Kawasaki disease in Kenya and review of the African literature

IF 2.8 3区 医学 Q1 PEDIATRICS
A. Migowa, CM. Njeru, E. Were, T. Ngwiri, I. Colmegna, C. Hitchon, R. Scuccimarri
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引用次数: 0

Abstract

Kawasaki disease has been described across the globe, although publications from Africa are limited. To our knowledge, there are no publications on Kawasaki disease from Kenya, which triggered this report. A retrospective cross-sectional study was undertaken to identify in-patients with a discharge diagnosis of Kawasaki disease, over 2 different 5-year periods, at two pediatric hospitals in Nairobi, Kenya. We reviewed the medical records of all patients and report their clinical findings, diagnostic workup and treatment. In addition, we undertook a detailed review of the literature. Twenty-three patients with Kawasaki disease were identified, of those 12 (52.2%) had incomplete disease. The mean age was 2.3 years (SD+/-2.2) (range 0.3–10.3) with a male to female ratio of 1:1. The mean duration of fever at diagnosis was 8.3 days (SD+/-4.7) (range 2–20). Oral changes were the most common clinical feature and conjunctivitis the least common. Thrombocytosis at diagnosis was seen in 52% (12/23). Twenty-one patients (91.3%) were treated with intravenous immunoglobulin and all except 1 received aspirin. Baseline echocardiograms were performed in 95.7% (22/23) and found to be abnormal in 3 (13.6%). Follow-up data was limited. Our literature review identified 79 publications with documented cases of Kawasaki disease in children from 22 countries across the African continent with a total of 1115 patients including those from this report. Only 153 reported cases, or 13.7%, are from sub-Saharan Africa. This is the first publication on Kawasaki disease from Kenya and one of the largest reports from sub-Saharan Africa. It is the first to have a complete review of the number of published cases from the African continent. Challenges in the diagnosis and management of Kawasaki disease in many African countries include disease awareness, infectious confounders, access and cost of intravenous immunoglobulin, access to pediatric echocardiography and follow-up. Increasing awareness and health care resources are important for improving outcomes of Kawasaki disease in Africa.
肯尼亚的川崎病和非洲文献综述
全球各地都有关于川崎病的描述,但来自非洲的出版物非常有限。据我们所知,肯尼亚没有关于川崎病的出版物,因此引发了本报告。我们开展了一项回顾性横断面研究,以确定肯尼亚内罗毕两家儿科医院在两个不同的 5 年期间出院诊断为川崎病的住院病人。我们查阅了所有患者的病历,并报告了他们的临床发现、诊断工作和治疗情况。此外,我们还详细查阅了相关文献。共发现 23 名川崎病患者,其中 12 人(52.2%)病情不完全。患者平均年龄为 2.3 岁(SD+/-2.2)(范围为 0.3-10.3),男女比例为 1:1。确诊时的平均发热时间为 8.3 天(SD+/-4.7)(范围为 2-20)。口腔变化是最常见的临床特征,结膜炎是最不常见的临床特征。52%的患者(12/23)在确诊时出现血小板减少。21名患者(91.3%)接受了静脉注射免疫球蛋白治疗,除1名患者外,其余患者均接受了阿司匹林治疗。95.7%的患者(22/23)接受了基线超声心动图检查,其中3例(13.6%)发现异常。随访数据有限。我们在文献综述中发现了79篇有川崎病儿童病例记录的文献,这些病例来自非洲大陆的22个国家,包括本报告在内共有1115名患者。撒哈拉以南非洲地区的报告病例仅有 153 例,占 13.7%。这是第一份关于肯尼亚川崎病的出版物,也是撒哈拉以南非洲最大的报告之一。这也是首次对非洲大陆已发表病例数量的完整回顾。许多非洲国家在川崎病的诊断和管理方面面临的挑战包括对疾病的认识、感染性混杂因素、静脉注射免疫球蛋白的获取途径和成本、儿科超声心动图检查和随访。提高认识和增加医疗资源对于改善非洲川崎病的治疗效果非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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