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Published in: BMC Public Health 1/2005

Open Access 01-12-2005 | Research article

Tissue classification for the epidemiological assessment of surgical transmission of sporadic Creutzfeldt-Jakob disease. A proposal on hypothetical risk levels

Authors: Alberto Rábano, Jesús de Pedro-Cuesta, Kåre Mølbak, Åke Siden, Miguel Calero, Henning Laursen, the EUROSURGYCJD Research Group

Published in: BMC Public Health | Issue 1/2005

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Abstract

Background

Epidemiological studies on the potential role of surgery in Creutzfeldt-Jakob Disease transmission have disclosed associations with history of specific surgical interventions or reported negative results.

Methods

Within the context of a case-control study designed to address surgical risk of sporadic Creutzfeldt-Jakob Disease in Nordic European countries (EUROSURGYCJD Project), a strategy was adopted to categorise reported surgical procedures in terms of potential risk of Creutzfeldt-Jakob Disease acquisition. We took into account elements of biological plausibility, either clinically or experimentally demonstrated, such as tissue infectivity, PrP expression content or successful route of infection.

Results

We propose a classification of exposed tissues and anatomic structures, drawn up on the basis of their specific putative role as entry site for prion transmission through contact with surgical instruments that are not fully decontaminated.

Conclusions

This classification can serve as a reference, both in our study and in further epidemiological research, for categorisation of surgical procedures in terms of risk level of Creutzfeldt-Jakob Disease acquisition.
Literature
1.
go back to reference Kondo K, Kuroiwa Y: A case control study of Creutzfeldt-Jakob disease: association with physical injuries. Ann Neurol. 1982, 11: 377-381. 10.1002/ana.410110410.CrossRefPubMed Kondo K, Kuroiwa Y: A case control study of Creutzfeldt-Jakob disease: association with physical injuries. Ann Neurol. 1982, 11: 377-381. 10.1002/ana.410110410.CrossRefPubMed
2.
go back to reference Davanipour Z, Alter M, Sobel E, Asher DM, Gajdusek DC: Creutzfeldt-Jakob disease: possible medical risk factors. Neurology. 1985, 35: 1483-1486.CrossRefPubMed Davanipour Z, Alter M, Sobel E, Asher DM, Gajdusek DC: Creutzfeldt-Jakob disease: possible medical risk factors. Neurology. 1985, 35: 1483-1486.CrossRefPubMed
3.
go back to reference Harries-Jones R, Knight RSG, Will RG, Cousens SN, Smith PG, Matthews WB: Creutzfeldt-Jakob disease in England and Wales, 1980-1984: a case-control study of potential risk factors. J Neurol Neurosurg Psychiatry. 1988, 51: 1113-1119.CrossRefPubMedPubMedCentral Harries-Jones R, Knight RSG, Will RG, Cousens SN, Smith PG, Matthews WB: Creutzfeldt-Jakob disease in England and Wales, 1980-1984: a case-control study of potential risk factors. J Neurol Neurosurg Psychiatry. 1988, 51: 1113-1119.CrossRefPubMedPubMedCentral
4.
go back to reference van Duijn CM, Delasnerie-Lauprêtre N, Masullo C, Zerr I, de Silva R, Wientjens DPWM, Brandel JP, Weber T, Bonavita V, Zeidler M, Alpérovitch A, Poser S, Granieri E, Hofman A, Will RG: Case-control study of risk factors of Creutzfeldt-Jakob disease in Europe during 1993-95. Lancet. 1998, 351: 1081-1085. 10.1016/S0140-6736(97)09468-3.CrossRefPubMed van Duijn CM, Delasnerie-Lauprêtre N, Masullo C, Zerr I, de Silva R, Wientjens DPWM, Brandel JP, Weber T, Bonavita V, Zeidler M, Alpérovitch A, Poser S, Granieri E, Hofman A, Will RG: Case-control study of risk factors of Creutzfeldt-Jakob disease in Europe during 1993-95. Lancet. 1998, 351: 1081-1085. 10.1016/S0140-6736(97)09468-3.CrossRefPubMed
