Evidence map›Paper›PMID 28235046›Full record

ArticlePloS one2017

Community recommendations on biobank governance: Results from a deliberative community engagement in California.

Sarah M Dry, Sarah B Garrett, Barbara A Koenig, Arleen F Brown, Michael M Burgess, Jen R Hult, Holly Longstaff, Elizabeth S Wilcox, Sigrid Karina Madrigal Contreras, Arturo Martinez and 2 more

Abstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Research data use in a digital society: a deliberative public engagement.International journal of population data science · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
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  11. Article
  12. Article
  13. Article
  14. The reported impact of public involvement in biobanks: A scoping review.Health expectations : an international journal of public participation in health care and health policy · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Hopeful and Concerned: Public Input on Building a Trustworthy Medical Information Commons.The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics · 2019
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Sarah M DryDepartment of Pathology and Laboratory Medicine, University of California Los Angeles, Los Angeles, California, United States of America.
Sarah B GarrettPhilip R. Lee Institute for Health Policy Studies, University of California San Francisco, San Francisco, California, United States of America.
Barbara A KoenigDepartment of Social and Behavioral Sciences, Institute for Health and Aging, University of California San Francisco, San Francisco, California, United States of America.
Arleen F BrownDivision of General Internal Medicine and Health Services Research, University of California Los Angeles, Los Angeles, California, United States of America.
Michael M BurgessDepartment of Biomedical Ethics, The University of British Columbia, Vancouver, B.C., Canada.
Jen R HultGenentech, Inc., South San Francisco, California, United States of America.
Holly LongstaffOffice of Research Ethics, Simon Fraser University, Burnaby, B.C., Canada.
Elizabeth S WilcoxSchool of Population and Public Health, The University of British Columbia, Vancouver, B.C., Canada.
Sigrid Karina Madrigal ContrerasIndependent Scholar, Torrance, California, United States of America.
Arturo MartinezCenter for Clinical and Translational Science Institute, University of California Los Angeles, Los Angeles, California, United States of America.
Elizabeth A BoydUniversity of California, Office of the President, Oakland, California, United States of America.
Daniel DohanPhilip R. Lee Institute for Health Policy Studies, University of California San Francisco, San Francisco, California, United States of America.

Funding

Engaging University of California Stakeholders for Biorespository ResearchUL1TR000004 · NCATS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRANDIS, JENNIFER RUBIN · 2012 to 2015
$78.0M
UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
Center for Transdisciplinary ELSI Research in Translational GenomicsP20HG007243 · NHGRI · KAISER FOUNDATION RESEARCH INSTITUTE · PI HARRIS-WAI, JULIE NOEL, KOENIG, BARBARA A. · 2013 to 2016
$958k
NCATS NIH HHS UL1 TR000004NCATS NIH HHS UL1 TR000124NHGRI NIH HHS P20 HG007243
6 · The paper itself

Abstract

United States-based biorepositories are on the cusp of substantial change in regulatory oversight at the same time that they are increasingly including samples and data from large populations, e.g. all patients in healthcare system. It is appropriate to engage stakeholders from these populations in new governance arrangements. We sought to describe community recommendations for biorepository governance and oversight using deliberative community engagement (DCE), a qualitative research method designed to elicit lay perspectives on complex technical issues. We asked for stakeholders to provide input on governance of large biorepositories at the University of California (UC), a public university. We defined state residents as stakeholders and recruited residents from two large metropolitan areas, Los Angeles (LA) and San Francisco (SF). In LA, we recruited English and Spanish speakers; in SF the DCE was conducted in English only. We recruited individuals who had completed the 2009 California Health Interview Survey and were willing to be re-contacted for future studies. Using stratified random sampling (by age, education, race/ethnicity), we contacted 162 potential deliberants of whom 53 agreed to participate and 51 completed the 4-day DCE in June (LA) and September-October (SF), 2013. Each DCE included discussion among deliberants facilitated by a trained staff and simultaneously-translated in LA. Deliberants also received a briefing book describing biorepository operations and regulation. During the final day of the DCE, deliberants voted on governance and oversight recommendations using an audience response system. This paper describes 23 recommendations (of 57 total) that address issues including: educating the public, sharing samples broadly, monitoring researcher behavior, using informative consent procedures, and involving community members in a transparent process of biobank governance. This project demonstrates the feasibility of obtaining meaningful input on biorepository governance from diverse lay stakeholders. Such input should be considered as research institutions respond to changes in biorepository regulation.

Indexed as

Community ParticipationAdultAgedBiological Specimen BanksBiomedical ResearchFemaleHealth Knowledge, Attitudes, PracticeHealth SurveysHumansInformed ConsentLos AngelesMaleMiddle AgedQualitative ResearchSan FranciscoUniversities

Identifiers

PMID28235046
PMCPMC5325297

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.