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慢性阻塞性肺疾病中的肺动脉高压和慢性肺源性心脏病

Pulmonary hypertension and chronic cor pulmonale in COPD.

作者信息

Shujaat Adil, Minkin Ruth, Eden Edward

机构信息

Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, St. Luke's and Roosevelt Hospitals, Columbia University, New York, NY, USA.

出版信息

Int J Chron Obstruct Pulmon Dis. 2007;2(3):273-82.

Abstract

Hypoxia and endothelial dysfunction play a central role in the development of pulmonary hypertension. Cor pulmonale is a maladaptive response to pulmonary hypertension. The presence of peripheral edema in cor pulmonale is almost invariably associated with hypercapnia. Correction of abnormalities of gas exchange and ventilation can ameliorate pulmonary hypertension and improve survival. This review focuses on new information about the pathogenesis and treatment of pulmonary hypertension in COPD including information derived from lung volume reduction surgery, the role of brain natriuretic peptide, exhaled nitric oxide for diagnosis, and the treatment of cor pulmonale with recently available specific pulmonary vasodilators.

摘要

缺氧和内皮功能障碍在肺动脉高压的发展中起核心作用。肺心病是对肺动脉高压的一种适应不良反应。肺心病患者出现外周水肿几乎总是与高碳酸血症相关。纠正气体交换和通气异常可改善肺动脉高压并提高生存率。本综述重点关注慢性阻塞性肺疾病(COPD)中肺动脉高压发病机制和治疗的新信息,包括肺减容手术获得的信息、脑钠肽的作用、呼出一氧化氮用于诊断以及使用最近可用的特异性肺血管扩张剂治疗肺心病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c2d/2695205/e534d8f10c3e/copd-2-273f1.jpg

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