Zhang Min, Cao Xiaoxiao, Ji Suqiong, Kosari Mohammadreza, Zhang Yong
Wuhan Maternal and Child Healthcare Hospital, Tongji Medical College, The Children's Heart Center, Wuhan Children's Hospital, Huazhong University of Science & Technology, 100 Hongkong Road, Jiangan District, Wuhan, Hubei, China.
Tongji Hospital, Tongji Medical College, Huazhong University of Science & Technology, Wuhan, Hubei, China.
J Cardiothorac Surg. 2025 Jan 7;20(1):41. doi: 10.1186/s13019-024-03148-1.
Tachycardia-induced cardiomyopathy refers to changes in cardiac structure and function that result from rapid arrhythmia and can manifest as a continuous or recurrent event. Cardiomyopathy induced by atrial tachycardia is typically reversible if the arrhythmia is effectively controlled. There are few literature reports of atrial tachycardia-induced cardiomyopathy in children, and fewer cases have been effectively treated by radiofrequency catheter ablation in children.
we conducted a clinical summary of 7 cases of atrial tachycardia-induced cardiomyopathy in children in Wuhan Children's Hospital to investigate the effectiveness and safety of radiofrequency catheter ablation for atrial tachycardia-induced cardiomyopathy.
A total of 7 children (4 girls and 3 boys) diagnosed with atrial tachycardia-induced cardiomyopathy and admitted to Wuhan Children's Hospital from January 2017 to April 2024 were selected. An intracardiac electrophysiological study was conducted on all 7 children to verify the origin of the atrial tachycardia and the presence of decreased cardiac function. All children were followed up for a period ranging from 2 to 12 months after RFCA or atrial appendectomy. During this follow-up, left ventricular end-diastolic diameter and left ventricular ejection fraction were monitored.
The age range was 3.6 to 13 years and the median age was 11.2 years. The weight range was from 15 to 92 kg, the average weight was 34 kg. The results of the intracardiac electrophysiological study of the 7 cases showed that the origin came from the right pulmonary vein in 2 cases, from the left pulmonary vein in 2 cases, from the left atrial appendage in one case, and from the right atrial appendage in 2 cases. Four cases of tachycardia-induced cardiomyopathy originating in the left and right pulmonary veins were successfully eliminated by radiofrequency catheter ablation (RFCA). The foci of atrial tachycardia were located in the atrial appendages of three children. For two of them, after precise positioning by the atrium three-dimensional electroanatomic mapping system and performing RFCA, the atrial tachycardia briefly stopped for approximately 24 h before reoccurring, and atrial appendectomy was subsequently performed. Nevertheless, in the other child, whose focus of atrial tachycardia was in the right atrial appendage, the lesion was successfully eliminated by RFCA. After RFCA or in combination with atrial appendectomy, 6 children were followed for more than 1 year and 1 child for 2 months. All children had sinus rhythm. At the same time, the left ventricular ejection fraction after RFCA or combined atrial appendectomy was significantly increased in 7 cases, indicating statistical significance (P = 0.018)), but the left ventricular end-diastolic diameter was not statistically significant in the treatment (P = 0.203)).
Sustained atrial tachycardia can lead to the occurrence of cardiomyopathy such as cardiac enlargement and heart failure. RFCA and combined atrial appendectomy can effectively stop tachycardia, eliminate the mechanism of tachycardia, and allow complete recovery of cardiac function.
心动过速性心肌病是指快速心律失常导致的心脏结构和功能改变,可表现为持续性或复发性事件。如果心律失常得到有效控制,房性心动过速所致的心肌病通常是可逆的。儿童房性心动过速性心肌病的文献报道较少,且儿童通过射频导管消融有效治疗的病例更少。
对武汉市儿童医院7例儿童房性心动过速性心肌病进行临床总结,探讨射频导管消融治疗儿童房性心动过速性心肌病的有效性和安全性。
选取2017年1月至2024年4月在武汉市儿童医院确诊为房性心动过速性心肌病并入院的7例儿童(4例女孩,3例男孩)。对所有7例儿童进行心内电生理检查,以验证房性心动过速的起源及心脏功能下降情况。所有儿童在射频导管消融术(RFCA)或心房附件切除术后进行2至12个月的随访。在此随访期间,监测左心室舒张末期内径和左心室射血分数。
年龄范围为3.6至13岁,中位年龄为11.2岁。体重范围为15至92千克,平均体重为34千克。7例心内电生理检查结果显示,起源于右肺静脉2例,左肺静脉2例,左心耳1例,右心耳2例。4例起源于左右肺静脉的心动过速性心肌病通过射频导管消融成功消除。3例儿童房性心动过速的病灶位于心耳。其中2例,经心房三维电解剖标测系统精确定位并进行RFCA后,房性心动过速短暂停止约24小时后复发,随后进行了心房附件切除术。然而,另1例儿童房性心动过速病灶位于右心耳,其病灶通过RFCA成功消除。RFCA或联合心房附件切除术后,6例儿童随访1年以上,1例儿童随访2个月。所有儿童均为窦性心律。同时,7例患者RFCA或联合心房附件切除术后左心室射血分数显著升高,差异有统计学意义(P = 0.018),但治疗后左心室舒张末期内径差异无统计学意义(P = 0.203)。
持续性房性心动过速可导致心脏扩大、心力衰竭等心肌病的发生。RFCA及联合心房附件切除术可有效终止心动过速,消除心动过速机制,使心脏功能完全恢复。