开发一个实时注册系统来跟踪整个波士顿市的乳腺癌患者。

IF 3.4 Q2 HEALTH CARE SCIENCES & SERVICES
JAMIA Open Pub Date : 2025-09-29 eCollection Date: 2025-10-01 DOI:10.1093/jamiaopen/ooaf099
Amy M LeClair, Clara A Chen, Marisa L Mizzoni, William G Adams, William F Harvey, Christopher W Shanahan, Jennifer S Haas, Stephenie C Lemon, Tracy Battaglia, Karen M Freund
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引用次数: 0

摘要

目的:患者导航旨在识别和解决患者在整个癌症治疗过程中的需求。在旨在提供标准化患者导航协议的临床试验的背景下,需要一个注册表,以允许来自多个卫生系统的用户输入患者数据,跟踪导航扩展,并实时协调癌症护理。设计一个注册表,使4个卫生系统的6个医疗中心的患者导航员(PNs)能够跟踪被确定为最有可能延迟治疗的乳腺癌患者。材料和方法:一个多学科团队选择REDCap作为注册中心。其目的是开发一个平台,该平台将(1)管理最容易受到延误的患者;(2)通过连续的癌症治疗实时跟踪患者;(3)允许执业医师优先考虑某些患者;(4)便于系统间通信;(5)允许研究团队监控导航员的活动(在研究研究的背景下,进行监督和反馈)。结果:通过与临床提供者、PNs、信息学专家和REDCap团队的专家开发人员合作,使用软件标准特性并使用SAS编程合并其他功能,构建了该注册表。结论:REDCap提供了一个可访问且可修改的平台,用于托管注册表以实时跟踪患者。然而,它并没有像预期的那样简化pn的工作流程或减少数据输入负担。一个主要的障碍是缺乏与现有系统导航器的互操作性,这导致了冗余并增加了文档的负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Developing a real-time registry to track breast cancer patients across the city of Boston.

Developing a real-time registry to track breast cancer patients across the city of Boston.

Developing a real-time registry to track breast cancer patients across the city of Boston.

Developing a real-time registry to track breast cancer patients across the city of Boston.

Objectives: Patient navigation is designed to identify and address patients' needs throughout their cancer treatment. In the context of a clinical trial designed to deliver a standardized patient navigation protocol, a registry was needed to allow users from across multiple health systems to input patient data, track navigation outreach, and coordinate cancer care in real time. To design a registry to allow patient navigators (PNs) at 6 medical centers across 4 health systems to track breast cancer patients determined to be most at risk for delays in treatment.

Materials and methods: A multi-disciplinary team chose REDCap to host the registry. The aim was to develop a platform that would (1) manage a caseload of patients who are most vulnerable for delays; (2) track patients through the continuum of cancer care in real time; (3) allow PNs to prioritize certain patients; (4) facilitate inter-system communication; and (5) allow the research team to monitor navigators' activities (in context of a research study, for supervision and feedback).

Results: The registry was built through collaboration with clinical providers, PNs, informatics specialists, and expert developers from the REDCap team, using the software standard features and incorporating additional functionality using SAS programming.

Conclusion: REDCap provided an accessible and modifiable platform for hosting a registry to track patients in real time. However, it did not streamline PNs' workflows or reduce data entry burdens as intended. A major barrier was the lack of interoperability with pre-existing systems navigators use, which led to redundancy and increased the burden of documentation.

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来源期刊
JAMIA Open
JAMIA Open Medicine-Health Informatics
CiteScore
4.10
自引率
4.80%
发文量
102
审稿时长
16 weeks
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