Zhu Rong, Chen Kan, Zheng Yuan-Yuan, Zhang Hua-Wei, Wang Jun-Shan, Xia Yu-Jing, Dai Wei-Qi, Wang Fan, Shen Miao, Cheng Ping, Zhang Yan, Wang Cheng-Fen, Yang Jing, Li Jing-Jing, Lu Jie, Zhou Ying-Qun, Guo Chuan-Yong
Rong Zhu, Kan Chen, Yuan-Yuan Zheng, Hua-Wei Zhang, Jun-Shan Wang, Yu-Jing Xia, Wei-Qi Dai, Fan Wang, Miao Shen, Ping Cheng, Yan Zhang, Cheng-Fen Wang, Jing Yang, Jing-Jing Li, Jie Lu, Ying-Qun Zhou, Chuan-Yong Guo, Department of Gastroenterology, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai 200072, China.
World J Gastroenterol. 2014 Dec 21;20(47):18013-21. doi: 10.3748/wjg.v20.i47.18013.
To evaluate the role of probiotics in the standard triple Helicobacter pylori therapy.
In this meta-analysis, we investigated the efficacy of probiotics in a standard triple H. pylori therapy in adults. Searches were mainly conducted in MEDLINE/PubMed, EMBASE, and the Cochrane Central Register of Controlled Trials. Fourteen studies met our criteria, and the quality of these studies was assessed using the Jadad scale. We used STATA version 12.0 to extract data and to calculate the odds ratios (ORs), which are presented with the corresponding 95% confidence intervals (CIs). The data are presented as forest plots.
The pooled ORs for the eradication rates calculated by intention-to-treat analysis and per-protocol analysis in the probiotic group vs the control group were 1.67 (95%CI: 1.38-2.02) and 1.68 (95%CI: 1.35-2.08), respectively, using the fixed-effects model. The sensitivity of the Asian studies was greater than that of the Caucasian studies (Asian: OR = 1.78, 95%CI: 1.40-2.26; Caucasian: OR = 1.48, 95%CI: 1.06-2.05). The pooled OR for the incidence of total adverse effects was significantly lower in the probiotic group (OR = 0.49, 95%CI: 0.26-0.94), using the random effects model, with significant heterogeneity (I (2) = 85.7%). The incidence of diarrhea was significantly reduced in the probiotic group (OR = 0.21, 95%CI: 0.06-0.74), whereas the incidence of taste disorders, metallic taste, vomiting, nausea, and epigastric pain did not differ significantly between the probiotic group and the control group.
Supplementary probiotic preparations during standard triple H. pylori therapy may improve the eradication rate, particularly in Asian patients, and the incidence of total adverse effects.
评估益生菌在标准三联疗法治疗幽门螺杆菌中的作用。
在这项荟萃分析中,我们研究了益生菌在成人标准三联疗法治疗幽门螺杆菌中的疗效。主要检索了MEDLINE/PubMed、EMBASE和Cochrane对照试验中心注册库。14项研究符合我们的标准,使用Jadad量表评估这些研究的质量。我们使用STATA 12.0版本提取数据并计算比值比(OR),并给出相应的95%置信区间(CI)。数据以森林图形式呈现。
使用固定效应模型,在意向性分析和符合方案分析中,益生菌组与对照组根除率的合并OR分别为1.67(95%CI:1.38 - 2.02)和1.68(95%CI:1.35 - 2.08)。亚洲研究的敏感性高于白种人研究(亚洲:OR = 1.78,95%CI:1.40 - 2.26;白种人:OR = 1.48,95%CI:1.06 - 2.05)。使用随机效应模型,益生菌组总不良反应发生率的合并OR显著更低(OR = 0.49,95%CI:0.26 - 0.94),异质性显著(I² = 85.7%)。益生菌组腹泻发生率显著降低(OR = 0.21,95%CI:0.06 - 0.74),而益生菌组与对照组在味觉障碍、金属味、呕吐、恶心和上腹部疼痛的发生率上无显著差异。
在标准三联疗法治疗幽门螺杆菌期间补充益生菌制剂可能提高根除率,尤其是在亚洲患者中,并且降低总不良反应发生率。