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三药联合治疗对甲氨蝶呤和皮质类固醇联合治疗抵抗的类风湿关节炎:单中心经验。

Triple DMARD combination for rheumatoid arthritis resistant to methotrexate and steroid combination: a single-center experience.

机构信息

Division of Rheumatology, Department of Internal Medicine, Hacettepe University Hospital, 06100 Sihhiye, Ankara, Turkey.

出版信息

Rheumatol Int. 2013 Jun;33(6):1425-7. doi: 10.1007/s00296-012-2546-6. Epub 2012 Nov 15.

Abstract

The mainstay of RA treatment is the disease-modifying antirheumatic drugs, and triple DMARD combination is now known to be better than monotherapies. Our aim in this trial was to report our clinical experience with triple DMARD therapy for resistant rheumatoid arthritis. Data of 140 patients with RA resistant to methotrexate and steroid combination were evaluated retrospectively. One hundred and nineteen (85 %) were female, and the median age at diagnosis was 56 (29-82) years. The median time between the diagnosis and beginning of triple therapy was 45.5 (6-564) months. Fifty-two (37.1 %) patients (group 1) on triple therapy protocol achieved remission, but the others (88; 62.9 %) (group 2) did not. The mean DAS28 scores for the study group before triple DMARD therapy and after 12 months under triple DMARD therapy were 4.93 and 3.24, respectively. The DAS28 scores after 12 months for groups 1 and 2 were 2.57 and 3.64. The median follow-up period for patients in group 1 was 60 months (23-118), and the mean DAS28 score at the time of the analysis for group 1 was 2.36. Triple DMARD combination may save one-third of the MTX-resistant RA patients from the serious side effects and the cost of anti-TNF.

摘要

类风湿关节炎治疗的主要药物是改善病情抗风湿药,目前已知三联 DMARD 治疗优于单药治疗。本试验旨在报告我们对三药联合治疗耐药性类风湿关节炎的临床经验。回顾性评估了 140 例对甲氨蝶呤和皮质类固醇联合治疗耐药的类风湿关节炎患者的数据。119 例(85%)为女性,诊断时的中位年龄为 56(29-82)岁。诊断后开始三联治疗的中位时间为 45.5(6-564)个月。52 例(37.1%)(第 1 组)患者接受三联治疗方案达到缓解,但其余 88 例(62.9%)(第 2 组)未达到缓解。研究组在开始三联 DMARD 治疗前和三联 DMARD 治疗 12 个月后的 DAS28 评分分别为 4.93 和 3.24。第 1 组和第 2 组治疗 12 个月后的 DAS28 评分分别为 2.57 和 3.64。第 1 组患者的中位随访时间为 60 个月(23-118),第 1 组分析时的平均 DAS28 评分为 2.36。三联 DMARD 联合治疗可能使三分之一的 MTX 耐药性 RA 患者免受严重副作用和抗 TNF 治疗的费用。

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