[Clinical characteristics of 42 children with focal atrial tachycardia originated from the right atrial appendage].

Y Zhang, X M Li, H Jiang, Y Q Jin, M T Li, Y L Gu, H M Zhou
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Abstract

Objective: To investigate the feature and treatment of atrial tachycardia (AT) originated from right atrial appendage (RAA) in children. Methods: The data of 42 children with AT originated from RAA, who were admitted the First Hospital of Tsinghua University from January 2010 to September 2022 were analyzed retrospectively.The clinical characteristics, treatment and efficacy were analyzed. The children were divided into tachycardia cardiomyopathy group and normal cardiac function group. The differences in the ablation age and the heart rate during AT between two groups were compared by independent sample t-test. Results: Among 42 children, there were 20 males and 22 females. The age of onset was 2.7 (0.6, 5.1) years. Their age at radiofrequency ablation was (6.5±3.6) years, and the weight was (23.4±10.0) kg. Thirty-two children (76%) had sustained AT. The incidence of tachycardia cardiomyopathy was 43% (18/42). Compared to that of the normal cardiac function group, the ablation age and the heart rate at atrial tachycardia of the tachycardia cardiomyopathy group were higher ((8.1±3.8) vs. (5.3±3.1) years, t=-2.63, P=0.012; (173±41) vs. (150±30) beats per minute, t=-2.05, P=0.047. Thirty-eight children (90%) responded poorly to two or more antiarrhythmic drugs. The immediate success rate of radiofrequency ablation (RFCA) was 57% (24/42), and the AT recurrence rate was 17% (4/24). Twenty-two children underwent RAA resection, and their AT were all converted to sinus rhythm after the surgery. During the RAA resection, 10 cases of right atrial appendage aneurysm were found, 9/18 of which failed the RFCA. Conclusions: The AT originated from the RAA in children tend to present with sustained AT, respond poorly to antiarrhythmic drugs, and has a low success rate of RFCA as well as high recurrence rate. Resection of the RAA is a safe and effective complementary treatment.

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[小儿局灶性房性心动过速42例临床特点]。
目的:探讨儿童右心房附件性房性心动过速(AT)的特点及治疗方法。方法:回顾性分析2010年1月至2022年9月清华大学第一医院收治的42例RAA源性AT患儿的资料。分析其临床特点、治疗方法及疗效。将患儿分为心动过速心肌病组和心功能正常组。采用独立样本t检验比较两组消融年龄和AT期间心率的差异。结果:42例患儿中,男20例,女22例。发病年龄为2.7(0.6,5.1)岁。患者射频消融年龄(6.5±3.6)岁,体重(23.4±10.0)kg。32例患儿(76%)持续AT。心动过速心肌病的发生率为43%(18/42)。与心功能正常组相比,心动过速心肌病组消融年龄和房性心动过速心率均增高((8.1±3.8)∶(5.3±3.1)年,t=-2.63, P=0.012;(173±41)vs(150±30)次/分,t=-2.05, P=0.047。38名儿童(90%)对两种或两种以上抗心律失常药物反应不佳。射频消融(RFCA)即刻成功率为57% (24/42),AT复发率为17%(4/24)。22例患儿行RAA切除术,术后AT均转化为窦性心律。在RAA切除术中发现10例右心房附件动脉瘤,其中9/18例RFCA手术失败。结论:儿童RAA源性AT多表现为持续性AT,抗心律失常药物反应差,RFCA成功率低,复发率高。RAA切除术是一种安全有效的辅助治疗方法。
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