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初级保健医生使用与电子健康记录集成的临床决策支持的家庭健康史工具的经验:一项实施过程评估。

Primary care physician experiences utilizing a family health history tool with electronic health record-integrated clinical decision support: an implementation process assessment.

作者信息

Lemke Amy A, Thompson Jennifer, Hulick Peter J, Sereika Annette W, Johnson Christian, Oshman Lauren, Dunnenberger Henry M

机构信息

Mark R. Neaman Center for Personalized Medicine, NorthShore University HealthSystem, 1001 University Place, Suite 160, Evanston, IL, 60201, USA.

Center for Medical Genetics, NorthShore University HealthSystem, 1000 Central Street, Suite 610, Evanston, IL, 60201, USA.

出版信息

J Community Genet. 2020 Jul;11(3):339-350. doi: 10.1007/s12687-020-00454-8. Epub 2020 Feb 4.

Abstract

Family health history (FHH) screening plays a key role in disease risk identification and tailored disease prevention strategies. Primary care physicians (PCPs) are in a frontline position to provide personalized medicine recommendations identified through FHH screening; however, adoption of FHH screening tools has been slow and inconsistent in practice. Information is also lacking on PCP facilitators and barriers of utilizing family history tools with clinical decision support (CDS) embedded in the electronic health record (EHR). This study reports on PCPs' initial experiences with the Genetic and Wellness Assessment (GWA), a patient-administered FHH screening tool utilizing the EHR and CDS. Semi-structured interviews were conducted with 24 PCPs who use the GWA in a network of community-based practices. Four main themes regarding GWA implementation emerged: benefits to clinical care, challenges in practice, CDS-specific issues, and physician-recommended improvements. Sub-themes included value in improving patient access to genetic services, inadequate time to discuss GWA recommendations, lack of patient follow-through with recommendations, and alert fatigue. While PCPs valued the GWA's clinical utility, a number of challenges were identified in the administration and use of the GWA in practice. Based on participants' recommendations, iterative changes have been made to the GWA and workflow to increase efficiency, upgrade the CDS process, and provide additional education to PCPs and patients. Future studies are needed to assess a diverse sample of physicians' and patients' perspectives on the utility of FHH screening utilizing EHR-based genomics recommendations.

摘要

家族健康史(FHH)筛查在疾病风险识别和量身定制的疾病预防策略中起着关键作用。初级保健医生(PCP)处于一线位置,能够提供通过FHH筛查确定的个性化医疗建议;然而,FHH筛查工具在实践中的采用一直缓慢且不一致。关于初级保健医生在电子健康记录(EHR)中嵌入临床决策支持(CDS)来使用家族史工具的促进因素和障碍的信息也很缺乏。本研究报告了初级保健医生使用遗传与健康评估(GWA)的初步经验,GWA是一种患者自主管理的FHH筛查工具,利用了EHR和CDS。对在社区实践网络中使用GWA的24名初级保健医生进行了半结构化访谈。出现了关于GWA实施的四个主要主题:对临床护理的益处、实践中的挑战、CDS特定问题以及医生建议的改进。子主题包括改善患者获得遗传服务的价值、讨论GWA建议的时间不足、患者对建议的后续跟进不足以及警报疲劳。虽然初级保健医生重视GWA的临床效用,但在实践中GWA的管理和使用方面发现了一些挑战。根据参与者的建议,已对GWA和工作流程进行了迭代更改,以提高效率、升级CDS流程,并为初级保健医生和患者提供额外教育。未来需要开展研究,以评估医生和患者对利用基于EHR的基因组学建议进行FHH筛查效用的不同观点。

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Family health history: underused for actionable risk assessment.家族健康史:在可操作的风险评估中未得到充分利用。
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