Literature DB >> 23514393

Does consent bias research?

Mark A Rothstein1, Abigail B Shoben.   

Abstract

Researchers increasingly rely on large data sets of health information, often linked with biological specimens. In recent years, the argument has been made that obtaining informed consent for conducting records-based research is unduly burdensome and results in "consent bias." As a type of selection bias, consent bias is said to exist when the group giving researchers access to their data differs from the group denying access. Therefore, to promote socially beneficial research, it is argued that consent should be unnecessary. After analyzing the biostatistics evidence and bioethics arguments, the article concludes that (1) claims about the amount of consent bias are overstated; (2) commonly used statistical methods usually can account for consent bias; and (3) any residual effects of consent bias are below an acceptable level of imprecision and constitute a reasonable social cost for conducting ethically responsible research.

Mesh:

Year:  2013        PMID: 23514393     DOI: 10.1080/15265161.2013.767955

Source DB:  PubMed          Journal:  Am J Bioeth        ISSN: 1526-5161            Impact factor:   11.229


  9 in total

1.  Ethical and practical challenges to studying patients who opt out of large-scale biorepository research.

Authors:  S Trent Rosenbloom; Jennifer L Madison; Kyle B Brothers; Erica A Bowton; Ellen Wright Clayton; Bradley A Malin; Dan M Roden; Jill Pulley
Journal:  J Am Med Inform Assoc       Date:  2013-07-25       Impact factor: 4.497

2.  Evaluation of a Computer-Based Recruitment System for Enrolling Men Who Have Sex With Men Into an Observational HIV Behavioral Risk Study.

Authors:  Christine M Khosropour; Julia C Dombrowksi; James P Hughes; Lisa E Manhart; Matthew R Golden
Journal:  Am J Epidemiol       Date:  2016-09-08       Impact factor: 4.897

3.  How electronic clinical data can improve health technology assessment.

Authors:  Jonathan R Treadwell; Eileen Erinoff; Vivian Coates
Journal:  EGEMS (Wash DC)       Date:  2013-10-28

4.  Rare disease research: Breaking the privacy barrier.

Authors:  Deborah Mascalzoni; Angelo Paradiso; Matts Hansson
Journal:  Appl Transl Genom       Date:  2014-04-18

5.  Facilitating the ethical use of health data for the benefit of society: electronic health records, consent and the duty of easy rescue.

Authors:  Sebastian Porsdam Mann; Julian Savulescu; Barbara J Sahakian
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2016-12-28       Impact factor: 4.226

6.  Eliciting meta consent for future secondary research use of health data using a smartphone application - a proof of concept study in the Danish population.

Authors:  Thomas Ploug; Søren Holm
Journal:  BMC Med Ethics       Date:  2017-08-15       Impact factor: 2.652

7.  RAADS-14 Screen: validity of a screening tool for autism spectrum disorder in an adult psychiatric population.

Authors:  Jonna M Eriksson; Lisa Mj Andersen; Susanne Bejerot
Journal:  Mol Autism       Date:  2013-12-09       Impact factor: 7.509

8.  Parental perspectives on consent for participation in large-scale, non-biological data repositories.

Authors:  Kiran Pohar Manhas; Stacey Page; Shawn X Dodd; Nicole Letourneau; Aleta Ambrose; Xinjie Cui; Suzanne C Tough
Journal:  Life Sci Soc Policy       Date:  2016-01-20

9.  In Defence of informed consent for health record research - why arguments from 'easy rescue', 'no harm' and 'consent bias' fail.

Authors:  Thomas Ploug
Journal:  BMC Med Ethics       Date:  2020-08-20       Impact factor: 2.652

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.