探索对遗传咨询学生开办的免费诊所的看法,将其作为一种创新的服务提供模式,以增加遗传咨询服务的可及性。

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY
Shayna Morgan, Clara Lajonchere, Michael Prelip, Christina G. S. Palmer
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引用次数: 0

摘要

代表性不足的群体缺乏获得遗传学服务的机会,这加剧了从精准医学进步中受益的人群之间的健康差距。在遗传咨询方面,学生开办的免费诊所(SRFCs)是解决这种医疗差距和提高健康公平性的一种创新方法。虽然文献中只报道了一家最近成立的遗传咨询 SRFC,但 SRFC 在护理、药学和物理治疗等其他健康专业学校中已有很长的历史,而且研究支持其为患者和学生带来的益处。本定性研究旨在探讨认证遗传咨询师(CGCs)和遗传咨询专业学生(GC students)对 SRFCs 作为一种创新服务模式的看法,以增加遗传咨询服务的可及性。研究人员对全美 10 名注册遗传咨询师和 10 名遗传咨询专业学生进行了半结构化 Zoom 访谈。他们就 SRFC 如何满足该领域的需求、创建和维护这些诊所的潜在挑战以及预期成果等问题向参与者提出了开放式问题。通过对访谈记录进行归纳主题分析,确定了三大主题:(1) SRFCs 可以互惠互利,因为与专业目标保持一致可能会为患者和学生带来积极的成果;(2) 学生的职责范围将因学生的能力而异,这与他们的培训时间表和所需的监督水平有关;(3) SRFCs 的成功实施和可持续发展需要在合作、基础设施支持、诊所运营、知名度和保护弱势群体等方面进行周到的规划。与会者认识到,通过扩大未参保和参保不足人群获得遗传咨询的机会,SRFC 有可能减少健康差异。实施 SRFCs 可以提高遗传咨询学生的培训质量,提供应用技能的机会,并获得与不同患者群体合作的经验。一个关键的次主题是,在从传统督导模式过渡的过程中,需要促进基因遗传学社区的支持。这项研究为进一步开发和实施遗传咨询 SRFC 提供了一个基础框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Exploring perceptions of genetic counseling student-run free clinics as an innovative service delivery model to increase access to genetic counseling services

Exploring perceptions of genetic counseling student-run free clinics as an innovative service delivery model to increase access to genetic counseling services

Underrepresented groups lack access to genetics services, heightening health disparities among those who benefit from advancements in precision medicine. An innovative approach to addressing this gap in care and increasing health equity in the context of genetic counseling is student-run free clinics (SRFCs). While only one recently established SRFC for genetic counseling is reported in the literature, SRFCs have a long-standing presence in other health professional schools, such as nursing, pharmacy and physical therapy, and research supports the benefits for patients and students. This qualitative study aims to explore the perspectives of certified genetic counselors (CGCs) and genetic counseling  students (GC students) regarding SRFCs as an innovative service delivery model to increase access to genetic counseling services. Semi-structured Zoom interviews were conducted with 10 CGCs and 10 GC students across the United States. Participants were asked open-ended questions about how SRFCs could meet needs of the field, potential challenges in creating and maintaining these clinics, and anticipated outcomes. Through abductive thematic analysis of interview transcripts, three main themes were identified: (1) SRFCs can be mutually beneficial as alignment with profession goals potentially leads to positive outcomes for patients and students; (2) student scope of duties will vary depending on student ability corresponding with their training timeline and level of required supervision; and (3) successful SRFC implementation and sustainability will require thoughtful planning regarding collaboration, infrastructure support, clinic operations, visibility, and protections for vulnerable groups. Participants recognized SRFCs' potential to reduce health disparities by expanding access to genetic counseling for uninsured and underinsured populations. Implementing SRFCs could enhance the quality of GC student training, providing opportunities to apply skills and gain experience working with diverse patient populations. A key subtheme was the need to foster support from the CGC community in transitioning from a traditional supervision model. This research provides a baseline framework from which to further develop and implement SRFCs for genetic counseling.

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来源期刊
Journal of Genetic Counseling
Journal of Genetic Counseling GENETICS & HEREDITY-
CiteScore
3.80
自引率
26.30%
发文量
113
审稿时长
6 months
期刊介绍: The Journal of Genetic Counseling (JOGC), published for the National Society of Genetic Counselors, is a timely, international forum addressing all aspects of the discipline and practice of genetic counseling. The journal focuses on the critical questions and problems that arise at the interface between rapidly advancing technological developments and the concerns of individuals and communities at genetic risk. The publication provides genetic counselors, other clinicians and health educators, laboratory geneticists, bioethicists, legal scholars, social scientists, and other researchers with a premier resource on genetic counseling topics in national, international, and cross-national contexts.
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