Cao Xinfu, Zhou Mingxue, Liu Hongxu, Chen Xiufen, Li Xiang, Jia Sihan
Department of Cardiology, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing Institute of Traditional Chinese Medicine, Beijing, China.
Front Pharmacol. 2021 Feb 22;12:613922. doi: 10.3389/fphar.2021.613922. eCollection 2021.
Shensong Yangxin capsule (SSYX) is a well-known traditional Chinese patent medicine for treating arrhythmia. Recently, a flurry of randomized controlled trials (RCTs) of SSYX combined with amiodarone (SSYX-amiodarone) was reported in the treatment of heart failure (HF) complicated by ventricular arrhythmia (VA) in China. However, these RCTs have not been systematically evaluated. Therefore, this study aimed to evaluate the efficacy and safety of SSYX-amiodarone in the treatment of heart failure complicated by ventricular arrhythmia (HF-VA). Seven electronic literature databases (the Cochrane Library, PubMed, EMBASE, China Biomedical database web, China National Knowledge Infrastructure Databases, Chinese Scientific Journal database and Wanfang database) were searched from their inceptions to June 1, 2020 to identify RCTs of SSYX-amiodarone in the treatment of HF-VA. The primary outcomes included the total effective rate and adverse events (ADRs). The secondary outcomes included the frequency of ventricular premature complexes, left ventricular ejection fraction, N terminal pro Btype natriuretic peptide (NT-proBNP), and QT dispersion (QTd). The quality of the included RCTs was assessed using the Cochrane risk-of-bias tool. All data was analyzed using RevMan 5.3 software. The registration number of this protocol is PROSPERO CRD42020196689. There are Eighteen trials involving 1,697 patients were included in this study. Meta-analysis showed that SSYX-amiodarone group was superior to the amiodarone group in improving the total effective rate [RR = 1.21; 95%CI (1.16, 1.27); < 0.01], meanwhile reducing the ADRs [RR = 0.65; 95%CI (0.45, 0.95); = 0.03], VPCs [MD = 170.96; 95%CI (159.88, 182.04); < 0.01] and QTd [MD = 8.39; 95%CI (6.91, 9.87); < 0.01]. No significant difference of enhancing LVEF [MD = 4.32; 95%CI (-0.56, 9.20); . Despite the apparent positive findings reported, the evidence provided by this meta-analysis was still insufficient to support the routine use of SSYX-amiodarone for HF-VA due to the poor methodological quality of included studies. The overall effect should to be verified in further through more well-design clinical studies with reasonable sample and good methodological quality.
参松养心胶囊(SSYX)是一种治疗心律失常的著名中成药。最近,中国有一系列关于参松养心胶囊联合胺碘酮(SSYX - 胺碘酮)治疗心力衰竭(HF)合并室性心律失常(VA)的随机对照试验(RCT)报道。然而,这些RCT尚未得到系统评价。因此,本研究旨在评估SSYX - 胺碘酮治疗心力衰竭合并室性心律失常(HF - VA)的疗效和安全性。检索了七个电子文献数据库(考克兰图书馆、PubMed、EMBASE、中国生物医学文献数据库、中国知网数据库、中国科技期刊数据库和万方数据库),从建库至2020年6月1日,以确定SSYX - 胺碘酮治疗HF - VA的RCT。主要结局包括总有效率和不良事件(ADR)。次要结局包括室性早搏的频率、左心室射血分数、N末端B型利钠肽原(NT - proBNP)和QT离散度(QTd)。使用考克兰偏倚风险工具评估纳入RCT的质量。所有数据使用RevMan 5.3软件进行分析。本方案的注册号为PROSPERO CRD42020196689。本研究纳入了18项试验,涉及1697例患者。荟萃分析表明,SSYX - 胺碘酮组在提高总有效率方面优于胺碘酮组[RR = 1.21;95%CI(1.16,1.27);P < 0.01],同时降低了ADR[RR = 0.65;95%CI(0.45,0.95);P = 0.03]、室性早搏[MD = 170.96;95%CI(159.88,182.04);P < 0.01]和QTd[MD = 8.39;95%CI(6.91,9.87);P < 0.01]。在提高左心室射血分数方面无显著差异[MD = 4.32;95%CI( - 0.56,9.20);P = 0.08](此处原文可能有误,推测应为P = 0.08,否则表述与前文不一致)。尽管报道了明显的阳性结果,但由于纳入研究的方法学质量较差,本荟萃分析提供的证据仍不足以支持SSYX - 胺碘酮常规用于HF - VA。总体效果应通过更多设计合理、样本量合适且方法学质量良好的临床研究进一步验证。