The Medical Device Unique Device Identifier as the Single Source of Truth in Healthcare Enterprises - Roadmap for Implementation of the Clinically Integrated Supply Chain.

IF 1.3 Q4 ENGINEERING, BIOMEDICAL
Medical Devices-Evidence and Research Pub Date : 2021-12-24 eCollection Date: 2021-01-01 DOI:10.2147/MDER.S344132
James E Tcheng, Miriam V Nguyen, Helen W Brann, Patricia A Clarke, Maureen Pfeiffer, Jane R Pleasants, Gregory W Shelton, Joseph F Kelly
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引用次数: 5

Abstract

Documentation and tracking of supplies, equipment and medical devices is central to operational, financial, and clinical aspects of safe, efficient, and effective patient care. The labeling of medical devices with a unique device identifier (UDI) creates the opportunity to tightly integrate device information across health information systems by using the UDI as the index "source of truth". Across 3 hospitals of the Duke University Health System, we executed a comprehensive implementation of UDI-based device and supply information management in our cardiac catheterization and electrophysiology laboratories. Following are our key insights. Implementing a UDI-centric environment is a complex undertaking requiring integration of information systems, management processes, and clinical workflows involving leadership, inventory management, supply chain, clinical and billing teams. Implementation involves the domains of procedure documentation, electronic health records (EHRs), charge capture and billing, and interface and information technology systems, including information systems vendors. Replacing manual processes with electronic messages is not simply an exercise in programming information systems - successful execution requires orchestrated re-engineering of clinical and operational workflows. Our initiative resulted in a more efficient and effective supply chain, eliminated operational and clinical documentation errors, automated the posting of device implant data to the EHR, reduced clinician burden, improved charge capture, and produced a substantial financial benefit, with return on investment recognized in well under 1 year. We believe our stepwise approach to accomplishing a clinically integrated supply chain can serve as a roadmap for other healthcare enterprises to follow.

Abstract Image

医疗器械唯一标识符作为医疗企业的单一真相来源——临床一体化供应链实施路线图。
物资、设备和医疗器械的记录和跟踪对于安全、高效和有效的患者护理的业务、财务和临床方面至关重要。使用唯一设备标识符(UDI)的医疗器械标签通过使用UDI作为索引“真相来源”,创造了在卫生信息系统中紧密集成设备信息的机会。在杜克大学卫生系统的3家医院中,我们在心导管和电生理实验室中全面实施了基于udi的设备和供应信息管理。以下是我们的主要见解。实现以uddi为中心的环境是一项复杂的工作,需要集成信息系统、管理流程和涉及领导层、库存管理、供应链、临床和计费团队的临床工作流程。实现涉及程序文档、电子健康记录(EHRs)、收费捕获和计费以及接口和信息技术系统(包括信息系统供应商)等领域。用电子信息代替手工流程并不是简单的信息系统编程——成功的执行需要对临床和操作工作流程进行精心的重新设计。我们的举措带来了更高效和有效的供应链,消除了操作和临床文件错误,将器械植入数据自动发布到电子病历,减轻了临床医生的负担,改善了收费记录,并产生了可观的经济效益,在不到一年的时间内实现了投资回报。我们相信,我们逐步实现临床整合供应链的方法可以作为其他医疗保健企业效仿的路线图。
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来源期刊
Medical Devices-Evidence and Research
Medical Devices-Evidence and Research ENGINEERING, BIOMEDICAL-
CiteScore
2.80
自引率
0.00%
发文量
41
审稿时长
16 weeks
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