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Short-term effect and adverse events of adalimumab versus placebo in inducing remission for moderate-to-severe ulcerative colitis: a meta-analysis

机译:阿达木单抗与安慰剂在诱导中度至重度溃疡性结肠炎缓解中的短期作用和不良事件:一项荟萃分析

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摘要

Background: Adalimumab is used in an attempt to maintain remission for Ulcerative colitis. This study was to evaluate the efficacy and adverse events of adalimumab compared with placebo in inducing remission of Ulcerative colitis. Methods: MEDLINE, EMBASE, the Cochrane Controlled Trials Register, OVID, BIOSIS, CNKI, and Google were searched. All randomized trials comparing adalimumab with placebo in inducing remission of moderate-to-severe ulcerative colitis were included. Results: Two randomized controlled trials with a total of 754 participants met the inclusion criteria. The pooled risk ratio (RR) of clinical remission was 1.85 (95% confidence interval (CI) 1.26 to 2.72) following adalimumab treatment. RR of clinical response was 1.40 (95% CI 1.19 to 1.65) while that of mucosal healing was 1.23 (95% CI 1.03 to 1.47). RR of any adverse events was 1.00 (95% CI 0.93 to 1.09). Conclusion: Compared with placebo, administration of adalimumab may increase the proportion of patients with moderate-to-severe ulcerative colitis attaining clinical remission, clinical response and mucosal healing. Adalimumab is also tolerated well in these patients.
机译:背景:阿达木单抗用于维持溃疡性结肠炎的缓解。本研究旨在评估阿达木单抗与安慰剂相比在诱导溃疡性结肠炎缓解中的功效和不良事件。方法:搜索MEDLINE,EMBASE,Cochrane对照试验注册,OVID,BIOSIS,CNKI和Google。纳入所有比较阿达木单抗和安慰剂诱导中度至重度溃疡性结肠炎缓解的随机试验。结果:两项共754名参与者的随机对照试验符合纳入标准。阿达木单抗治疗后临床缓解的合并风险比(RR)为1.85(95%置信区间(CI)为1.26至2.72)。临床反应的RR为1.40(95%CI为1.19至1.65),而粘膜愈合的RR为1.23(95%CI为1.03至1.47)。任何不良事件的RR为1.00(95%CI为0.93至1.09)。结论:与安慰剂相比,阿达木单抗的给药可增加中度至重度溃疡性结肠炎患者的临床缓解,临床反应和黏膜愈合的比例。这些患者对阿达木单抗的耐受性也很好。

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