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他克莫司和霉酚酸酯作为自身免疫性肝炎的二线治疗:证据质量是否足以制定推荐意见?

Tacrolimus and mycophenolate mofetil as second-line treatment in autoimmune hepatitis: Is the evidence of sufficient quality to develop recommendations?

机构信息

Department of Epidemiology, University of Groningen, Groningen 9700 RB, Netherlands.

Research Center for Evidence Based Medicine, Tabriz University of Medical Sciences, Tabriz 5166614766, Iran.

出版信息

World J Gastroenterol. 2020 Oct 14;26(38):5896-5910. doi: 10.3748/wjg.v26.i38.5896.

Abstract

BACKGROUND

The standard management of autoimmune hepatitis (AIH) is based on corticosteroids, alone or in combination with azathioprine. Second-line treatments are needed for patients who have refractory disease. However, high-quality data on the alternative management of AIH are scarce.

AIM

To evaluate the efficacy and safety of tacrolimus and mycophenolate mofetil (MMF) and the quality of evidence by using the Grading of Recommendations Assessment, Development and Evaluation approach (GRADE).

METHODS

A systematic review and meta-analysis of the available data were performed. We calculated pooled event rates for three outcome measures: Biochemical remission, adverse events, and mortality, with their corresponding 95% confidence intervals (CI).

RESULTS

The pooled biochemical remission rate was 68.9% (95%CI: 60.4-76.2) for tacrolimus, and 59.6% (95%CI: 54.8-64.2) for MMF, and rates of adverse events were 25.5% (95%CI: 12.4-45.3) for tacrolimus and 24.1% (95%CI: 15.4-35.7) for MMF. The pooled mortality rate was estimated at 11.5% (95%CI: 7.1-18.1) for tacrolimus and 9.01% (95%CI: 6.2-12.8) for MMF. Pooled biochemical remission rates for tacrolimus and MMF in patients with intolerance to standard therapy were 56.6% (CI: 43.4-56.6) 73.5% (CI: 58.1-84.7), and among non-responders were 59.1% (CI: 48.7-68.8) 40.8% (CI: 32.3-50.0), respectively. Moreover, the overall quality assessments using GRADE proved to be very low for all our outcomes in both treatment groups.

CONCLUSION

Tacrolimus and MMF are in practice considered effective for patients with AIH who are non-responders or intolerant to first-line treatment, but we found no high-quality evidence to support this statement.

摘要

背景

自身免疫性肝炎(AIH)的标准治疗方法是使用单独或联合使用皮质类固醇和硫唑嘌呤。对于患有难治性疾病的患者,需要二线治疗。然而,替代 AIH 管理的高质量数据非常有限。

目的

使用推荐评估、制定和评估方法(GRADE)评估他克莫司和霉酚酸酯(MMF)的疗效和安全性以及证据质量。

方法

对现有数据进行系统评价和荟萃分析。我们计算了三种结局指标的汇总事件发生率:生化缓解、不良事件和死亡率,及其相应的 95%置信区间(CI)。

结果

他克莫司的汇总生化缓解率为 68.9%(95%CI:60.4-76.2),MMF 为 59.6%(95%CI:54.8-64.2),他克莫司的不良事件发生率为 25.5%(95%CI:12.4-45.3),MMF 为 24.1%(95%CI:15.4-35.7)。他克莫司的汇总死亡率估计为 11.5%(95%CI:7.1-18.1),MMF 为 9.01%(95%CI:6.2-12.8)。对标准治疗不耐受的患者,他克莫司和 MMF 的汇总生化缓解率分别为 56.6%(CI:43.4-56.6)和 73.5%(CI:58.1-84.7),对无应答者分别为 59.1%(CI:48.7-68.8)和 40.8%(CI:32.3-50.0)。此外,使用 GRADE 进行的总体质量评估在两个治疗组的所有结局中均被证明为极低质量。

结论

他克莫司和 MMF 被认为对不耐受或对一线治疗无应答的 AIH 患者有效,但我们没有发现高质量的证据支持这一说法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6232/7579758/6444b910ba6c/WJG-26-5896-g001.jpg

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