Adolescents' and Parents' Perspectives on a Novel Decision-Making Process for Return of Results in Genomic Research

被引:2
作者
Matula, Kelly A. [1 ]
Blumling, Amy A. [2 ]
Myers, Melanie F. [2 ,3 ]
McGowan, Michelle L. [4 ,5 ]
Lipstein, Ellen A. [1 ,3 ,6 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, James M Anderson Ctr Hlth Syst Excellence, Cincinnati, OH USA
[2] Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH USA
[3] Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH USA
[4] Univ Cincinnati, Coll Arts & Sci, Dept Womens Gender & Sexual Studies, Cincinnati, OH USA
[5] Mayo Clin, Dept Quantitat Hlth Sci, Biomed Eth Res Program, Rochester, MN USA
[6] Cincinnati Childrens Hosp Med Ctr, T Bldg,240 Albert Sabin Way, Cincinnati, OH 45229 USA
关键词
bioethics; children and adolescent; Pediatrics; communication in research; decision making capacity; Surrogate decision makers; genetic research; parental consent; Child assent; qualitative methods; EXOME; AUTONOMY; BELIEFS; RISK;
D O I
10.1177/15562646231190826
中图分类号
B82 [伦理学(道德学)];
学科分类号
摘要
To understand whether they found a two-step decision process helpful and why, adolescent-parent dyads participating in a study investigating return of genomic testing results were asked about their decision-making experience. Responses were qualitatively coded and analyzed using thematic analysis. Adolescents and parents found both joint and independent decision-making stages helpful. Regarding independent decision-making, adolescents appreciated exercising independence, while parents valued both adolescent and parental independence. Joint decision-making allowed each to hear the other's viewpoints. Some found joint decision-making irrelevant but recognized it might help others. Overall, adolescents and parents had similar reasons for finding the two-step decision-making process helpful. Our findings support using such a process for engaging parents and adolescents in challenging research and clinical decisions.
引用
收藏
页码:278 / 283
页数:6
相关论文
共 23 条
[1]   Pediatric clinical exome/genome sequencing and the engagement process: encouraging active conversation with the older child and adolescent: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG) [J].
Bush, Lynn W. ;
Bartoshesky, Louis E. ;
David, Karen L. ;
Wilfond, Benjamin ;
Williams, Janet L. ;
Holm, Ingrid A. .
GENETICS IN MEDICINE, 2018, 20 (07) :692-694
[2]   Preferences for the Return of Individual Results From Research on Pediatric Biobank Samples [J].
Christensen, Kurt D. ;
Savage, Sarah K. ;
Huntington, Noelle L. ;
Weitzman, Elissa R. ;
Ziniel, Sonja I. ;
Bacon, Phoebe L. ;
Cacioppo, Cara N. ;
Green, Robert C. ;
Holm, Ingrid A. .
JOURNAL OF EMPIRICAL RESEARCH ON HUMAN RESEARCH ETHICS, 2017, 12 (02) :97-106
[3]   Self and Others in Adolescence [J].
Crone, Eveline A. ;
Fuligni, Andrew J. .
ANNUAL REVIEW OF PSYCHOLOGY, VOL 71, 2020, 71 :447-469
[4]   Informed consent for enrolling minors in genetic susceptibility research: A qualitative study of at-risk children's and parents' views about children's role in decision-making [J].
Geller, G ;
Tambor, ES ;
Bernhardt, BA ;
Fraser, G ;
Wissow, LS .
JOURNAL OF ADOLESCENT HEALTH, 2003, 32 (04) :260-271
[5]   ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing [J].
Green, Robert C. ;
Berg, Jonathan S. ;
Grody, Wayne W. ;
Kalia, Sarah S. ;
Korf, Bruce R. ;
Martin, Christa L. ;
McGuire, Amy L. ;
Nussbaum, Robert L. ;
O'Daniel, Julianne M. ;
Ormond, Kelly E. ;
Rehm, Heidi L. ;
Watson, Michael S. ;
Williams, Marc S. ;
Biesecker, Leslie G. .
GENETICS IN MEDICINE, 2013, 15 (07) :565-574
[6]  
Guest G., 2012, Applied thematic analysis
[7]   The beliefs, motivations, and expectations of parents who have enrolled the children in a genetic biorepository [J].
Harris, Erin D. ;
Ziniel, Sonja I. ;
Amatruda, Jonathan G. ;
Clinton, Catherine M. ;
Savage, Sarah K. ;
Taylor, Patrick L. ;
Huntington, Noelle L. ;
Green, Robert C. ;
Holm, Ingrid A. .
GENETICS IN MEDICINE, 2012, 14 (03) :330-337
[8]   Three approaches to qualitative content analysis [J].
Hsieh, HF ;
Shannon, SE .
QUALITATIVE HEALTH RESEARCH, 2005, 15 (09) :1277-1288
[9]   Informed Consent in Decision-Making in Pediatric Practice [J].
Katz, Aviva L. ;
Webb, Sally A. .
PEDIATRICS, 2016, 138 (02)
[10]   Stakeholders' Opinions on the Implementation of Pediatric Whole Exome Sequencing: Implications for Informed Consent [J].
Levenseller, Brooke L. ;
Soucier, Danielle J. ;
Miller, Victoria A. ;
Harris, Diana ;
Conway, Laura ;
Bernhardt, Barbara A. .
JOURNAL OF GENETIC COUNSELING, 2014, 23 (04) :552-565