Enhanced geographically restricted surveillance simulates sporadic Creutzfeldt-Jakob disease cluster

被引:29
作者
Klug, Genevieve M. [1 ,5 ]
Wand, Handan [2 ]
Boyd, Alison [1 ,5 ]
Law, Matthew [2 ]
Whyte, Scott [3 ,4 ]
Kaldor, John [2 ]
Masters, Colin L. [1 ,5 ]
Collins, Steven [1 ,5 ]
机构
[1] Univ Melbourne, Dept Pathol, Australian Natl Creutzfeldt Jakob Dis Registry, Parkville, Vic 3010, Australia
[2] Univ New S Wales, Natl Ctr HIV Epidemiol & Clin Res, Sydney, NSW, Australia
[3] N Sydney & Cent Coast Area Hlth, Sydney, NSW, Australia
[4] Univ Newcastle, Newcastle, NSW 2308, Australia
[5] Mental Hlth Res Inst Victoria, Parkville, Vic, Australia
关键词
CJD; cluster analysis; epidemiology; surveillance; incidence; 14-3-3; PROTEIN; PRION DISEASE; EPIDEMIOLOGY; FRANCE; RISK; DIAGNOSIS; AUSTRALIA; MORTALITY; SURGERY; HUNGARY;
D O I
10.1093/brain/awn303
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Spatio-temporal clustering of sporadic Creutzfeldt-Jakob disease (sCJD) has been recognized and investigated previously in various global settings including Australia. Generally, despite often extensive investigation, explanations such as point source outbreaks and plausible case-to-case transmission links have not been identified to explain the apparently higher case rates than expected. In the context of national surveillance during the period 19932006, an increased number of cases of sCJD were recognized in a circumscribed coastal region of eastern Australia. To assess the significance of this apparent clustering, the Spatial Scan Statistic was used to examine for geographic excess of CJD mortality at spatial and temporal combined, spatial only and temporal only levels. A significant spatial cluster was confirmed, encompassing three contiguous statistical local areas within the state of New South Wales (NSW). Detailed epidemiological analysis did not reveal a plausible cross-over or point source transmission event. Further evaluation prompted the conclusion that vigilant and motivated managing clinicians in this geographically circumscribed area of NSW evinced a sustained higher level of clinical awareness for the broad phenotypic spectrum of CJD with reliable referral of suspect cases for further investigation. In addition, these physicians established and maintained a well-coordinated and active approach to suspect CJD autopsy. This combination of factors translated into a higher intensity of surveillance at approximately twice the rate per population observed in the entire state, culminating in twice the incidence of sCJD at around 2.28 cases/million population/year. The hypothesis that intensity of surveillance for rare disorders can be objectively measured and that this can positively correlate with disease incidence deserves further exploration. It may prove to be an important insight into the varying incidence rates over periods of time within individual nations and between different countries.
引用
收藏
页码:493 / 501
页数:9
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