Volume 26, Number 8—August 2020
CME ACTIVITY - Research
Sporadic Creutzfeldt-Jakob Disease among Physicians, Germany, 1993–2018
Table 4
Review of studies about health professionals and CJD*
Study or report |
Observation or sCJD patient |
---|---|
Case–control study | |
Wientjens et al., 1996 (34) | Observation: 1975–1984 (Japan, United Kingdom, United States), meta-analysis of 3 case–control studies |
•178 cases, 333 controls (hospital based, community based, and spouses) | |
•Nonsignificantly increased risk for health professionals (OR 1.5 [95% CI 0.5–4.1]) | |
Van Duijn et al., 1998 (24) | Observation: 1993–1995 (France, Germany, Italy, Netherlands, United Kingdom) |
•405 cases, 405 controls (hospital-based) | |
•No increased risk for health professionals (OR 0.92 [95% CI 0.69–1.32]) | |
Cocco et al., 2003 (35) | Observation: 1984–1995 (United States) |
•636 cases, 3,180 controls (population-based from a death registry) | |
•Increased risk for workers in physicians’ offices (OR 4.6 [95% CI 1.2–17.6]) | |
Ruegger et al., 2009 (32) | Observation: 2001–2004 (Switzerland) |
•69 cases, 224 controls (from general practitioners and random digit telephone dialing) | |
•Nonsignificantly increased risk for medical professionals (OR 1.46 [95% CI 0.43–5.15]) |
|
Case report | |
Schoene et al., 1981 (36) | 1 neurosurgeon |
Miller, 1988 (37) | 1 histopathologist |
Sitwell, 1988 (38) | 1 histopathologist |
Gorman et al., 1992 (39) | 1 pathologist |
Berger et al., 1993 (40) | 1 internist (with training in pathology 30 y before disease onset) |
Weber et al., 1993 (41) | 1 orthopedic surgeon (handling dura 20–24 y before onset) |
Mitrova et al., 2000 (42) | 1 physician, 5 nurses, 1 medical technician, 1 ambulance driver |
Alcalde-Cabero et al., 2012 (25) | Observation: 1965–2010; case reports and literature review |
•202 health professionals (among 8,321 cases) | |
•65 physicians (9 general practitioners, 7 surgeons, 7 internists, 4 dentists, 3 ophthalmologists, 2 pathologists), and 137 other health professionals |
*OR, odds ratio; sCJD, sporadic Creutzfeldt-Jakob disease.
References
- Prusiner SB. Novel proteinaceous infectious particles cause scrapie. Science. 1982;216:136–44. DOIPubMedGoogle Scholar
- Zerr I, Kallenberg K, Summers DM, Romero C, Taratuto A, Heinemann U, et al. Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. [Erratum in: Brain. 2012;135] [Pt 4]. Brain. 2009;132:2659–68. DOIPubMedGoogle Scholar
- Ladogana A, Puopolo M, Croes EA, Budka H, Jarius C, Collins S, et al. Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada. Neurology. 2005;64:1586–91. DOIPubMedGoogle Scholar
- Glatzel M, Rogivue C, Ghani A, Streffer JR, Amsler L, Aguzzi A. Incidence of Creutzfeldt-Jakob disease in Switzerland. Lancet. 2002;360:139–41. DOIPubMedGoogle Scholar
- Hermann P, Laux M, Glatzel M, Matschke J, Knipper T, Goebel S, et al. Validation and utilization of amended diagnostic criteria in Creutzfeldt-Jakob disease surveillance. Neurology. 2018;91:e331–8. DOIPubMedGoogle Scholar
- Colby DW, Prusiner SB. Prions. Cold Spring Harb Perspect Biol. 2011;3:
