[To accumulate clinical evidence and improve the diagnosis and treatment of connective tissue disease associated pulmonary hypertension in China]

Zhonghua Nei Ke Za Zhi. 2021 May 1;60(5):396-399. doi: 10.3760/cma.j.cn112138-20210209-00122.
[Article in Chinese]

Abstract

第一大类肺动脉高压(pulmonary arterial hypertension,PAH)是影响结缔组织病(CTD)远期预后的决定性因素,需要风湿免疫科、心脏科、呼吸科、影像科、重症医学科和康复科等多学科紧密协作,才能及时、准确及有效的诊治。目前各相关专科医师急需可供遵循的符合我国国情的CTD相关PAH诊疗指南,以提高CTD相关PAH患者的规范化诊治水平。中国医师协会风湿免疫科医师分会风湿病相关肺血管/间质病学组、国家风湿病数据中心和国家皮肤与免疫疾病临床医学研究中心组织制定“2020中国结缔组织病相关肺动脉高压诊治专家共识”,纳入了更多我国的循证医学证据,充分反映了近年来的学术进展,有助于提高我国CTD相关PAH的诊疗水平,改善患者预后。.

MeSH terms

  • China
  • Connective Tissue Diseases* / complications
  • Connective Tissue Diseases* / diagnosis
  • Connective Tissue Diseases* / therapy
  • Humans
  • Hypertension, Pulmonary* / diagnosis
  • Hypertension, Pulmonary* / therapy