大流行期间儿童多系统炎症综合征与川崎病的鉴别。

IF 1.3 Q3 PEDIATRICS
Seher Şener, Ezgi Deniz Batu, Ümmüşen Kaya Akca, Erdal Atalay, Müşerref Kasap Cüceoğlu, Zeynep Balık, Özge Başaran, Tevfik Karagöz, Yasemin Özsürekçi, Yelda Bilginer, Seza Özen
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引用次数: 0

摘要

目的:材料与方法: 我们对大流行期间(2021年1月至2022年12月)收治的川崎病(KD)患者和有KD样表现的儿童多系统炎症综合征(MIS-C)患者进行了评估:我们对大流行期间(2021 年 1 月至 2022 年 12 月)收治的 KD 患者和有 KD 类似症状的 MIS-C 患者进行了评估:结果:共纳入 33 名 MIS-C 患者和 15 名 KD 患者。川崎病患者比 MIS-C 患者年轻(3.4 岁对 7.6 岁)。川崎病患者更常见皮疹(P = .044,100% 对 75.7%)、口腔粘膜变化(P = .044,100% 对 75.7%)和颈淋巴结病(P = .001,93.3% 对 42.4%)。儿童多系统炎症综合征:患者有更多的低血压(P = .002,45.4% 对 0)、胃肠道症状(P .001,72.7% 对 13.3%)和呼吸道症状(P = .044,24.2% 对 0)。与 KD 患者不同的是,儿童多系统炎症综合征患者的淋巴细胞和血小板计数偏低,d-二聚体、铁蛋白和心脏参数水平升高。在超声心动图检查中,儿童多系统炎症综合征患者的左心室收缩功能明显下降。在治疗方面的另一个明显差异是,MIS-C 患者需接受阿那金拉治疗:结论:虽然 MIS-C 患者的临床表现可能与 KD 相似,但有几个特征有助于区分 MIS-C 和传统 KD。特定的临床(低血压、胃肠道和呼吸道症状)和实验室(低淋巴细胞和血小板计数,较高的 C 反应蛋白、铁蛋白、二聚体和心脏参数)特征是 MIS-C 的特征。此外,这两种疾病的治疗策略也存在明显差异,MIS-C 患者比传统 KD 患者更倾向于使用生物药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differentiating Multisystem Inflammatory Syndrome in Children from Kawasaki Disease During the Pandemic.

Objective: We aimed to delineate the distinctive characteristics that aid in distinguishing between Kawasaki disease (KD) and multisystem inflammatory syndrome in children (MIS-C) with KD-like manifestations during the pandemic.

Materials and methods: We evaluated KD patients and MIS-C patients with KD-like symptoms admitted during the pandemic (between January 2021 and December 2022).

Results: Thirty-three MIS-C patients and 15 KD patients were included. Kawasaki disease patients were younger than MIS-C patients (3.4 vs. 7.6 years). Rash (P = .044, 100% vs. 75.7%), oral mucosal changes (P = .044, 100% vs. 75.7%), and cervical lymphadenopathy (P = .001, 93.3% vs. 42.4%) were more common in KD. Multisystem inflammatory syndrome in children: patients had more hypotension (P = .002, 45.4% vs. 0), gastrointestinal (P .001, 72.7% vs. 13.3%), and respiratory symptoms (P = .044, 24.2% vs. 0). Multisystem inflammatory syndrome in children patients also had low lymphocyte and thrombocyte counts and elevated levels of d-dimer, ferritin, and cardiac parameters, unlike KD patients. Multisystem inflammatory syndrome in children patients exhibited a notable reduction in left ventricular systolic function in echocardiography. Another significant difference with regard to management was the anakinra treatment, which was prescribed for MIS-C patients.

Conclusion: Although MIS-C patients might display a clinical resemblance to KD, several features could help differentiate between MIS-C and classical KD. Specific clinical (hypotension, gastrointestinal, and respiratory symptoms) and laboratory (low lymphocyte and thrombocyte counts with higher C-reactive protein, ferritin, d-dimer, and cardiac parameters) features are characteristic of MIS-C. In addition, divergence in management strategies is evident between the 2 diseases, as biologic drugs were more prevalently employed in MIS-C patients than in classical KD patients.

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