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人类免疫缺陷病毒相关的肺动脉高压:一个会持续存在的临床问题?

HIV-associated pulmonary arterial hypertension: a clinical problem that is here to stay?

作者信息

Murphy D, Girgis R E

机构信息

Department of Respiratory Medicine, Mater Misericordiae University Hospital, University College Dublin, Dublin, Ireland.

出版信息

Int J Clin Pract Suppl. 2009 Mar(161):19-21. doi: 10.1111/j.1742-1241.2008.01959.x.

Abstract

HIV-associated pulmonary arterial hypertension (PAH) is a serious complication of HIV infection and associated with high patient mortality. There are multiple similarities between HIV-associated PAH and idiopathic PAH and standard PAH medications have been used to treat the condition with reported success. Prior to the advent of highly active antiretroviral treatments (HAART), the prevalence of the condition in the HIV-infected population was estimated at 0.5%. In a recently published, large, prospective, multi-centre study performed in the HIV-population across France, the prevalence of HIV-associated PAH was estimated at 0.46%. In this article, we provide an overview of HIV-associated PAH and summarise the methodology, pertinent findings and implications of this important paper.

摘要

人类免疫缺陷病毒相关的肺动脉高压(PAH)是HIV感染的一种严重并发症,与患者的高死亡率相关。HIV相关PAH与特发性PAH有诸多相似之处,标准的PAH药物已被用于治疗该疾病,且有报道称取得了成功。在高效抗逆转录病毒治疗(HAART)出现之前,估计HIV感染人群中该疾病的患病率为0.5%。在法国针对HIV人群进行的一项最近发表的大型前瞻性多中心研究中,HIV相关PAH的患病率估计为0.46%。在本文中,我们概述了HIV相关PAH,并总结了这篇重要论文的方法、相关发现及意义。

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