Suppr超能文献

[慢性血栓栓塞性肺动脉高压诊断和治疗指南(2024年版)]

[Guidelines for the diagnosis and treatment of chronic thromboembolic pulmonary hypertension (2024 edition)].

出版信息

Zhonghua Yi Xue Za Zhi. 2024 Jun 25;104(24):2200-2221. doi: 10.3760/cma.j.cn112137-20240116-00117.

Abstract

Chronic thromboembolic pulmonary hypertension (CTEPH) is classified as group 4 pulmonary hypertension, characterized by pulmonary arterial thrombotic occlusion leading to vascular stenosis or obstruction, progressive elevation of pulmonary vascular resistance and pulmonary arterial pressure, ultimately leading to right heart failure and even death. Recent years have seen rapid progress in the diagnostic and therapeutic in CTEPH field. More and more patients with CTEPH have been accurately diagnosed and assessed in time. Nevertheless, there is still a lot of work to do in the popularization of CTEPH diagnostic and therapeutic technique and the building of CTEPH expert center. To better guide clinical practice in our country, Pulmonary Embolism & Pulmonary Vascular Diseases Group of the Chinese Thoracic Society, Pulmonary Embolism & Pulmonary Vascular Disease Working Group of Chinese Association of Chest Physicians, National Cooperation Group on Prevention & Treatment of Pulmonary Embolism & Pulmonary Vascular Disease, National Expert Panel on the Development of a Standardized Framework for Pulmonary Arterial Hypertension, convened multidisciplinary experts for deliberation and Delphi expert consensus to develop the "Guidelines for the Diagnosis and Treatment of Chronic Thromboembolic Pulmonary Hypertension (2024 edition) ". These guidelines systematically evaluate domestic and international evidence-based medical research on CTEPH and propose recommendations tailored to clinical practice in our country. The key areas covered include definitions, epidemiology, pathogenesis, diagnosis and assessment, treatment, and management, with the aim of further standardizing the clinical diagnosis and treatment of CTEPH in our country.

摘要

慢性血栓栓塞性肺动脉高压(CTEPH)被归类为第4组肺动脉高压,其特征是肺动脉血栓性闭塞导致血管狭窄或阻塞、肺血管阻力和肺动脉压力进行性升高,最终导致右心衰竭甚至死亡。近年来,CTEPH领域的诊断和治疗取得了快速进展。越来越多的CTEPH患者得到了及时准确的诊断和评估。然而,在CTEPH诊断和治疗技术的普及以及CTEPH专家中心的建设方面仍有许多工作要做。为更好地指导我国临床实践,中华医学会呼吸病学分会肺栓塞与肺血管病学组、中国医师协会呼吸医师分会肺栓塞与肺血管病工作委员会、国家肺栓塞与肺血管病防治协作组、国家肺动脉高压标准化诊疗框架制定专家委员会,召集多学科专家进行审议并通过德尔菲专家共识制定了《慢性血栓栓塞性肺动脉高压诊断与治疗指南(2024版)》。这些指南系统评价了国内外关于CTEPH的循证医学研究,并提出了适合我国临床实践的建议。涵盖的关键领域包括定义、流行病学、发病机制、诊断与评估、治疗以及管理,旨在进一步规范我国CTEPH的临床诊断和治疗。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验