Human prion diseases and the risk of their transmission during anatomical dissection. Issue 6 (17th April 2014)
- Record Type:
- Journal Article
- Title:
- Human prion diseases and the risk of their transmission during anatomical dissection. Issue 6 (17th April 2014)
- Main Title:
- Human prion diseases and the risk of their transmission during anatomical dissection
- Authors:
- Bradford, Barry M.
Piccardo, Pedro
Ironside, James W.
Mabbott, Neil A. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Prion diseases (or transmissible spongiform encephalopathies) are a unique group of fatal progressive neurodegenerative diseases of the central nervous system. The infectious agent is hypothesized to consist solely of a highly protease‐resistant misfolded isoform of the host prion protein. Prions display a remarkable degree of resistance to chemical and physical decontamination. Many common forms of decontamination or neutralization used in infection control are ineffective against prions, except chaotropic agents that specifically disrupt proteins. Human cadaveric prosection or dissection for the purposes of teaching and demonstration of human anatomy has a distinguished history and remains one of the fundamentals of medical education. Iatrogenic transmission of human prion diseases has been demonstrated from the inoculation or implantation of human tissues. Therefore, although the incidence of human prion diseases is rare, restrictions exist upon the use of tissues from patients reported with dementia, specifically the brain and other central nervous system material. A current concern is the potential for asymptomatic variant Creutzfeldt–Jakob disease transmission within the UK population. Therefore, despite the preventative measures, the transmission of prion disease through human tissues remains a potential risk to those working with these materials. In this review, we aim to<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Prion diseases (or transmissible spongiform encephalopathies) are a unique group of fatal progressive neurodegenerative diseases of the central nervous system. The infectious agent is hypothesized to consist solely of a highly protease‐resistant misfolded isoform of the host prion protein. Prions display a remarkable degree of resistance to chemical and physical decontamination. Many common forms of decontamination or neutralization used in infection control are ineffective against prions, except chaotropic agents that specifically disrupt proteins. Human cadaveric prosection or dissection for the purposes of teaching and demonstration of human anatomy has a distinguished history and remains one of the fundamentals of medical education. Iatrogenic transmission of human prion diseases has been demonstrated from the inoculation or implantation of human tissues. Therefore, although the incidence of human prion diseases is rare, restrictions exist upon the use of tissues from patients reported with dementia, specifically the brain and other central nervous system material. A current concern is the potential for asymptomatic variant Creutzfeldt–Jakob disease transmission within the UK population. Therefore, despite the preventative measures, the transmission of prion disease through human tissues remains a potential risk to those working with these materials. In this review, we aim to summarize the current knowledge on human prion disease relevant to those working with human tissues in the context of anatomical dissection. Clin. Anat. 27:821–832, 2014. © 2014 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- Clinical anatomy. Volume 27:Issue 6(2014:Sep.)
- Journal:
- Clinical anatomy
- Issue:
- Volume 27:Issue 6(2014:Sep.)
- Issue Display:
- Volume 27, Issue 6 (2014)
- Year:
- 2014
- Volume:
- 27
- Issue:
- 6
- Issue Sort Value:
- 2014-0027-0006-0000
- Page Start:
- 821
- Page End:
- 832
- Publication Date:
- 2014-04-17
- Subjects:
- Anatomy -- Periodicals
Anatomy -- Periodicals
611 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-2353 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ca.22403 ↗
- Languages:
- English
- ISSNs:
- 0897-3806
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.247300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3759.xml