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扩张型肥厚型心肌病室性心动过速的导管消融:基质特征和消融结果。

Catheter ablation of ventricular tachycardia in dilated-phase hypertrophic cardiomyopathy: Substrate characterization and ablation outcome.

机构信息

Department of Cardiology, Faculty of Medicine, University of Tsukuba, Tsukuba, Tennodai, Japan.

出版信息

Pacing Clin Electrophysiol. 2022 Jun;45(6):773-785. doi: 10.1111/pace.14508. Epub 2022 May 2.

DOI:10.1111/pace.14508
PMID:35430753
Abstract

INTRODUCTION

Catheter ablation is a therapeutic option to suppress ventricular tachycardia (VT) in the setting of dilated-phase hypertrophic cardiomyopathy (DHCM). However, the characteristics of the arrhythmogenic substrate and the ablation outcome are not fully illustrated.

METHOD

A total of 23 ablation procedures for drug-refractory sustained monomorphic VTs in 13 DHCM patients (60 ± 11 years, one female, the left ventricular [LV] ejection fraction 39% ± 9%, the LV mass index 156 ± 39 g/m ) were performed. The distribution of VT substrate as endocardial or epicardial/intramural was based on detailed mapping and ablation response during VT.

RESULT

Two patients underwent ablation of sustained monomorphic VT that was not scar-mediated tachycardia. Of the remaining 11 patients, eight (73%) patients had VT substrate in the basal regions, most frequently at the epicardial and/or intramural basal antero-septum. None of the patients had VT substrate located at the LV inferolateral region. Ablation at the right ventricular septum and the aortic cusps was done in four and five patients, respectively. Other approaches including bipolar and chemical ablations, were done in three and two patients, respectively. Six (55%) out of 11 patients (two patients lost follow-up) had VT recurrence. All the six patients had basal substrate. However, anti-tachycardia pacing was sufficient for VT termination except in one patient.

CONCLUSION

Catheter ablation of VT in patients with DHCM is challenging because of the predominant basal anteroseptal epicardial/intramural location of arrhythmogenic substrate. An ablation approach from multiple sites and/or adjunctive interventional techniques are often required.

摘要

简介

导管消融是治疗扩张型肥厚型心肌病(DHCM)患者室性心动过速(VT)的一种治疗选择。然而,致心律失常基质的特征和消融效果尚未完全阐明。

方法

对 13 例 DHCM 患者(60±11 岁,1 例女性,左心室射血分数 39%±9%,左心室质量指数 156±39 g/m )共进行了 23 例药物难治性持续性单形 VT 的消融治疗。VT 基质的分布为心内膜或心外膜/心室内膜,基于 VT 期间的详细标测和消融反应。

结果

2 例患者进行了持续性单形 VT 的消融治疗,而不是瘢痕介导的心动过速。在其余 11 例患者中,8 例(73%)患者的 VT 基质位于基底区,最常见于心外膜和/或心室内膜基底前间隔。没有患者的 VT 基质位于左心室下外侧区域。右心室间隔和主动脉瓣环分别在 4 例和 5 例患者中进行消融。其他方法包括双极和化学消融,分别在 3 例和 2 例患者中进行。11 例患者中有 6 例(55%)(2 例患者失访)出现 VT 复发。所有 6 例患者均有基底基质。然而,除 1 例患者外,抗心动过速起搏足以终止 VT。

结论

由于致心律失常基质主要位于基底前间隔心外膜/心室内膜,DHCM 患者 VT 的导管消融具有挑战性。通常需要从多个部位进行消融方法和/或辅助介入技术。

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