Surveillance of Creutzfeldt-Jakob disease in Australia: 2008.

Genevieve M Klug, Alison Boyd, Victoria Lewis, Amelia R McGlade, Helene Roberts, Samantha L Douglass, Colin L Masters, Steven J Collins
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Abstract

Australia-wide surveillance of all human transmissible spongiform encephalopathies (TSEs) is performed by the Australian National Creutzfeldt-Jakob Disease Registry (ANCJDR), since establishment in October 1993. During the surveillance period 1 April 2007 to 31 March 2008, the ANCJDR received 78 new suspect case notifications of TSEs (67 in 2007, 13 in 2008). This level of suspect case notification aligns with the previous 2006/2007 surveillance period, which was elevated in comparison to the previous 5 years. Based on the total number of probable and definite Creutzfeldt-Jakob disease (CJD) cases, encompassing retrospective cases to 1970 and prospectively ascertained cases from 1993 to 31 March 2008, the average age-adjusted mortality rate is 1.16 deaths per million per year. In this short report, we provide updated Australian TSE figures and describe recent changes in surveillance mechanisms and review their impact on case notifications and eventual CJD classification.

澳大利亚克雅氏病监测:2008。
自1993年10月成立以来,澳大利亚国家克雅氏病登记处(ANCJDR)在澳大利亚范围内对所有人类传染性海绵状脑病(tse)进行监测。在2007年4月1日至2008年3月31日的监测期间,国家传染病预防和预防中心收到了78例新的tse疑似病例通报(2007年67例,2008年13例)。这一疑似病例通报水平与2006/2007年监测期间一致,与前5年相比有所提高。根据可能和确诊的克雅氏病(CJD)病例总数,包括1970年的回顾性病例和1993年至2008年3月31日的前瞻性确定病例,年龄调整后的平均死亡率为每年每百万人死亡1.16例。在这份简短的报告中,我们提供了最新的澳大利亚TSE数据,描述了监测机制的最新变化,并回顾了它们对病例报告和最终CJD分类的影响。
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