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首页> 外文期刊>Clinical and experimental rheumatology >The ability of disease modifying antirheumatic drugs to induce and maintain improvement in patients with rheumatoid arthritis. epidemiology of DMARDs treatment in Japan.
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The ability of disease modifying antirheumatic drugs to induce and maintain improvement in patients with rheumatoid arthritis. epidemiology of DMARDs treatment in Japan.

机译:疾病改良抗风湿药诱导和维持类风湿关节炎患者病情改善的能力。日本DMARDs治疗的流行病学。

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OBJECTIVE: The effectiveness of the disease-modifying antirheumatic drugs (DMARDs) methotrexate (MTX), bucillamine (BUC), salazosulphapyridine (SASP) and gold sodium thiomalate (GST) over two courses of treatment with a follow-up period of at least 12 months was evaluated in 425 patients with rheumatoid arthritis. METHODS: Clinical efficacy was evaluated on the basis of the numbers of painful and swollen joints, morning stiffness, grip strength, erythrocyte sedimentation rate, C-reactive protein and rheumatoid factor levels before and after treatment. Results were evaluated on the basis of the survival rate (Kaplan-Meier method) and the incidence and types of adverse drug reactions (ADR) following single and combined therapies. RESULTS: In the first course of treatment, the survival rates for MTX, GST, BUC and SASP were 52.3%, 40.4%, 33.0% and 24.8%, respectively. The rates of development of ADR were 22.9%, 23.5%, 26.3% and 30.0% for BUC, SASP, GST and MTX, respectively. In the second course, the survival rates for MTX, BUC and SASP were 36.6%, 14.1% and 10%, respectively. CONCLUSION: DMARDs used in the first course of treatment improved the clinical parameters until the 6th month after initiation of treatment. Combination treatments showed some effectiveness, but because of the high incidence of ADR the survival rate was low. DMARDs used in the second course of treatment were not efficacious and there was no improvement in the survival rate compared to the first course of treatment.
机译:目的:疾病改善型抗风湿药(DMARDs)甲氨蝶呤(MTX),布西拉明(BUC),Salazosulphapyridine(SASP)和硫代苹果酸金钠(GST)在两个疗程中的随访时间至少为12在425名类风湿关节炎患者中评估了10个月。方法:根据治疗前后疼痛和肿胀的关节数,晨僵,握力,红细胞沉降率,C反应蛋白和类风湿因子水平评估临床疗效。根据存活率(Kaplan-Meier方法)以及单一和联合疗法后药物不良反应的发生率和类型(ADR)评估结果。结果:在第一疗程中,MTX,GST,BUC和SASP的存活率分别为52.3%,40.4%,33.0%和24.8%。 BUC,SASP,GST和MTX的ADR发生率分别为22.9%,23.5%,26.3%和30.0%。在第二个疗程中,MTX,BUC和SASP的生存率分别为36.6%,14.1%和10%。结论:在治疗的第一个疗程中使用的DMARD改善了临床参数,直到开始治疗后的第6个月为止。联合治疗显示出一定的效果,但是由于ADR的高发率,生存率很低。与第一疗程相比,在第二疗程中使用的DMARD无效,并且存活率没有改善。

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