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在先天性心脏缺陷患者中,用于完全消融典型心房扑动的进入手术排除的腔静脉三尖瓣峡部的方法。

Methods to access the surgically excluded cavotricuspid isthmus for complete ablation of typical atrial flutter in patients with congenital heart defects.

作者信息

El Yaman Malek M, Asirvatham Samuel J, Kapa Suraj, Barrett Renee A, Packer Douglas L, Porter Co-Burn

机构信息

Division of Pediatric Cardiology, Department of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota 55905, USA.

出版信息

Heart Rhythm. 2009 Jul;6(7):949-56. doi: 10.1016/j.hrthm.2009.03.017. Epub 2009 Mar 11.

Abstract

BACKGROUND

Cavotricuspid isthmus (CVTI)-dependent flutter in postoperative congenital heart disease patients is common and difficult to treat.

OBJECTIVE

The purpose of this study was to evaluate techniques for accessing excluded portions of the CVTI after Fontan or atrial switch procedures and completely ablating flutter.

METHODS

Patients who had undergone Fontan or atrial switch procedures and had CVTI-dependent flutter requiring ablation between 1990 and 2007 were identified. Flutters induced, methods for accessing the CVTI, use of intracardiac echocardiography, complications, and success rates were noted.

RESULTS

Sixteen patients (44% males, mean age at ablation 28 years) were identified: 14 prior Fontan and 2 Mustard repair, with a total of 19 ablation procedures. In 13 (81%) of 16 patients, access to the entire CVTI could not be achieved via a systemic venous route. The excluded CVTI was accessed by retrograde transaortic approach in 6 and by anterograde transconduit puncture in 1 patient, with termination and lack of reinducibility of CVTI-dependent flutter achieved in all cases. One patient developed high-grade AV block requiring pacemaker therapy. Follow-up data (range 1-89 months, mean 29 months) were available for 18 of 19 procedures. CVTI atrial flutter recurred in 1 of 7 patients involving access to the pulmonary venous side.

CONCLUSION

Even when surgical procedures exclude a portion of the CVTI, complete ablation of "typical" atrial flutter, including documentation of bidirectional block, can be achieved by novel approaches targeting the surgically excluded arrhythmogenic atrial tissue.

摘要

背景

先天性心脏病术后患者中,依赖腔静脉三尖瓣峡部(CVTI)的房扑很常见且难以治疗。

目的

本研究旨在评估在Fontan或心房调转术后进入CVTI被分隔部分并完全消融房扑的技术。

方法

确定1990年至2007年间接受Fontan或心房调转术且有依赖CVTI的房扑需要消融的患者。记录诱发的房扑、进入CVTI的方法、心内超声心动图的使用、并发症及成功率。

结果

确定了16例患者(44%为男性,消融时平均年龄28岁):14例曾行Fontan手术,2例曾行Mustard修复术,共进行了19次消融手术。16例患者中有13例(81%)无法通过体静脉途径进入整个CVTI。6例通过逆行经主动脉途径、1例通过顺行经导管穿刺进入被分隔的CVTI,所有病例均实现了依赖CVTI的房扑终止且不能再诱发。1例患者发生高度房室传导阻滞,需要起搏器治疗。19例手术中有18例有随访数据(范围1 - 89个月,平均29个月)。7例涉及进入肺静脉侧的患者中有1例CVTI房扑复发。

结论

即使手术操作分隔了部分CVTI,通过针对手术分隔的致心律失常心房组织的新方法,也可实现“典型”房扑的完全消融,包括记录双向阻滞。

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