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临床决策支持系统可以进行修改,以减少“警报疲劳”,同时将法律诉讼风险降至最低。

Clinical decision support systems could be modified to reduce 'alert fatigue' while still minimizing the risk of litigation.

机构信息

Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.

出版信息

Health Aff (Millwood). 2011 Dec;30(12):2310-7. doi: 10.1377/hlthaff.2010.1111.

Abstract

Clinical decision support systems--interactive computer systems that help doctors make clinical choices--can reduce errors in drug prescribing by offering real-time alerts about possible adverse reactions. But physicians and other users often suffer "alert fatigue" caused by excessive numbers of warnings about items such as potentially dangerous drug interactions. As a result, they may pay less attention to or even ignore some vital alerts, thus limiting these systems' effectiveness. Designers and vendors sharply limit the ability to modify alert systems because they fear being exposed to liability if they permit removal of a warning that could have prevented a harmful prescribing error. Our analysis of product liability principles and existing research into the use of clinical decision support systems, however, finds that more finely tailored or parsimonious warnings could ease alert fatigue without imparting a high risk of litigation for vendors, purchasers, and users. Even so, to limit liability in this area, we recommend stronger government regulation of clinical decision support systems and development of international practice guidelines highlighting the most important warnings.

摘要

临床决策支持系统——帮助医生做出临床决策的交互式计算机系统——可以通过实时提醒可能出现的不良反应来减少药物处方错误。但是,医生和其他用户经常会因为大量关于潜在危险药物相互作用等项目的警告而出现“警报疲劳”。因此,他们可能会较少关注甚至忽略一些重要的警报,从而限制了这些系统的效果。由于担心如果允许删除可能防止有害处方错误的警告,他们会面临责任风险,因此设计者和供应商会严格限制修改警报系统的能力。然而,我们对产品责任原则的分析和对临床决策支持系统使用情况的现有研究发现,更精细或更节省的警告可以减轻警报疲劳,而不会给供应商、购买者和用户带来高诉讼风险。即便如此,为了限制这一领域的责任,我们建议对临床决策支持系统进行更严格的政府监管,并制定国际实践指南,突出最重要的警告。

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