在电子病历中生成和实现以患者为中心和面向患者的基因组检测报告。

Jessica M Goehringer, Michele A Bonhag, Laney K Jones, Tara Schmidlen, Marci Schwartz, Alanna Kulchak Rahm, Janet L Williams, Marc S Williams
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引用次数: 15

摘要

背景:由于结果和报告的复杂性,遗传实验室结果与患者和提供者的沟通受到阻碍。这可能导致对结果的误解,造成不适当的护理。患者通常不会收到报告的副本,这可能导致误解。为了解决这些问题,我们进行了以患者为中心的研究,为解释性报告的设计提供信息。在这里,我们描述了一个特定的以患者为中心的临床决策支持(CDS)工具的开发和部署,这是一个多用途的以患者为中心的基因组测试报告(PGR),它与电子健康记录(EHR)接口。实施过程:使用本地开发的软件(COMPASS™)来管理安全数据交换和访问,配置了带有配套提供商报告的PGR,以便在EHR中实施。研究结果:我们对患者、家庭成员和临床医生进行了半结构化访谈,表明他们寻求明确的信息,包括研究结果、家庭影响、资源、预后和与基因组结果相关的下一步。提供者要求获得适用的、可用的临床指南。初步结果表明,患者和医疗服务提供者都认为PGR包含有用的、有价值的信息,并将为患者、医疗服务提供者和家庭之间的结果相关对话提供基础。主要主题:患者直接参与PGR确定的格式和表现偏好的设计和开发,并向患者和提供者提供相关信息,促进CDS工具的创建。结论:以患者为中心的CDS工具的研究和开发旨在支持改善患者的预后,通过患者早期和大量参与工具设计和开发的各个阶段,可以加强研究和开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Generation and Implementation of a Patient-Centered and Patient-Facing Genomic Test Report in the EHR.

Generation and Implementation of a Patient-Centered and Patient-Facing Genomic Test Report in the EHR.

Generation and Implementation of a Patient-Centered and Patient-Facing Genomic Test Report in the EHR.

Context: Communication of genetic laboratory results to patients and providers is impeded by the complexity of results and reports. This can lead to misinterpretation of results, causing inappropriate care. Patients often do not receive a copy of the report leading to possible miscommunication. To address these problems, we conducted patient-centered research to inform design of interpretive reports. Here we describe the development and deployment of a specific patient-centered clinical decision support (CDS) tool, a multi-use patient-centered genomic test report (PGR) that interfaces with an electronic health record (EHR).

Implementation process: A PGR with a companion provider report was configured for implementation within the EHR using locally developed software (COMPASS™) to manage secure data exchange and access.

Findings: We conducted semi-structured interviews with patients, family members, and clinicians that showed they sought clear information addressing findings, family implications, resources, prognosis and next steps relative to the genomic result. Providers requested access to applicable, available clinical guidelines. Initial results indicated patients and providers found the PGR contained helpful, valuable information and would provide a basis for result-related conversation between patients, providers and family.

Major themes: Direct patient involvement in the design and development of a PGR identified format and presentation preferences, and delivery of relevant information to patients and providers, prompting the creation of a CDS tool.

Conclusions: Research and development of patient-centered CDS tools designed to support improved patient outcomes, are enhanced by early and substantial engagement of patients in contributing to all phases of tool design and development.

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