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Definition and classification of pulmonary arterial hypertension Until 2018, pulmonary arterial hypertension (PAH) was formally defined as a mean pulmonary artery pressure (mPAP) of greater than or equal to 25 mm Hg at rest, accompanied by a pulmonary vascular resistance…
Drug Class Overview and Guidelines Pulmonary arterial hypertension (PAH) is a rare, heterogenous family of disease states marked by pathologic remodeling of the pulmonary vascular system, leading to increased pulmonary artery pressure and ultimately right ventricular failure, hypoxia, and death.…