heart catheterization. (1, 2) In PAH, the pulmonary vasculature is obstructed by vasocons
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