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系统评价:他克莫司在克罗恩病治疗中的作用。

Systematic review: the role of tacrolimus in the management of Crohn's disease.

机构信息

Division of Paediatric Gastroenterology, Hepatology and Nutrition, Alder Hey Children's NHS Foundation Trust, Liverpool, UK.

出版信息

Aliment Pharmacol Ther. 2011 Dec;34(11-12):1282-94. doi: 10.1111/j.1365-2036.2011.04873.x. Epub 2011 Oct 17.

Abstract

BACKGROUND  Several published studies have evaluated the efficacy of tacrolimus in the management of Crohn's disease with variable conclusions. AIM  To review systematically the evidence examining the efficacy and safety of tacrolimus in treating Crohn's disease. METHODS  The Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE (PUBMED) and EMBASE (1984 to January 2011) were searched. Also, references from selected articles were examined. Case series (five or more patients), cohort and randomised controlled trials were eligible for inclusion, incorporating oral, intravenous or topical tacrolimus therapy. The primary outcome was induction of remission of active Crohn's disease. RESULTS  Eleven studies met the inclusion criteria which included 163 patients, of which 127 received tacrolimus therapy. In patients with luminal Crohn's disease, the crude pooled remission rate for tacrolimus was 44.3% (range, 7-69%) and the crude pooled response rate was 37.1% (range, 14-57%). For patients with perianal disease using systemic tacrolimus, crude pooled remission rate was 28.6% (range, 0-64%) and crude pooled response rate was 38.8% (range, 0-57%). Combining data from two studies using topical tacrolimus, 35.7% of patients achieved remission and 28.6% partial response. Nonserious adverse effects are common, particularly tremor, paraesthesia and headache. Reversible nephrotoxity occurred in 16% of patients. CONCLUSIONS  The current evidence; although of a poor quality, appears to support the use of tacrolimus in Crohn's disease. High quality randomised controlled trials are needed.

摘要

背景

有几项已发表的研究评估了他克莫司治疗克罗恩病的疗效,但结论不一。

目的

系统评价他克莫司治疗克罗恩病的疗效和安全性。

方法

检索 Cochrane 中央对照试验注册库(CENTRAL)、MEDLINE(PUBMED)和 EMBASE(1984 年至 2011 年 1 月),并查阅入选文献的参考文献。纳入标准为:纳入研究采用口服、静脉或局部他克莫司治疗,病例系列(5 例或以上患者)、队列研究和随机对照试验。主要结局为诱导缓解活动期克罗恩病。

结果

11 项研究符合纳入标准,共纳入 163 例患者,其中 127 例接受他克莫司治疗。对于肠腔克罗恩病患者,他克莫司的总体缓解率为 44.3%(范围 7-69%),总体应答率为 37.1%(范围 14-57%)。对于接受全身他克莫司治疗的肛周疾病患者,总体缓解率为 28.6%(范围 0-64%),总体应答率为 38.8%(范围 0-57%)。两项局部用他克莫司的研究数据合并后,35.7%的患者达到缓解,28.6%部分缓解。常见不良反应为非严重不良反应,尤其以震颤、感觉异常和头痛多见。可逆性肾毒性发生率为 16%。

结论

目前的证据质量较差,但似乎支持将他克莫司用于克罗恩病。需要开展高质量的随机对照试验。

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