Developing a taxonomy for research in adverse drug events: potholes and signposts

J. Nebeker, John F. Hurdle, Jennifer M. Hoffman, Beverly Roth, C. Weir, M. Samore
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引用次数: 65

Abstract

Computerized decision support and order entry shows great promise for reducing adverse drug events (ADEs). The evaluation of these solutions depends on a framework of definitions and classifications that is clear and practical. Unfortunately the literature does not always provide a clear path to defining and classifying adverse drug events. While not a systematic review, this paper uses examples from the literature to illustrate problems that investigators will confront as they develop a conceptual framework for their research. It also proposes a targeted taxonomy that can facilitate a clear and consistent approach to the research of ADEs and aid in the comparison to results of past and future studies. The taxonomy addresses the definition of ADE, types, seriousness, error, and causality.
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制定药物不良事件研究的分类:坑洼和路标
计算机化的决策支持和订单输入显示了减少药物不良事件(ADEs)的巨大希望。对这些解决办法的评价取决于明确和实际的定义和分类框架。不幸的是,文献并不总是提供一个明确的途径来定义和分类药物不良事件。虽然不是一个系统的回顾,本文从文献中使用的例子来说明问题,调查人员将面临,因为他们发展的概念框架,为他们的研究。本文还提出了一种有针对性的分类方法,可以为ADEs的研究提供一个明确和一致的方法,并有助于与过去和未来的研究结果进行比较。该分类法涉及ADE的定义、类型、严重性、错误和因果关系。
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