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肺动脉高压的流行病学和治疗。

Epidemiology and treatment of pulmonary arterial hypertension.

机构信息

Department of Respiratory Medicine, Royal Prince Alfred Hospital, Missenden Road, Camperdown, NSW 2050, Australia.

Computational Genomics Laboratory, Victor Chang Cardiac Research Institute, Liverpool Street, Darlinghurst, NSW 2010, Australia.

出版信息

Nat Rev Cardiol. 2017 Oct;14(10):603-614. doi: 10.1038/nrcardio.2017.84. Epub 2017 Jun 8.

Abstract

In the past 2 decades, major changes have occurred in the epidemiological and treatment landscape of pulmonary arterial hypertension (PAH). Previously regarded as a disease of the young and middle-aged, contemporary registries from the Western world have demonstrated an increase in the age of patients with PAH, many of whom are elderly with multiple comorbidities. Another important observation is the improvement in survival of patients with PAH in the modern treatment era compared with historical cohorts, before the availability of advanced therapy. The management of PAH has also become more complex, and numerous drugs are now approved that target the endothelin 1, nitric oxide, and prostacyclin pathways. Combining drugs from different classes is now considered the standard of care and has been demonstrated to improve outcomes. Furthermore, the current treatment paradigm is the early use of combination therapy, often at the time of diagnosis, particularly in patients with severe disease. This Review provides a comprehensive update on the epidemiology and pharmacotherapy of PAH.

摘要

在过去的 20 年中,肺动脉高压 (PAH) 的流行病学和治疗格局发生了重大变化。此前被认为是年轻人和中年人易患的疾病,来自西方世界的当代登记处显示,PAH 患者的年龄不断增加,其中许多是患有多种合并症的老年人。另一个重要的观察结果是,与先进治疗方法出现之前的历史队列相比,在现代治疗时代,PAH 患者的生存率有所提高。PAH 的治疗也变得更加复杂,现在有许多药物被批准用于靶向内皮素 1、一氧化氮和前列环素途径。现在联合使用来自不同类别的药物被认为是标准的治疗方法,并已被证明可以改善预后。此外,目前的治疗模式是早期使用联合治疗,通常在诊断时,特别是在患有严重疾病的患者中。这篇综述全面介绍了 PAH 的流行病学和药物治疗。

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