Safety and Efficacy of Ustekinumab in the Treatment of Crohn Disease: A Systematic Review and Meta-analysis

Q4 Medicine
M. Khorshid, A. Cordie, S. Abd-Elsalam
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Abstract

Background and Aims The present systematic review and meta-analysis was designed to estimate the safety and effectiveness of ustekinumab in the treatment of Crohn disease (CD) in clinical trials and observational studies. Methods We retrieved all the related publications from the PubMed, Cochrane, EBSCO, Google Scholar and EMBASE databases using a systematic search strategy. We only included clinical trials and observational studies that were published in English. Results Only 31 studies that met the eligibility criteria out of the 733 identified studies were included. The overall clinical response rate in the cohort studies was of 0.539 (95% confidence interval [95%CI]: 0.419–0.659), and in the clinical trials it was of 0.428 (95%CI: 0.356–0.501). The pooled clinical remission rate was of 0.399 (95%CI: 0.295–0.503) in randomized control trials (RCTs,) and of 0.440 (95%CI: 0.339–0.542) in cohort studies. The rate of adverse effects was of 0.158 (95%CI: 0.109–0.207) in cohort studies and of 0.690 (95%CI: 0.633–0.748) in RCTs. Conclusion Ustekinumab is effective in the treatment of CD. However, more research is required on the safety profiles because there was considerable variation among the included studies.
Ustekinumab治疗克罗恩病的安全性和有效性:系统评价和荟萃分析
背景和目的 本系统综述和荟萃分析旨在评估ustekinumab在临床试验和观察性研究中治疗克罗恩病(CD)的安全性和有效性。方法 我们使用系统搜索策略从PubMed、Cochrane、EBSCO、Google Scholar和EMBASE数据库中检索了所有相关出版物。我们只包括以英文发表的临床试验和观察性研究。后果 在733项已确定的研究中,只有31项符合资格标准。队列研究中的总体临床缓解率为0.539(95%置信区间[95%CI]:0.419-0.659),临床试验中为0.428(95%CI:0.356–0.501)。随机对照试验(RCTs)中的合并临床缓解率是0.399(95%CI:0.295-0.503),队列研究中是0.440(95%CI:0.339-0.542)。在队列研究中,不良反应发生率为0.158(95%CI:0.109–0.207),在随机对照试验中为0.690(95%CI:0.633–0.748)。结论 Ustekinumab对CD的治疗是有效的。然而,由于纳入的研究之间存在相当大的差异,因此需要对安全性进行更多的研究。
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
Journal of Coloproctology
Journal of Coloproctology Medicine-Gastroenterology
CiteScore
0.60
自引率
0.00%
发文量
41
审稿时长
47 weeks
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