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小儿患者麻醉术后心肌顿抑——病例报告

Stunned myocardium after an anesthetic procedure in a pediatric patient - case report.

作者信息

Faleiro Oliveira Joana, Rebelo Pacheco Susana, Moniz Marta, Nunes Pedro, Abadesso Clara, Rebelo Mónica, Loureiro Helena, Almeida Helena

机构信息

Departamento de Pediatria, Hospital Prof. Doutor Fernando Fonseca, Amadora, Portugal.

Departamento de Pediatria, Hospital Prof. Doutor Fernando Fonseca, Amadora, Portugal.

出版信息

Rev Port Cardiol. 2016 Jun;35(6):375.e1-5. doi: 10.1016/j.repc.2015.09.003. Epub 2016 May 11.

Abstract

Takotsubo syndrome (TTS) is an acquired transient type of systolic dysfunction which mimics myocardial infarction clinically and electrocardiographically. TTS is also known as stress cardiomyopathy, broken heart syndrome, apical ballooning, reversible acute heart failure, neurogenic stunned myocardium or acute catecholamine cardiomyopathy. This case report describes an uncommon presentation of myocardial stunning after an anesthetic procedure. A 14-year-old girl with a history of pineal cyst and hemiplegic migraine was admitted for control brain magnetic resonance imaging. During anesthesia induction with propofol she suffered bradycardia, which was reversed with atropine, followed by tachyarrhythmia, reversed with lidocaine and precordial thump. Within hours she developed pulmonary edema and global respiratory failure due to acute left ventricular dysfunction. A transthoracic echocardiogram showed a dilated left ventricle with global hypokinesia and depressed left ventricular systolic function (ejection fraction <30%). The electrocardiogram showed persistent sinus tachycardia and nonspecific ST-T wave abnormalities. Cardiac biomarkers were elevated (troponin 2.42 ng/ml, proBNP 8248 pg/ml). She was placed on diuretics, angiotensin-converting enzyme inhibitors, digoxin and dopamine. The clinical course was satisfactory with clinical, biochemical and echocardiographic improvement within four days. Subsequent echocardiograms showed no ventricular dysfunction. The patient was discharged home on carvedilol, which was discontinued after normalization of cardiac function on cardiac magnetic resonance imaging. Few cases of TTS have been described in children, some of them triggered by acute central nervous system disorders and others not fulfilling all the classical diagnostic criteria. In this case the anesthetic procedure probably triggered the TTS.

摘要

Takotsubo综合征(TTS)是一种后天获得性的短暂性收缩功能障碍,在临床和心电图表现上类似心肌梗死。TTS也被称为应激性心肌病、心碎综合征、心尖球囊样变、可逆性急性心力衰竭、神经源性心肌顿抑或急性儿茶酚胺性心肌病。本病例报告描述了一例麻醉手术后出现心肌顿抑的罕见表现。一名有松果体囊肿和偏瘫性偏头痛病史的14岁女孩因控制脑磁共振成像入院。在使用丙泊酚进行麻醉诱导期间,她出现了心动过缓,使用阿托品后得以纠正,随后又出现了快速心律失常,使用利多卡因和胸前区叩击后得以纠正。数小时内,她因急性左心室功能障碍出现了肺水肿和全身呼吸衰竭。经胸超声心动图显示左心室扩张,整体运动减弱,左心室收缩功能降低(射血分数<30%)。心电图显示持续性窦性心动过速和非特异性ST-T波异常。心脏生物标志物升高(肌钙蛋白2.42 ng/ml,脑钠肽前体8248 pg/ml)。她接受了利尿剂、血管紧张素转换酶抑制剂、地高辛和多巴胺治疗。临床过程令人满意,四天内临床、生化和超声心动图均有改善。随后的超声心动图显示没有心室功能障碍。患者出院时服用卡维地洛,心脏磁共振成像显示心脏功能恢复正常后停用。儿童中TTS病例报道较少,其中一些由急性中枢神经系统疾病引发,另一些则不完全符合所有经典诊断标准。在本病例中,麻醉过程可能触发了TTS。

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