Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091,China.
The First Affiliated Hospital of the Henan University of Chinese Medicine, Henan 450046, China.
Pharmacol Res. 2020 Aug;158:104883. doi: 10.1016/j.phrs.2020.104883. Epub 2020 May 22.
Xinyue capsule, a patented Chinese herbal medicine, has been used to manage coronary artery disease (CAD) for over a decade in China, but whether it can further reduce risk of cardiovascular events beyond conventional treatment is unknown.
In this multicenter, randomized, placebo-controlled trial, we randomly assigned patients with stable CAD who underwent percutaneous coronary intervention (PCI) within the preceding 3-12 months to receive Xinyue capsule (100 mg panax quinquefolius saponins, three times a day) or placebo for 24 weeks in addition to conventional treatment. The primary endpoint was a composite that included cardiac death, nonfatal myocardial infarction and urgent revascularization with either PCI or coronary artery bypass grafting. The secondary composite endpoints included stroke, re-hospitalization due to acute coronary syndrome (ACS), pulmonary embolism, peripheral vascular events and all-cause mortality. Quality of life was assessed using a 36-item Short-Form Health Survey (SF-36).
A total of 1054 participants were included in the analyses. The median follow up was 1 year. The primary endpoint events occurred in 16 patients (3.02%) in the Xinyue group and 34 patients (6.49%) in the placebo group (hazard ratio [HR] 0.455, 95% confidence interval [CI] 0.25 to 0.825; P = 0.009). Secondary end-point events occurred in 5.47% of patients in the Xinyue group and 10.31% in the placebo group (HR 0.515, 95% CI 0.328 to 0.809; P = 0.004). SF-36 subscale scores at 12 months were significantly higher in the Xinyue group than placebo group for general health (P = 0.048) and vitality (P = 0.008).
In patients with stable CAD after PCI within the preceding 3 to 12 months, Xinyue capsule added on conventional treatment reduced the incidence of primary composite endpoint (cardiac death, nonfatal myocardial infarction and urgent revascularization).
心悦胶囊是一种专利中草药,已在中国用于治疗冠心病 (CAD) 超过十年,但它是否能在常规治疗基础上进一步降低心血管事件的风险尚不清楚。
在这项多中心、随机、安慰剂对照试验中,我们将在过去 3-12 个月内行经皮冠状动脉介入治疗 (PCI) 的稳定型 CAD 患者随机分为接受心悦胶囊(100mg 西洋参总皂苷,每日三次)或安慰剂治疗 24 周,同时接受常规治疗。主要终点是包括心脏死亡、非致死性心肌梗死和紧急血运重建(PCI 或冠状动脉旁路移植术)的复合终点。次要复合终点包括卒中和因急性冠状动脉综合征 (ACS) 再住院、肺栓塞、外周血管事件和全因死亡率。使用 36 项简明健康调查问卷 (SF-36) 评估生活质量。
共有 1054 名患者纳入分析。中位随访时间为 1 年。主要终点事件在心悦组发生 16 例(3.02%),安慰剂组发生 34 例(6.49%)(风险比 [HR] 0.455,95%置信区间 [CI] 0.25 至 0.825;P=0.009)。次要终点事件在心悦组发生 5.47%的患者,安慰剂组发生 10.31%的患者(HR 0.515,95%CI 0.328 至 0.809;P=0.004)。12 个月时,心悦组的 SF-36 量表评分在一般健康(P=0.048)和活力(P=0.008)方面明显高于安慰剂组。
在 PCI 后 3 至 12 个月内稳定型 CAD 患者中,心悦胶囊联合常规治疗可降低主要复合终点(心脏死亡、非致死性心肌梗死和紧急血运重建)的发生率。