Informed consent for biobanking: consensus-based guidelines for adequate comprehension

被引:44
作者
Beskow, Laura M. [1 ,2 ]
Dombeck, Carrie B. [1 ]
Thompson, Cole P. [1 ]
Watson-Ormond, J. Kemp [1 ]
Weinfurt, Kevin P. [1 ,3 ]
机构
[1] Duke Univ, Sch Med, Duke Clin Res Inst, Durham, NC 27708 USA
[2] Duke Univ, Sch Med, Dept Med, Durham, NC 27706 USA
[3] Duke Univ, Sch Med, Dept Psychiat & Behav Sci, Durham, NC USA
关键词
biobanking; comprehension; Delphi process; informed consent; research ethics; PARTICIPANTS; ETHICS; BIOREPOSITORIES; GENOMICS; DELPHI; TRIBE;
D O I
10.1038/gim.2014.102
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose: Federal regulations and best practice guidelines identify categories of information that should be communicated to prospective biobank participants during the informed consent process. However, uncertainty remains about which of this information participants must understand to provide valid consent. Methods: We conducted a Delphi process to define "adequate comprehension" in the context of biobanking consent. The process involved an iterative series of three online surveys of a diverse panel of 51 experts, including genome scientists, biobank managers, ethics and policy experts, and community and participant representatives. We sought consensus (>70% agreement) concerning what specific details participants should know about 16 biobank consent topics. Results: Consensus was achieved for 15 of the 16 consent topics. The exception was the comprehension needed regarding the Genetic Information Nondiscrimination Act. Conclusion: Our Delphi process was successful in identifying a concise set of key points that prospective participants must grasp to provide valid consent for biobanking. Specifying the level of knowledge sufficient for individuals to make an informed choice provides a basis for improving consent forms and processes, as well as an absolute metric for assessing the effectiveness of other interventions to improve comprehension.
引用
收藏
页码:226 / 233
页数:8
相关论文
共 36 条
  • [1] Appelbaum PS., 2010, AJOB Prim Res, V1, P1, DOI [10.1080/21507716.2010.499322, DOI 10.1080/21507716.2010.499322]
  • [2] BUILDING BETTER BIOBANKS
    Baker, Monya
    [J]. NATURE, 2012, 486 (7401) : 141 - 146
  • [3] Beauchamp Tom, 1994, Principles of biomedical ethics, V4th
  • [4] Beskow Laura M, 2014, AJOB Prim Res, V5, P12
  • [5] Developing a Simplified Consent Form for Biobanking
    Beskow, Laura M.
    Friedman, Joelle Y.
    Hardy, N. Chantelle
    Lin, Li
    Weinfurt, Kevin P.
    [J]. PLOS ONE, 2010, 5 (10):
  • [6] Simplifying informed consent for biorepositories: Stakeholder perspectives
    Beskow, Laura M.
    Friedman, Joelle Y.
    Hardy, N. Chantelle
    Lin, Li
    Weinfurt, Kevin P.
    [J]. GENETICS IN MEDICINE, 2010, 12 (09) : 567 - 572
  • [7] Black N, 1999, J Health Serv Res Policy, V4, P236
  • [8] ETHICS DNA Returned to Tribe, Raising Questions About Consent
    Couzin-Frankel, Jennifer
    [J]. SCIENCE, 2010, 328 (5978) : 558 - 558
  • [9] Assessing the quality of democratic deliberation: A case study of public deliberation on the ethics of surrogate consent for research
    De Vries, Raymond
    Stanczyk, Aimee
    Wall, Ian F.
    Uhlmann, Rebecca
    Damschroder, Laura J.
    Kim, Scott Y.
    [J]. SOCIAL SCIENCE & MEDICINE, 2010, 70 (12) : 1896 - 1903
  • [10] Department of Health and Human Services, 2011, FED REG S143, V76, P44512