Methods to Minimize the Risks of Creutzfeldt‐Jakob Disease Transmission by Surgical Procedures: Where to Set the Standard?
Health Protection Agency, Centre for Emergency Preparedness and Response, Porton Down, Salisbury, United Kingdom
New prion‐related disorders have emerged over the past 20 years, of which the most notable in the human context is variant Creutzfeldt‐Jakob disease (CJD). This disorder is a challenge to medical and public health professionals seeking early detection and diagnosis, provision of therapy, and support for persons affected and a better understanding of transmission risks. The risk of iatrogenic transmission of the disease remains a significant threat, given the well documented cases of CJD transmission via surgery, organ transplantation, and blood transfusion. This review discusses our current understanding of the prevalence of variant CJD, the distribution of tissue infectivity, and new methods for the decontamination of surgical instruments. A comparison of emerging technologies is provided on the basis of our current perception of surgical risk to identify methods that are likely to provide sufficient safety margins and to stimulate debate about the standards needed to protect against variant CJD and CJD transmission.
Received 1 February 2006; accepted 23 May 2006; electronically published 11 August 2006.
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Online publication date: 1-Feb-2008.
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The views expressed in this article are those of the authors and not necessarily those of the United Kingdom Department of Health or any other funding institution.



