Consent for the linkage of data for public health research: Is it (or should it be) an absolute pre-requisite?

Australian and New Zealand Journal of Public Health

Volumn 25, Issue 5, 2001, Pages 423-425

  Breen, Kerry J ^a,b  

^a Young Carers Research Advisory Group with Carers NSW   (Australia)

^b NATIONAL HEALTH AND MEDICAL RESEARCH COUNCIL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

DATA ANALYSIS; HEALTH CARE MANAGEMENT; HEALTH SERVICE; HEALTH SERVICES RESEARCH; HEALTH STATISTICS; INFORMED CONSENT; LEGAL ASPECT; MEDICAL ETHICS; MEDICAL INFORMATION; NOTE; PRACTICE GUIDELINE; PUBLIC HEALTH SERVICE;

EID: 0034794490     PISSN: 13260200     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1467-842X.2001.tb00286.x     Document Type: Note

References (4)

1. Health services research using linked records: Who consents and what is the gain?
2. The impracticable nature of consent for research use of linked administrative health records
3. National Statement on Ethical Conduct of Research Involving Humans. Commonwealth of Australia