Hui Jiaqi, Yuan Rong, Li Pengqi, Xin Qiqi, Miao Yu, Shen Xiaoxu, Xu Fengqin, Cong Weihong
Laboratory of Cardiovascular Diseases, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.
National Clinical Research Center for Chinese Medicine Cardiology, Beijing 100091, China.
J Clin Med. 2022 May 25;11(11):2991. doi: 10.3390/jcm11112991.
Tongxinluo capsule (TXLC) is a widely used traditional Chinese medicine for coronary heart disease (CHD). However, the efficacy and safety of different courses of TXLC for CHD after percutaneous coronary intervention (PCI) have not been systematically evaluated yet. The Cochrane Library, PubMed, Embase, China National Knowledge Infrastructure, Wanfang Database, and Chinese Scientific Journal Database were searched from the inception to 26 August 2021. A meta-analysis was performed using a fixed- or random-effects model. The risk of adverse cardiovascular events, mortality, or adverse effects was evaluated by risk ratio (RR) with 95% confidence interval (CI). Thirty-four studies involving 3652 patients were finally included. After the 6-month treatment, compared with conventional treatment alone, TXLC combined with conventional treatment achieved better efficacy in lowering the risk of angiographic restenosis (RR = 0.37, 95% CI = 0.28−0.48, p < 0.001), myocardial infarction (RR = 0.38, 95% CI = 0.25−0.60, p < 0.001), heart failure (RR = 0.32, 95% CI = 0.18−0.56, p < 0.001), angina (RR = 0.26, 95% CI = 0.17−0.38, p < 0.001), revascularization (RR = 0.20, 95% CI = 0.09−0.46, p < 0.001), all-cause mortality (RR = 0.24, 95% CI = 0.10−0.58, p = 0.001), and mortality due to any cardiovascular event (RR = 0.27, 95% CI = 0.09−0.80, p = 0.018). After the 12-month treatment, TXLC reduced the recurrence risk of angina (RR = 0.40, 95% CI = 0.20−0.80, p = 0.009). However, there was no difference in any outcomes after the 3-month treatment. Besides, no difference was found in the incidence of adverse effects after the 3-month and 6-month treatments (3 months: RR = 0.73, 95% CI = 0.35−1.56, p = 0.418; 6 months: RR = 1.71, 95% CI = 0.74−3.93, p = 0.209). The certainty of evidence ranged from very low to moderate due to the risk of bias, inconsistency, and imprecision. TXLC showed beneficial effects on reducing the adverse cardiovascular events without compromising safety for CHD patients after PCI on the 6-month course. However, due to the unavoidable risk of bias, more high-quality and long-term studies are still needed to further evaluate the efficacy and safety of TXLC in many countries, not only in China.
通心络胶囊(TXLC)是一种广泛用于治疗冠心病(CHD)的中药。然而,经皮冠状动脉介入治疗(PCI)后不同疗程的通心络胶囊治疗冠心病的疗效和安全性尚未得到系统评估。检索了Cochrane图书馆、PubMed、Embase、中国知网、万方数据库和中国科技期刊数据库,检索时间从建库至2021年8月26日。采用固定效应或随机效应模型进行荟萃分析。通过风险比(RR)及95%置信区间(CI)评估不良心血管事件、死亡率或不良反应的风险。最终纳入34项研究,共3652例患者。治疗6个月后,与单纯常规治疗相比,通心络胶囊联合常规治疗在降低血管造影再狭窄风险(RR = 0.37,95%CI = 0.28−0.48,p < 0.001)、心肌梗死(RR = 0.38,95%CI = 0.25−0.60,p < 0.001)、心力衰竭(RR = 0.32,95%CI = 0.18−0.56,p < 0.001)、心绞痛(RR = 0.26,95%CI = 0.17−0.38,p < 0.001)、血运重建(RR = 0.20,95%CI = 0.09−0.46,p < 0.001)、全因死亡率(RR = 0.24,95%CI = 0.10−0.58,p = 0.001)以及任何心血管事件导致的死亡率(RR = 0.27,95%CI = 0.09−0.80,p = 0.018)方面疗效更佳。治疗12个月后,通心络胶囊降低了心绞痛的复发风险(RR = 0.40,95%CI = 0.20−0.80,p = 0.009)。然而,治疗3个月后在任何结局方面均无差异。此外,治疗3个月和6个月后不良反应发生率无差异(3个月:RR = 0.73,95%CI = 0.35−1.56,p = 0.418;6个月:RR = 1.71,95%CI = 0.74−3.93,p = 0.209)。由于存在偏倚、不一致性和不精确性风险,证据的确定性从中等到非常低不等。通心络胶囊在6个月疗程中对降低冠心病PCI术后患者不良心血管事件具有有益作用且不影响安全性。然而,由于不可避免的偏倚风险,不仅在中国,在许多国家仍需要更多高质量的长期研究来进一步评估通心络胶囊的疗效和安全性。