Coronary artery dilation in children with MIS-C: prevalence, risk factor, and progression.

IF 2.6 3区 医学 Q1 PEDIATRICS European Journal of Pediatrics Pub Date : 2025-03-03 DOI:10.1007/s00431-025-06051-6
Phung Nguyen The Nguyen, Tran Thanh Thuc, Nguyen Thanh Hung, Nguyen Tri Hao, Nguyen Minh Tri Viet, Nguyen Thi Ngoc Phuong, Vu Thi Thuy Trang, Le Minh Hieu, Phan Dai Bang, Nguyen Thi Mai Thao, Huynh Nguyen Anh Thu
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Abstract

Cardiac injury is the critical issue in children with MIS-C, particularly coronary artery dilation. This study aimed to describe the prevalence, risk factors associated with coronary artery abnormalities, and their progression after 3 months of follow-up in MIS-C children in Vietnam. A prospective multicenter case series study was conducted on MIS-C patients diagnosed per WHO criteria from September 2021 to February 2023 at the two largest pediatric hospitals in southern Vietnam. Data on demographics, clinical features, laboratory findings, and treatments during the acute phase of MIS-C were collected. Patients were followed for 3 months post-discharge and categorized into normal and abnormal coronary artery groups for comparative analysis. Among 195 patients (mean age 6.3 years; male to female ratio 1.5:1), 33.3% exhibited coronary artery abnormalities at admission. Treatment included a combination of intravenous immunoglobulin (IVIG) and corticosteroids (53.3%), corticosteroids alone (42.6%), and IVIG alone (4.1%). After 3 months, only 3.6% of patients had persistent coronary artery abnormalities. Independent risk factors for coronary artery dilation included male sex (OR 4.59; 95% CI 1.62-12.94; p = 0.004), Kawasaki-like phenotype (OR 6.42; 95% CI 2.25-18.33; p = 0.001), and mesenteric lymphadenitis (OR 8.79; 95% CI 1.74-44.31; p = 0.008).

Conclusion: Coronary artery dilation in MIS-C patients shows a favorable recovery trajectory after a 3-month follow-up. Male sex, Kawasaki-like MIS-C, and mesenteric lymphadenitis are independent risk factors for coronary artery dilation in MIS-C patients.

What is known: • Multisystem inflammatory syndrome in children (MIS-C) is a severe inflammatory syndrome following SARS-CoV-2 infection, often leading to cardiac complications, particularly coronary artery dilation.

What is new: • Coronary artery dilation in MIS-C patients mostly resolves within three months of follow-up. Factors associated with coronary artery dilation in MIS-C patients include: male sex, Kawasaki-like phenotype and mesenteric lymphadenitis.

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misc患儿冠状动脉扩张:患病率、危险因素和进展。
心脏损伤是misc患儿的关键问题,尤其是冠状动脉扩张。本研究旨在描述越南misc儿童的患病率、与冠状动脉异常相关的危险因素及其随访3个月后的进展情况。2021年9月至2023年2月,在越南南部两家最大的儿科医院对按照世卫组织标准诊断的misc患者进行了一项前瞻性多中心病例系列研究。收集了MIS-C急性期的人口统计学、临床特征、实验室结果和治疗数据。出院后随访3个月,将患者分为冠状动脉正常组和异常组进行对比分析。195例患者(平均年龄6.3岁;男女比例为1.5:1),入院时冠状动脉异常占33.3%。治疗包括静脉注射免疫球蛋白(IVIG)联合皮质类固醇(53.3%)、单独使用皮质类固醇(42.6%)和单独使用IVIG(4.1%)。3个月后,只有3.6%的患者出现持续的冠状动脉异常。冠状动脉扩张的独立危险因素包括男性(OR 4.59;95% ci 1.62-12.94;p = 0.004),川崎样表型(OR 6.42;95% ci 2.25-18.33;p = 0.001)和肠系膜淋巴结炎(OR 8.79;95% ci 1.74-44.31;p = 0.008)。结论:经3个月随访,misc患者冠状动脉扩张恢复良好。男性、川崎样misc和肠系膜淋巴结炎是misc患者冠状动脉扩张的独立危险因素。•儿童多系统炎症综合征(MIS-C)是SARS-CoV-2感染后的一种严重炎症综合征,通常导致心脏并发症,特别是冠状动脉扩张。最新进展:•misc患者的冠状动脉扩张大多在随访3个月内消退。与MIS-C患者冠状动脉扩张相关的因素包括:男性、川崎样表型和肠系膜淋巴结炎。
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来源期刊
CiteScore
5.90
自引率
2.80%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The European Journal of Pediatrics (EJPE) is a leading peer-reviewed medical journal which covers the entire field of pediatrics. The editors encourage authors to submit original articles, reviews, short communications, and correspondence on all relevant themes and topics. EJPE is particularly committed to the publication of articles on important new clinical research that will have an immediate impact on clinical pediatric practice. The editorial office very much welcomes ideas for publications, whether individual articles or article series, that fit this goal and is always willing to address inquiries from authors regarding potential submissions. Invited review articles on clinical pediatrics that provide comprehensive coverage of a subject of importance are also regularly commissioned. The short publication time reflects both the commitment of the editors and publishers and their passion for new developments in the field of pediatrics. EJPE is active on social media (@EurJPediatrics) and we invite you to participate. EJPE is the official journal of the European Academy of Paediatrics (EAP) and publishes guidelines and statements in cooperation with the EAP.
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