亨廷顿氏病的预测性基因检测:探索参与者在门诊预约之间的不确定性和矛盾体验。

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY
L M Ballard, S Doheny, R Dimond, A M Lucassen, A J Clarke
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引用次数: 0

摘要

矛盾和不确定性是贯穿医疗保健心理学文献的关键主题。对于亨廷顿氏病(HD)的高危人群来说,尤其如此,因为目前还没有任何治疗方法可以改变疾病的进展,所以他们在考虑是否要进行基因检测。更好地了解做出基因预测决定的经历将有助于从业人员在这一过程中为患者提供支持和指导。我们的目的是捕捉参与者在基因咨询预约间隙的不确定性和矛盾体验。我们通过英格兰和威尔士四个地区遗传学服务机构转介进行预测性 HD 检测的九名参与者的经历来探讨这些问题。数据包括门诊咨询录音、日记以及在检测过程结束时进行的深入访谈。对数据进行了专题分析。确定了四个主题,分别代表四种可能的未来,每种未来都取决于接受检测的决定和检测的结果。我们的结果表明,参与者除了更多地关注代表他们目前没有接受预测性检测的未来,也更多地关注预测性检测结果呈阳性且症状已经开始的遥远未来。参加者较少关注检测后两个更直接的未来(得到阳性结果但症状尚未开始的未来和得到阴性结果的未来)。日记的使用让我们对参与者的矛盾和不确定性体验、心理困扰和情感负担有了独特的了解。这些发现有助于为门诊中的讨论提供信息,并鼓励研究人员考虑将日记作为一种方法,用于探索个人在门诊之外的情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predictive genetic testing for Huntington's disease: Exploring participant experiences of uncertainty and ambivalence between clinic appointments.

Ambivalence and uncertainty are key themes throughout the psychology of healthcare literature. This is especially so for individuals at risk of Huntington's disease (HD) deliberating the decision to undergo genetic testing because there is currently no treatment that modifies disease progression. A better understanding of the experience of making a decision about genetic prediction will help practitioners support and guide individuals through this process. Our aim was to capture participants' experiences of uncertainty and ambivalence in between their genetic counseling appointments. We explored these issues through the experiences of nine participants who were referred for predictive HD testing at four regional genetics services in England and Wales. Data consisted of recordings of clinic consultations, diaries, and an in-depth interview conducted at the end of the testing process. Data were analyzed thematically. Four themes were identified representing four possible futures, each future dependent on the decision to undergo testing and the result of that test. Our results showed that participants, as well as attending more to a future that represents their current situation of not having undergone predictive testing, also attended more to a distant future where a positive predictive result is received and symptoms have started. Participants attended less to the two futures that were more immediate once testing was undertaken (a future where a positive result is received and symptoms have not started and a future where a negative result is received). The use of diaries gave us a unique insight into these participants' experiences of ambivalence and uncertainty, psychological distress, and the emotional burden experienced. These findings help inform discussions within the clinic appointment as well as encourage researchers to consider diary use as a method of exploring what happens for individuals outside of clinical encounters.

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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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