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12例儿童心动过速性心肌病的临床特征及随访研究

[Clinical characteristics and follow-up study of tachycardia-induced cardiomyopathy in 12 children].

作者信息

Qi Jian-guang, Xing Chang-qing, Liu Xue-qin, Zhang Qing-you, Chen Yong-hong, DU Jun-bao

机构信息

Department of Pediatrics, Peking University First Hospital, Beijing 100034, China.

出版信息

Zhonghua Er Ke Za Zhi. 2011 Dec;49(12):933-8.

Abstract

OBJECTIVE

Tachycardia induced cardiomyopathy (TIC), secondary to various tachyarrhythmias, is a reversible condition which can lead to cardiac enlargement and heart failure. The impairment of both structure and function of heart can be reverted completely or partially if tachyarrhythmias are ceased without delay. This study aimed to explore the clinical characteristics, therapeutic regimen and outcome of TIC in children.

METHODS

Clinical data of 12 children with TIC, who came from Peking University First Hospital from Feb. 2003 to Jun. 2009, were retrospectively analyzed and followed up. The echocardiogram data on admission were compared with those from 12 homochronous cases with idiopathic dilated cardiomyopathy matched with 12 TIC cases in age and gender.

RESULTS

Atrial tachycardia is the commonest arrhythmia in 12 TIC cases (75%). Four cases underwent catheterization for radiofrequency ablation and all succeeded. The cardiac rhythm of 6 out of 8 cases treated with drugs became sinus rhythm after 3 days to 2 weeks antiarrhythmic drugs treatment. The remaining 2 cases still retained atrial rhythm, but the ventricular heart rates declined to normal. The left ventricular end-diastolic dimensions of the 12 cases were decreased compared with those of pretherapy [(37.5 ± 5.3) mm vs. (43.0 ± 5.7) mm, P < 0.01], and the left ventricular ejection fractions were increased [(60.5% ± 5.6%) vs. (33.7% ± 10.3%), P < 0.01], after (3.4 ± 2.3) months. In our (4.3 ± 2.4) year-follow-up, all cases were fine, except in one case the tachyarrhythmia relapsed because of discontinuation of the drug treatment by her parents. The left ventricular end-diastolic dimensions in 12 TIC cases were smaller than those of the 12 age- and gender-matched idiopathic dilated cardiomyopathy [(43.0 ± 5.7) mm vs. (54.8 ± 7.5) mm, t = 7.9, P < 0.01], and the ejection fractions were higher [(33.7% ± 10.3%) vs. (21.8% ± 7.5%), t = 3.7, P < 0.01].

CONCLUSION

The diagnosis of TIC should be considered for the children with tachycardia, cardiac enlargement and cardiac insufficiency. The degree of cardiac enlargement and cardiac insufficiency might be of value for the differential diagnosis between TIC and idiopathic dilated cardiomyopathy. The rhythm control and ventricular rates control could all result in a favorite therapeutic efficacy.

摘要

目的

心动过速性心肌病(TIC)继发于各种快速性心律失常,是一种可逆性病症,可导致心脏扩大和心力衰竭。如果快速性心律失常能及时终止,心脏的结构和功能损害可完全或部分恢复。本研究旨在探讨儿童TIC的临床特征、治疗方案及预后。

方法

回顾性分析并随访2003年2月至2009年6月来自北京大学第一医院的12例儿童TIC患者的临床资料。将入院时的超声心动图数据与12例年龄和性别相匹配的特发性扩张型心肌病的同期病例进行比较。

结果

12例TIC患者中最常见的心律失常是房性心动过速(75%)。4例行导管射频消融术,均成功。8例接受药物治疗的患者中,6例在抗心律失常药物治疗3天至2周后转为窦性心律。其余2例仍维持房性心律,但心室率降至正常。12例患者治疗后左心室舒张末期内径较治疗前减小[(37.5±5.3)mm对(43.0±5.7)mm,P<0.01],左心室射血分数增加[(60.5%±5.6%)对(33.7%±10.3%),P<0.01],时间为(3.4±2.3)个月。在我们(4.3±2.4)年的随访中,除1例因家长停药导致快速性心律失常复发外,所有病例情况良好。12例TIC患者的左心室舒张末期内径小于12例年龄和性别相匹配的特发性扩张型心肌病患者[(43.0±5.7)mm对(54.8±7.5)mm,t=7.9,P<0.01],射血分数更高[(33.7%±10.3%)对(21.8%±7.5%),t=3.7,P<0.01]。

结论

对于有心动过速、心脏扩大和心功能不全的儿童应考虑TIC的诊断。心脏扩大和心功能不全的程度对TIC与特发性扩张型心肌病的鉴别诊断可能有价值。节律控制和心室率控制均可产生良好的治疗效果。

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