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本文引用的文献

1
'It's a nightmare': informed consent in paediatric genome-wide sequencing. A qualitative expert interview study from Germany and Switzerland.“这是一场噩梦”:儿科全基因组测序中的知情同意。来自德国和瑞士的定性专家访谈研究。
Eur J Hum Genet. 2023 Dec;31(12):1398-1406. doi: 10.1038/s41431-023-01468-9. Epub 2023 Sep 29.
2
Whole genome sequencing diagnostic yield for paediatric patients with suspected genetic disorders: systematic review, meta-analysis, and GRADE assessment.疑似遗传疾病儿科患者的全基因组测序诊断率:系统评价、荟萃分析和GRADE评估
Arch Public Health. 2023 May 25;81(1):93. doi: 10.1186/s13690-023-01112-4.
3
Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study.参与 10 万基因组计划中罕见病基因组测序的体验:一项混合方法研究。
Eur J Hum Genet. 2022 May;30(5):604-610. doi: 10.1038/s41431-022-01065-2. Epub 2022 Mar 9.
4
Informed consent practices for exome sequencing: An interview study with clinical geneticists in the Netherlands.外显子组测序知情同意实践:荷兰临床遗传学家的访谈研究。
Mol Genet Genomic Med. 2022 Mar;10(3):e1882. doi: 10.1002/mgg3.1882. Epub 2022 Feb 11.
5
The long-term impact of receiving incidental findings on parents undergoing genome-wide sequencing.接受全基因组测序的父母所受意外发现的长期影响。
J Genet Couns. 2022 Aug;31(4):887-900. doi: 10.1002/jgc4.1558. Epub 2022 Feb 6.
6
Return of individual research results from genomic research: A systematic review of stakeholder perspectives.基因组研究中个体研究结果的返还:利益相关者观点的系统评价。
PLoS One. 2021 Nov 8;16(11):e0258646. doi: 10.1371/journal.pone.0258646. eCollection 2021.
7
Lessons learned from unsolicited findings in clinical exome sequencing of 16,482 individuals.从 16482 例临床外显子组测序中的意外发现中吸取的经验教训。
Eur J Hum Genet. 2022 Feb;30(2):170-177. doi: 10.1038/s41431-021-00964-0. Epub 2021 Oct 25.
8
Parental experiences of rapid exome sequencing in cases with major ultrasound anomalies during pregnancy.父母在胎儿孕期出现主要超声异常时对快速外显子组测序的体验。
Prenat Diagn. 2022 May;42(6):762-774. doi: 10.1002/pd.6056. Epub 2021 Oct 22.
9
Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression.参与美国新生儿基因组测序试验对有抑郁风险的父母的影响。
J Genet Couns. 2022 Feb;31(1):218-229. doi: 10.1002/jgc4.1475. Epub 2021 Jul 26.
10
After genomic testing results: Parents' long-term views.基因检测结果出来后:家长的长远看法。
J Genet Couns. 2022 Feb;31(1):82-95. doi: 10.1002/jgc4.1454. Epub 2021 Jun 24.

抱有希望,但不要期望过高?比较父母在对孩子进行外显子组测序诊断后披露结果前后的态度。

Hope, but never expect? Comparing parents' pre- and post-disclosure attitudes toward return of results from diagnostic exome sequencing for their child.

机构信息

Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

Department of Medical Humanities, Julius Center, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

Mol Genet Genomic Med. 2024 Mar;12(3):e2341. doi: 10.1002/mgg3.2341. Epub 2024 Feb 17.

DOI:10.1002/mgg3.2341
PMID:38366804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10958177/
Abstract

BACKGROUND

Counseling for whole-exome sequencing (WES) could benefit from aligning parents' pre- and post-disclosure attitudes. A few studies have qualitatively compared parents' pre- and post-disclosure attitudes toward receiving WES results for their child in a diagnostic setting. This study explored these attitudes in the context of children with a developmental delay.

METHODS

Semi-structured interviews were conducted with parents (n = 27) of 16 children undergoing diagnostic WES in trio-analysis, both before and after receiving results.

RESULTS

Three key insights emerged. First, the distinction between hoping and expecting was relevant for shaping parents' experiences with receiving results related to the primary indication. Second, parents of young children whose development of autonomous capacities was uncertain sometimes found themselves in a situation resembling a Catch-22 when confronted with decisions about unsolicited findings (UFs): an important reason for consenting to WES was to gain a better picture of how the child might develop, but in order to make responsible choices about UFs, some ideas of their child's development is needed. Third, default opt-ins and opt-outs helped parents fathom new kinds of considerations for accepting or declining UFs in different categories, thereby aiding decision-making.

CONCLUSION

Results from this study are relevant for counseling and policy development.

摘要

背景

咨询全外显子组测序(WES)可以通过使父母在披露前和披露后的态度保持一致来获益。一些研究已经定性比较了父母在诊断环境中接受子女 WES 结果的披露前和披露后的态度。本研究在儿童发育迟缓的背景下探讨了这些态度。

方法

对正在进行三联分析的 16 名儿童的父母(n=27)进行了半结构化访谈,在接受结果之前和之后都进行了访谈。

结果

出现了三个关键见解。首先,希望和期望之间的区别对于塑造父母接受与主要指征相关的结果的经验是相关的。其次,当面对关于未请求发现(UFs)的决策时,年幼的孩子自主能力发展不确定的父母有时会发现自己处于类似于两难境地的情况:同意 WES 的一个重要原因是为了更清楚地了解孩子的发展情况,但为了对 UFs 做出负责任的选择,需要了解一些关于孩子发展的想法。第三,默认的选择加入和选择退出帮助父母理解接受或拒绝不同类别 UFs 的新考虑因素,从而有助于决策。

结论

本研究的结果与咨询和政策制定有关。