Understanding the psychological impact of identifying carrier status on young adults: A qualitative study exploring peer reactions.

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY Journal of Genetic Counseling Pub Date : 2024-04-26 DOI:10.1002/jgc4.1903
Edie Bowen, John Langston, Harriet Fletcher, Julia Domek, Fiona Ulph
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Abstract

The benefits and harms of identifying carriers in childhood have long been debated with European Guidelines advising against this practice. Yet over a thousand carriers are identified via newborn bloodspot screening per year in the United Kingdom alone. One of the concerns about identification is the impact it has on an individual's identity. This, in part, will be determined by how parents and peers view carriers, particularly during young adulthood. To address the paucity of research looking at how carriers are perceived by peers, this study sought to explore the views of young adults, who themselves are not carriers, toward carriers. As the narratives around COVID-19 increased, the salience of the term "carrier", the impact of such narratives on perceptions, was also explored. Twenty-five 18-25 year olds participated in a diary-interview study in the United Kingdom during 2021 to explore their perceptions of carriers via hypothetical scenarios. Data were analyzed using thematic analysis. Interviewees believed carriers would experience stigma-including societal and self-stigma. This was because people used existing illness beliefs to make sense of carrier status about which they had low levels of understanding. Interviewees believed carriers would experience challenges in familial and romantic relationships due to others' judgments. They also believed parents of carriers would experience a burden around making reproductive decisions, with clear views on what society would view as acceptable choices. Importantly interviewees felt knowledge of ones' own carrier status conferred complex communication challenges within relationships. These findings suggest an urgent need for more research and support for young adults entering a key stage in life for identity formation who have knowledge of their carrier status. The results suggest that support targeted toward the carrier regarding navigating complex communication and targeted more broadly to avoid stigma based on misunderstanding should be researched and developed.
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了解确认携带者身份对青少年的心理影响:探索同伴反应的定性研究。
长期以来,人们一直在争论在儿童期发现病毒携带者的利弊,欧洲指南也建议不要这样做。然而,仅在英国,每年就有一千多名携带者通过新生儿血斑筛查被识别出来。对身份识别的担忧之一是它对个人身份的影响。这在一定程度上取决于父母和同龄人对携带者的看法,尤其是在青年时期。针对同龄人如何看待携带者的研究较少这一问题,本研究试图探讨本身不是携带者的年轻人对携带者的看法。随着有关 COVID-19 的报道越来越多,"携带者 "一词的显著性以及此类报道对人们看法的影响也被纳入了研究范围。2021 年期间,25 名 18-25 岁的年轻人在英国参加了一项日记访谈研究,通过假设情景探讨他们对携带者的看法。研究采用主题分析法对数据进行了分析。受访者认为携带者会遭受污名化,包括社会和自我污名化。这是因为人们利用现有的疾病观念来理解携带者身份,而他们对携带者身份的理解程度很低。受访者认为,由于他人的判断,携带者在家庭和恋爱关系中会遇到挑战。他们还认为,携带者的父母在做出生育决定时会有负担,因为他们不清楚社会认为哪些选择是可以接受的。重要的是,受访者认为了解自己的携带者身份会给人际交往带来复杂的挑战。这些研究结果表明,对于进入人生中身份形成关键阶段的、知道自己携带者身份的年轻人来说,迫切需要更多的研究和支持。研究结果表明,应研究和开发针对携带者的支持服务,帮助他们驾驭复杂的沟通方式,并在更大范围内避免因误解而产生的耻辱感。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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