Department of Bioethics, The Hospital for Sick Children, Toronto, Canada.
Holland Bloorview Kids Rehabilitation Hospital, University of Toronto, Toronto, Canada.
J Med Ethics. 2017 Aug;43(8):535-539. doi: 10.1136/medethics-2016-103564. Epub 2016 Nov 25.
To better understand the consequences of returning whole genome sequencing (WGS) results in paediatrics and facilitate its evidence-based clinical implementation, we studied parents' experiences with WGS and their preferences for the return of adult-onset secondary variants (SVs)-medically actionable genomic variants unrelated to their child's current medical condition that predict adult-onset disease.
We conducted qualitative interviews with parents whose children were undergoing WGS as part of the SickKids Genome Clinic, a research project that studies the impact of clinical WGS on patients, families, and the healthcare system. Interviews probed parents' experience with and motivation for WGS as well as their preferences related to SVs. Interviews were analysed thematically.
Of 83 invited, 23 parents from 18 families participated. These parents supported WGS as a diagnostic test, perceiving clear intrinsic and instrumental value. However, many parents were ambivalent about receiving SVs, conveying a sense of self-imposed obligation to take on the 'weight' of knowing their child's SVs, however unpleasant. Some parents chose to learn about adult-onset SVs for their child but not for themselves.
Despite general enthusiasm for WGS as a diagnostic test, many parents felt a duty to learn adult-onset SVs. Analogous to 'inflicted insight', we call this phenomenon 'inflicted ought'. Importantly, not all parents of children undergoing WGS view the best interests of their child in relational terms, thereby challenging an underlying justification for current ACMG guidelines for reporting incidental secondary findings from whole exome and WGS.
为了更好地了解儿科全基因组测序(WGS)结果返还的后果,并促进其基于证据的临床实施,我们研究了父母对 WGS 的经验及其对成人发病的次要变体(SVs)-与子女当前病情无关但可预测成人发病疾病的可操作基因组变体的返回偏好。
我们对正在接受 WGS 的儿童的父母进行了定性访谈,这些儿童是 SickKids 基因组诊所的一部分,该研究项目研究了临床 WGS 对患者、家庭和医疗保健系统的影响。访谈探讨了父母对 WGS 的体验和动机,以及与 SVs 相关的偏好。访谈进行了主题分析。
在 83 名受邀者中,有 18 个家庭的 23 名父母参与了研究。这些父母支持 WGS 作为一种诊断测试,认为其具有明显的内在和工具价值。然而,许多父母对接受 SVs 感到矛盾,他们感到有一种自我强加的义务,即承担了解孩子 SVs 的“重担”,无论多么不愉快。一些父母选择为孩子了解成人发病的 SVs,但不为自己了解。
尽管普遍对 WGS 作为诊断测试感到热情,但许多父母感到有责任了解成人发病的 SVs。类似于“强加的洞察力”,我们称这种现象为“强加的应该”。重要的是,并非所有接受 WGS 的儿童的父母都将孩子的最佳利益视为关系性的,从而对当前 ACMG 指南报告全外显子组和 WGS 偶然次要发现的指导原则提出了挑战。