Exploring preferences and support needs for disclosing 47, XXY status: A qualitative study of adults with XXY.

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY
Cassandra Oeckinghaus, Kimberly Zayhowski, Kayla Horowitz, Darius Haghighat
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引用次数: 0

Abstract

There are minimal guidelines regarding the disclosure of XXY, otherwise called Klinefelter syndrome, in healthcare or within the family. The increased use of cell-free DNA (cfDNA) to screen for fetal aneuploidy and sex chromosomes bolsters the importance of providing genetic counselors, other healthcare professionals (HCPs), and parents with XXY-led disclosure information. The aim of this qualitative study was to discern the preferences of adults of XXY in the disclosure of XXY status across the lifespan to best inform the clinical and social aspects of their care. Fifteen semi-structured interviews were conducted with adults with XXY to gain their perspective on healthcare and support needs, the impact their care has had on their perception and acceptance of XXY, as well as their disclosure preferences across age groups. Interviews were coded and analyzed using reflexive thematic analysis through a social constructivist lens, from which four themes were generated: (1) lack of support within the healthcare system affects quality of care; (2) stigma and shame impacts XXY individuals' decisions to disclose information to others; (3) communication of XXY genetic results to children should be thoughtful and age-appropriate; and (4) attention to psychosocial needs is integral to comprehensive care. Novel findings of this study, which include the detrimental impacts of negative disclosure experiences on relationships with HCPs and self-identity, underscore specific clinical and social support needs for individuals with XXY. This study highlights the need for specialized support across one's lifespan, particularly within interdisciplinary clinics staffed by HCPs knowledgeable about the overall health of individuals with XXY. Participants stress the importance of empathetic delivery of XXY status and discussions on sex and gender to mitigate shame and stigma. Advocating for ongoing support services, including referrals to specialists and mental health resources, participants also endorse a personalized approach to childhood disclosure by parents, or in collaboration with HCPs, aiming to preserve trust, empower the child, and consider their maturity level. This study emphasizes the importance of providing tailored support to individuals with XXY, prioritizing informed decision-making, emotional well-being, and holistic care.

探索披露 47、XXY 状态的偏好和支持需求:对患有 XXY 的成年人的定性研究。
关于在医疗保健或家庭中披露 XXY(又称 Klinefelter 综合征)的指导原则少之又少。由于越来越多地使用无细胞 DNA(cfDNA)来筛查胎儿非整倍体和性染色体,因此向遗传咨询师、其他医疗保健专业人员(HCPs)和父母提供以 XXY 为主导的披露信息就显得尤为重要。这项定性研究旨在了解 XXY 成年人在整个生命周期中披露 XXY 状况的偏好,以便为他们的临床和社会护理提供最佳信息。研究人员对患有 XXY 的成年人进行了 15 次半结构式访谈,以了解他们对医疗保健和支持需求的看法、护理对他们对 XXY 的认知和接受程度产生的影响,以及他们在不同年龄段对披露信息的偏好。通过社会建构主义视角,采用反思性主题分析法对访谈进行了编码和分析,并从中产生了四个主题:(1)医疗保健系统内缺乏支持会影响护理质量;(2)耻辱感和羞耻感会影响 XXY 患者向他人披露信息的决定;(3)与儿童沟通 XXY 遗传结果时应考虑周到并与年龄相适应;以及(4)关注社会心理需求是全面护理不可或缺的一部分。本研究的新发现包括负面信息披露经历对与 HCPs 关系和自我认同的不利影响,强调了 XXY 患者在临床和社会支持方面的特殊需求。这项研究强调了在人的一生中需要专门的支持,尤其是在由了解 XXY 患者整体健康的保健医生组成的跨学科诊所中。参与者强调了以感同身受的方式告知 XXY 状态以及讨论性和性别以减轻羞耻感和耻辱感的重要性。参与者提倡提供持续的支持服务,包括转介到专家和心理健康资源,他们还赞同由父母或与保健医生合作,采用个性化的方法来披露儿童的情况,目的是维护信任、增强儿童的能力并考虑到他们的成熟程度。这项研究强调了为 XXY 患者提供量身定制的支持的重要性,并将知情决策、情感健康和整体护理放在了首位。
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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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