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首页> 外文期刊>The Lancet >Incidence of Henoch-Schonlein purpura, Kawasaki disease, and rare vasculitides in children of different ethnic origins.
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Incidence of Henoch-Schonlein purpura, Kawasaki disease, and rare vasculitides in children of different ethnic origins.

机译:不同种族血统的儿童患上过敏性紫癜,川崎病和罕见血管炎的发生率。

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摘要

BACKGROUND: The frequency and ethnic variation of Henoch-Schonlein purpura, Kawasaki disease, and rarer vasculitides during childhood are not well characterised. Our aim was to ascertain the incidence and ethnic distribution of these conditions in children resident in a region of the UK with a diverse ethnic mix. METHODS: 1.1 million children younger than age 17 years live in the West Midlands. Between Sept 1, 1996, and Aug 31, 1999, we surveyed this population with monthly questionnaires sent to 321 consultants, a single questionnaire sent to 2860 family doctors, and review of 406 case notes with diagnostic codes for vasculitis. We included in the analyses children who fulfilled established criteria for vasculitis with disease onset during the study, and calculated incidence rates from population rates derived from the census of 1991. FINDINGS: We identified 586 new instances of vasculitis and connective tissue disease. The estimated annual incidence of Henoch-Schonlein purpura was 20.4 per 100000, and was highest between the ages of 4 years and 6 years (70.3 per 100000). The estimated annual incidence of Kawasaki disease was 5.5 per 100000 in children younger than 5 years, and was highest in Indian subcontinent Asian children (14.6 per 100000). Indian subcontinent Asian and black children had the highest incidence of systemic lupus erythematosus, juvenile dermatomyositis, and other primary systemic vasculitides. INTERPRETATION: Childhood Henoch-Schonlein purpura is more frequent in the West Midlands than previously reported, and Kawasaki disease has a higher incidence than previously indicated in the UK, with the highest incidence in Indian subcontinental Asian children. Other vasculitis is rare in childhood.
机译:背景:儿童期Henoch-Schonlein紫癜,川崎病和稀有血管炎的发生频率和种族变异尚无很好的特征。我们的目标是确定居住在英国不同种族混合地区的儿童中这些疾病的发生率和种族分布。方法:西米德兰兹州居住着110万名17岁以下的儿童。在1996年9月1日至1999年8月31日期间,我们通过向321位顾问发送的每月调查表,向2860位家庭医生发送的一份调查表以及406例带有血管炎诊断代码的病例注释对这一人群进行了调查。在研究中,我们纳入了符合既定疾病发作标准的血管炎的儿童,并根据1991年的人口普查计算出的发病率,计算出发病率。结果:我们确定了586例新的血管炎和结缔组织病病例。过敏性紫癜的估计年发病率为每100000例20.4,在4岁至6岁之间最高(每100000例70.3)。据估计,川崎病的年发病率在5岁以下的儿童中为每10万人中5.5例,在印度次大陆亚洲儿童中最高(每10万人中为14.6例)。印度次大陆亚洲和黑人儿童的系统性红斑狼疮,青少年皮肌炎和其他原发性系统性血管炎的发生率最高。解释:西米德兰兹地区儿童时期的过敏性紫癜比以前报道的更为频繁,川崎病的发病率高于英国,而印度次大陆亚洲儿童的发病率最高。其他血管炎在儿童时期很少见。

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