“可接受风险”的概念:效用在药物管理中的作用

David A. Lane , Tom A. Hutchinson
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引用次数: 15

摘要

本文提出了基于效用概念的“可接受风险”的定义。如果在相关患者群体中没有比使用该药物相关的替代治疗具有更高的累积预期效用,则该药物特定使用的不良反应构成可接受的风险。该定义对药品上市后管理的影响进行了探讨。特别是,上市后监督应该扩大到包括患者价值的量化,药物的有益作用和不良影响。管理行动应针对具有不可接受风险的特定药物使用,而不是针对药物本身。这可能需要使用教育和服务行动方案,以及针对开处方者和分发者的管制行动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The notion of “acceptable risk”: The role of utility in drug management

This paper presents a definition of “acceptable risk” that is based on the concept of utility. The adverse effects of a specific use of a drug pose an acceptable risk if no alternative treatment has a higher cumulated expected utility in the relevant patient population than that associated with the use of the drug. The implications of this definition for postmarketing management of drugs are explored. In particular, postmarketing surveillance should be expanded to include the quantification of patients' values, a drug's beneficial effects, and its adverse effects. Management actions should be targeted at specific drug uses with unacceptable risks rather than at drugs themselves. This may require the use of education and service action options, as well as regulatory actions aimed at prescribers and dispensers.

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