‘We Should View Him as an Individual’: The Role of the Child’s Future Autonomy in Shared Decision-Making About Unsolicited Findings in Pediatric Exome Sequencing

被引:0
作者
W. Dondorp
I. Bolt
A. Tibben
G. De Wert
M. Van Summeren
机构
[1] Maastricht University,Department of Health, Ethics and Society, Faculty of Health, Medicine and Life Sciences
[2] Erasmus Medical Centre,Department of Medical Ethics, Philosophy and History of Medicine
[3] Leiden University Medical Centre,Department of Clinical Genetics
[4] University Medical Centre Utrecht,Department of General Pediatrics
[5] UMC Utrecht,undefined
来源
Health Care Analysis | 2021年 / 29卷
关键词
Pediatrics; Clinical sequencing; Unsollicited findings; Future autonomy; Shared decision making; Ethics;
D O I
暂无
中图分类号
学科分类号
摘要
In debates about genetic testing of children, as well as about disclosing unsolicited findings (UFs) of pediatric exome sequencing, respect for future autonomy should be regarded as a prima facie consideration for not taking steps that would entail denying the future adult the opportunity to decide for herself about what to know about her own genome. While the argument can be overridden when other, morally more weighty considerations are at stake, whether this is the case can only be determined in concrete cases. Importantly, when children grow into adolescents, respect for future autonomy will have to give way to respecting their emerging autonomy. When pediatric exome sequencing is done for complex conditions not involving developmental delay, respect for the child’s future or emerging autonomy should be a primary consideration for those charged with deciding on behalf of the child. Building on what Emanuel and Emanuel have termed the ‘deliberative model’ of shared decision making, we argue that if parents fail to give these considerations their due, professionals should actively invite them to do so. Taking a directive stance may be needed in order to make sure that the future or emerging autonomy of the child are duly considered in the decision-making process, but also to help the parents and themselves to shape their respective roles as responsible care-givers.
引用
收藏
页码:249 / 261
页数:12
相关论文
共 151 条
  • [1] Bertier G(2015)ACMG policy statement: Updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing Genetics in Medicine 17 68-69
  • [2] Senecal K(2001)Ethical issues with genetic testing in pediatrics Pediatrics 107 1451-1455
  • [3] Borry P(2013)Ethical and policy issues in genetic testing and screening of children Pediatrics 131 620-622
  • [4] Vears DF(2017)Unsolved challenges in pediatric whole-exome sequencing: A literature analysis Critical Reviews in Clinical Laboratory Sciences 54 134-142
  • [5] Bloch M(1990)Predictive testing for Huntington disease in childhood—Challenges and implications—Opinion American Journal of Human Genetics 46 1-4
  • [6] Hayden MR(2009)Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations European Journal of Human Genetics 17 711-719
  • [7] Borry P(2006)Presymptomatic and predictive genetic testing in minors: A systematic review of guidelines and position papers Clinical Genetics 70 374-381
  • [8] Evers-Kiebooms G(2016)Ethical issues in pediatric genetic testing and screening Current Opinion in Pediatrics 28 700-704
  • [9] Cornel MC(2015)Points to consider: Ethical, legal, and psychosocial implications of genetic testing in children and adolescents American Journal of Human Genetics 97 6-21
  • [10] Clarke A(2013)Next-generation sequencing: Does the next generation still have a right to an open future? Nature Reviews Genetics 14 306-335