阿巴拉契亚会议系列的遗传服务。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Kimberly M. Kelly, Trupti Dhumal, Virginia G. Scott, Nadia Falah, Rebecca Kronk, Alissa Bovee Terry, Kristi Graves, Justine Pickarski, Margaret Au
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引用次数: 0

摘要

这项研究检查了作为七次网络研讨会系列的一部分产生的数据,该系列关注的是医疗服务不足的阿巴拉契亚农村地区的遗传学护理提供,并检查了这些服务如何适应具有挑战性的实践环境。审议了本地区护理的障碍和促进因素。数据包括注册者的基线调查、会议记录和会议反馈。我们使用顺序和并发混合方法分析数据。登记者(n = 137)是不成比例的具有遗传服务专业知识的医疗保健提供者(37.2%)。大约一半(43.8%)的注册人来自阿巴拉契亚中部地区的肯塔基州、西弗吉尼亚州和田纳西州。我们的基线调查发现,最明显的障碍是服务成本、缺乏提供者和获得护理的机会。最常见的促进因素是远程保健。对成绩单的分析确定了与基线调查中指出的一致的障碍,但讨论了额外的支持和网络机会,以允许跨服务学习。指出了提供服务的许多障碍;然而,尽管面临挑战,参与者还是发现了社区中的机会和资源。这些见解将为研究议程提供信息,旨在推进阿巴拉契亚农村的遗传学服务,应对挑战,并利用资产来改善医疗保健的获取和结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic Services in Appalachia Conference Series

This study examined the data generated as part of a seven-session webinar series that focused on genetics care provision in the medically underserved, rural Appalachian region and examined how these services have adapted to challenging practice environments. Barriers and facilitators to care in our region were considered. Data included a baseline survey of registrants, transcripts of sessions, and feedback about sessions. We analyzed data with a sequential and concurrent mixed methods approach. Registrants (n = 137) were disproportionately healthcare providers with genetic services expertise (37.2%). Approximately half (43.8%) of registrants were from KY, WV, and TN in the central Appalachian region. Our baseline survey found that the most noted barriers were the cost of services, lack of providers, and access to care. The most common facilitator was telehealth. Analysis of transcripts identified barriers that were consistent with those noted in the baseline survey, but additional support and network opportunities were discussed to allow for learning across services. Numerous barriers to service delivery were noted; however, despite challenges, participants identified opportunities and resources in the community. These insights will inform a research agenda aimed at advancing genetics services in rural Appalachia, addressing challenges, and leveraging assets for improved healthcare access and outcomes.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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