Efficacy and safety of Chinese herbal medicine Wenxin Keli for ventricular premature be ats: A systematic review

医学 普罗帕酮 胺碘酮 随机对照试验 美托洛尔 内科学 不利影响 替代医学 安慰剂 心房颤动 病理
作者
Mei He,Zhan Lv,Zheng‐Wei Yang,Jiu-Ling Huang,Liu Fu
出处
期刊:Complementary Therapies in Medicine [Elsevier]
卷期号:29: 181-189 被引量:7
标识
DOI:10.1016/j.ctim.2016.10.007
摘要

Abstract Background To evaluate the efficacy and safety of the Chinese herbal extract Wenxin Keli, alone or in combination with Western medicine, for ventricular premature beats. Methods This systematic review was registered at PROSPERO (registration number CRD42013003200). A systematic literature search of 8 core electronic databases and 3 clinical trial registries in Chinese and English, yielded 10 trials whose randomness verified by contacting the authors. The included trials were assessed by the Cochrane risk of bias tool. Results Wenxin Keli might be more efficacious than placebo (Change of VPBs numbers, RR, 1.61, 95%CI, 1.48–1.76, P 2 =0%;VPBs- related symptom, RR, 2.10, 95%CI, 1.91–2.30, P 2 =0%), and the dual therapy of Wenxin Keli plus amiodarone might also be more effective than the monotherapy of amiodarone (Change of VPBs numbers, RR, 1.23, 95%CI, 1.10–1.39, P=0.0005, I 2 =0%; VPBs- related symptom, RR, 1.51., 95%CI, 1.30–1.76, P 2 =0%), whereas Wenxin Keli might be comparable to metoprolol, propafenone or mexiletine (Change of VPBs numbers: metoprolol, RR, 1.01, 95%CI, 0.91–1.11, P=0.88, I 2 =0%; propafenone, RR, 1.05, 95%CI, 0.93–1.19, P=0.44, I 2 =0%; mexiletine, RR, 1.06, 95%CI, 0.96–1.17, P=0.28. VPBs- related symptom: metoprolol, RR, 0.95, 95%CI, 0.87–1.04, P=0.27, I 2 =0%, propafenone. RR, 1.10, 95%CI, 0.93–1.30, P=0.29, I 2 =29%, mexiletine,RR, 0.94, 95%CI, 0.78–1.12, P=0.47). Participants with ventricular premature beats' numbers 2 =44%; RR, 1.71, 95%CI, 1.18–2.49, P=0.005, I 2 =54%, respectively). The safety analysis revealed that Wenxin Keli did not statistically significant differed from the Western medicine in respect of the incidence of total adverse drug reactions (RR, 0.59, 95%CI, 0.35–1.01, P=0.05, I 2 =0%), but Wenxin Keli might be associated with a reduced risk of proarrhythmic reactions (P=0.007). The quality of the methodology of included trials was generally low. Several limitations existed that affected the validity of the findings, including the small sample size, insufficient randomization methods, poorly defined eligibility criteria, short duration of follow-up, absence of hard endpoints, and high risk of publication bias(P=0.013). Conclusions Wenxin Keli might be a promising alternative and complementary medicine for ventricular premature beats.
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