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普瑞巴林治疗纤维肌痛:来自公司临床试验报告的疗效和安全性的荟萃分析。

Pregabalin in fibromyalgia: meta-analysis of efficacy and safety from company clinical trial reports.

机构信息

Department of Occupational and Social Medicine, University of Göttingen, Göttingen, Germany.

出版信息

Rheumatology (Oxford). 2010 Apr;49(4):706-15. doi: 10.1093/rheumatology/kep432. Epub 2010 Jan 7.

Abstract

OBJECTIVES

Meta-analysis of pregabalin trials in FM using company trial reports, which provide more detailed information about trials than published papers. FM is a common condition with a significant impact on quality of life.

METHODS

Reports of five high-quality randomized trials (3808 patients) of pregabalin in FM were obtained from Pfizer. Four trials (2754 patients) were of classical trial design and one was an enriched enrolment randomized withdrawal design. Outcomes for meta-analysis from the four trials with classical design were pooled in an intention-to-treat analysis.

RESULTS

Significant benefit of pregabalin over placebo was seen for a variety of outcomes including mean pain and sleep scores, the proportion of patients achieving at least 50% pain relief and most of the individual domains of short-form 36. Only a minority of patients achieve moderate or substantial pain relief. The proportions of patients with any adverse event, somnolence or dizziness were also significantly greater with pregabalin than with placebo. There was no difference with regard to serious adverse events. A dose-response relationship was apparent for at least 50% pain relief and for adverse event outcomes.

CONCLUSIONS

Pregabalin is effective in treating FM and is relatively safe. The size of therapeutic effect is similar to that with other recent interventions such as duloxetine and the combination of tramadol and paracetamol. Enriched enrolment randomized withdrawal design gives similar results to classical trial designs in FM.

摘要

目的

使用公司试验报告对纤维肌痛(FM)的普瑞巴林试验进行荟萃分析,这些报告提供了比已发表论文更详细的试验信息。FM 是一种常见病症,对生活质量有重大影响。

方法

从辉瑞公司获得了五篇高质量随机试验(3808 例患者)的普瑞巴林治疗 FM 的报告。其中四项试验(2754 例患者)采用经典试验设计,一项为富集入组随机撤药设计。四项采用经典设计的试验中,从所有结局进行意向治疗分析,对试验结果进行荟萃分析。

结果

普瑞巴林与安慰剂相比,在各种结局方面均有显著获益,包括平均疼痛和睡眠评分、达到至少 50%疼痛缓解的患者比例以及简明 36 项健康调查简表的大多数单项领域。只有少数患者获得中度或明显的疼痛缓解。普瑞巴林治疗组患者发生任何不良事件、嗜睡或头晕的比例也明显高于安慰剂组。但在严重不良事件方面两组无差异。至少 50%疼痛缓解和不良事件结局均呈现出剂量反应关系。

结论

普瑞巴林治疗 FM 有效且相对安全。治疗效果的大小与其他最近的干预措施如度洛西汀以及曲马多和对乙酰氨基酚联合治疗相似。富集入组随机撤药设计在 FM 中与经典试验设计产生的结果相似。

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