Suppr超能文献

甲氨蝶呤与硫唑嘌呤治疗类风湿关节炎的疗效比较。一项为期48周的随机双盲试验。

Methotrexate versus azathioprine in the treatment of rheumatoid arthritis. A forty-eight-week randomized, double-blind trial.

作者信息

Jeurissen M E, Boerbooms A M, van de Putte L B, Doesburg W H, Mulder J, Rasker J J, Kruijsen M W, Haverman J F, van Beusekom H J, Muller W H

机构信息

Department of Rheumatology, University Hospital Nijmegen, The Netherlands.

出版信息

Arthritis Rheum. 1991 Aug;34(8):961-72. doi: 10.1002/art.1780340805.

Abstract

We conducted a double-blind, randomized trial comparing azathioprine (AZA) and methotrexate (MTX) in the treatment of patients with rheumatoid arthritis in whom parenteral gold and/or D-penicillamine treatment had been unsuccessful. Patients were randomly assigned to receive either AZA (100 mg daily) or oral MTX (7.5 mg weekly). After 8 weeks, the dosage was increased depending on the clinical improvement. Sixty-four patients were followed up for 48 weeks (33 AZA, 31 MTX). Comparison of values at week 24 with baseline values revealed significant improvement in 12 of 13 disease variables in the MTX group and in 6 of 13 in the AZA group. Comparison between the 2 treatment groups at 24 weeks, by area-under-the-curve analysis, showed significantly more improvement in the MTX group in terms of the swollen joint count, pain score, erythrocyte sedimentation rate, C-reactive protein level, hemoglobin level, thrombocyte level, and disease activity score. A significant overall clinical improvement (disease activity score) was found in 7 of 20 patients treated with AZA and 18 of 30 patients treated with MTX after 24 weeks of therapy, and in 6 of 12 AZA-treated patients and 19 of 25 MTX-treated patients after 48 weeks. The number of withdrawals due to side effects was significantly higher in the AZA group. After 48 weeks, only 12 patients from the AZA group (36%), but 25 from the MTX group (81%), were still using the initial drug. These results demonstrate MTX to be superior to AZA in the treatment of rheumatoid arthritis, with a more rapid clinical improvement which is sustained after 1 year, accompanied by a lower rate of serious adverse reactions.

摘要

我们进行了一项双盲随机试验,比较硫唑嘌呤(AZA)和甲氨蝶呤(MTX)对接受肠胃外金制剂和/或青霉胺治疗无效的类风湿性关节炎患者的治疗效果。患者被随机分配接受AZA(每日100毫克)或口服MTX(每周7.5毫克)治疗。8周后,根据临床改善情况增加剂量。64例患者接受了48周的随访(33例使用AZA,31例使用MTX)。将第24周时的值与基线值进行比较,结果显示MTX组13项疾病变量中有12项显著改善,AZA组13项中有6项显著改善。通过曲线下面积分析比较两个治疗组在第24周时的情况,结果显示MTX组在肿胀关节计数、疼痛评分、红细胞沉降率、C反应蛋白水平、血红蛋白水平、血小板水平和疾病活动评分方面有更显著的改善。治疗24周后,使用AZA治疗的20例患者中有7例、使用MTX治疗的30例患者中有18例出现显著的总体临床改善(疾病活动评分);治疗48周后,使用AZA治疗的12例患者中有6例、使用MTX治疗的25例患者中有19例出现显著的总体临床改善。AZA组因副作用而停药的人数显著更高。48周后,AZA组只有12例患者(36%)仍在使用初始药物,而MTX组有25例患者(81%)仍在使用。这些结果表明,在类风湿性关节炎的治疗中,MTX优于AZA,临床改善更快,且在1年后仍能持续,同时严重不良反应发生率更低。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验