2009
DOI: 10.1186/1471-2458-9-18
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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

Abstract: Background: In 2001, the observed annual mortality from Creutzfeldt-Jakob disease (CJD) in Switzerland increased from less than 1.5 to 2.6 per million inhabitants. An underlying cause could not be identified.

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Cited by 37 publications
(68 citation statements)
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“…Seventeen reports focused on surgical history [4,9,10,13,14,15,16,27,28,29,30,31,32,33,34,35,36] and 14 also included data on BT [4,13,14,15,16,27,28,29,30,31,32,34,35,36]. Two UK studies addressed BT only [17,26].…”
Section: Resultsmentioning
confidence: 99%
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“…Seventeen reports focused on surgical history [4,9,10,13,14,15,16,27,28,29,30,31,32,33,34,35,36] and 14 also included data on BT [4,13,14,15,16,27,28,29,30,31,32,34,35,36]. Two UK studies addressed BT only [17,26].…”
Section: Resultsmentioning
confidence: 99%
“…The 20 papers assessed in this report included 1 on CJD (all forms included) [30], 3 on vCJD [4,5,33], 17 on sCJD [9,10,13,14,15,16,17,26,27,28,29,31,32,33,34,35,36] and 1 on gCJD [16]. Seventeen reports focused on surgical history [4,9,10,13,14,15,16,27,28,29,30,31,32,33,34,35,36] and 14 also included data on BT [4,13,14,15,16,27,28,29,30,31,32,34,35,36].…”
Section: Resultsmentioning
confidence: 99%
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“…This has occurred in parallel with methodological enhancements such as establishment of national registries, application of a prospective approach, formulation of standard case definitions, recognition of disease subtypes, development and validation of diagnostic tools, and increased awareness among collaborating health professionals, all strengthening the plausibility of improved ascertainment, particularly in older patients and/or patients with less typical presentations (5,32). In Switzerland, a temporary increase in CJD mortality in the years 2001 to 2004 was ultimately attributed to heightened awareness of the disease as a result of the vCJD epidemic in the United Kingdom; the authors went so far as to suggest that the "true" mortality rate for sCJD may exceed two per million per year (33). In a recent study incorporating data from 10 countries, significant statistical correlations were demonstrated between observed sCJD mortality rate and several indices of surveillance intensity, including rates of case notification to the central registry as well as rates of autopsy and other laboratory investigations (34).…”
Section: Discussionmentioning
confidence: 99%