Myocardial Infarction in Kawasaki Disease.

IF 3.9 2区 医学 Q1 PEDIATRICS
Sunil J Ghelani, Annette L Baker, Kevin Friedman, Audrey Dionne, Sarah de Ferranti, Kelly Fitzgerald Cohen, Jane W Newburger
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Abstract

Objective: To evaluate the clinical features, diagnostic methods, treatment courses, and outcomes of myocardial infarction (MI) among patients with Kawasaki disease (KD).

Study design: This retrospective, single-center study reviewed patients with a history of KD who experienced MI from 1984 to 2023. Data collection included demographics, clinical presentation, imaging findings, interventions, and outcomes.

Results: Among 22 patients, 86% were male, with a median KD onset of 14 months (range: 3 months-15 years). MI was diagnosed at the time of the event in seven patients, through surveillance magnetic resonance imaging in eight asymptomatic cases, and by other diagnostic tests in four. Nearly half (48%) of MIs occurred within three months of acute KD, and 81% within two years. All patients had at least one large or giant coronary artery aneurysm, most commonly in the proximal left anterior descending artery. Seven patients underwent coronary artery bypass grafting, one had percutaneous coronary intervention, and one was listed for heart transplantation. Two patients died from MI-related complications in the 1980s, and 23% had left ventricular dysfunction on follow-up.

Conclusions: A high prevalence of missed MI diagnoses and adverse outcomes highlight the need for improved early detection and management. Although MI occurred only in patients with giant aneurysms, additional risk factors remain unclear. Future studies exploring computational modeling and genetic predispositions may help personalize antithrombotic regimens and optimize care for high-risk patients.

川崎病的心肌梗死。
目的:探讨川崎病(Kawasaki disease, KD)患者心肌梗死(MI)的临床特点、诊断方法、治疗过程及转归。研究设计:这项回顾性、单中心研究回顾了1984年至2023年间有KD病史的心肌梗死患者。数据收集包括人口统计学、临床表现、影像学表现、干预措施和结果。结果:22例患者中,86%为男性,KD发病中位数为14个月(范围:3个月-15年)。7例患者在事件发生时诊断为心肌梗死,8例无症状病例通过监测磁共振成像诊断为心肌梗死,4例通过其他诊断测试诊断为心肌梗死。近一半(48%)的MIs发生在急性KD的三个月内,81%发生在两年内。所有患者至少有一个大或巨大的冠状动脉动脉瘤,最常见于左前降支近端。7例患者行冠状动脉旁路移植术,1例行经皮冠状动脉介入治疗,1例列心脏移植。20世纪80年代,两名患者死于心肌梗死相关并发症,23%的患者在随访中出现左心室功能障碍。结论:心肌梗死的高漏诊率和不良后果突出了改善早期发现和管理的必要性。尽管心肌梗死仅发生在巨大动脉瘤患者中,其他危险因素尚不清楚。未来的研究探索计算模型和遗传易感性可能有助于个性化抗血栓治疗方案和优化对高危患者的护理。
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
Journal of Pediatrics
Journal of Pediatrics 医学-小儿科
CiteScore
6.00
自引率
2.00%
发文量
696
审稿时长
31 days
期刊介绍: The Journal of Pediatrics is an international peer-reviewed journal that advances pediatric research and serves as a practical guide for pediatricians who manage health and diagnose and treat disorders in infants, children, and adolescents. The Journal publishes original work based on standards of excellence and expert review. The Journal seeks to publish high quality original articles that are immediately applicable to practice (basic science, translational research, evidence-based medicine), brief clinical and laboratory case reports, medical progress, expert commentary, grand rounds, insightful editorials, “classic” physical examinations, and novel insights into clinical and academic pediatric medicine related to every aspect of child health. Published monthly since 1932, The Journal of Pediatrics continues to promote the latest developments in pediatric medicine, child health, policy, and advocacy. Topics covered in The Journal of Pediatrics include, but are not limited to: General Pediatrics Pediatric Subspecialties Adolescent Medicine Allergy and Immunology Cardiology Critical Care Medicine Developmental-Behavioral Medicine Endocrinology Gastroenterology Hematology-Oncology Infectious Diseases Neonatal-Perinatal Medicine Nephrology Neurology Emergency Medicine Pulmonology Rheumatology Genetics Ethics Health Service Research Pediatric Hospitalist Medicine.
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