Article info
PDFBrief report
Informed consent for record linkage: a systematic review
- Correspondence to Márcia Elizabeth Marinho da Silva, General Management of Information Systems, Agency for Health Plans and Insurance (ANS), Av. Augusto Severo, 84, 10°. Andar, Glória, Rio de Janeiro, Rio de Janeiro 22021040, Brazil; marcia.marinho.silva{at}gmail.com
Citation
Informed consent for record linkage: a systematic review
Publication history
- Received September 5, 2011
- Revised February 7, 2012
- Accepted February 13, 2012
- First published March 8, 2012.
Online issue publication
April 27, 2016
Article Versions
- Previous version (27 April 2016).
- You are viewing the most recent version of this article.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions
Other content recommended for you
- Written informed consent and selection bias in observational studies using medical records: systematic review
- Access to medical records for research purposes: varying perceptions across research ethics boards
- A randomised controlled trial to compare opt-in and opt-out parental consent for childhood vaccine safety surveillance using data linkage
- Holding personal information in a disease-specific register: the perspectives of people with multiple sclerosis and professionals on consent and access
- Routine health information use among healthcare providers in Ethiopia: a systematic review and meta-analysis
- Consent for the use of human biological samples for biomedical research: a mixed methods study exploring the UK public's preferences
- The biobank consent debate: Why ‘meta-consent’ is not the solution?
- Obtaining informed consent for genomics research in Africa: analysis of H3Africa consent documents
- Taking it to the bank: the ethical management of individual findings arising in secondary research
- Lumos: a statewide linkage programme in Australia integrating general practice data to guide system redesign