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中药逍遥散治疗功能性胃肠病的疗效与安全性:随机对照试验的Meta分析和试验序贯分析

Efficacy and Safety of Chinese Herbal Medicine Xiao Yao San in Functional Gastrointestinal Disorders: A meta-Analysis and Trial Sequential Analysis of Randomized Controlled Trials.

作者信息

Liu Qian, Shi Zongming, Zhang Tao, Jiang Tianyuan, Luo Xiaoying, Su Xiaolan, Yang Yang, Wei Wei

机构信息

Wangjing Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

Beijing University of Chinese Medicine, Beijing, China.

出版信息

Front Pharmacol. 2022 Jan 20;12:821802. doi: 10.3389/fphar.2021.821802. eCollection 2021.

Abstract

Functional gastrointestinal disorders are now named disorders of gut-brain interaction (DGBI) according to the Rome IV criteria, characterized by the interaction of gastrointestinal symptoms and dysregulation of central nervous systems. Xiao-Yao-San (XYS) is effective in the treatment of gastrointestinal symptoms in China, especially in patients with concurrent mood disorders. A meta-analysis was designed to evaluate the efficacy and safety of Xiao-Yao-San for FGIDs. We searched randomized controlled trials in seven databases from their inception till November 22, 2021. Pooled analysis included therapeutic efficacy, symptom score, Self-Rating Anxiety Scale (SAS) score, Self-Rating Depression Scale (SDS) score, and the recurrence rate. Conventional meta-analysis with random-effects model or fixed-effects model and trial sequential analysis (TSA) were performed. A total of 48 RCTs were eligible for inclusion ( = 4,403). Meta-analysis results showed that XYS could improve the effective rate of FGIDs compared with western drugs [RR = 1.23; (95%CI, 1.19-1.27); < 0.00001], and XYS combined with western medicine could also improve the effective rate [RR = 1.26; (95%CI, 1.21-1.33); < 0.00001]. In addition, XYS could reduce the symptom score [SMD = -1.07; (95%CI -1.42, -0.72); Z = 6.03; < 0.00001], SAS score [MD = -6.24; (95%CI -7.48, -4.99); Z = 9.81; < 0.00001] and SDS score [MD = -6.70; (95%CI -8.18, -5.21); Z = 8.83; < 0.00001] of FGIDs patients, and reduce the recurrence rate [MD = -6.70; (95%CI -8.18, -5.21); Z = 8.83; < 0.00001]. XYS was safe in most cases and no serious adverse events were observed in any of the included trials. TAS showed adequate "information size" for the primary outcome, and further confirmed the efficacy of XYS in the treatment of FGIDs. XYS could improve symptoms and reduce recurrence rates in FGIDs patients, and XYS may be a potential candidate for the treatment of FGIDs. However, due to the limited quality of current studies, more long-term, randomized, double-blinded clinical trials are needed in future studies. https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=284308, identifier CRD42021284308.

摘要

根据罗马IV标准,功能性胃肠疾病现在被命名为肠-脑互动障碍(DGBI),其特征是胃肠道症状与中枢神经系统失调之间的相互作用。逍遥散(XYS)在中国对胃肠道症状的治疗有效,尤其是对并发情绪障碍的患者。本荟萃分析旨在评估逍遥散治疗功能性胃肠疾病的疗效和安全性。我们检索了7个数据库从建库至2021年11月22日的随机对照试验。汇总分析包括治疗效果、症状评分、自评焦虑量表(SAS)评分、自评抑郁量表(SDS)评分和复发率。采用随机效应模型或固定效应模型进行传统荟萃分析以及试验序贯分析(TSA)。共有48项随机对照试验符合纳入标准(n = 4403)。荟萃分析结果显示,与西药相比,逍遥散可提高功能性胃肠疾病的有效率[相对危险度(RR)= 1.23;(95%置信区间,1.19 - 1.27);P < 0.00001],逍遥散联合西药也可提高有效率[RR = 1.26;(95%置信区间,1.21 - 1.33);P < 0.00001]。此外,逍遥散可降低功能性胃肠疾病患者的症状评分[标准化均数差(SMD)= -1.07;(95%置信区间 -1.42, -0.72);Z = 6.03;P < 0.00001]、SAS评分[平均差(MD)= -6.24;(95%置信区间 -7.48, -4.99);Z = 9.81;P < 0.00001]和SDS评分[MD = -6.70;(95%置信区间 -8.18, -5.21);Z = 8.83;P < 0.00001],并降低复发率[MD = -6.70;(95%置信区间 -8.18, -5.21);Z = 8.83;P < 0.00001]。逍遥散在大多数情况下是安全的,纳入的任何试验中均未观察到严重不良事件。试验序贯分析显示主要结局有足够的“信息量”,并进一步证实了逍遥散治疗功能性胃肠疾病的疗效。逍遥散可改善功能性胃肠疾病患者的症状并降低复发率,逍遥散可能是治疗功能性胃肠疾病的潜在候选药物。然而,由于当前研究质量有限,未来研究需要更多长期、随机、双盲临床试验。https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=284308,标识符CRD42021284308

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a0b/8811448/1b12a87c9b3b/fphar-12-821802-g001.jpg

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