[Network Meta-analysis of oral Chinese patent medicine combined with conventional western medicine in treatment of gastro-esophageal reflux disease].

Q3 Pharmacology, Toxicology and Pharmaceutics Zhongguo Zhongyao Zazhi Pub Date : 2024-09-01 DOI:10.19540/j.cnki.cjcmm.20240523.501
Jia-Xu Zhu, Bin-Yang Yu, Xian Li, Rui Gao
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Abstract

The effectiveness and safety of various oral Chinese patent medicines combined with conventional western medicine in treatment of gastro-esophageal reflux disease(GERD) were evaluated using network Meta-analysis. CNKI, Wanfang, VIP, SinoMed, PubMed, Cochrane Library, EMbase, and Web of Science were searched for randomized controlled trial(RCT) of oral Chinese patent medicines combined with conventional western medicine in treatment of GERD from inception to September 2023. The quality of the included studies was assessed using the Cochrane risk-of-bias tool, and data analysis was conducted using RevMan 5.4 and Stata 16 software. Forty-seven RCTs were included, involving 10 oral Chinese patent medicines, including Jianwei Yuyang Tablets, Qizhi Weitong Granules, Dalitong Granules, Liuwei Anxiao Capsules, Kangfuxin Liquid, Weisu Granules, Zhizhu Kuanzhong Capsules, Xiaochaihu Granules, Xiaoyao Pills, and Danweikang Capsules. Network Meta-analysis showed that:(1)in terms of effective rate of clinical symptoms, intervention measure ranked first by SUCRA was Dalitong Granules + conventional western medicine.(2)In terms of endoscopic effective rate, intervention measure ranked first by SUCRA was Liuwei Anxiao Capsules + conventional western medicine.(3)In terms of increasing serum gastrin levels, intervention measure ranked first by SUCRA was Weisu Granules + conventional western medicine.(4)In terms of increasing plasma motilin level, intervention measure ranked first by SUCRA was Xiaoyao Pills + conventional western medicine. In terms of symptom scores, quality of life and recurrence rate, only descriptive analyses were performed due to the heterogeneity of the studies, but all studies reported that oral Chinese patent medicines combined with conventional western medicine improved the outcome indicators better than conventional western medicine alone, and the differences were statistically significant. In terms of adverse reactions, there was no significant difference between oral Chinese patent medicine combined with conventional western medicine and conventional western medicine alone. Through cluster analysis, it was found that the comprehensive efficacy of Dalitong Granules + conventional western medicine, Danweikang Capsules + conventional western medicine, Qizhi Weitong Granules + conventional western medicine, Kangfuxin Liquid + conventional western medicine, and Liuwei Anxiao Capsules + conventional western medicine were more prominent, and could improve clinical symptoms and endoscopic inflammation at the same time. The results indicated that oral Chinese patent medicines combined with conventional western medicine in treatment of GERD could improve comprehensive efficacy, alleviate clinical symptoms, and regulate gastrointestinal motility. However, due to limitations such as sample size and quality of the included literature, the conclusions need to be further verified by more large-sample, high-quality studies.

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[口服中成药联合常规西药治疗胃食管反流病的网络 Meta 分析]。
采用网络 Meta 分析评价了多种口服中成药联合常规西药治疗胃食管反流病(GERD)的有效性和安全性。在 CNKI、万方、VIP、SinoMed、PubMed、Cochrane Library、EMbase 和 Web of Science 中检索了从开始到 2023 年 9 月口服中成药联合常规西药治疗胃食管反流病的随机对照试验(RCT)。使用Cochrane偏倚风险工具评估了纳入研究的质量,并使用RevMan 5.4和Stata 16软件进行了数据分析。共纳入 47 项 RCT,涉及 10 种口服中成药,包括健脾益阳片、芪微通颗粒、达力通颗粒、六味安消胶囊、康复欣液、味苏颗粒、枳壳宽中胶囊、小柴胡颗粒、消渴丸和丹鳖康胶囊。网络 Meta 分析表明:(1)在临床症状有效率方面,SUCRA 排名第一的干预措施是达力通颗粒+常规西药;(2)在内镜有效率方面,SUCRA 排名第一的干预措施是六味安消胶囊+常规西药。(3)在提高血清胃泌素水平方面,SUCRA 排名第一的干预措施是味苏颗粒+常规西药。 (4)在提高血浆动情素水平方面,SUCRA 排名第一的干预措施是消遥丸+常规西药。在症状评分、生活质量和复发率方面,由于研究的异质性,仅进行了描述性分析,但所有研究均报告口服中成药联合常规西药对结果指标的改善优于常规西药单独治疗,且差异有统计学意义。在不良反应方面,口服中成药联合常规西药与单纯常规西药无明显差异。通过聚类分析发现,达力通颗粒+常规西药、丹微康胶囊+常规西药、芪微通颗粒+常规西药、康复欣液+常规西药、六味安消胶囊+常规西药的综合疗效较为突出,能同时改善临床症状和内镜下炎症。结果表明,口服中成药联合常规西药治疗胃食管反流病可提高综合疗效,缓解临床症状,调节胃肠动力。然而,由于样本量和收录文献质量等方面的限制,结论还需要更多的大样本、高质量的研究来进一步验证。
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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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