Kawasaki disease in children: a retrospective cross-sectional study.

IF 1.4 Q3 RHEUMATOLOGY
Reumatologia Pub Date : 2023-01-01 DOI:10.5114/reum/163170
Ali Hosseininasab, Fahime Pashang, Mohammad Rezaei Zadeh Rukerd, Hanieh Mirkamali, Mohsen Nakhaie, Amin Sayyadi
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引用次数: 0

Abstract

Introduction: Kawasaki disease (KD) is a systemic vasculitis, seen mostly in children. Epidemiology of KD is dependent on geographical location and seasonality. Although many years have passed since the first report of KD, multiple related factors are still unknown.

Material and methods: We investigated the clinical, paraclinical, and therapeutic aspects of KD in Kerman, Iran by performing a retrospective, descriptive, cross-sectional study on all children hospitalized due to KD between 2007 and 2020.

Results: A total of 340 patients with mean ±SD age of 29.83 ±22.55 months participated in the study. Most of our patients were two to five years old. The male : female ratio was ~ 1.4 : 1. A few of our patients had a family history of KD or vasculitis (0.3%, 1.7%). Typical KD was more common by a large margin (316 patients with typical KD). More than half of our patients had a duration of hospitalization of under ten days. All of our patients were febrile. Hand/foot and lip/mouth changes were the second and third most common clinical findings in more than 60% of our patients. Other manifestations were conjunctivitis in 40%, skin rashes in 34.8%, gastrointestinal manifestations in 33.9%, and lymphadenopathy in 25.3%. Echocardiography revealed abnormalities in 78.6% of the participants; coronary artery aneurysm (CAA) was the most frequent (22.5%) and follow-up echocardiography revealed that all of them regressed within 6 months after treatment. The two laboratory tests with the highest ratio of abnormality were erythrocyte sedimentation rate (95%) and hemoglobin (83.3%). C-reactive protein and liver function tests were also abnormal in most patients. All of our patients received intravenous immunoglobulin and acetylsalicylic acid.

Conclusions: Kawasaki disease must be considered in every febrile child, especially those with risk factors, because timely diagnosis and treatment are essential to prevent complications. Health policies should focus on appropriate diagnosis and treatment to prevent the occurrence of sequelae.

Abstract Image

儿童川崎病:一项回顾性横断面研究
川崎病(Kawasaki disease, KD)是一种全身性血管炎,多见于儿童。KD的流行病学与地理位置和季节性有关。虽然KD的首次报道已经过了许多年,但许多相关因素仍然未知。材料和方法:我们通过对2007年至2020年期间因KD住院的所有儿童进行回顾性、描述性、横断面研究,调查了伊朗Kerman患者KD的临床、临床旁和治疗方面。结果:共有340例患者参与研究,平均±SD年龄为29.83±22.55个月。我们的大多数病人都是2到5岁。男女比例为~ 1.4:1。少数患者有KD或血管炎家族史(0.3%,1.7%)。典型KD更为常见(316例为典型KD)。超过一半的病人住院时间少于十天。我们所有的病人都发烧了。在超过60%的患者中,手/脚和嘴唇/嘴的变化是第二和第三常见的临床表现。其他表现为结膜炎占40%,皮疹占34.8%,胃肠道表现占33.9%,淋巴结病占25.3%。超声心动图显示78.6%的参与者异常;冠状动脉动脉瘤(CAA)最为常见(22.5%),随访超声心动图显示治疗后6个月内全部消退。血沉率(95%)和血红蛋白(83.3%)是异常率最高的两项实验室检查。大多数患者的c反应蛋白和肝功能检查也异常。所有患者均静脉注射免疫球蛋白和乙酰水杨酸。结论:川崎病必须在每一个发热儿童,特别是那些有危险因素,因为及时诊断和治疗是预防并发症的关键。卫生政策应侧重于适当的诊断和治疗,以防止后遗症的发生。
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
Reumatologia
Reumatologia Medicine-Rheumatology
CiteScore
2.70
自引率
0.00%
发文量
44
审稿时长
10 weeks
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