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Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment
The book on iatrogenic Creutzfeldt-Jakob disease (CJD) in humans is almost closed. This form of CJD transmission via medical misadventures was first detected in 1974. Today, only occasional CJD cases with exceptionally long incubation periods still appear. The main sources of the largest outbreaks w...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Centers for Disease Control and Prevention
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358170/ https://www.ncbi.nlm.nih.gov/pubmed/22607808 http://dx.doi.org/10.3201/eid1806.120116 |
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author | Brown, Paul Brandel, Jean-Philippe Sato, Takeshi Nakamura, Yosikazu MacKenzie, Jan Will, Robert G. Ladogana, Anna Pocchiari, Maurizio Leschek, Ellen W. Schonberger, Lawrence B. |
author_facet | Brown, Paul Brandel, Jean-Philippe Sato, Takeshi Nakamura, Yosikazu MacKenzie, Jan Will, Robert G. Ladogana, Anna Pocchiari, Maurizio Leschek, Ellen W. Schonberger, Lawrence B. |
author_sort | Brown, Paul |
collection | PubMed |
description | The book on iatrogenic Creutzfeldt-Jakob disease (CJD) in humans is almost closed. This form of CJD transmission via medical misadventures was first detected in 1974. Today, only occasional CJD cases with exceptionally long incubation periods still appear. The main sources of the largest outbreaks were tissues from human cadavers with unsuspected CJD that were used for dura mater grafts and growth hormone extracts. A few additional cases resulted from neurosurgical instrument contamination, corneal grafts, gonadotrophic hormone, and secondary infections from blood transfusions. Although the final solution to the problem of iatrogenic CJD is still not available (a laboratory test to identify potential donors who harbor the infectious agent), certain other measures have worked well: applying special sterilization of penetrating surgical instruments, reducing the infectious potential of donor blood and tissue, and excluding donors known to have higher than normal risk for CJD. |
format | Online Article Text |
id | pubmed-3358170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-33581702012-06-01 Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment Brown, Paul Brandel, Jean-Philippe Sato, Takeshi Nakamura, Yosikazu MacKenzie, Jan Will, Robert G. Ladogana, Anna Pocchiari, Maurizio Leschek, Ellen W. Schonberger, Lawrence B. Emerg Infect Dis Synopsis The book on iatrogenic Creutzfeldt-Jakob disease (CJD) in humans is almost closed. This form of CJD transmission via medical misadventures was first detected in 1974. Today, only occasional CJD cases with exceptionally long incubation periods still appear. The main sources of the largest outbreaks were tissues from human cadavers with unsuspected CJD that were used for dura mater grafts and growth hormone extracts. A few additional cases resulted from neurosurgical instrument contamination, corneal grafts, gonadotrophic hormone, and secondary infections from blood transfusions. Although the final solution to the problem of iatrogenic CJD is still not available (a laboratory test to identify potential donors who harbor the infectious agent), certain other measures have worked well: applying special sterilization of penetrating surgical instruments, reducing the infectious potential of donor blood and tissue, and excluding donors known to have higher than normal risk for CJD. Centers for Disease Control and Prevention 2012-06 /pmc/articles/PMC3358170/ /pubmed/22607808 http://dx.doi.org/10.3201/eid1806.120116 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited. |
spellingShingle | Synopsis Brown, Paul Brandel, Jean-Philippe Sato, Takeshi Nakamura, Yosikazu MacKenzie, Jan Will, Robert G. Ladogana, Anna Pocchiari, Maurizio Leschek, Ellen W. Schonberger, Lawrence B. Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment |
title | Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment |
title_full | Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment |
title_fullStr | Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment |
title_full_unstemmed | Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment |
title_short | Iatrogenic Creutzfeldt-Jakob Disease, Final Assessment |
title_sort | iatrogenic creutzfeldt-jakob disease, final assessment |
topic | Synopsis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358170/ https://www.ncbi.nlm.nih.gov/pubmed/22607808 http://dx.doi.org/10.3201/eid1806.120116 |
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