Wilson Natalia A, Tcheng James E, Graham Jove, Drozda Joseph P
College of Health Solutions, Arizona State University, Phoenix, AZ, USA.
Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
Med Devices (Auckl). 2022 Jun 21;15:177-186. doi: 10.2147/MDER.S364539. eCollection 2022.
The requirement for medical device manufacturers to label their devices with a unique device identifier (UDI) was formalized by the 2013 US Food and Drug Administration Unique Device Identification System Rule. However, parallel regulatory requirement for US health systems to use UDIs, particularly the electronic documentation of UDIs during patient care is lacking. Despite the lack of regulation, some health systems have implemented and are using UDIs. To assess the current state, we studied representative health system UDI implementation experiences, including barriers and the strategies to overcome them, and identified next steps to advance UDI adoption.
Semi-structured interviews were performed with health system personnel involved in UDI implementation in their cardiac catheterization labs or operating rooms. Interviews were transcribed and analyzed using the framework methodology of Ritchie and Spencer. An expert panel evaluated findings and informed barriers, strategies, and next steps.
Twenty-four interviews at ten health systems were performed. Identified barriers were internal (lack of organizational support, information technology gaps, clinical resistance) and external (information technology vendor resistance, limitations in manufacturer support, gaps in reference data, lack of an overall UDI system). Identified strategies included relationship building, education, engagement, and communication. Next steps to advance UDI adoption focus on education, research, support, and policy.
Delineation of UDI implementation barriers and strategies provides guidance and support for health systems to adopt the UDI standard and electronically document UDIs during clinical care. Next steps illuminate critical areas for attention to advance UDI adoption and achieve a comprehensive UDI system in health care to strengthen patient care and safety.
2013年美国食品药品监督管理局的《医疗器械唯一标识系统规则》将医疗器械制造商为其产品标注唯一设备标识符(UDI)的要求正式化。然而,美国卫生系统在使用UDI方面缺乏相应的监管要求,尤其是在患者护理期间对UDI进行电子记录的要求。尽管缺乏监管,但一些卫生系统已经实施并正在使用UDI。为评估当前状况,我们研究了具有代表性的卫生系统UDI实施经验,包括障碍及克服这些障碍的策略,并确定了推进UDI采用的后续步骤。
对参与心脏导管实验室或手术室UDI实施的卫生系统人员进行了半结构化访谈。访谈内容进行了转录,并使用里奇和斯宾塞的框架方法进行分析。一个专家小组对研究结果进行了评估,并明确了障碍、策略和后续步骤。
在10个卫生系统进行了24次访谈。确定的障碍包括内部障碍(缺乏组织支持、信息技术差距、临床抵触)和外部障碍(信息技术供应商抵触、制造商支持有限、参考数据差距、缺乏整体UDI系统)。确定的策略包括建立关系、教育、参与和沟通。推进UDI采用的后续步骤集中在教育、研究、支持和政策方面。
明确UDI实施的障碍和策略可为卫生系统采用UDI标准并在临床护理期间对UDI进行电子记录提供指导和支持。后续步骤阐明了推进UDI采用并在医疗保健领域实现全面UDI系统以加强患者护理和安全所需关注的关键领域。