摘要
肺动脉高压是以肺小动脉的血管痉挛、内膜增生和重构为主要特征的一种疾病。它是一进展性疾病,生存期为2.8年,早期诊断和治疗干预是改善患者预后的重要措施,现将新近的治疗进展综述。
Pulmonary arterial hypertension is characterized by pulmonary artery vasospasm, intimal hyperplasia, and remoldeling lesions. Pulmonary arterial hypertension is a progressive disease and has a prognosis of 2.8 years of life, on average, after diagnosis. Early diagnosis and treatment are imperative for improved prognosis. This article reviews recent progress in the treatment of pulmonary arterial hypertension.
出处
《心血管病学进展》
CAS
2010年第2期219-222,共4页
Advances in Cardiovascular Diseases
关键词
肺动脉高压
治疗
pulmonary arterial hypertension
treatment
