Can Mortality Data Provide Reliable Indicators for Creutzfeldt-Jakob Disease Surveillance? A Study in France from 2000 to 2008

被引:5
作者
Brandel, Jean-Philippe [1 ,2 ,3 ,4 ,5 ]
Welaratne, Arlette [1 ]
Salomon, Dominique [6 ,7 ]
Capek, Isabelle [8 ]
Vaillant, Veronique [8 ]
Aouaba, Albertine [9 ]
Haik, Stephane [1 ,2 ,3 ,4 ,5 ]
Alperovitch, Annick [6 ,7 ]
机构
[1] Grp Hosp Pitie Salpetriere, AP HP, FR-75013 Paris, France
[2] INSERM, UMR S 975, Equipe Malad Alzheimer Malad Prions, Paris, France
[3] CNRS, UMR 7225, Paris, France
[4] Univ Paris 06, CRICM, UMR 7225, S 975, Paris, France
[5] CNR ATNC, Paris, France
[6] INSERM, U708, Paris, France
[7] Univ Paris 06, UMR S708, Paris, France
[8] Inst Veille Sanit, St Maurice, France
[9] INSERM CepiDc, Le Vesinet, France
关键词
Creutzfeldt-Jakob disease; Mortality register; Active surveillance; Evaluation of surveillance systems; CHRONIC WASTING DISEASE; BLOOD-TRANSFUSION; RISK; PATIENT; ENCEPHALOPATHY; TRANSMISSION; DIAGNOSIS; VCJD;
D O I
10.1159/000332764
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Surveillance of Creutzfeldt-Jakob disease (CJD) is still an important issue because of the variant CJD epidemic, which is in decline and also because of the emergence of novel forms of animal transmissible spongiform encephalopathy with zoonotic potential and the risk of nosocomial and blood transfusion-related transmission. Active surveillance has been implemented in most European countries and requires important human resources and funding. Here, we studied whether national mortality and morbidity statistics can be used as reliable indicators. Methods: CJD data collected by the French national CJD surveillance centre were compared with data registered in the national mortality statistics. Results: From 2000 to 2008, the two sources reported fairly similar numbers of CJD deaths. However, analysis of individual data showed important between-sources disagreement. Nearly 24% of CJD reported by the mortality register were false-positive diagnoses and 21.6% of the CJD cases diagnosed by the surveillance centre were not registered as CJD in the national mortality statistics. One out of 22 variant CJD cases was not reported as having any type of CJD in the mortality statistics. Conclusions: These findings raise doubt about the possibility of a reliable CJD surveillance only based on mortality data. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:188 / 192
页数:5
相关论文
共 22 条
[1]   Wernicke encephalopathy and Creutzfeldt-Jakob disease [J].
Bertrand, A. ;
Brandel, J. P. ;
Grignon, Y. ;
Sazdovitch, V. ;
Seilhean, D. ;
Faucheux, B. ;
Privat, N. ;
Brault, J. L. ;
Vital, A. ;
Uro-Coste, E. ;
Pluot, M. ;
Chapon, F. ;
Maurage, C. A. ;
Letournel, F. ;
Vespignani, H. ;
Place, G. ;
Degos, C. F. ;
Peoc'h, K. ;
Haik, S. ;
Hauw, J. J. .
JOURNAL OF NEUROLOGY, 2009, 256 (06) :904-909
[2]   Identification of a second bovine amyloidotic spongiform encephalopathy: Molecular similarities with sporadic Creutzfeldt-Jakob disease [J].
Casalone, C ;
Zanusso, G ;
Acutis, P ;
Ferrari, S ;
Capucci, L ;
Tagliavini, F ;
Monaco, S ;
Caramelli, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :3065-3070
[3]   Atypical BSE (BASE) Transmitted from Asymptomatic Aging Cattle to a Primate [J].
Comoy, Emmanuel E. ;
Casalone, Cristina ;
Lescoutra-Etchegaray, Nathalie ;
Zanusso, Gianluigi ;
Freire, Sophie ;
Marce, Dominique ;
Auvre, Frederic ;
Ruchoux, Marie-Magdeleine ;
Ferrari, Sergio ;
Monaco, Salvatore ;
Sales, Nicole ;
Caramelli, Maria ;
Leboulch, Philippe ;
Brown, Paul ;
Lasmezas, Corinne I. ;
Deslys, Jean-Philippe .
PLOS ONE, 2008, 3 (08)
[4]   Predicting the CJD epidemic in humans [J].
Cousens, SN ;
Vynnycky, E ;
Zeidler, M ;
Will, RG ;
Smith, PG .
NATURE, 1997, 385 (6613) :197-198
[5]   Nosocomial transmission of sporadic Creutzfeldt-Jakob disease: results from a risk-based assessment of surgical interventions [J].
de Pedro-Cuesta, Jesus ;
Mahillo-Fernandez, Ignacio ;
Rabano, Alberto ;
Calero, Miguel ;
Cruz, Mabel ;
Siden, Ake ;
Laursen, Henning ;
Falkenhorst, Gerhard ;
Molbak, Kare .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2011, 82 (02) :204-212
[6]   Uncertainty in the Tail of the Variant Creutzfeldt-Jakob Disease Epidemic in the UK [J].
Garske, Tini ;
Ghani, Azra C. .
PLOS ONE, 2010, 5 (12)
[7]   Predicted vCJD mortality in Great Britain - Modelling the latest data puts a ceiling on the likely number of vCJD cases. [J].
Ghani, AC ;
Ferguson, NM ;
Donnelly, CA ;
Anderson, RM .
NATURE, 2000, 406 (6796) :583-584
[8]  
Health Protection Agency, 2007, HLTH PROTECTION REPO, V1
[9]   Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion [J].
Llewelyn, CA ;
Hewitt, PE ;
Knight, RSG ;
Amar, K ;
Cousens, S ;
Mackenzie, J ;
Will, RG .
LANCET, 2004, 363 (9407) :417-421
[10]   Surgery and Risk of Sporadic Creutzfeldt-Jakob Disease in Denmark and Sweden: Registry-Based Case-Control Studies [J].
Mahillo-Fernandez, Ignacio ;
de Pedro-Cuesta, Jesus ;
Jose Bleda, Maria ;
Cruz, Mabel ;
Molbak, Kare ;
Laursen, Henning ;
Falkenhorst, Gerhard ;
Martinez-Martin, Pablo ;
Siden, Ake .
NEUROEPIDEMIOLOGY, 2008, 31 (04) :229-240