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Clinical decision support systems: a discussion of quality safety and legal liability issues.

机译:临床决策支持系统:有关质量安全性和法律责任问题的讨论。

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摘要

Developers of Clinical Decision Support Systems (CDSSs) have to date been more concerned with the efficacy of systems (e.g. measurable improvements in clinical outcomes) than with safety (e.g. potential for harmful side-effects). In future CDSS developers will be required (by the courts etc.) to acknowledge a "duty of care" covering all aspects of design, development and deployment. Experience in the transport, power and other safety-critical industries has led to a range of quality and safety assurance methods whose adoption may be needed before CDSSs can safely become an integral part of routine patient care, and before the trust of healthcare professionals, patients and other stakeholders can be gained. No single method will be sufficient for safe development and deployment; a range of techniques will be needed and used selectively. This paper is a contribution to discussion of quality, safety and legal liability issues in the medical informatics community.
机译:迄今为止,临床决策支持系统(CDSS)的开发人员更关注系统的功效(例如,临床结果的可衡量的改进),而不是安全性(例如,潜在的有害副作用)。将来,CDSS开发人员将被(法院等)要求承认涵盖设计,开发和部署各个方面的“谨慎义务”。在交通,电力和其他对安全至关重要的行业中的经验导致了一系列质量和安全保证方法,在CDSS可以安全地成为常规患者护理的组成部分之前以及在医疗保健专业人员信任之前,可能需要采用这些方法。并获得其他利益相关者。没有任何一种方法足以进行安全的开发和部署;需要并选择性地使用一系列技术。本文对医学信息学界对质量,安全性和法律责任问题的讨论做出了贡献。

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