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Is hydroxychloroquine effective in treating primary Sjogren’s syndrome: a systematic review and meta-analysis

机译:羟氯喹对治疗原发性干燥综合征有效吗:系统评价和荟萃分析

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Background To systematically review and assess the efficacy and safety of hydroxychloroquine (HCQ) for treating primary Sjogren’s syndrome (pSS). Methods Five electronic databases (Pubmed, EMBASE, Web of science, Ovid, Cochrane Library) were searched for randomized controlled trials and retrospective or prospective studies published in English that reported the effect of HCQ on pSS. The subjective symptoms (?sicca symptoms, fatigue and pain) and the objective indexes (erythrocyte sedimentation rate and Schirmer test) were assessed as main outcome measures. A meta-analysis and descriptive study on the efficacy and safety of HCQ were conducted. The estimate of the effect of HCQ treatment was expressed as a proportion together with 95% confidence interval, and plotted on a forest plot. Results Four trials with totals of 215 SS patients, including two randomized controlled trials, one double blind crossover trial and one retrospective open-label study, were analyzed in this review. For dry mouth and dry eyes, the effectiveness of HCQ treatment was essentially the same as placebo treatment. For fatigue, the effectiveness of HCQ was lower than placebo. The efficacy of HCQ in treating pain associated with pSS was superior to that of the placebo. There was no significant difference between HCQ-treated groups and controls in terms of Schirmer test results, but HCQ could reduce the erythrocyte sedimentation rate compare with placebo. A descriptive safety assessment showed that gastrointestinal adverse effects were the most common adverse effects associated with HCQ. Conclusions This systematic review showed that there is no significant difference between HCQ and placebo in the treatment of dry mouth and dry eye in pSS. Well-designed, randomized, controlled trials are needed to provide higher-quality evidence to confirm our findings, and future studies should focus on some other ?i?n?dex ?or? extraglandular measures, such as cutaneous manifestations, to further explore the therapeutic effect of HCQ in pSS.
机译:背景技术系统地审查和评估羟氯喹(HCQ)治疗原发性干燥综合征(pSS)的疗效和安全性。方法检索五个电子数据库(Pubmed,EMBASE,Web of science,Ovid,Cochrane图书馆),以随机对照试验以及以英语发表的回顾性或前瞻性研究报告HCQ对pSS的影响。评估主观症状(干燥症状,疲劳和疼痛)和客观指标(红细胞沉降率和Schirmer试验)作为主要结局指标。对HCQ的有效性和安全性进行了荟萃分析和描述性研究。 HCQ处理效果的估计值用比例和95%置信区间表示,并绘制在森林图上。结果本研究分析了总共215名SS患者的四项试验,包括两项随机对照试验,一项双盲交叉试验和一项回顾性开放标签研究。对于口干和眼睛干燥,HCQ治疗的有效性与安慰剂治疗基本相同。对于疲劳,HCQ的有效性低于安慰剂。 HCQ在治疗与pSS相关的疼痛方面的疗效优于安慰剂。在Schirmer测试结果方面,HCQ治疗组与对照组之间无显着差异,但HCQ与安慰剂相比可降低红细胞沉降率。描述性安全性评估表明,胃肠道不良反应是与HCQ相关的最常见不良反应。结论这项系统评价表明HCQ和安慰剂在治疗pSS的口干和眼干方面没有显着差异。需要设计良好的随机对照试验来提供高质量的证据,以证实我们的发现,而未来的研究应侧重于其他一些“右旋”或“右旋”研究。腺外措施,例如皮肤表现,以进一步探讨HCQ对pSS的治疗作用。

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