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Side Effects Associated with Probiotic Use in Adult Patients with Inflammatory Bowel Disease: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

机译:成年炎性肠病患者与益生菌使用相关的副作用:随机对照试验的系统评价和荟萃分析

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摘要

Probiotics demonstrated to be effective in the treatment of inflammatory bowel disease (IBD). However, the safety profile of probiotics is insufficiently explored. In the present systematic review and meta-analysis, we examined the occurrence of side effects related to probiotic/synbiotic use in randomized controlled trials (RCTs) of IBD patients as compared with placebo. Eligible RCTs in adult patients with IBD were identified by accessing the Medline database via PubMed, EMBASE, CENTRAL and the Cochrane central register of controlled trials up to December 2018. Occurrence of side effects was retrieved and recorded. Data were pooled and the relative risks (RRs) with their 95% confidence intervals (CIs) were calculated. The low-moderate study heterogeneity, assessed by the I statistic, allowed to use of a fixed-effects modelling for meta-analysis. Nine RCTs among 2337, including 826 patients (442 treated with probiotics/symbiotic and 384 with placebo) were analyzed. Eight were double-blind RCTs, and six enrolled ulcerative colitis (UC) patients. Although the risk for the overall side effects (RR 1.35, 95%CI 0.93–1.94; = 25%) and for gastrointestinal symptoms (RR 1.78, 95%CI 0.99–3.20; = 20%) was higher in IBD patients taking probiotics than in those exposed to placebo, statistical significance was achieved only for abdominal pain (RR 2.59, 95%CI 1.28–5.22; = 40%). In conclusion, despite the small number of RCTs and the variety of probiotic used and schedule across studies, these findings highlight the level of research effort still required to identify the most appropriate use of probiotics in IBD.
机译:益生菌被证明可有效治疗炎症性肠病(IBD)。然而,未充分探索益生菌的安全性。在本系统综述和荟萃分析中,我们检查了与安慰剂相比,IBD患者的随机对照试验(RCT)中与益生菌/合生元使用相关的副作用的发生。通过截至2018年12月的PubMed,EMBASE,CENTRAL和Cochrane中央对照试验注册中心访问Medline数据库,鉴定了成年IBD患者的合格RCT。检索并记录了副作用的发生。汇总数据并计算其95%置信区间(CI)的相对风险(RR)。通过I统计量评估的低中度研究异质性允许使用固定效应模型进行荟萃分析。分析了2337例患者中的9例RCT,包括826例患者(442例用益生菌/共生药治疗,384例用安慰剂治疗)。 8例为双盲RCT,6例为溃疡性结肠炎(UC)患者。尽管服用益生菌的IBD患者的总体副作用(RR 1.35,95%CI 0.93–1.94; = 25%)和胃肠道症状(RR 1.78,95%CI 0.99–3.20; = 20%)的风险高于使用益生菌的患者在那些接受安慰剂的人群中,只有腹部疼痛才具有统计学意义(RR 2.59,95%CI 1.28-5.22; = 40%)。总之,尽管随机对照试验的数量很少,并且在整个研究中使用的益生菌种类和时间表各异,但这些发现凸显了确定IBD中最合适的益生菌用法仍需要进行的研究。

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