Unexpected and atypical clinical presentation of myocardial infarction in infants and children: complex pathogenesis of progressive and lethal disease.

IF 0.9 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Amr Matoq, Gina Patel, Takeshi Tsuda
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引用次数: 0

Abstract

Background: Myocardial infarction is rare in children but frequently occurs unexpectedly with atypical presentation. It can cause a progressive lethal course unless prompt treatment is initiated.

Methods: Paediatric cases of myocardial infarction diagnosed by the presence of ischaemic myocardial insults and symptomatic ventricular dysfunction were reviewed retrospectively.

Results: Eighteen patients (5 days to 14 years of age; median 3 months) with myocardial infarction were studied. The aetiology was variable, including congenital coronary anomalies: anomalous left coronary artery from pulmonary artery (five patients), pulmonary atresia with intact ventricular septum with right ventricle-dependent coronary circulation (four), anomalous aortic origin of left coronary artery (three), and Williams syndrome with supravalvar aortic stenosis (one). Two acquired coronary anomalies occurred in one patient with undiagnosed Kawasaki disease with complete thrombotic obstruction of the left coronary artery and another with post-transplant cardiac allograft microangiopathy. Three patients developed thromboembolic coronary artery incidents in normal coronary anatomy. Fourteen patients were less than 1 year of age (78%). Electrocardiographic abnormalities were noted in all patients. Four patients required extracorporeal membrane oxygenation support for severe ventricular dysfunction, none of whom survived. Five patients underwent heart transplant. Five patients died during the same hospitalisation, and one patient died after discharge (overall mortality 33%). Transplant-free survival was 39%.

Conclusion: Most myocardial infarction occurred in infants who presented with abrupt onset of non-specific clinical manifestations with progressively deteriorating haemodynamic status resulting in poor transplant-free survival rate. Early diagnosis and treatment are essential to prevent catastrophic outcomes.

婴幼儿心肌梗死的意外和非典型临床表现:进展性致命疾病的复杂发病机制。
背景:心肌梗死在儿童中非常罕见,但经常以不典型的表现意外发生。除非得到及时治疗,否则心肌梗死可导致进行性死亡:方法:对根据缺血性心肌损伤和无症状心室功能障碍诊断的儿童心肌梗死病例进行回顾性研究:研究了 18 名心肌梗死患者(5 天至 14 岁,中位数为 3 个月)。病因多种多样,包括先天性冠状动脉异常:肺动脉左冠状动脉异常(5 例)、肺动脉闭锁伴完整室间隔和右心室依赖性冠状动脉循环(4 例)、左冠状动脉主动脉起源异常(3 例)和威廉姆斯综合征伴瓣上主动脉狭窄(1 例)。两名后天性冠状动脉畸形患者中,一名是左冠状动脉完全血栓性阻塞的未确诊川崎病患者,另一名是移植后心脏同种异体微血管病变患者。三名患者的冠状动脉解剖结构正常,但发生了血栓栓塞性冠状动脉事件。14名患者的年龄不到1岁(78%)。所有患者均出现心电图异常。四名患者因严重心室功能障碍而需要体外膜氧合支持,但无一存活。五名患者接受了心脏移植手术。五名患者在住院期间死亡,一名患者在出院后死亡(总死亡率为33%)。无移植存活率为39%:结论:大多数心肌梗死发生在婴儿身上,他们突然出现非特异性临床表现,血流动力学状况逐渐恶化,导致无移植存活率很低。为避免灾难性后果,早期诊断和治疗至关重要。
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
Cardiology in the Young
Cardiology in the Young 医学-小儿科
CiteScore
1.70
自引率
10.00%
发文量
715
审稿时长
4-8 weeks
期刊介绍: Cardiology in the Young is devoted to cardiovascular issues affecting the young, and the older patient suffering the sequels of congenital heart disease, or other cardiac diseases acquired in childhood. The journal serves the interests of all professionals concerned with these topics. By design, the journal is international and multidisciplinary in its approach, and members of the editorial board take an active role in the its mission, helping to make it the essential journal in paediatric cardiology. All aspects of paediatric cardiology are covered within the journal. The content includes original articles, brief reports, editorials, reviews, and papers devoted to continuing professional development.
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