"I Didn't Have to Worry about It": Patient and Family Experiences with Health System Involvement in Notifying Relatives of Genetic Test Results.

IF 1.3 4区 医学 Q4 GENETICS & HEREDITY
Public Health Genomics Pub Date : 2024-01-01 Epub Date: 2024-09-30 DOI:10.1159/000541532
Paula Rae Blasi, Jamilyn M Zepp, Aaron Scrol, John Ewing, Melissa L Anderson, James D Ralston, Stephanie M Fullerton, Kathleen Leppig, Nora B Henrikson
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引用次数: 0

Abstract

Introduction: In the USA, patients who undergo genetic testing for hereditary cancer risk are responsible for informing relatives about their genetic test results, but many relatives never find out they might be at risk. A health system-mediated relative notification program might help fill this gap, but questions remain about the acceptability of this approach.

Methods: We analyzed qualitative data from a single-arm, nonrandomized, mixed-methods study to understand how patients and families experienced a new health system-mediated relative notification program. We invited all study participants to participate in semi-structured telephone interviews at 6-8 weeks after return of genetic test results. We used a template analysis approach to thematically analyze interview transcripts.

Results: We interviewed 32 participants, including 17 probands and 15 relatives. Relatives reported positive experiences with the notification program, noting they felt in control of decisions and appreciated genetic counselor involvement in communicating the proband's test results. Benefits of direct contact included reduced burden for probands, increased family discussions about health, and notification of relatives who otherwise would not have learned results. No participants reported adverse effects from the program.

Conclusion: Overall, the relative notification program was acceptable to participants and supported probands in reaching at-risk relatives who otherwise might not have been notified. These findings could inform the implementation of future genetic risk family notification programs with the potential to improve uptake of cascade testing and advance cancer prevention and early detection efforts.

"我不必为此担心":患者和家属对医疗系统参与通知亲属基因检测结果的体验。
导言:在美国,接受遗传性癌症风险基因检测的患者有责任将基因检测结果告知亲属,但许多亲属从未发现自己可能有风险。以医疗系统为媒介的亲属通知计划可能有助于填补这一空白,但这种方法的可接受性仍存在问题:我们对一项单臂、非随机、混合方法研究的定性数据进行了分析,以了解患者和家属是如何体验一项新的以医疗系统为媒介的亲属通知计划的。我们邀请所有研究参与者在基因检测结果返回后 6-8 周参加半结构化电话访谈。我们采用模板分析法对访谈记录进行了专题分析:我们对 32 名参与者进行了访谈,其中包括 17 名准患者和 15 名亲属。亲属们报告了他们在通知项目中的积极体验,指出他们感觉自己能够控制决定,并感谢遗传咨询师参与告知遗嘱检验结果。直接联系的好处包括减轻了遗嘱人的负担,增加了家庭对健康问题的讨论,以及通知了原本不会得知结果的亲属。没有参与者报告该计划的不良影响:总的来说,亲属通知计划是可以被参与者接受的,并能帮助受试者联系到高风险亲属,否则这些亲属可能不会得到通知。这些发现可为未来遗传风险家庭通知计划的实施提供参考,并有可能提高级联检测的接受率,推进癌症预防和早期检测工作。
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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.
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