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Meridian-sinew release therapy for the treatment of refractory rheumatoid arthritis

机译:经络-新释放疗法治疗难治性类风湿关节炎

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摘要

Objective: To evaluate the efficacy and safety of Meridian-sinew Release therapy in Chinese patients with refractory active Rheumatoid Arthritis (RA). Summary of Background Data: Few studies focused on the effect of combination of Meridian-sinew Release therapy and Methotrexate (MTX) on refractory active RA of Chinese patients. Methods: Eighty refractory active rheumatoid arthritis patients were randomized to receive Meridian-sinew Release+MTX 10 mg (n=40), MTX 10 mg (n=40) every week for 12 weeks. The primary end point was the proportion of patients achieving ≥20% improvement in the American College of Rheumatology criteria (ACR20) at week 12. Secondary efficacy endpoints included 28-joint disease activity score with ESR (DAS28-ESR), simplified disease activity index (SDAI), clinical disease activity index (CDAI) and Health Assessment Questionnaire-Disability Index (HAQ-DI). Results: Week 12 ACR20 response rates were significantly greater in Meridian-sinew Release+MTX group (30/38 (78.9%)) than in MTX group (19/37 (51.3%)), (P<0.001), as were ACR50 and ACR70 response rates. Patients treated with Meridian-sinew Release+MTX were significantly more likely to achieve clinical remission, using various definitions, at 12 weeks versus MTX alone. A larger percentage of Meridian-sinew+MTX patients than MTX alone patients were in states of low disease activity or remission for DAS28-ESR, SDAI and CDAI after 12 weeks of treatment. Conclusion: Our study suggests that Meridian-sinew Release therapy was well tolerated and efficacious in improving clinical outcomes in Chinese patients with refractory active RA.
机译:目的:评价经络-新释放疗法在中国难治性活动性类风湿关节炎(RA)患者中的疗效和安全性。背景数据摘要:很少有研究关注经络-新释放疗法和甲氨蝶呤(MTX)联合治疗对中国患者难治性活动性RA的影响。方法:将80名难治性活动性类风湿关节炎患者随机分为12周,每周接受经络-新释放+ MTX 10 mg(n = 40),MTX 10 mg(n = 40)。主要终点是在第12周时达到美国风湿病学会标准(ACR20)≥20%的患者比例。次要疗效终点包括ESR的28个关节疾病活动评分(DAS28-ESR),简化的疾病活动指数(SDAI),临床疾病活动指数(CDAI)和健康评估问卷-残疾指数(HAQ-DI)。结果:Meridian-sinew Release + MTX组第12周的ACR20响应率(30/38(78.9%))显着高于MTX组(19/37(51.3%)),与ACR50相比(P <0.001)和ACR70响应率。与单独使用MTX相比,使用各种定义的Meridian-sinew Release + MTX治疗的患者在12周时更有可能实现临床缓解。经12周治疗后,DAS28-ESR,SDAI和CDAI的疾病活动性或缓解程度较低的子午线-sinew + MTX患者比例高于单独的MTX患者。结论:我们的研究表明,经络-新释放疗法对中国难治性活动性RA患者的临床结局具有良好的耐受性和有效性。

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