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肺动脉高压的新型治疗方法

Novel Therapeutic Approaches of Pulmonary Arterial Hypertension.

作者信息

Tyagi Sanjay, Batra Vishal

机构信息

Department of Cardiology, Maulana Azad Medical College, New Delhi, India.

Department of Cardiology, G.B. Pant Institute of Postgraduate Medical Education and Research, New Delhi, India.

出版信息

Int J Angiol. 2019 Jun;28(2):112-117. doi: 10.1055/s-0039-1692140. Epub 2019 Jul 12.

Abstract

Pulmonary arterial hypertension (PAH) is an uncommon disease characterized progressive remodeling of pulmonary vasculature. Although treatment for PAH have improved in last two decades but the outcome remains fatal. Currently, the therapies for PAH target three well-established pathways the nitric oxide (NO) pathway, endothelin receptors, and prostanoids. There are multiple potential targets for development of newer drugs in PAH which requires meticulous research and clinical trials.

摘要

肺动脉高压(PAH)是一种罕见的疾病,其特征是肺血管进行性重塑。尽管在过去二十年中PAH的治疗有所改善,但结果仍然是致命的。目前,PAH的治疗针对三个已确立的途径:一氧化氮(NO)途径、内皮素受体和前列腺素。PAH中有多个新药开发的潜在靶点,这需要细致的研究和临床试验。

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本文引用的文献

1
Risk stratification and medical therapy of pulmonary arterial hypertension.肺动脉高压的风险分层与药物治疗。
Eur Respir J. 2019 Jan 24;53(1). doi: 10.1183/13993003.01889-2018. Print 2019 Jan.

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