Literature DB >> 23514396

A review of evidence on consent bias in research.

Khaled El Emam1, Elizabeth Jonker, Ester Moher, Luk Arbuckle.   

Abstract

Mesh:

Year:  2013        PMID: 23514396     DOI: 10.1080/15265161.2013.767958

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


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  11 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.  Seeing Beyond the Margins: Challenges to Informed Inclusion of Vulnerable Populations in Research.

Authors:  Sarah Gehlert; Jessica Mozersky
Journal:  J Law Med Ethics       Date:  2018-03-27       Impact factor: 1.718

3.  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

4.  Association of Race/Ethnicity With Oral Anticoagulant Use in Patients With Atrial Fibrillation: Findings From the Outcomes Registry for Better Informed Treatment of Atrial Fibrillation II.

Authors:  Utibe R Essien; DaJuanicia N Holmes; Larry R Jackson; Gregg C Fonarow; Kenneth W Mahaffey; James A Reiffel; Benjamin A Steinberg; Larry A Allen; Paul S Chan; James V Freeman; Rosalia G Blanco; Karen S Pieper; Jonathan P Piccini; Eric D Peterson; Daniel E Singer
Journal:  JAMA Cardiol       Date:  2018-12-01       Impact factor: 14.676

5.  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

6.  Anonymising and sharing individual patient data.

Authors:  Khaled El Emam; Sam Rodgers; Bradley Malin
Journal:  BMJ       Date:  2015-03-20

7.  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

8.  Optimizing the synthesis of clinical trial data using sequential trees.

Authors:  Khaled El Emam; Lucy Mosquera; Chaoyi Zheng
Journal:  J Am Med Inform Assoc       Date:  2021-01-15       Impact factor: 4.497

9.  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

10.  Can synthetic data be a proxy for real clinical trial data? A validation study.

Authors:  Zahra Azizi; Chaoyi Zheng; Lucy Mosquera; Louise Pilote; Khaled El Emam
Journal:  BMJ Open       Date:  2021-04-16       Impact factor: 2.692

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