遗传咨询师对在初级保健诊所试点整合一年期间所获经验、挑战和成功的反思。

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY Public Health Genomics Pub Date : 2023-01-01 Epub Date: 2023-06-12 DOI:10.1159/000530683
Prescilla B Carrion, Jehannine Austin, Alison M Elliott
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引用次数: 0

摘要

这篇与实践相关的见解文章介绍了遗传咨询师融入加拿大不列颠哥伦比亚省维多利亚市一家多学科初级保健诊所的经历,该诊所主要为边缘化患者群体提供医疗服务。遗传咨询师分享了在为期一年的试点整合过程中的经验教训,包括面临的挑战和取得的成功,并探讨了遗传咨询师融入初级保健诊所后可提供的潜在价值。探讨了临床遗传咨询实践与初级保健中文化安全和创伤知情方法之间的关系,并介绍了可采取的其他步骤,以促进服务不足和弱势患者群体更公平、更包容地获得遗传咨询服务。
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A Genetic Counselor's Reflections on Lessons Learned, Challenges, and Successes Experienced during a One-Year Pilot Integration in a Primary Care Clinic.

This practice-related insight article describes the experience of a genetic counselor being integrated into a multidisciplinary primary care clinic that provides care for a predominantly marginalized patient population in Victoria, British Columbia, Canada. Reflections on the lessons learned, including challenges and successes during this 1-year pilot integration are shared by the genetic counselor in the context of exploring the potential value a genetic counselor can provide while embedded in a primary care clinic. The relationship between clinical genetic counseling practice and a culturally safe and trauma-informed approach in primary care is explored, and additional steps are described that can be taken to facilitate more equitable and inclusive access to genetic counseling services for underserved and vulnerable patient populations.

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来源期刊
Public Health Genomics
Public Health Genomics 医学-公共卫生、环境卫生与职业卫生
CiteScore
2.90
自引率
0.00%
发文量
14
审稿时长
>12 weeks
期刊介绍: ''Public Health Genomics'' is the leading international journal focusing on the timely translation of genome-based knowledge and technologies into public health, health policies, and healthcare as a whole. This peer-reviewed journal is a bimonthly forum featuring original papers, reviews, short communications, and policy statements. It is supplemented by topic-specific issues providing a comprehensive, holistic and ''all-inclusive'' picture of the chosen subject. Multidisciplinary in scope, it combines theoretical and empirical work from a range of disciplines, notably public health, molecular and medical sciences, the humanities and social sciences. In so doing, it also takes into account rapid scientific advances from fields such as systems biology, microbiomics, epigenomics or information and communication technologies as well as the hight potential of ''big data'' for public health.
期刊最新文献
"The Biggest Struggle:" Navigating Trust and Uncertainty in Genetic Variant Interpretation. "Should I let them know I have this?": Multifaceted genetic discrimination and limited awareness of legal protections amongst individuals with hereditary cancer syndromes. Who's on your genomics research team? Consumer experiences from Australia. Development and Pilot Testing of Evidence-Based Interventions to Improve Adherence after Receiving a Genetic Result. Co-creating the experience of consent for newborn genome sequencing (The Generation Study).
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