Esmonde T G, Will R G
Department of Clinical Neurosciences, Western General Hospital, Edinburgh.
Scott Med J. 1992 Dec;37(6):181-4. doi: 10.1177/003693309203700607.
The epidemiological and clinical features of Creutzfeldt-Jakob disease have never before been studied in Scotland and Northern Ireland. Case records for those dying with this diagnosis were obtained for the period 1980-89. Over the ten year period, 25 definite or probable cases were identified, giving an annual incidence of 0.37 cases/million. There were more cases in the second half of the decade, and this was most likely due to increased ascertainment. One pair of cases occurred in close proximity to each other. Sex distribution showed an excess of males (male:female ratio = 1.8:1). Mean age at onset was 65.2 years, and mean duration of disease was 5.3 months. The presenting symptoms and clinical features were similar to those noted in previous studies of other populations. There was no excess of cases in occupations linked to food, farming, or medical/paramedical work.
此前从未在苏格兰和北爱尔兰对克雅氏病的流行病学和临床特征进行过研究。获取了1980年至1989年期间因该诊断死亡者的病例记录。在这十年期间,共确定了25例确诊或疑似病例,年发病率为每百万人口0.37例。该十年的后半期病例更多,这很可能是由于确诊率提高所致。有一对病例彼此距离很近。性别分布显示男性过多(男:女比例 = 1.8:1)。发病时的平均年龄为65.2岁,疾病平均持续时间为5.3个月。出现的症状和临床特征与之前其他人群的研究中所记录的相似。与食品、农业或医疗/医护工作相关的职业中病例并无过多情况。