Literature DB >> 16424468

Using personal health information in medical research.

Tom Walley.   

Abstract

Mesh：

Year:  2006        PMID： 16424468      PMCID： PMC1336750          DOI： 10.1136/bmj.332.7534.130

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


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  6 in total

1.  Consent, confidentiality, and the threat to public health surveillance.

Authors:  Chris Verity; Angus Nicoll
Journal:  BMJ       Date:  2002-05-18

Review 2.  Obstacles to conducting epidemiological research in the UK general population.

Authors:  Hester J T Ward; Simon N Cousens; Blaire Smith-Bathgate; Margaret Leitch; Dawn Everington; Robert G Will; Peter G Smith
Journal:  BMJ       Date:  2004-07-31

3.  Consent, confidentiality, and the Data Protection Act.

Authors:  Amy Iversen; Kathleen Liddell; Nicola Fear; Matthew Hotopf; Simon Wessely
Journal:  BMJ       Date:  2006-01-21

4.  Over-regulation of clinical research: a threat to public health.

Authors:  Charles Warlow
Journal:  Clin Med (Lond)       Date:  2005 Jan-Feb       Impact factor: 2.659

5.  Public attitudes towards the use of primary care patient record data in medical research without consent: a qualitative study.

Authors:  M R Robling; K Hood; H Houston; R Pill; J Fay; H M Evans
Journal:  J Med Ethics       Date:  2004-02       Impact factor: 2.903

Review 6.  Confidentiality and the public interest in medical research--will we ever get it right?

Authors:  Michel P Coleman; Barry G Evans; Geraldine Barrett
Journal:  Clin Med (Lond)       Date:  2003 May-Jun       Impact factor: 2.659
  6 in total
  7 in total

1.  Personal privacy and public health: potential impacts of privacy legislation on health research in Canada.

Authors:  M Anne Harris; Adrian R Levy; Kay E Teschke
Journal:  Can J Public Health       Date:  2008 Jul-Aug

2.  National survey of British public's views on use of identifiable medical data by the National Cancer Registry.

Authors:  Geraldine Barrett; Jackie A Cassell; Janet L Peacock; Michel P Coleman
Journal:  BMJ       Date:  2006-04-28

3.  Challenges in evaluating Welfare to Work policy interventions: would an RCT design have been the answer to all our problems?

Authors:  Kathryn Skivington; Gerry McCartney; Hilary Thomson; Lyndal Bond
Journal:  BMC Public Health       Date:  2010-05-17       Impact factor: 3.295

4.  The social licence for research: why care.data ran into trouble.

Authors:  Pam Carter; Graeme T Laurie; Mary Dixon-Woods
Journal:  J Med Ethics       Date:  2015-01-23       Impact factor: 2.903

5.  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

6.  Participant recruitment in sensitive surveys: a comparative trial of 'opt in' versus 'opt out' approaches.

Authors:  Katherine J Hunt; Natalie Shlomo; Julia Addington-Hall
Journal:  BMC Med Res Methodol       Date:  2013-01-11       Impact factor: 4.615

7.  Ethical issues in implementation research: a discussion of the problems in achieving informed consent.

Authors:  Jane L Hutton; Martin P Eccles; Jeremy M Grimshaw
Journal:  Implement Sci       Date:  2008-12-17       Impact factor: 7.327
  7 in total

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