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肺动脉高压的肺功能改变及临床预后的评估 被引量:7

Changes of the lung function of pulmonary artery hypertension and clinical prognosis evaluation
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摘要 肺动脉高压(pulmonary artery hypertension,PAH)指静息时肺动脉平均压〉25 mmH g(1 mmH g=0.133 kP a)或运动时〉30 mmH g,是一类以肺血管阻力(pulmonary vascular resistance,PVR)和肺动脉压(pulmonary artery pressure,PAP)进行性升高为主要特征的肺血管疾病[1]。PAH分为原发性和继发性两类。
出处 《中华肺部疾病杂志(电子版)》 CAS 2016年第3期239-243,共5页 Chinese Journal of Lung Diseases(Electronic Edition)
基金 国家科技支撑计划资助项目(2009BA185B003) 青海省应用基础研究计划资助项目(2011-Z-710)
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