以人为本的方法优化Lynch综合征携带者的降低风险手术和阿司匹林决策辅助:一项有声思考访谈研究。

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY
Kelly Kohut, Kate Morton, Lesley Turner, Rebecca Foster, Elizabeth K Bancroft, John Burn, Emma J Crosbie, Mev Dominguez-Valentin, Mary Jane Esplen, Helen Hanson, Karen Hurley, Pål Moller, Neil Ryan, Katie Snape, Diana Eccles, Claire Foster
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引用次数: 0

摘要

林奇综合征“携带者”携带一种种系致病变异,使基因、性别和器官特异性的癌症风险增加。在他们的一生中,他们面临着困难的、相互关联的选择。该研究是共同设计健康干预项目Lynch Choices™https://canchoose.org.uk的一部分,该项目为携带者、其家庭成员和临床医生提供信息中心和决策支持。本研究旨在回答研究问题:基因癌症风险管理决策辅助的哪些内容、框架和设计元素对Lynch综合征携带者很重要?成年携带者被邀请参加一个有声思考访谈,听取他们对包含价值观澄清练习的Lynch Choices™原型版本的想法。前半部分的访谈集中在妇科降低风险的手术,后半部分集中在阿司匹林的决策辅助。20名携带者(8名男性)接受了采访,其中一半有个人癌症病史。Lynch Choices™内容和设计的迭代改进在访谈之间完成,使用基于人的方法的透明更改表。访谈之后,反身性专题分析应用于整个定性数据集。构建了三个主题,以指导进一步优化,并为临床实践中改进癌症风险沟通提出建议。三个主题是:(1)解释基因特异性癌症风险和“这对我意味着什么?”措辞很重要:谨慎的措辞对于感觉被理解很重要;(3)辅助决策:它们可以提供帮助,但可能会引发情绪。有声思考访谈提供了对携带者心理社会背景的深入了解。这种明智的决策优化有助于支持参与并促进与医疗保健专业人员的共享决策。从这项研究中学习到的知识除了决策辅助开发之外,还具有更广泛的意义,可以理解关于遗传癌症风险沟通和决策支持的偏好、需求和经验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Optimizing risk-reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person-based approach: A think-aloud interview study.

Optimizing risk-reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person-based approach: A think-aloud interview study.

Optimizing risk-reducing surgery and aspirin decision aids for Lynch syndrome carriers using the person-based approach: A think-aloud interview study.

Lynch syndrome "carriers" carry a germline pathogenic variant conferring gene-, sex-, and organ-specific increased cancer risks. They are presented with difficult, interrelated choices over their lifetime. This study was part of a larger project to codesign a health intervention, Lynch Choices™ https://canchoose.org.uk to provide an information hub and decision support for carriers, their family members, and clinicians. This study aimed to answer the research question: What content, framing, and design elements of a decision aid for genetic cancer risk management are important to Lynch syndrome carriers? Adult carriers were invited to a think-aloud interview to hear their thoughts about a prototype version of Lynch Choices™ containing values-clarification exercises. The first half of interviews focused on the gynecological risk-reducing surgery and the second half on the aspirin decision aid. Twenty carriers (eight men) were interviewed, half of whom had a personal history of cancer. Iterative refinement of Lynch Choices™ content and design was completed between interviews using a transparent table of changes from the person-based approach. Following the interviews, reflexive thematic analysis was applied to the entire qualitative dataset. Three themes were constructed to guide further optimization and make recommendations for improved cancer risk communication in clinical practice. The three themes were: (1) Interpreting gene-specific cancer risks and "What does it mean to me?"; (2) Words matter: Careful phrasing is important to feel understood; (3) Decision aids: They can help but might trigger emotions. Think-aloud interviews provided in-depth insight into the psychosocial context of carriers. This informed optimization of the decision aid to support engagement and promote shared decision making with healthcare professionals. The learning from this study had broader implications beyond decision aid development, to understanding preferences, needs, and experiences regarding genetic cancer risk communication and decision support.

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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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