Savage Erica L, Fairbanks Rollin J, Ratwani Raj M
National Center for Human Factors in Healthcare, MedStar Health, Washington, DC, USA.
J Am Med Inform Assoc. 2017 Jul 1;24(4):769-775. doi: 10.1093/jamia/ocw185.
Despite federal policies put in place by the Office of the National Coordinator (ONC) to promote safe and usable electronic health record (EHR) products, the usability of EHRs continues to frustrate providers and have patient safety implications. This study sought to compare government policies on usability and safety, and methods of examining compliance to those policies, across 3 federal agencies: the ONC and EHRs, the Federal Aviation Administration (FAA) and avionics, and the Food and Drug Administration (FDA) and medical devices. Our goal was to identify whether differences in policies exist and, if they do exist, how policies and enforcement mechanisms from other industries might be applied to optimize EHR usability.
We performed a qualitative study using publicly available governing documents to examine similarities and differences in usability and safety policies across agencies.
The policy review and analysis revealed several consistencies within each agency's usability policies. Critical differences emerged in the usability standards and policy enforcement mechanisms utilized by the 3 agencies. The FAA and FDA look at evidence of usability processes and are more prescriptive when it comes to testing final products as compared to the ONC, which relies on attestation and is less prescriptive.
A comparison of usability policies across industries illustrates key differences between the ONC and other federal agencies. These differences could be contributing to the usability challenges associated with EHRs.
Our analysis highlights important areas of usability and safety policy from other industries that can better inform ONC policies on EHRs.
尽管国家协调员办公室(ONC)制定了联邦政策以推广安全且易用的电子健康记录(EHR)产品,但EHR的易用性仍使医疗服务提供者感到沮丧,并对患者安全产生影响。本研究旨在比较3个联邦机构在可用性和安全性方面的政府政策,以及检查这些政策合规性的方法,这3个机构分别是:ONC与EHR、联邦航空管理局(FAA)与航空电子设备、食品药品监督管理局(FDA)与医疗设备。我们的目标是确定政策是否存在差异,如果存在差异,其他行业的政策和执行机制如何应用于优化EHR的可用性。
我们进行了一项定性研究,使用公开可用的管理文件来检查各机构在可用性和安全政策方面的异同。
政策审查和分析揭示了每个机构可用性政策中的若干一致性。3个机构在使用的可用性标准和政策执行机制方面出现了重大差异。与ONC相比,FAA和FDA关注可用性流程的证据,在测试最终产品时更具规范性,而ONC依赖认证且规范性较低。
跨行业可用性政策的比较说明了ONC与其他联邦机构之间的关键差异。这些差异可能导致了与EHR相关的可用性挑战。
我们的分析突出了其他行业在可用性和安全政策方面的重要领域,这些领域可以为ONC关于EHR的政策提供更好的参考。