Pulmonary arterial hypertension (PAH)

肺动脉高压是肺动脉高压

英文解释

Pulmonary arterial hypertension (PAH) is a subtype of pulmonary hypertension (PH), characterized by pulmonary arterial remodeling. Pulmonary arterial hypertension (PAH) leads to progressive increases in pulmonary vascular resistance (PVR), right heart failure, and even lethality of life.

中文解释

肺动脉高压是肺动脉高压 (PAH) 的一种亚型，其特征是肺动脉重构。肺动脉高压导致肺血管阻力 (PVR) 进行性增加，右心衰，甚至使生命体致命。

参考文献

[1]. Ruopp NF, et al. Diagnosis and Treatment of Pulmonary Arterial Hypertension: A Review. JAMA. 2022 Apr 12;327(14):1379-1391.
[2]. Coons JC, et al. Pulmonary Arterial Hypertension: a Pharmacotherapeutic Update. Curr Cardiol Rep. 2019 Nov 22;21(11):141.