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Adolescent engagement during assent for exome sequencing

机译:在exame测序的同意期间青少年接合

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Background: Research focused on describing the content of informed consent interactions has shed little light on how to best to encourage, support, and nurture adolescent participation in genomic sequencing. Research addressing adolescents' comprehension and agency is needed because sequencing may have significant implications for an adolescent's own future health status, as well as for other members of the adolescent's family. This article explores adolescent participation and decision making during informed consent for exome sequencing. Methods: Investigators recruited 25 adolescents with unexplained hearing loss, cardiac arrhythmias, mitochondria! disease, or neurodevelopmental disorders from an urban teaching and research hospital for participation in a research project offering whole exome sequencing. Twenty-five adolescents ages 12-19 years and their parents completed informed consent sessions with study clinicians lasting up to 90 minutes. Sessions were digitally recorded, transcribed, and analyzed using grounded theory's "constant comparative" method. Results: Adolescent participants were briefly active when asked direct questions. Otherwise, they stayed mostly quiet. Parents functioned as protectors and information holders. Clinicians used proscriptive language to direct families to consider adolescents' preferences, to balance the interests of multiple caregivers, and to give families time to consider their options before making decisions. In two cases of significant family disagreement, providers maintained a nondirective stance toward all parties and excused themselves from the intense discussion by deferring decisions to a later date. Conclusions: Conventional approaches to informed consent may be insufficient to the risks, benefits, and possibilities offered by genomic sequencing. Rather than target autonomy, enhancing the agency of adolescents in decision making may more appropriately address their needs so that all stakeholders provide input and are respected throughout the informed consent process.
机译:背景:研究重点是描述知情同意互动的内容对如何最好地鼓励,支持和培养青少年参与基因组测序来阐明。需要研究涉及青少年的理解和机构,因为测序可能对青少年未来的健康状况以及青少年家庭的其他成员具有重大影响。本文探讨了在exome序列的知情同意期间的青少年参与和决策。方法:调查人员招募了25名青少年,具有无法解释的听力丧失,心脏心律失常,线粒体!来自城市教学和研究医院的疾病,或神经发育障碍参与研究项目,提供全面exome测序。二十五岁的青少年12-19岁及其父母完成了知情同意会,研究临床医生最多90分钟。使用接地理论的“常数比较”方法进行数字记录,转录和分析会话。结果:当询问直接问题时,青少年参与者短暂积极。否则,他们大多保持安静。家长作为保护者和信息持有人发挥作用。临床医生使用披露语言来指导家庭考虑青少年的偏好,以平衡多个护理人员的利益,并在做出决定之前给家庭时间考虑他们的选择。在两个重要的家庭分歧的案例中,提供者对所有缔约方保持着一种非展望的立场,并通过推迟到以后的决定,从激烈的讨论中解除自我讨论。结论:对知情同意的常规方法可能不足以基因组测序提供的风险,福利和可能性。在决策中加强青少年的机构而不是目标自治可能会更适当地解决他们的需求,以便所有利益相关者提供投入,并在整个知情同意过程中尊重。

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