医学
工作队
重症监护医学
临床实习
右心导管插入术
临床试验
肺动脉高压
叙述性评论
任务(项目管理)
随机对照试验
确定性
梅德林
疾病
临床研究
循证医学
风险评估
最佳实践
疾病管理
死因
临床判断
心脏病学
系统回顾
呼吸系统
作者
Gábor Kovács,Katarina Zeder,Marc Humbert,Robin Condliffe,Ingrid Toews,Athénaïs Boucly,Micheala Aldred,Roberto Badagliacca,Wendy Chung,Frances De Man,Peter Dorfmüller,Pisana Ferrari,George Giannakoulas,Sergio Harari,T. Kotsimbos,Nicole Ngai Yung Tsang,Rozenn Quarck,Antenor Rodrigues,Stephan Rosenkranz,Olivier Sitbon
出处
期刊:The European respiratory journal
[European Respiratory Society]
日期:2026-09-07
卷期号:: 2601178-2601178
标识
DOI:10.1183/13993003.01178-2026
摘要
Background Pulmonary arterial hypertension (PAH) is a severe, progressive disease of the small pulmonary arteries. These guidelines provide updated evidence-based recommendations for the treatment of PAH focusing on the latest scientific evidence on sotatercept, an activin signalling inhibitor targeting a novel pathway for the treatment of PAH, and on the role of right heart catheterisation (RHC) in the management of PAH patients during follow-up. Methods A European Respiratory Society (ERS) Task Force, comprising global experts, methodologists and a patient representative, developed these clinical practice guidelines in accordance with ERS methodology and the GRADE (Grading of Recommendations, Assessment, Development and Evaluations) approach. Four PICO (Patients, Intervention, Comparator, Outcomes) questions and one narrative question have been addressed. Recommendations The Task Force recommends add-on treatment with sotatercept in PAH patients who already receive PAH drugs and are at intermediate-low, intermediate-high or high risk of death during follow-up; this recommendation is based on a high certainty of evidence available from randomised controlled trials (RCTs). In PAH patients at low risk of death, the Task Force does not provide a recommendation due to the low certainty of evidence and the limited number of such patients included in RCTs. To monitor safety and efficacy, patients receiving sotatercept should be treated in pulmonary hypertension centres and their management should include regular follow-up and appropriate examinations. To guide treatment strategy, the Task Force suggests performing RHC during follow-up in PAH patients who receive PAH drugs and are at intermediate-low, intermediate-high or high risk of death, when therapeutic consequences are expected. The Task Force does not provide a recommendation for this question in PAH patients at low risk of death, due to the very low certainty of evidence. Conclusion The ERS guidelines on the treatment of PAH provide an updated evidence-based framework for the optimal management of patients with PAH.