Literature DB >> 23514398

How and when does consent bias research?

R H H Groenwold1, R van der Graaf, J J M van Delden.   

Abstract

Mesh：

Year:  2013        PMID： 23514398     DOI： 10.1080/15265161.2013.767961

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


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  5 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.  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

4.  Blockchain, consent and prosent for medical research.

Authors:  Sebastian Porsdam Mann; Julian Savulescu; Philippe Ravaud; Mehdi Benchoufi
Journal:  J Med Ethics       Date:  2020-05-04       Impact factor: 2.903

5.  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
  5 in total

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