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由一名初级保健医生倡导者管理的临床遗传学电子咨询服务的流程与结果。

Processes and outcomes from a clinical genetics e-consultation service managed by a primary care physician champion.

作者信息

Kerman Benjamin J, Zawatsky Carrie B L, Fieg Elizabeth, Frank Natasha Y, Donnelly Roseann S, Green Robert C, Kennedy John C, Lakdawala Neal, Licurse Adam M, Perez Emma F, Preys Charlene L, Krier Joel B, Rana Huma Q, Zettler Bethany, Vassy Jason L

机构信息

Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA.

Harvard Medical School, Boston, MA.

出版信息

Genet Med Open. 2024 Feb 21;2:101831. doi: 10.1016/j.gimo.2024.101831. eCollection 2024.

Abstract

PURPOSE

Timely access to clinical genetics consultations remains a barrier to timely genomic medicine services, which new service delivery models might help address.

METHODS

We implemented a genetics electronic consultation (eConsult) service staffed by a primary care physician (PCP) champion, supervised by genetics specialists. Chart reviews from July 2018 to January 2022 examined categories of questions received, e-consultant's recommendations, and outcomes of any conventional genetics referrals. Providers were surveyed on likelihood of ordering a conventional genetics consultation before eConsult and satisfaction with eConsult responses.

RESULTS

Conventional genetics consultation was recommended for 338 out of 462 (73%) eConsults received, among whom 254 out of 338 (75%) had an order placed for a conventional consult by the provider requesting the eConsult. Among all 462 eConsults, including in cases which conventional consult was not recommended, 279 (60%) were referred for conventional genetics consultation, of which 171 out of 279 (61%) completed a consult. Of these, 122 out of 171 (71%) were recommended for genetic testing, and 84 out of 122 (69%) completed testing. The genetic testing of 23 out of 84 (27%) patients identified informative actionable findings. Supervising genetics specialists made substantive revisions to PCP draft responses for only 8% (36/462) of eConsults.

CONCLUSION

This case series demonstrates that a PCP champion eConsult model can feasibly triage and respond to genetics questions with PCP-relevant content and yield high provider satisfaction. Such a model warrants further evaluation as an addition to the genetic services of health care systems.

摘要

目的

及时获得临床遗传学咨询仍然是及时提供基因组医学服务的障碍,新的服务提供模式可能有助于解决这一问题。

方法

我们实施了一项遗传学电子咨询(eConsult)服务,由一名初级保健医生(PCP)倡导者负责,并由遗传学专家监督。对2018年7月至2022年1月的病历审查,检查了收到的问题类别、电子咨询师的建议以及任何常规遗传学转诊的结果。对提供者进行了调查,了解他们在使用eConsult之前订购常规遗传学咨询的可能性以及对eConsult回复的满意度。

结果

在收到的462次eConsult中,有338次(73%)被建议进行常规遗传学咨询,其中338次中有254次(75%)由请求eConsult的提供者下达了常规咨询订单。在所有462次eConsult中,包括那些不建议进行常规咨询的病例,有279次(60%)被转诊进行常规遗传学咨询,其中279次中有171次(61%)完成了咨询。在这些病例中,171次中有122次(71%)被建议进行基因检测,122次中有84次(69%)完成了检测。84名患者中有23名(27%)的基因检测发现了有意义的可采取行动的结果。遗传学专家监督员仅对8%(36/462)的eConsult中初级保健医生的回复草案进行了实质性修订。

结论

这个病例系列表明,由初级保健医生倡导的eConsult模式可以切实可行地对遗传学问题进行分类,并以与初级保健医生相关的内容做出回应,从而获得较高的提供者满意度。作为医疗保健系统遗传服务的补充,这种模式值得进一步评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98cc/11613873/5f347471f556/gr1.jpg

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