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| Research article summary (published 30 Jan 2003): |
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Common sense and common consent in communicable disease surveillance.
Full Abstract
The need to protect the public against the spread of communicable (infectious) disease provides a good example of the need for a commonsense approach to the use of confidential data. Laboratories need to notify different professionals in order to trace the sources of outbreaks of infection and eradicate the cause. It is often not possible to obtain consent from individual patients, given the rapid time scale required. In doing so, however, laboratory staff and others would contravene the Data Protection Act in passing on information without consent. Section 60 of the Health and Social Care Act was designed to overcome barriers to research relying on data accumulated in the past and this type of public health work. But this is proving a sluggish procedure. It is an awkward solution to the problem of data use without specific consent. This problem will be overcome only when the public can have sufficient trust in safeguards that are in place to protect their safety and confidentiality so that these important activities can be pursued without specific informed consent.
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Author information
Author/s: Turnberg, L (L);
Affiliation: Public Health Laboratory Service, House of Lords, London, UK. turnberg@parliament.uk
Journal and publication information
Publication Type: Journal Article
Journal: Journal of medical ethics (J Med Ethics), published in England. (Language: eng)
Reference: 2003-Feb; vol 29 (issue 1) : pp 27-9
Dates: Created 2003/02/05; Completed 2003/05/06; Revised 2004/11/17;
PMID: 12569191, status: MEDLINE (last retrieval date: 11/6/2008)
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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