欧洲实施先进临床数字决策支持系统面临的法律挑战。

Colin Mitchell, Corrette Ploem
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引用次数: 0

摘要

基于人工智能和机器学习的系统有助于医疗保健决策,是“个性化”或“精确”医疗时代有前途的新工具。随着患者数据和科学证据数量的增长,这些计算机化决策支持系统(DSS)在帮助医疗专业人员改进对个别患者的诊断和护理方面具有巨大潜力。然而,这些工具在临床护理中的实施给欧洲的医疗保健提供者和DSS供应商带来了一些可预见的法律挑战:复杂和新颖的DSS的使用如何与提供合理护理标准的专业标准相关?在DSS可用于常规实践之前,应在测试方面做些什么?如果DSS不能正常运行,医疗保健提供者和DSS公司的潜在责任是什么?保护患者数据和一般隐私权的法律要求如何适用于可能的DSS场景?在这篇文章中,我们从欧洲的角度概述了现行法律及其对DSS使用的一般影响。我们得出的结论是,如果医疗保健提供者和DSS供应商首先在患者明确知情同意的情况下在转化研究中接受测试,他们将最有可能遇到法律挑战;DSS供应商和医疗保健提供者能够澄清并就其个人法律责任达成一致,以及;患者被适当告知隐私风险,并能够自行决定他们的数据是否可以用于其他目的,或者在欧盟之外存储和处理。DSS开发人员和医疗保健提供者需要密切合作,以确保符合合理和安全的患者护理所需的国家和欧洲法规和标准。与患者的相关性:先进的数字决策支持系统有可能改善患者的诊断和护理。在这篇文章中,我们讨论了关键的法律问题,以支持使用DSS的转化研究,并确保它们符合欧洲保护患者安全和隐私的高标准。
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Legal challenges for the implementation of advanced clinical digital decision support systems in Europe.

Systems based on artificial intelligence and machine learning that facilitate decision making in health care are promising new tools in the era of 'personalized' or 'precision' medicine. As the volume of patient data and scientific evidence grows, these computerised decision support systems (DSS) have great potential to help healthcare professionals improve diagnosis and care for individual patients. However, the implementation of these tools in clinical care raises some foreseeable legal challenges for healthcare providers and DSS-suppliers in Europe: How does the use of complex and novel DSS relate to professional standards to provide a reasonable standard of care? What should be done in terms of testing before DSS can be used in regular practice? What are the potential liabilities of health care providers and DSS companies if a DSS fails to function well? How do legal requirements for the protection of patient data and general privacy rights apply to likely DSS scenarios? In this article, we provide an overview of the current law and its general implications for the use of DSS, from a European perspective. We conclude that healthcare providers and DSS-suppliers will have the best chance of meeting legal challenges if: they are first tested in translational research with the patients' explicit, informed consent; DSS-suppliers and healthcare providers are able to clarify and agree on their individual legal responsibilities, and; patients are properly informed about privacy risks and able to decide themselves whether their data can be used for other purposes, or are stored and processed outside the EU. DSS developers and healthcare providers will need to work together closely to ensure compliance with national and European regulations and standards required for reasonable and safe patient care.

Relevance for patients: Advanced digital decision support systems have the potential to improve patient diagnosis and care. In this article we discuss key legal issues to support translational research using DSS and ensure that they meet the high standards for protection of patient safety and privacy in Europe.

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