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改进用药错误报告系统。错误为何会发生?

Improving medication administration error reporting systems. Why do errors occur?

作者信息

Wakefield B J, Wakefield D S, Uden-Holman T

机构信息

Iowa City VA Medical Center, and College of Nursing, at The University of Iowa, in Iowa City, IA, USA.

出版信息

Ambul Outreach. 2000 Spring:16-20.

Abstract

Monitoring medication administration errors (MAE) is often included as part of the hospital's risk management program. While observation of actual medication administration is the most accurate way to identify errors, hospitals typically rely on voluntary incident reporting processes. Although incident reporting systems are more economical than other methods of error detection, incident reporting can also be a time-consuming process depending on the complexity or "user-friendliness" of the reporting system. Accurate incident reporting systems are also dependent on the ability of the practitioner to: 1) recognize an error has actually occurred; 2) believe the error is significant enough to warrant reporting; and 3) overcome the embarrassment of having committed a MAE and the fear of punishment for reporting a mistake (either one's own or another's mistake).

摘要

监测用药差错(MAE)通常是医院风险管理计划的一部分。虽然观察实际用药过程是识别差错最准确的方法,但医院通常依赖自愿的事件报告流程。尽管事件报告系统比其他差错检测方法更经济,但根据报告系统的复杂性或“用户友好性”,事件报告也可能是一个耗时的过程。准确的事件报告系统还取决于从业者的能力:1)识别差错实际已经发生;2)认为该差错严重到足以报告;3)克服因犯了用药差错而产生的尴尬以及因报告错误(自己的或他人的错误)而产生的受罚恐惧。

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