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Decision Support for Patient Consent Management

机译:病人同意管理的决策支持

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摘要

Patients are given more and more control on the access to their medical information. In many situations, the regulation rules require the acquisition of patients' consent before one can access the patients' medical information. However, in practice, patients oftentimes have difficulties determining whether they should permit a certain access request. In this article, we propose a quantitative approach to assist patients in consent management of their medical information. Our system evaluates access requests based on three factors (importance, sensitivity, normalcy) and makes personalized suggestion to patients. Our design is capable to handle requests in different categories. In situations where patients expect their data to be accessible to the requesters, our solution will make the consent management task effortless for patients. In less critical usage scenarios, our solution will recommend an informed decision by comparing risks and benefits associated with data access. Furthermore, our solution intends to enable patients to review past access activities periodically and can automatically detect potential over-accessing activities from various parties. We have implemented a prototype of our solution and performed simulations on real-world medical history records. We hope our work lays some technical ground for policy makers to derive best practices for health care organizations and enable enforcements of compliance laws such as HIPAA.
机译:越来越多地让患者对他们的医疗信息的访问有所控制。在许多情况下,监管规则要求在获得患者的医疗信息之前必须征得患者的同意。然而,在实践中,患者通常难以确定他们是否应允许某个进入请求。在本文中,我们提出了一种定量方法来协助患者对其医疗信息进行同意管理。我们的系统基于三个因素(重要性,敏感性,正常性)评估访问请求,并向患者提出个性化建议。我们的设计能够处理不同类别的请求。在患者希望其数据可被请求者访问的情况下,我们的解决方案将使患者的同意管理任务毫不费力。在不太关键的使用场景中,我们的解决方案将通过比较与数据访问相关的风险和收益来建议明智的决策。此外,我们的解决方案旨在使患者能够定期回顾过去的访问活动,并可以自动检测各方的潜在过度访问活动。我们已经实现了解决方案的原型,并在现实世界中的病历记录上进行了模拟。我们希望我们的工作为决策者奠定一些技术基础,以便他们为医疗保健组织制定最佳实践并促进诸如HIPAA之类的合规性法律的执行。

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