Arrhythmia-Induced Cardiomyopathy Presented Cardiogenic Shock Caused by Multifocal Atrial Tachycardia in a 4-Month-Old Boy

Akira Sato, S. Fujita, K. Usuda, Keiichi Hirono, K. Hatasaki
{"title":"Arrhythmia-Induced Cardiomyopathy Presented Cardiogenic Shock Caused by Multifocal Atrial Tachycardia in a 4-Month-Old Boy","authors":"Akira Sato, S. Fujita, K. Usuda, Keiichi Hirono, K. Hatasaki","doi":"10.9794/JSPCCS.36.321","DOIUrl":null,"url":null,"abstract":"Multifocal atrial tachycardia (MAT) is generally diagnosed in infants under one year of age; a few of these infants may also present with arrhythmia-induced cardiomyopathy. We report the case of 4-month-old boy diagnosed with cardiogenic shock secondary to MAT who responded to antiarrhythmic medications. e child was delivered by caesarean section at gestational age of 36 weeks due to fetal distress; his birth weight was 2,362 g. He was referred to our hospital at four months of age with chief complaints of poor feeding and tachyarrhythmias detected during a previous examination. A 12-lead electrocardiogram (ECG) revealed a narrow QRS complex and irregular tachycardia at a rate of 200‒240 beats per minute, leading to the diagnosis of MAT. Echocardiography revealed severe functional decline, including an 11% shortening fraction (SF) and a dilated le ventricle. Amiodarone (5 mg/kg injection) was administered in an attempt to normalize the atrial tachycardia; this resulted in a substantial drop in blood pressure. e patient was intubated and provided with inotropic support, including dopamine and milrinone. Landiolol (10 μg/kg/min by continuous infusion) and oral aprindine (1.5 mg/kg/day) were initiated on hospital day 8. e frequency of tachycardia decreased and cardiac function gradually recovered over a period of 2‒3 weeks. e patient was discharged on hospital day 43 with improved cardiac function and a SF of 30%. Results from a follow-up visit revealed the cardiac function had returned to near-normal with no recurrence of MAT. We conclude that it is critical to control MAT in pediatric patients with arrhythmia-induced cardiomyopathy.","PeriodicalId":89701,"journal":{"name":"Nihon Shoni Junkanki Gakkai zasshi = Pediatric cardiology and cardiac surgery","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nihon Shoni Junkanki Gakkai zasshi = Pediatric cardiology and cardiac surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9794/JSPCCS.36.321","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Multifocal atrial tachycardia (MAT) is generally diagnosed in infants under one year of age; a few of these infants may also present with arrhythmia-induced cardiomyopathy. We report the case of 4-month-old boy diagnosed with cardiogenic shock secondary to MAT who responded to antiarrhythmic medications. e child was delivered by caesarean section at gestational age of 36 weeks due to fetal distress; his birth weight was 2,362 g. He was referred to our hospital at four months of age with chief complaints of poor feeding and tachyarrhythmias detected during a previous examination. A 12-lead electrocardiogram (ECG) revealed a narrow QRS complex and irregular tachycardia at a rate of 200‒240 beats per minute, leading to the diagnosis of MAT. Echocardiography revealed severe functional decline, including an 11% shortening fraction (SF) and a dilated le ventricle. Amiodarone (5 mg/kg injection) was administered in an attempt to normalize the atrial tachycardia; this resulted in a substantial drop in blood pressure. e patient was intubated and provided with inotropic support, including dopamine and milrinone. Landiolol (10 μg/kg/min by continuous infusion) and oral aprindine (1.5 mg/kg/day) were initiated on hospital day 8. e frequency of tachycardia decreased and cardiac function gradually recovered over a period of 2‒3 weeks. e patient was discharged on hospital day 43 with improved cardiac function and a SF of 30%. Results from a follow-up visit revealed the cardiac function had returned to near-normal with no recurrence of MAT. We conclude that it is critical to control MAT in pediatric patients with arrhythmia-induced cardiomyopathy.
一例4个月大男孩多灶性房性心动过速致心律失常性心肌病伴心源性休克
多灶性房性心动过速(MAT)通常诊断为一岁以下的婴儿;其中一些婴儿也可能出现心律失常引起的心肌病。我们报告了一例4个月大的男孩被诊断为继发于MAT的心源性休克,他对抗心律失常药物有反应。e胎龄36周时因胎儿窘迫通过剖腹产分娩;他的出生体重为2362克。他在四个月大时被转诊到我们医院,主要症状是在之前的检查中发现进食不良和快速心律失常。12导联心电图(ECG)显示QRS波群狭窄,心动过速不规则,每分钟200-240次,诊断为MAT。超声心动图显示功能严重下降,包括11%的缩短分数(SF)和扩张的左心室。胺碘酮(5 mg/kg注射)用于尝试使房性心动过速正常化;这导致血压大幅度下降。e患者插管并接受包括多巴胺和米力农在内的肌力支持。Landiool(10μg/kg/min,连续输注)和口服阿必定(1.5mg/kg/天)于住院第8天开始。在2-3周的时间里,心动过速的频率降低,心功能逐渐恢复。e患者在第43天出院,心功能改善,SF为30%。随访结果显示,心脏功能已恢复到接近正常水平,无MAT复发。我们得出结论,在心律失常诱导型心肌病的儿童患者中,控制MAT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。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信