Ussher R, Yeong M L, Stace N
Wellington Medical School.
N Z Med J. 1994 May 25;107(978):195-7.
A retrospective study was carried out in the greater Wellington area. The objectives of this study were to identify an incidence rate, presenting symptoms and clinical features of coeliac disease.
Histology archives from the Wellington hospital department of pathology over the last eight years (1985-92) were retrieved and analysed. Abnormal duodenal and jejunal histological sections were reviewed. One hundred and seventy seven biopsy specimens from 127 patients were identified for further study from a total of 367 abnormal duodenal and jejunal biopsy specimens. Diagnosis of coeliac disease was based on information from hospital notes, biopsy request forms, and histology reports. Diagnostic criteria used for coeliac disease were evidence of malabsorption, abnormal histology consistent with coeliac disease and clinical improvement following a gluten free diet.
Thirty eight patients were diagnosed with coeliac disease 1985-92 in a population of 267,252. Of these 38 only four were children (0-12 years). Overall incidence was 1.8 per 100,000. The estimated overall prevalence was 70 per 100,000, with 14 per 100,000 for children. The live birth rate was 0.1 per 1000. There was a female predominance of 3:1. Patients presented with a diverse range of problems, most commonly diarrhoea, anaemia, weight loss and steatorrhoea. Three out of the 6 patients who had a single problem had anaemia.
The study has demonstrated an overall incidence and prevalence of coeliac disease in the Wellington region similar to overseas figures. However only 11% of the total were children, which is a very low proportion compared to the 50% reported in Sweden and 25% in Edinburgh. Patients presented with a wide range of clinical features. The threshold for small bowel biopsy should be relatively low in any patient considered to have clinical features of malabsorption.
在大惠灵顿地区开展一项回顾性研究。本研究的目的是确定乳糜泻的发病率、症状表现和临床特征。
检索并分析了惠灵顿医院病理科过去八年(1985 - 1992年)的组织学档案。对十二指肠和空肠的异常组织学切片进行了复查。从总共367份异常十二指肠和空肠活检标本中,确定了127例患者的177份活检标本用于进一步研究。乳糜泻的诊断基于医院记录、活检申请表和组织学报告中的信息。乳糜泻的诊断标准为吸收不良的证据、与乳糜泻一致的异常组织学以及无麸质饮食后的临床改善。
在1985 - 1992年期间,在267,252人的人群中,有38例被诊断为乳糜泻。其中38例中只有4例是儿童(0 - 12岁)。总体发病率为每10万人中有1.8例。估计总体患病率为每10万人中有70例,儿童患病率为每10万人中有14例。活产率为每1000例中有0.1例。女性占主导,比例为3:1。患者表现出各种各样的问题,最常见的是腹泻、贫血、体重减轻和脂肪泻。6例仅有单一问题的患者中有3例患有贫血。
该研究表明,惠灵顿地区乳糜泻的总体发病率和患病率与海外数据相似。然而,儿童仅占总数的11%,与瑞典报告的50%和爱丁堡报告的25%相比,这一比例非常低。患者表现出广泛的临床特征。对于任何被认为有吸收不良临床特征的患者,小肠活检的阈值应该相对较低。