a006833 . DOIPubMedGoogle Scholar - Imran M, Mahmood S. An overview of animal prion diseases. Virol J. 2011;8:493. DOIPubMedGoogle Scholar
- The National CJD Research & Surveillance Unit. Current data on variant CJD cases worldwide [cited 2019 Aug 8]. http://www.cjd.ed.ac.uk/sites/default/files/worldfigs.pdf
- Andrews NJ, Farrington CP, Ward HJT, Cousens SN, Smith PG, Molesworth AM, et al. Deaths from variant Creutzfeldt-Jakob disease in the UK. Lancet. 2003;361:751–2. DOIPubMedGoogle Scholar
- Brown P, Preece M, Brandel JP, Sato T, McShane L, Zerr I, et al. Iatrogenic Creutzfeldt-Jakob disease at the millennium. Neurology. 2000;55:1075–81. DOIPubMedGoogle Scholar
- Heinemann U, Krasnianski A, Meissner B, Varges D, Kallenberg K, Schulz-Schaeffer WJ, et al. Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance. Brain. 2007;130:1350–9. DOIPubMedGoogle Scholar
- Brown P, Brandel J-P, Sato T, Nakamura Y, MacKenzie J, Will RG, et al. Iatrogenic Creutzfeldt-Jakob disease, final assessment. Emerg Infect Dis. 2012;18:901–7. DOIPubMedGoogle Scholar
- World Health Organization. Global surveillance, diagnosis and therapy of human transmissible spongiform encephalopathies: report of a WHO consultation, Geneva, Switzerland. 1998 Feb 9–11 [cited 2019 Aug 8]. https://apps.who.int/iris/handle/10665/65516
- Kobayashi A, Parchi P, Yamada M, Mohri S, Kitamoto T. Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases. Neuropathology. 2016;36:305–10. DOIPubMedGoogle Scholar
- Takeuchi A, Kobayashi A, Parchi P, Yamada M, Morita M, Uno S, et al. Distinctive properties of plaque-type dura mater graft-associated Creutzfeldt-Jakob disease in cell-protein misfolding cyclic amplification. Lab Invest. 2016;96:581–7. DOIPubMedGoogle Scholar
- Ward HJ, Everington D, Cousens SN, Smith-Bathgate B, Gillies M, Murray K, et al. Risk factors for sporadic Creutzfeldt-Jakob disease. Ann Neurol. 2008;63:347–54. DOIPubMedGoogle Scholar
- López FJG, Ruiz-Tovar M, Almazán-Isla J, Alcalde-Cabero E, Calero M, de Pedro-Cuesta J. Risk of transmission of sporadic Creutzfeldt-Jakob disease by surgical procedures: systematic reviews and quality of evidence. Euro Surveill. 2017;22:16–00806. DOIPubMedGoogle Scholar
- Puopolo M, Ladogana A, Vetrugno V, Pocchiari M. Transmission of sporadic Creutzfeldt-Jakob disease by blood transfusion: risk factor or possible biases. Transfusion. 2011;51:1556–66. DOIPubMedGoogle Scholar
- Urwin PJ, Mackenzie JM, Llewelyn CA, Will RG, Hewitt PE. Creutzfeldt-Jakob disease and blood transfusion: updated results of the UK Transfusion Medicine Epidemiology Review Study. Vox Sang. 2016;110:310–6. DOIPubMedGoogle Scholar
- Crowder LA, Schonberger LB, Dodd RY, Steele WR. Creutzfeldt-Jakob disease lookback study: 21 years of surveillance for transfusion transmission risk. Transfusion. 2017;57:1875–8. DOIPubMedGoogle Scholar
- Brown P, Cervenáková L, McShane L, Goldfarb LG, Bishop K, Bastian F, et al. Creutzfeldt-Jakob disease in a husband and wife. Neurology. 1998;50:684–8. DOIPubMedGoogle Scholar
- Rudge P, Jaunmuktane Z, Adlard P, Bjurstrom N, Caine D, Lowe J, et al. Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years. Brain. 2015;138(Pt 11):3386–99, 20, 21, 22.
