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用于患者安全的健康信息技术以及提高健康信息技术的安全性

Health IT for Patient Safety and Improving the Safety of Health IT.

作者信息

Magrabi Farah, Ong Mei-Sing, Coiera Enrico

机构信息

Centre for Health Informatics, Australian Institute of Health Innovation, Macquarie University, Sydney, Australia.

出版信息

Stud Health Technol Inform. 2016;222:25-36.

Abstract

Alongside their benefits health IT applications can pose new risks to patient safety. Problems with IT have been linked to many different types of clinical errors including prescribing and administration of medications; as well as wrong-patient, wrong-site errors, and delays in procedures. There is also growing concern about the risks of data breach and cyber-security. IT-related clinical errors have their origins in processes undertaken to design, build, implement and use software systems in a broader sociotechnical context. Safety can be improved with greater standardization of clinical software and by improving the quality of processes at different points in the technology life cycle, spanning design, build, implementation and use in clinical settings. Oversight processes can be set up at a regional or national level to ensure that clinical software systems meet specific standards. Certification and regulation are two mechanisms to improve oversight. In the absence of clear standards, guidelines are useful to promote safe design and implementation practices. Processes to identify and mitigate hazards can be formalised via a safety management system. Minimizing new patient safety risks is critical to realizing the benefits of IT.

摘要

除了带来益处外,健康信息技术应用也可能给患者安全带来新风险。信息技术问题已与许多不同类型的临床错误相关联,包括药物处方和给药;以及错误患者、错误部位的错误和手术延误。人们还越来越担心数据泄露和网络安全风险。与信息技术相关的临床错误源于在更广泛的社会技术背景下设计、构建、实施和使用软件系统所进行的流程。通过提高临床软件的标准化程度以及改善技术生命周期不同阶段(包括设计、构建、实施和临床环境中的使用)的流程质量,可以提高安全性。可以在区域或国家层面建立监督流程,以确保临床软件系统符合特定标准。认证和监管是改善监督的两种机制。在缺乏明确标准的情况下,指南有助于促进安全的设计和实施实践。识别和减轻危害的流程可以通过安全管理系统来正式化。将新的患者安全风险降至最低对于实现信息技术的益处至关重要。

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