Safety comparison of single-donor and pooled fecal microbiota transfer product preparation in ulcerative colitis: systematic review and meta-analysis.

IF 2.5 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Bastien Laperrousaz, Benoît Levast, Mathieu Fontaine, Stéphane Nancey, Pierre Dechelotte, Joël Doré, Philippe Lehert
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引用次数: 0

Abstract

Background: Multiple studies have evaluated fecal microbiota transfer (FMT) in patients with ulcerative colitis (UC) using single-donor (SDN) and multidonor (MDN) products. Systematic review and meta-analysis were performed to compare the safety of SDN and MDN products.

Methods: Systematic searches were performed in Web of Science, Scopus, PubMed, and Orbit Intelligence to identify studies that compared FMT products manufactured using SDN or MDN strategies against control treatment in patients with UC. Fifteen controlled studies were selected for meta-analysis (11 randomized controlled trials and 4 controlled cohort trials). Safety of each treatment type was assessed using the counts of adverse events and serious adverse events using fixed- and random-effects models. Significance of the indirect difference between FMT preparations was assessed using a network approach. Benefit-risk ratios were calculated by multiplicative utility model, incorporating geometric mean of risk ratios (RRs) of efficacy and safety.

Results: Safety data was collected for a total of 587 patients (193 exposed to SDN products, 114 exposed to MDN products and 280 exposed to control treatment). The 12 studies showed similar overall safety event counts for MDN and SDN versus placebo (RRs: 0.90 and 1.09, respectively [P = 0.206 and P = 0.420, respectively]). Results indicated similar risk of safety events for MDN compared to SDN (RR: 0.83, P = 0.159). Positive benefit-risk ratios were demonstrated for MDN and SDN versus placebo (RRs: 1.70 and 1.16, respectively [P = 0.003 and P = 0.173, respectively]). MDN had a greater benefit-risk ratio compared to SDN (RR: 1.46, P = 0.072).

Conclusion: Similar safety profiles were observed for MDN and SDN strategies. Alongside previously described superior efficacy, treatment with MDN has greater benefit-risk ratio than SDN in patients with UC. Further development of MDN FMT treatment for UC should be considered.

溃疡性结肠炎中单供体和集合粪便微生物群转移产品制剂的安全性比较:系统综述和荟萃分析。
背景:多项研究评估了使用单供体(SDN)和多供体(MDN)产品对溃疡性结肠炎(UC)患者进行粪便微生物群转移(FMT)的效果。为了比较 SDN 和 MDN 产品的安全性,我们进行了系统回顾和荟萃分析:在 Web of Science、Scopus、PubMed 和 Orbit Intelligence 中进行了系统检索,以确定将采用 SDN 或 MDN 策略生产的 FMT 产品与 UC 患者的对照治疗进行比较的研究。荟萃分析选择了 15 项对照研究(11 项随机对照试验和 4 项对照队列试验)。采用固定效应和随机效应模型,通过不良事件和严重不良事件的计数来评估每种治疗类型的安全性。采用网络方法评估了FMT制剂之间间接差异的显著性。采用乘法效用模型计算效益风险比,并纳入疗效和安全性风险比(RRs)的几何平均数:共收集了 587 名患者的安全数据(193 名接受 SDN 产品治疗,114 名接受 MDN 产品治疗,280 名接受对照治疗)。12 项研究显示,MDN 和 SDN 与安慰剂相比,总体安全事件计数相似(RRs:分别为 0.90 和 1.09 [P = 0.206 和 P = 0.420])。结果表明,与 SDN 相比,MDN 的安全事件风险相似(RR:0.83,P = 0.159)。与安慰剂相比,MDN 和 SDN 的获益风险比呈正值(RR 分别为 1.70 和 1.16 [P = 0.003 和 P = 0.173])。与 SDN 相比,MDN 的获益风险比更高(RR:1.46,P = 0.072):结论:MDN 和 SDN 策略具有相似的安全性。结论:在 UC 患者中,MDN 和 SDN 的安全性相似,除了之前描述的卓越疗效外,MDN 治疗的收益风险比也高于 SDN。应考虑进一步开发 MDN FMT 治疗 UC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Gastroenterology
BMC Gastroenterology 医学-胃肠肝病学
CiteScore
4.20
自引率
0.00%
发文量
465
审稿时长
6 months
期刊介绍: BMC Gastroenterology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of gastrointestinal and hepatobiliary disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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