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Meta-Analysis on Efficacy and Safety of Modified Guizhi Shaoyao Zhimu Tang with the Western Medicines in Treating Rheumatoid Arthritis

机译:桂枝Sha药止痛汤加西药治疗类风湿关节炎疗效及安全性的Meta分析

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Objective: To assess the efficacy and safety of modified Guizhi Shaoyao Zhimu Tang (GSZT) with the Western medicines in treating rheumatoid arthritis. Methods: All the relevant studies were collected by searching the Pubmed, Web of science, Embase, Cochrane Library, SpringerLink, China National Knowledge Infrastructure (CNKI), VIP Journals database, and Wanfang database from their inception to October 2017. After the assessment, the eligible ones were subject to Jadad score. The meta-analysis was conducted by RevMan 5.3 software. Results: Totally 10 randomized controlled trials (RCTs) involving 962 patients were enrolled. The clinical efficacy of analysis showed that modified GSZT with the Western medicines can significantly improve the clinical total effective rate [OR = 4.64, 95%CI (3.03, 7.12), P < 0.00001], the duration of morning stiff [MD = − 14.58, 95%CI ( − 16.49, − 12.68), P < 0.00001], erythrocyte sedimentation rate (ESR) [MD = − 12.62 95%CI ( − 18.69, − 6.54), P < 0.001], rheumatoid factor (RF) [MD = − 49.88, 95%CI ( − 77.6, − 22.09), P < 0.001], C-reactive protein (CRP) [MD = − 5.34, 95%CI ( − 5.86, − 4.82), P < 0.001]. The adverse events had been seen in both of the two groups, however, the clinical symptoms of the group on modified GSZT with the Western medicines were obviously reduced than the other one [OR = 0.25, 95%CI (0.10, 0.61), Z = 3.06, P < 0.01]. This system review shows that the modified GSZT with the Western medicines improved the clinical efficacy, symptoms and the blood biochemical indicators were improved significantly than that of Western medicines alone on rheumatoid arthritis. At the same time, it can reduce adverse effects and enhance safety.
机译:目的:探讨西药桂枝Sha药止痛汤(GSZT)的改良疗效和安全性。方法:从开始到2017年10月,通过搜索Pubmed,科学Web,Embase,Cochrane图书馆,SpringerLink,中国国家知识基础设施(CNKI),VIP Journals数据库和Wanfang数据库收集所有相关研究。评估后,符合条件的人会受到Jadad评分。荟萃分析由RevMan 5.3软件进行。结果:共纳入10项涉及962例患者的随机对照试验(RCT)。分析的临床疗效表明,用西药修饰的GSZT可以显着提高临床总有效率[OR = 4.64,95%CI(3.03,7.12),P <0.00001],僵硬的早晨持续时间[MD =-14.58 ,95%CI(-16.49,-12.68),P <0.00001],红细胞沉降率(ESR)[MD =-12.62 95%CI(-18.69,-6.54),P <0.001],类风湿因子(RF)[ MD = − 49.88,95%CI(− 77.6,− 22.09),P <0.001],C反应蛋白(CRP)[MD = − 5.34,95%CI(− 5.86,− 4.82),P <0.001]。两组均出现了不良事件,但是,西药改良GSZT组的临床症状明显较另一组减轻[OR = 0.25,95%CI(0.10,0.61),Z = 3.06,P <0.01]。该系统评价表明,用西药改良的GSZT治疗类风湿性关节炎的临床疗效,症状和血液生化指标均明显优于单用西药。同时,它可以减少不良影响并提高安全性。

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