Literature DB >> 12848254

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

Michel P Coleman1, Barry G Evans, Geraldine Barrett.   

Abstract

Developments over the last decade in legislation and professional guidance on confidentiality and medical research in the UK are reviewed. Despite the General Medical Council's guidance, and recent changes to the common law on confidentiality in England and Wales, confusion remains about what is lawful and professionally acceptable in the handling of identifiable data. The GMC has contributed to this confusion. Professional bodies should jointly produce new guidance. The Health and Social Care Act 2001 is a temporary legislative solution. Public consensus is required on an acceptable balance between the citizen's right to privacy and the responsibility of society--to which all citizens belong--to protect the public health. The Government should survey public opinion, inform NHS patients better, initiate wide public debate, and legislate to protect both citizens' rights and medical research that is demonstrably in the public interest. Registration of cancer and communicable diseases should become statutory.

Entities:  

Keywords:  Biomedical and Behavioral Research; General Medical Council (Great Britain)

Mesh:

Year:  2003        PMID: 12848254      PMCID: PMC4952445          DOI: 10.7861/clinmedicine.3-3-219

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


  10 in total

1.  Legal aspects of records based medical research.

Authors:  S E Parkes
Journal:  Arch Dis Child       Date:  2004-10       Impact factor: 3.791

2.  Public opinions about participating in health research.

Authors:  Kay Teschke; Suhail Marino; Rong Chu; Joseph K C Tsui; M Anne Harris; Stephen A Marion
Journal:  Can J Public Health       Date:  2010 Mar-Apr

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.  Using personal health information in medical research.

Authors:  Tom Walley
Journal:  BMJ       Date:  2006-01-21

5.  A feasibility study of signed consent for the collection of patient identifiable information for a national paediatric clinical audit database.

Authors:  Patricia A McKinney; Samantha Jones; Roger Parslow; Nicola Davey; Mark Darowski; Bill Chaudhry; Charles Stack; Gareth Parry; Elizabeth S Draper
Journal:  BMJ       Date:  2005-03-18

6.  Linking survey data with computerised records to predict consulting by older people.

Authors:  Tess Harris; Derek G Cook; Christina R Victor; Carole Beighton; Stephen Dewilde; Iain M Carey
Journal:  Br J Gen Pract       Date:  2004-12       Impact factor: 5.386

7.  Epidemic investigations within an arm's reach - role of google maps during an epidemic outbreak.

Authors:  Roman Sonkin; Evan Avraham Alpert; Eli Jaffe
Journal:  Health Technol (Berl)       Date:  2020-07-12

Review 8.  Research governance: regulating risk and reducing harm?

Authors:  Sara Shaw; Geraldine Barrett
Journal:  J R Soc Med       Date:  2006-01       Impact factor: 18.000

9.  Eurocan plus report: feasibility study for coordination of national cancer research activities.

Authors: 
Journal:  Ecancermedicalscience       Date:  2008-05-20

10.  Guidelines for confidentiality and cancer registration.

Authors:  H Storm; D H Brewster; M P Coleman; D Deapen; A Oshima; T Threlfall; E Démaret
Journal:  Br J Cancer       Date:  2005-06-06       Impact factor: 7.640

  10 in total

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