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Guidance on conducting systematic reviews/meta-analyses of pharmacoepidemiological studies of safety outcomes: the gap is now filled

机译:有关进行安全结果的药物遗传学研究的系统评价/荟萃分析的指导:现在填补了差距

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摘要

Until recently, no comprehensive guidance specifically on the conduction of systematic reviews and meta-analyses of pharmacoepidemiological studies of safety outcomes was available. In December 2015, the European Network of Centres for Pharmacoepidemiology and Pharamacovigilance (ENCePP), a network coordinated by the European Medicines Agency, published their ‘Guidance on conducting systematic reviews and meta-analyses of completed comparative pharmacoepidemiological studies of safety outcomes’, filling an important gap in the field. This paper highlights the ENCePP recommendations in terms of study identification, data extraction, study quality appraisal and analytical plan. Although the ENCePP document should not be considered as definitive, since it will likely be refined following researchers’ feedback, it is expected that it will be highly influential and useful for the field, with the ultimate goal to improve and standardise the conduction and reporting of systematic reviews/meta-analyses of pharmacoepidemiological studies of safety outcomes.
机译:直到最近,没有专门针对安全结果的药物病态研究的系统评价和荟萃分析的全面指导。 2015年12月,欧洲药物病毒学和PharamacovilecaCE网络(Encepp),由欧洲药物局协调的网络,发表了“关于进行系统评价和荟萃分析的指导,对安全结果的完善的比较药物化学研究”,填补了领域的重要差距。本文以研究识别,数据提取,学习质量评估和分析计划来介绍encepp建议。虽然Encepp文件不应被视为最终,但由于研究人员的反馈可能会被提炼,预计这将是对该领域的高度影响力和有用的,因此最终目标是改进和标准化的传导和报告系统评价/荟萃分析安全结果的药物病态学研究。

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