5.
go back to reference Collins S, Law MG, Fletcher A, Boyd A, Kaldor J, Masters CL: Surgical treatment and risk of sporadic Creutzfeldt-Jakob disease: a case-control study. Lancet. 1999, 353: 693-697. 10.1016/S0140-6736(98)08138-0.CrossRefPubMed Collins S, Law MG, Fletcher A, Boyd A, Kaldor J, Masters CL: Surgical treatment and risk of sporadic Creutzfeldt-Jakob disease: a case-control study. Lancet. 1999, 353: 693-697. 10.1016/S0140-6736(98)08138-0.CrossRefPubMed
6.
go back to reference Zerr I, Brandel JP, Masullo C, Wientjens DPWM, de Silva R, Zeidler M, Granieri E, Sampaolo S, van Duijn CM, Delasnerie-Lauprêtre N, Will RG, Poser S: European surveillance on Creutzfeldt-Jakob disease: a case-control study for medical risk factors. J Clin Epidemiol. 2000, 53: 747-754. 10.1016/S0895-4356(99)00207-3.CrossRefPubMed Zerr I, Brandel JP, Masullo C, Wientjens DPWM, de Silva R, Zeidler M, Granieri E, Sampaolo S, van Duijn CM, Delasnerie-Lauprêtre N, Will RG, Poser S: European surveillance on Creutzfeldt-Jakob disease: a case-control study for medical risk factors. J Clin Epidemiol. 2000, 53: 747-754. 10.1016/S0895-4356(99)00207-3.CrossRefPubMed
7.
go back to reference Ward HJT, Everington D, Croes EA, Alpérovitch A, Delasnerie-Lauprêtre N, Zerr I, Poser CM, van Duijn CM: Sporadic Creutzfeldt-Jakob disease and surgery: a case-control study using community controls. Neurology. 2002, 59: 543-548.CrossRefPubMed Ward HJT, Everington D, Croes EA, Alpérovitch A, Delasnerie-Lauprêtre N, Zerr I, Poser CM, van Duijn CM: Sporadic Creutzfeldt-Jakob disease and surgery: a case-control study using community controls. Neurology. 2002, 59: 543-548.CrossRefPubMed
8.
go back to reference Wientjens DPWM, Davanipour Z, Hofman A, Kondo K, Matthews WB, Will RG, van Duijn CM: Risk factors for Creutzfeldt-Jakob disease: a reanalysis of case-control studies. Neurology. 1996, 46: 1287-1291.CrossRefPubMed Wientjens DPWM, Davanipour Z, Hofman A, Kondo K, Matthews WB, Will RG, van Duijn CM: Risk factors for Creutzfeldt-Jakob disease: a reanalysis of case-control studies. Neurology. 1996, 46: 1287-1291.CrossRefPubMed
9.
go back to reference Brown P, Preece MA, Brandel JP, Sato T, McShane L, Zerr I, Fletcher A, Will RG, Pocchiari M, Cashman NR, Huillard d'Aignaux J, Cervenáková L, Fradkin J, Schonberger LB, Collins SJ: Iatrogenic Creutzfeldt-Jakob disease at the millenium. Neurology. 2000, 55: 1075-1081. [http://www.neurology.org]CrossRefPubMed Brown P, Preece MA, Brandel JP, Sato T, McShane L, Zerr I, Fletcher A, Will RG, Pocchiari M, Cashman NR, Huillard d'Aignaux J, Cervenáková L, Fradkin J, Schonberger LB, Collins SJ: Iatrogenic Creutzfeldt-Jakob disease at the millenium. Neurology. 2000, 55: 1075-1081. [http://​www.​neurology.​org]CrossRefPubMed
10.
go back to reference Weissmann C, Enari M, Klohn PC, Rossi D, Flechsig E: Transmission of prions. J Infect Dis. 2002, 186 Suppl 2: S157-S165. 10.1086/344575.CrossRefPubMed Weissmann C, Enari M, Klohn PC, Rossi D, Flechsig E: Transmission of prions. J Infect Dis. 2002, 186 Suppl 2: S157-S165. 10.1086/344575.CrossRefPubMed
12.
go back to reference Prusiner SB: Scrapie prions. Annu Rev Microbiol. 1989, 43: 345-374. 10.1146/annurev.mi.43.100189.002021.CrossRefPubMed Prusiner SB: Scrapie prions. Annu Rev Microbiol. 1989, 43: 345-374. 10.1146/annurev.mi.43.100189.002021.CrossRefPubMed
13.
