Literature DB >> 16873867

Consent for the use of personal medical data in research.

Peter Singleton1, Michael Wadsworth.   

Abstract

Mesh：

Year:  2006        PMID： 16873867      PMCID： PMC1523480          DOI： 10.1136/bmj.333.7561.255

Source DB:  PubMed          Journal:  BMJ        ISSN： 0959-8138


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  3 in total

1.  Association of road-traffic accidents with benzodiazepine use.

Authors:  F Barbone; A D McMahon; P G Davey; A D Morris; I C Reid; D G McDevitt; T M MacDonald
Journal:  Lancet       Date:  1998-10-24       Impact factor: 79.321

2.  Antidepressants and suicide.

Authors:  S S Jick; A D Dean; H Jick
Journal:  BMJ       Date:  1995-01-28

Review 3.  Confidentiality of personal health information used for research.

Authors:  Dipak Kalra; Renate Gertz; Peter Singleton; Hazel M Inskip
Journal:  BMJ       Date:  2006-07-22
  3 in total
  15 in total

1.  Governance of research that uses identifiable personal data.

Authors:  Robert Souhami
Journal:  BMJ       Date:  2006-08-12

2.  Improving access to research data in Europe.

Authors:  Philipa Mladovsky; Elias Mossialos; Martin McKee
Journal:  BMJ       Date:  2008-02-09

3.  Alternatives to project-specific consent for access to personal information for health research: what is the opinion of the Canadian public?

Authors:  Donald J Willison; Lisa Schwartz; Julia Abelson; Cathy Charles; Marilyn Swinton; David Northrup; Lehana Thabane
Journal:  J Am Med Inform Assoc       Date:  2007-08-21       Impact factor: 4.497

4.  Selection bias resulting from the requirement for prior consent in observational research: a community cohort of people with ischaemic heart disease.

Authors:  Brian Buckley; Andrew W Murphy; Molly Byrne; Liam Glynn
Journal:  Heart       Date:  2007-05-13       Impact factor: 5.994

5.  Opt-out as an acceptable method of obtaining consent in medical research: a short report.

Authors:  Akke Vellinga; Martin Cormican; Belinda Hanahoe; Kathleen Bennett; Andrew W Murphy
Journal:  BMC Med Res Methodol       Date:  2011-04-06       Impact factor: 4.615

6.  A randomised controlled trial to compare opt-in and opt-out parental consent for childhood vaccine safety surveillance using data linkage: study protocol.

Authors:  Jesia G Berry; Philip Ryan; Annette J Braunack-Mayer; Katherine M Duszynski; Vicki Xafis; Michael S Gold
Journal:  Trials       Date:  2011-01-04       Impact factor: 2.279

7.  Consent for use of personal information for health research: do people with potentially stigmatizing health conditions and the general public differ in their opinions?

Authors:  Donald J Willison; Valerie Steeves; Cathy Charles; Lisa Schwartz; Jennifer Ranford; Gina Agarwal; Ji Cheng; Lehana Thabane
Journal:  BMC Med Ethics       Date:  2009-07-24       Impact factor: 2.652

8.  Low risk research using routinely collected identifiable health information without informed consent: encounters with the Patient Information Advisory Group.

Authors:  C Metcalfe; R M Martin; S Noble; J A Lane; F C Hamdy; D E Neal; J L Donovan
Journal:  J Med Ethics       Date:  2008-01       Impact factor: 2.903

Review 9.  "Let's get the best quality research we can": public awareness and acceptance of consent to use existing data in health research: a systematic review and qualitative study.

Authors:  Elizabeth M Hill; Emma L Turner; Richard M Martin; Jenny L Donovan
Journal:  BMC Med Res Methodol       Date:  2013-06-04       Impact factor: 4.615

10.  The ethics of unlinked anonymous testing of blood: views from in-depth interviews with key informants in four countries.

Authors:  Anthony S Kessel; Jessica Datta; Kaye Wellings; Sarah Perman
Journal:  BMJ Open       Date:  2012-12-20       Impact factor: 2.692
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