The Storage and Use of Biological Tissue Samples from Minors for Research: A Focus Group Study

K. Hens*, H. Nys, J.J. Cassiman, K. Dierickx

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review


Genetic research on pediatric stored tissue samples raises specific ethical questions that differ from those raised when adults are the donors. To investigate opinions on this matter, we conducted 10 focus group discussions. Five focus groups were conducted with adult participants and 5 had teenage participants between 15 and 19 years old. The discussions were analyzed with NVIVO 8 (qualitative research software). We found the following recurrent categories: the requirement that research should not pose any burden on children and that it should benefit other children, the trust people had in the role of parents, the need for information and the growth towards autonomy. Both the adults and teenagers we interviewed thought that the inclusion of tissue samples from minors in research had ethical implications. A major concern was that nontherapeutic research would pose no extra burden on children, which would assume the use of nonintrusive methods of gathering samples and the use of samples that were gathered in a diagnostic context. Participants, however, also understood the necessity of such research. The overall impression was that parents would be the best persons to make decisions on behalf of a small child and that the same parents would engage their children in the decision-making when they grew older. People thought that there was a duty to recontact minors when they reached the age of competence but on a best-effort basis. Copyright (C) 2010 S. Karger AG, Basel

Original languageEnglish
Pages (from-to)68-76
Number of pages9
JournalPublic Health Genomics
Issue number2
Publication statusPublished - 1 Jan 2011


  • Biobank
  • Ethics
  • Focus group
  • Minors
  • Stored tissue samples

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