- de Pedro-Cuesta J, Glatzel M, Almazán J, Stoeck K, Mellina V, Puopolo M, et al. Human transmissible spongiform encephalopathies in eleven countries: diagnostic pattern across time, 1993-2002. BMC Public Health. 2006;6:278. DOIPubMedGoogle Scholar
- van Duijn CM, Delasnerie-Lauprêtre N, Masullo C, Zerr I, de Silva R, Wientjens DP, et al. Case-control study of risk factors of Creutzfeldt-Jakob disease in Europe during 1993-95. European Union (EU) Collaborative Study Group of Creutzfeldt-Jakob disease (CJD). Lancet. 1998;351:1081–5. DOIPubMedGoogle Scholar
- Alcalde-Cabero E, Almazan-Isla J, Brandel JP, Breithaupt M, Catarino J, Collins S, et al. Health professions and risk of sporadic Creutzfeldt-Jakob disease, 1965 to 2010. Euro Surveill. 2012;17:20144.PubMedGoogle Scholar
- Bradford BM, Piccardo P, Ironside JW, Mabbott NA. Human prion diseases and the risk of their transmission during anatomical dissection. Clin Anat. 2014;27:821–32. DOIPubMedGoogle Scholar
- Worsley KJ. The power of likelihood ratio and cumulative sum tests for a change in a binomial probability. Biometrika. 1983;70:455–64. DOIGoogle Scholar
- Bundesärztekammer (BÄK). Ärztinnen und Ärzte mit Schwerpunktbezeichnung, BÄK. 2019 [cited 2019 Dec 2]. http://www.gbe-bund.de/oowa921-install/servlet/oowa/aw92/dboowasys921.xwdevkit/xwd_init?gbe.isgbetol/xs_start_neu/&p_aid=3&p_aid=66737473&nummer=614&p_sprache=D&p_indsp=99999999&p_aid=29100768
- Bundesärztekammer (BÄK). Ärztinnen und Ärzte mit Gebiets- und Facharztbezeichnung, BÄK. 2019 [cited 2019 Feb 27]. http://www.gbe-bund.de/oowa921-install/servlet/oowa/aw92/dboowasys921.xwdevkit/xwd_init?gbe.isgbetol/xs_start_neu/&p_aid=i&p_aid=7768273&nummer=656&p_sprache=D&p_indsp=99999999&p_aid=70341618
- Statistisches Bundesamt (DESTATIS). Bevölkerung: Deutschland, Stichtag, Altersjahre. 2019 [cited 2019 Feb 27]. http://www-genesis.destatis.de/genesis/online/link/tabellen/12411*
- Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol. 1999;46:224–33. DOIPubMedGoogle Scholar
- Ruegger J, Stoeck K, Amsler L, Blaettler T, Zwahlen M, Aguzzi A, et al. A case-control study of sporadic Creutzfeldt-Jakob disease in Switzerland: analysis of potential risk factors with regard to an increased CJD incidence in the years 2001-2004. BMC Public Health. 2009;9:18. DOIPubMedGoogle Scholar
- Zerr I, Brandel JP, Masullo C, Wientjens D, de Silva R, Zeidler M, et al. European surveillance on Creutzfeldt-Jakob disease: a case-control study for medical risk factors. J Clin Epidemiol. 2000;53:747–54. DOIPubMedGoogle Scholar
- Wientjens DP, Davanipour Z, Hofman A, Kondo K, Matthews WB, Will RG, et al. Risk factors for Creutzfeldt-Jakob disease: a reanalysis of case-control studies. Neurology. 1996;46:1287–91. DOIPubMedGoogle Scholar
- Cocco PL, Caperna A, Vinci F. Occupational risk factors for the sporadic form of Creutzfeldt-Jakob disease. Med Lav. 2003;94:353–63.PubMedGoogle Scholar
- Schoene WC, Masters CL, Gibbs CJ Jr, Gajdusek DC, Tyler HR, Moore FD, et al. Transmissible spongiform encephalopathy (Creutzfeldt-Jakob disease). Atypical clinical and pathological findings. Arch Neurol. 1981;38:473–7. DOIPubMedGoogle Scholar
- Creutzfeldt-Jakob disease in histopathology technicians. N Engl J Med. 1988;318:853–4. DOIPubMedGoogle Scholar
- Creutzfeldt-Jakob disease in histopathology technicians. N Engl J Med. 1988;318:853–4. DOIPubMedGoogle Scholar
- Gorman DG, Benson DF, Vogel DG, Vinters HV. Creutzfeldt-Jakob disease in a pathologist. Neurology. 1992;42:463. DOIPubMedGoogle Scholar
- Berger JR, David NJ. Creutzfeldt-Jakob disease in a physician: a review of the disorder in health care workers. Neurology. 1993;43:205–6. DOIPubMedGoogle Scholar
- Weber T, Tumani H, Holdorff B, Collinge J, Palmer M, Kretzschmar HA, et al. Transmission of Creutzfeldt-Jakob disease by handling of dura mater. Lancet. 1993;341:123–4. DOIPubMedGoogle Scholar
- Mitrová E, Belay G. Creutzfeldt-Jakob disease in health professionals in Slovakia. Eur J Epidemiol. 2000;16:353–5. DOIPubMedGoogle Scholar
- de Pedro Cuesta J, Ruiz Tovar M, Ward H, Calero M, Smith A, Verduras CA, et al. Sensitivity to biases of case-control studies on medical procedures, particularly surgery and blood transfusion, and risk of Creutzfeldt-Jakob disease. Neuroepidemiology. 2012;39:1–18. DOIPubMedGoogle Scholar
1These authors contributed equally to this article.