go back to reference Glatzel M, Aguzzi A: Peripheral pathogenesis of prion diseases. Microbes Infect. 2000, 2: 613-619. 10.1016/S1286-4579(00)00364-6.CrossRefPubMed Glatzel M, Aguzzi A: Peripheral pathogenesis of prion diseases. Microbes Infect. 2000, 2: 613-619. 10.1016/S1286-4579(00)00364-6.CrossRefPubMed
14.
go back to reference WHO guidelines on transmissible spongiform encephalopathies in relation to biological and pharmaceutical products. 2003, Geneva, World Health Organization, 1-26. WHO/BCT/QSD/03.01 WHO guidelines on transmissible spongiform encephalopathies in relation to biological and pharmaceutical products. 2003, Geneva, World Health Organization, 1-26. WHO/BCT/QSD/03.01
15.
go back to reference Ford MJ, Burton LJ, Morris RJ, Hall SM: Selective expression of prion protein in peripheral tissues of the adult mouse. Neuroscience. 2002, 113: 177-192. 10.1016/S0306-4522(02)00155-0.CrossRefPubMed Ford MJ, Burton LJ, Morris RJ, Hall SM: Selective expression of prion protein in peripheral tissues of the adult mouse. Neuroscience. 2002, 113: 177-192. 10.1016/S0306-4522(02)00155-0.CrossRefPubMed
16.
go back to reference Kimberlin RH, Walker CA: Pathogenesis of scrapie (strain 263K) in hamsters infected intracerebrally, intraperitoneally or intraocularly. J Gen Virol. 1986, 67: 255-263.CrossRefPubMed Kimberlin RH, Walker CA: Pathogenesis of scrapie (strain 263K) in hamsters infected intracerebrally, intraperitoneally or intraocularly. J Gen Virol. 1986, 67: 255-263.CrossRefPubMed
17.
go back to reference Race R, Oldstone M, Chesebro B: Entry versus blockade of brain infection following oral or intraperitoneal scrapie administration:role of prion protein expressin in peripheral nerves and spleen. J Virol. 2000, 74: 828-833. 10.1128/JVI.74.2.828-833.2000.CrossRefPubMedPubMedCentral Race R, Oldstone M, Chesebro B: Entry versus blockade of brain infection following oral or intraperitoneal scrapie administration:role of prion protein expressin in peripheral nerves and spleen. J Virol. 2000, 74: 828-833. 10.1128/JVI.74.2.828-833.2000.CrossRefPubMedPubMedCentral
18.
go back to reference Bradley R: Animal prion diseases. Prion diseases. Edited by: Collinge J and Palmer MS. 1997, Oxford, Oxford University Press Bradley R: Animal prion diseases. Prion diseases. Edited by: Collinge J and Palmer MS. 1997, Oxford, Oxford University Press
19.
go back to reference Scott JR, Foster JD, Fraser H: Conjunctival instillation of scrapie in mice can produce disease. Vet Microbiol. 1993, 34: 305-309. 10.1016/0378-1135(93)90055-C.CrossRefPubMed Scott JR, Foster JD, Fraser H: Conjunctival instillation of scrapie in mice can produce disease. Vet Microbiol. 1993, 34: 305-309. 10.1016/0378-1135(93)90055-C.CrossRefPubMed
20.
go back to reference Glatzel M, Abela E, Maissen M, Aguzzi A: Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease. N Engl J Med. 2003, 349: 1812-1820. 10.1056/NEJMoa030351.CrossRefPubMed Glatzel M, Abela E, Maissen M, Aguzzi A: Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease. N Engl J Med. 2003, 349: 1812-1820. 10.1056/NEJMoa030351.CrossRefPubMed
Metadata
Title
Tissue classification for the epidemiological assessment of surgical transmission of sporadic Creutzfeldt-Jakob disease. A proposal on hypothetical risk levels
Authors
Alberto Rábano
Jesús de Pedro-Cuesta
Kåre Mølbak
Åke Siden
Miguel Calero
Henning Laursen
the EUROSURGYCJD Research Group
Publication date
01-12-2005
Publisher
BioMed Central
Published in
BMC Public Health / Issue 1/2005
Electronic ISSN: 1471-2458
DOI
https://doi.org/10.1186/1471-2458-5-9

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