Literature DB >> 21802790

[Research and protection of personal data in Primary Care].

Sofía Garrido Elustondo1, Luisa Cabello Ballesteros, Inés Galende Domínguez, Rosario Riesgo Fuertes, Ricardo Rodríguez Barrientos, Elena Polentinos Castro.   

Abstract

Research is one of the fundamental functions that have to be carried out in Primary Care. The clinical information stored in different records arising from medical care is a basic tool for this activity. The use of personal data for the purposes of research is legitimate according to our laws; however, this information must be treated confidentially at all times. Two alternatives are available for this. One is to obtain the informed consent of the patient, and the other is to dissociate the handling of the information. But in some situations, the compliance to legal demands when obtaining data for research is not easy, there being a series of obstacles which in many cases makes it impossible to carry out research. In this article, we will give guidance on how to access the information contained in records while respecting the rights of the patient and the current legislation. Copyright Â
© 2011 Elsevier España, S.L. All rights reserved.

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Year:  2011        PMID: 21802790      PMCID: PMC7025257          DOI: 10.1016/j.aprim.2011.02.009

Source DB:  PubMed          Journal:  Aten Primaria        ISSN: 0212-6567            Impact factor:   1.137


  10 in total

1.  [Investigation and primary care].

Authors:  J Jiménez Villa
Journal:  Aten Primaria       Date:  1999-05       Impact factor: 1.137

2.  Data protection legislation: interpretation and barriers to research.

Authors:  J Strobl; E Cave; T Walley
Journal:  BMJ       Date:  2000-10-07

3.  [Research in primary care?].

Authors:  I Fernández Fernández
Journal:  Aten Primaria       Date:  2003-03-31       Impact factor: 1.137

4.  Patient records. Privacy rule creates bottleneck for U.S. biomedical researchers.

Authors:  Jocelyn Kaiser
Journal:  Science       Date:  2004-07-09       Impact factor: 47.728

5.  Registry research and medical privacy.

Authors:  Julie R Ingelfinger; Jeffrey M Drazen
Journal:  N Engl J Med       Date:  2004-04-01       Impact factor: 91.245

6.  Research on medical records without informed consent.

Authors:  Franklin G Miller
Journal:  J Law Med Ethics       Date:  2008       Impact factor: 1.718

7.  [Ethics guidelines for the creation and use of registries for biomedical research purposes].

Authors:  Francisco J de Abajo Iglesias; Lydia Feito Grande; Javier Júdez Gutiérrez; M Concepción Martín Arribas; Benedetto Terracini; Teresa Pàmpols Ros; Jaime Campos Castelló; Amelia Martín Uranga; Moisés Abascal Alonso; Joaquín Herrera Carranza; María José Sánchez Martínez
Journal:  Rev Esp Salud Publica       Date:  2008 Jan-Feb

8.  Whose interest? British newspaper reporting of use of medical records for research.

Authors:  Lindsey Brown; Michael Parker; Mary Dixon-Woods
Journal:  J Health Serv Res Policy       Date:  2008-07

Review 9.  Written informed consent and selection bias in observational studies using medical records: systematic review.

Authors:  Michelle E Kho; Mark Duffett; Donald J Willison; Deborah J Cook; Melissa C Brouwers
Journal:  BMJ       Date:  2009-03-12

10.  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

  10 in total

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