Literature DB >> 9563980

Maintaining privacy and the health of the public. Should not be seen as in opposition.

J P Vandenbroucke.   

Abstract

Keywords:  Biomedical and Behavioral Research; Legal Approach

Mesh：

Year:  1998        PMID： 9563980      PMCID： PMC1113066          DOI： 10.1136/bmj.316.7141.1331

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


× No keyword cloud information.
  8 in total

1.  Confidential medical records and epidemiological research.

Authors:  E G Knox
Journal:  BMJ       Date:  1992-03-21

2.  The threat to medical-records research.

Authors:  L J Melton
Journal:  N Engl J Med       Date:  1997-11-13       Impact factor: 91.245

3.  Informed consent for publication.

Authors:  P B Fontanarosa; R M Glass
Journal:  JAMA       Date:  1997-08-27       Impact factor: 56.272

4.  Obtain informed consent before publishing information about patients.

Authors:  L H Clever
Journal:  JAMA       Date:  1997-08-27       Impact factor: 56.272

5.  Patient consent for publication and the health of the public.

Authors:  D E Snider
Journal:  JAMA       Date:  1997-08-27       Impact factor: 56.272

6.  The ethics of learning from patients.

Authors: 
Journal:  Lancet       Date:  1994-07-09       Impact factor: 79.321

7.  European directive on confidential data: a threat to epidemiology.

Authors:  E Lynge
Journal:  BMJ       Date:  1994-02-19

8.  The patient record in epidemiology.

Authors:  L T Kurland; C A Molgaard
Journal:  Sci Am       Date:  1981-10       Impact factor: 2.142
  8 in total
  5 in total

1.  The CMA's Health Information Privacy Code: does it go too far?

Authors:  J Hoey
Journal:  CMAJ       Date:  1998-10-20       Impact factor: 8.262

2.  Do income questions and seeking consent to link medical records reduce survey response rates? A randomised controlled trial among older people.

Authors:  S Shah; T J Harris; E Rink; S DeWilde; C R Victor; D G Cook
Journal:  Br J Gen Pract       Date:  2001-03       Impact factor: 5.386

3.  Patient/family views on data sharing in rare diseases: study in the European LeukoTreat project.

Authors:  Sylviane Darquy; Grégoire Moutel; Anne-Sophie Lapointe; Diane D'Audiffret; Julie Champagnat; Samia Guerroui; Marie-Louise Vendeville; Odile Boespflug-Tanguy; Nathalie Duchange
Journal:  Eur J Hum Genet       Date:  2015-06-17       Impact factor: 4.246

4.  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

5.  A proposed architecture and method of operation for improving the protection of privacy and confidentiality in disease registers.

Authors:  Tim Churches
Journal:  BMC Med Res Methodol       Date:  2003-01-06       Impact factor: 4.615
  5 in total

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