Arslan Alev, Erdoğan İlkay, Varan Birgül, Yılmaz Mustafa, Özin Mehmet Bülent, Tokel Niyazi Kürşad
Division of Pediatric Cardiology, Başkent University Faculty of Medicine, Turkey.
Department of Pediatrics and Cardiology, Başkent University Faculty of Medicine, Turkey.
Turk J Pediatr. 2019;61(4):552-559. doi: 10.24953/turkjped.2019.04.012.
Arslan A, Erdoğan İ, Varan B, Yılmaz M, Özin MB, Tokel NK. Reversible cardiomyopathy-tachycardiomyopathy in children. Turk J Pediatr 2019; 61: 552-559. Tachycardia-induced cardiomyopathy (tachycardiomyopathy) is defined by the presence of a sustained tachycardia that results in left ventricular systolic dysfunction. Restoration of cardiac function is dependent on the control of tachyarrhythmias. We report a series including ten children with tachycardia-induced cardiomyopathy with different etiologies. The medical records of patients with tachycardiomyopathy who were managed in a Pediatric Cardiology Clinic between the years of 2014-2017 were reviewed retrospectively. Ten children (3 female, 7 male) were diagnosed with tachycardiomyopathy. The median age of the patients was 12 years (range: 4-15.8). Five had atrial tachycardia, two had ventricular tachycardia, the others had Mahaim fiber tachycardia, permanent junctional reciprocating tachycardia and atrioventricular reentrant tachycardia. Seven patients had catheter ablation and three patients who had previous heart surgery were treated with antiarrhythmic drugs. Median ejection fraction was 33% (range: 10-48), median left ventricle end-diastolic diameter was 55 mm (range: 30-78). All showed complete recovery with median ejection fraction 60% (range: 55- 78). Two patient with severe heart failure required extracorporeal membrane oxygenation support, one of them had ventricular assist device support but the device was removed after successful ablation. After two years this patient required permanent pacemaker implantation due to complete atrioventricular block. Tachycardia-induced cardiomyopathy is a rare and treatable cause of heart failure. Early recognition is critical, aggressive treatment aimed at controlling the arrhythmia results in symptom resolution and recovery of ventricular function.
阿尔斯兰·A、埃尔多安·İ、瓦兰·B、伊尔马兹·M、厄津·MB、托克尔·NK。儿童可逆性心肌病——心动过速性心肌病。《土耳其儿科学杂志》2019年;61:552 - 559。心动过速性心肌病是由持续性心动过速导致左心室收缩功能障碍所定义的。心脏功能的恢复取决于快速心律失常的控制。我们报告了一组包括10名病因各异的心动过速性心肌病患儿的病例。回顾性分析了2014年至2017年在儿科心脏病诊所接受治疗的心动过速性心肌病患者的病历。10名儿童(3名女性,7名男性)被诊断为心动过速性心肌病。患者的中位年龄为12岁(范围:4 - 15.8岁)。5例患有房性心动过速,2例患有室性心动过速,其他患者分别患有Mahaim纤维性心动过速、永久性交界性折返性心动过速和房室折返性心动过速。7例患者接受了导管消融术,3例曾接受心脏手术的患者接受了抗心律失常药物治疗。中位射血分数为33%(范围:10 - 48),左心室舒张末期内径中位值为55毫米(范围:30 - 78)。所有患者均完全恢复,中位射血分数为60%(范围:55 - 78)。2例严重心力衰竭患者需要体外膜肺氧合支持,其中1例患者接受了心室辅助装置支持,但在成功消融后该装置被移除。两年后,该患者因完全性房室传导阻滞需要植入永久性起搏器。心动过速性心肌病是一种罕见但可治疗的心力衰竭病因。早期识别至关重要,旨在控制心律失常的积极治疗可导致症状缓解和心室功能恢复。