The Eighth Affiliated Hospital of Sun Yat-Sen University, Shenzhen, Guangdong Province, China.
The Eighth Affiliated Hospital of Sun Yat-Sen University Cardiology Department, Shenzhen, China.
BMJ Open. 2024 Aug 25;14(8):e086901. doi: 10.1136/bmjopen-2024-086901.
Coronary microcirculation dysfunction (CMD) is prevalent in patients with coronary artery disease (CAD). Current therapies for CMD are focused on pharmacotherapy, non-pharmacological treatments such as enhanced external counterpulsation (EECP) have shown favourable results in patients with CAD. However, whether EECP can improve CMD remains unknown. This study is designed to evaluate the effectiveness of EECP on CMD in patients with CAD, and to assess the feasibility of conducting a multicentre randomised controlled trial.
This study is a single-centre, outcome-assessor-blinded, parallel randomised controlled trial. A total of 110 participants with CAD will be included and randomly assigned to either the intervention group (EECP plus optimal medical therapy (OMT)) or the control group (OMT alone). EECP will be administered by operators for 60 min, 5 times per week for 7 weeks (35 times in total). Outcomes include patients' retention rates, the primary outcome and secondary outcomes. The primary outcome is the change in Myocardial Perfusion Reserve Index with cardiac MRI from baseline to the end of follow-up. The planned study duration is from 2024 to 2026.
Ethical approval was obtained from the Ethics Committee of the Eighth Affiliated Hospital, Sun Yat-sen University (ID: 2023-045-03). The findings will be disseminated in peer-reviewed publications.
ChiCTR2300076231.
冠状动脉微循环功能障碍(CMD)在冠心病(CAD)患者中较为常见。目前CMD 的治疗方法侧重于药物治疗,体外反搏(EECP)等非药物治疗方法已在 CAD 患者中显示出良好的效果。然而,EECP 是否能改善 CMD 尚不清楚。本研究旨在评估 EECP 对 CAD 患者 CMD 的有效性,并评估进行多中心随机对照试验的可行性。
这是一项单中心、结局评估者盲法、平行随机对照试验。共纳入 110 名 CAD 患者,并随机分为干预组(EECP+最佳药物治疗(OMT))和对照组(单独 OMT)。EECP 将由操作人员进行,每次 60 分钟,每周 5 次,共 7 周(共 35 次)。结局包括患者保留率、主要结局和次要结局。主要结局是心脏 MRI 从基线到随访结束时心肌灌注储备指数的变化。计划的研究时间为 2024 年至 2026 年。
中山大学第八附属医院伦理委员会已批准(ID:2023-045-03)。研究结果将在同行评议的出版物中公布。
ChiCTR2300076231。