Combination of Chinese Herbal Medicines and Conventional Treatment versus Conventional Treatment Alone in Patients with Acute Coronary Syndrome after Percutaneous Coronary Intervention (5C Trial): An Open-Label Randomized Controlled, Multicenter Study
机构:[1]China Acad Chinese Med Sci, Guanganmen Hosp, Beijing 100053, Peoples R China;[2]China Acad Chinese Med Sci, Xiyuan Hosp, Beijing 100091, Peoples R China;[3]Fudan Univ, Zhongshan Hosp, Shanghai 200032, Peoples R China;[4]Capital Med Univ, Beijing Inst Resp Med, Beijing Anzhen Hosp, Beijing 10029, Peoples R China;研究所/中心(本部)呼吸疾病研究所首都医科大学附属安贞医院北京朝阳医院[5]Chinese Acad Med Sci, Cardiovasc Inst, Beijing 100037, Peoples R China;[6]Chinese Acad Med Sci, Fuwai Hosp, Beijing 100037, Peoples R China;[7]Peking Union Med Coll, Beijing 100037, Peoples R China;[8]Capital Med Univ, Beijing Tongren Hosp, Beijing 100730, Peoples R China;首都医科大学附属同仁医院[9]Beijing Univ Chinese Med, Dongzhimen Hosp, Beijing 100007, Peoples R China;[10]Liaoning Tradit Chinese Med Univ, Affiliated Hosp, Shenyang 110033, Peoples R China;[11]Capital Med Univ, Beijing Chinese Med Hosp, Beijing 100010, Peoples R China;[12]Tianjin Univ Tradit Chinese Med, Teaching Hosp 1, Tianjin 300193, Peoples R China;[13]Beijing Chuiyangliu Hosp, Beijing 100022, Peoples R China;[14]Second Peoples Hosp Fujian Prov, Fuzhou 350100, Peoples R China;[15]Nanjing Univ Tradit Chinese Med, Wuxi Tradit Chinese Med Hosp, Wuxi 214001, Peoples R China
Aims. To evaluate the efficacy of Chinese herbal medicines (CHMs) plus conventional treatment in patients with acute coronary syndrome (ACS) after percutaneous coronary intervention (PCI). Methods and Results. Participants (n = 808) with ACS who underwent PCI from thirteen hospitals of mainland China were randomized into two groups: CHMs plus conventional treatment group (treatment group) or conventional treatment alone group (control group). All participants received conventional treatment, and participants in treatment group additionally received CHMs for six months. The primary endpoint was the composite of cardiac death, nonfatal recurrent MI, and ischemia-driven revascularization. Secondary endpoint was the composite of readmission for ACS, stroke, or congestive heart failure. The safety endpoint involved occurrence of major bleeding events. The incidence of primary endpoint was 2.7% in treatment group versus 6.2% in control group (HR, 0.43; 95% CI, 0.21 to 0.87; n = 0.015). The incidence of secondary endpoint was 3.5% in treatment group versus 8.7% in control group (HR, 0.39; 95% CI, 0.21 to 0.72; P = 0.002). No major bleeding events were observed in any participant. Conclusion. Treatment with CHMs plus conventional treatment further reduced the occurrence of cardiovascular events in patients with ACS after PCI without increasing risk of major bleeding.
基金:
Supporting Program of the "Eleventh Five-year Plan" for Sci & Tech Research of China [2006BA104A01]
第一作者机构:[1]China Acad Chinese Med Sci, Guanganmen Hosp, Beijing 100053, Peoples R China;
通讯作者:
通讯机构:[2]China Acad Chinese Med Sci, Xiyuan Hosp, Beijing 100091, Peoples R China;
推荐引用方式(GB/T 7714):
Wang Shao-Li,Wang Cheng-Long,Wang Pei-Li,et al.Combination of Chinese Herbal Medicines and Conventional Treatment versus Conventional Treatment Alone in Patients with Acute Coronary Syndrome after Percutaneous Coronary Intervention (5C Trial): An Open-Label Randomized Controlled, Multicenter Study[J].EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE.2013,2013:-.doi:10.1155/2013/741518.
APA:
Wang, Shao-Li,Wang, Cheng-Long,Wang, Pei-Li,Xu, Hao,Liu, Hong-Ying...&Chen, Ke-Ji.(2013).Combination of Chinese Herbal Medicines and Conventional Treatment versus Conventional Treatment Alone in Patients with Acute Coronary Syndrome after Percutaneous Coronary Intervention (5C Trial): An Open-Label Randomized Controlled, Multicenter Study.EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE,2013,
MLA:
Wang, Shao-Li,et al."Combination of Chinese Herbal Medicines and Conventional Treatment versus Conventional Treatment Alone in Patients with Acute Coronary Syndrome after Percutaneous Coronary Intervention (5C Trial): An Open-Label Randomized Controlled, Multicenter Study".EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE 2013.(2013):-