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甲氨蝶呤治疗慢性活动性溃疡性结肠炎:一项以色列多中心双盲随机试验

Methotrexate in chronic active ulcerative colitis: a double-blind, randomized, Israeli multicenter trial.

作者信息

Oren R, Arber N, Odes S, Moshkowitz M, Keter D, Pomeranz I, Ron Y, Reisfeld I, Broide E, Lavy A, Fich A, Eliakim R, Patz J, Bardan E, Villa Y, Gilat T

机构信息

Department of Gastroenterology, Ichilov Medical Center, Tel Aviv, Israel.

出版信息

Gastroenterology. 1996 May;110(5):1416-21. doi: 10.1053/gast.1996.v110.pm8613046.

Abstract

BACKGROUND & AIMS: Uncontrolled studies have suggested that methotrexate may be effective in patients with active ulcerative colitis. The aim of this study was to evaluate the effectiveness of oral methotrexate in chronic steroid-dependent ulcerative colitis in a randomized, double-blind multicenter trial.

METHODS

Patients with active ulcerative colitis who have received steroids and/or immunosuppressives for at least 4 months during the preceding 12 months with a current Mayo Clinic score of > or = 7 were included in the study. Methotrexate (12.5 mg) or placebo was added to their treatment once weekly for 9 months.

RESULTS

Sixty-seven patients were included (methotrexate, 30 patients, placebo, 37 patients). The proportion of patients entering first remission (methotrexate, 46.7%; placebo, 48.6%), the time to reach first remission (methotrexate, 4.1 +/- 1.9 months; placebo, 3.4 +/- 1.7 months), as well as the proportions of patients having a relapse after first remission (methotrexate, 64.3%; placebo, 44.4%) were not significantly different between the two groups. The mean Mayo Clinic score, the mean monthly steroid dose, and the proportion of abnormal laboratory results during the study were also similar.

CONCLUSIONS

Methotrexate at a weekly oral dose of 12.5 mg was not found to be better than placebo in the induction or maintenance of remission in patients with chronic active ulcerative colitis.

摘要

背景与目的

非对照研究表明甲氨蝶呤可能对活动性溃疡性结肠炎患者有效。本研究旨在通过一项随机、双盲多中心试验评估口服甲氨蝶呤对慢性激素依赖型溃疡性结肠炎的疗效。

方法

纳入在过去12个月中接受类固醇和/或免疫抑制剂治疗至少4个月且当前梅奥诊所评分≥7分的活动性溃疡性结肠炎患者。每周一次给予甲氨蝶呤(12.5毫克)或安慰剂,持续9个月。

结果

共纳入67例患者(甲氨蝶呤组30例,安慰剂组37例)。两组患者首次缓解的比例(甲氨蝶呤组46.7%;安慰剂组48.6%)、达到首次缓解的时间(甲氨蝶呤组4.1±1.9个月;安慰剂组3.4±1.7个月)以及首次缓解后复发的比例(甲氨蝶呤组64.3%;安慰剂组44.4%)均无显著差异。研究期间的平均梅奥诊所评分、平均每月类固醇剂量以及实验室检查结果异常的比例也相似。

结论

对于慢性活动性溃疡性结肠炎患者,每周口服12.5毫克甲氨蝶呤在诱导或维持缓解方面并不优于安慰剂。

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