肺动脉高压的临床药物治疗及药物开发。

Massimiliano Mulè, Marilena Scarabelli, Davide Capodanno, Gian P Ussia, Corrado Tamburino
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引用次数: 1

摘要

肺动脉高压(PAH)是一种罕见但严重的疾病,如果不治疗,则与生存率低有关。目前,即使几项试验已经导致许多治疗多环芳烃的药物获得批准,也没有确定的治疗这种疾病的方法。然而,批准的PAH药物已显著改善了这些患者的症状、运动能力、生活质量和生存率。本综述的目的是概述多环芳烃的标准治疗方法,并就目前正在研究的新治疗方法以及最近专利的讨论提供一些见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical pharmacotherapy and drug development for pulmonary arterial hypertension.

Pulmonary arterial hypertension (PAH) is a rare, but serious condition which, if untreated, is associated with a poor survival. Currently, even if several trials have led to the approval of many drugs for PAH, there is no established cure for this disease. However, approved drugs for PAH have contributed to significantly improve symptoms, exercise capacity, quality of life and survival of these patients. The aim of this review is to overview the standard treatment of PAH and to give some insights about new treatments that are currently under investigation along with the discussion of recent patents.

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