Epidemiological Profile and Management of Kawasaki Syndrome at Rabat Children’s Hospital: A retrospective study from Morocco

N. Mebrouk, L. Chtouki, A. Bentahila
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Abstract

Kawasaki disease (KD) is a common pediatric vasculitis with a risk of coronary artery aneurysm. In this report, we review some particularities of KD disease, especially coronary involvement, and highlight its aspects during the COVID-19 epidemic which saw the emergence of a syndrome named multisystem inflammatory syndrome in children (MIS-C). Because of its many similarities with KD, MIS-C is often referred to as Kawasaki-like disease (KLD) or pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS).We report on a retrospective study on the different epidemiological, clinical, and evolutionary aspects of KD and the coronary involvement resulting from this disease before and after the pandemic. The study is based on the echocardiography records of the P4 Department at Rabat Children’s Hospital, from January 2002 to December 2021. A total of 379 patients were diagnosed with KD during that period.  This includes 47 cases that were reported during the first year of the COVID-19 epidemic in Morocco (March 2020). Echocardiography results for our series show that cardiac complications wererelatively more frequent among KD patients during the COVID-19 period, perhaps because they were relatively older (67 months on average) than classic KD patients (37 months on average).  However, all patients had a favorable outcome after treatment with a combination of intravenous immunoglobulin (IVIG) and aspirin. The few patients who did not respond to standard treatment received corticosteroids, and no mortality occurred. We conclude that as far as cardiac complications,KD, KLD, and MIS-C are the same core disease that is triggered under different conditions for different age groups.The emergence of the Sars-Cov-2 virus changed the epidemiologic profile of KD but not its treatment. Insights from this study would help in the decision to initiate targeted immunotherapy quickly and reduce the risk factors associated with KD.
拉巴特儿童医院川崎综合征的流行病学概况和管理:来自摩洛哥的回顾性研究
川崎病(KD)是一种常见的儿童血管炎,有冠状动脉瘤的危险。在本报告中,我们回顾了KD疾病的一些特殊性,特别是冠状动脉受累,并强调了其在COVID-19流行期间出现的一种名为儿童多系统炎症综合征(MIS-C)的综合征。由于与KD有许多相似之处,misc通常被称为川崎样病(KLD)或与SARS-CoV-2暂时相关的儿科炎症多系统综合征(PIMS-TS)。我们报告了一项回顾性研究,研究了大流行前后KD的不同流行病学、临床和进化方面以及由该疾病引起的冠状动脉受累。该研究基于2002年1月至2021年12月拉巴特儿童医院P4科的超声心动图记录。在此期间,共有379名患者被诊断为KD。这包括在摩洛哥2019冠状病毒病流行第一年(2020年3月)报告的47例病例。我们系列的超声心动图结果显示,在COVID-19期间,KD患者的心脏并发症相对更频繁,这可能是因为他们的年龄(平均67个月)比典型KD患者(平均37个月)大。然而,所有患者在静脉注射免疫球蛋白(IVIG)和阿司匹林联合治疗后都有良好的结果。少数对标准治疗无效的患者接受皮质类固醇治疗,无死亡发生。我们的结论是,就心脏并发症而言,KD、KLD和MIS-C是相同的核心疾病,不同年龄组在不同条件下触发。Sars-Cov-2病毒的出现改变了KD的流行病学概况,但没有改变其治疗方法。这项研究的见解将有助于快速启动靶向免疫治疗的决定,并减少与KD相关的危险因素。
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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