Literature DB >> 15244364

Accountability, trust and informed consent in medical practice and research.

Onora O'Neill1.   

Abstract

During the last 25 years public policy in the UK has aimed to replace 'club' cultures and their supposedly suspect reliance on trust between professionals and public with a new public culture based on accountability and 'transparency'. These transformations have changed both clinical practice and public health policy in deep ways. Are the new conceptions of accountability adequate? Are obligations to be 'transparent' any more than requirements to disclose information which overlook the need for genuine communication? Can demands for ever fuller informed consent improve accountability to individual patients and research subjects? Could we devise more intelligent conceptions of accountability that support more intelligent placing and refusal of trust? What might intelligent conceptions of accountability suggest about proper clinical practice, public health medicine and professional responsibilities?

Entities:  

Keywords:  Biomedical and Behavioral Research; Professional Patient Relationship

Mesh:

Year:  2004        PMID: 15244364      PMCID: PMC4953592          DOI: 10.7861/clinmedicine.4-3-269

Source DB:  PubMed          Journal:  Clin Med (Lond)        ISSN: 1470-2118            Impact factor:   2.659


  23 in total

1.  Frontline ethical issues in pediatric clinical research: ethical and regulatory aspects of seven current bottlenecks in pediatric clinical research.

Authors:  Wim Pinxten; Herman Nys; Kris Dierickx
Journal:  Eur J Pediatr       Date:  2010-07-29       Impact factor: 3.183

Review 2.  Ethics, audit, and research: all shades of grey.

Authors:  Derick T Wade
Journal:  BMJ       Date:  2005-02-26

3.  A new role for the royal colleges?

Authors:  Ian Gilmore
Journal:  BMJ       Date:  2006-11-04

4.  Regulation and the social licence for medical research.

Authors:  Mary Dixon-Woods; Richard E Ashcroft
Journal:  Med Health Care Philos       Date:  2008-07-17

5.  Regulating trust in pediatric clinical trials.

Authors:  Wim Pinxten; Herman Nys; Kris Dierickx
Journal:  Med Health Care Philos       Date:  2008-07-18

6.  A defense of compulsory vaccination.

Authors:  Jessica Flanigan
Journal:  HEC Forum       Date:  2014-03

7.  Surrogate Informed Consent: A Qualitative Analysis of Surrogate Decision Makers' Perspectives.

Authors:  Trevor Lane; Elinor Brereton; Carolyn Nowels; Jeffrey McKeehan; Marc Moss; Daniel D Matlock
Journal:  Ann Am Thorac Soc       Date:  2021-07

Review 8.  Ethical aspects of clinical research with minors.

Authors:  Wendy Bos; Krista Tromp; Dick Tibboel; Wim Pinxten
Journal:  Eur J Pediatr       Date:  2012-10-17       Impact factor: 3.183

9.  How IRBs view and make decisions about consent forms.

Authors:  Robert L Klitzman
Journal:  J Empir Res Hum Res Ethics       Date:  2013-02       Impact factor: 1.742

10.  Tailoring consent to context: designing an appropriate consent process for a biomedical study in a low income setting.

Authors:  Fasil Tekola; Susan J Bull; Bobbie Farsides; Melanie J Newport; Adebowale Adeyemo; Charles N Rotimi; Gail Davey
Journal:  PLoS Negl Trop Dis       Date:  2009-07-21
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