Radiofrequency Catheter Ablation of Ventricular Tachycardia in Patients With Hypertrophic Cardiomyopathy and Apical Aneurysm

被引:54
作者
Igarashi, Miyako [1 ]
Nogami, Akihiko [1 ]
Kurosaki, Kenji [1 ]
Hanaki, Yuichi [1 ]
Komatsu, Yuki [1 ]
Fukamizu, Seiji [1 ]
Morishima, Itsuro [1 ]
Kaitani, Kazuaki [1 ]
Nishiuchi, Suguru [1 ]
Talib, Ahmed Karim [1 ]
Machino, Takeshi [1 ]
Kuroki, Kenji [1 ]
Yamasaki, Hiro [1 ]
Murakoshi, Nobuyuki [1 ]
Sekiguchi, Yukio [1 ]
Kuga, Keisuke [1 ]
Aonuma, Kazutaka [1 ]
机构
[1] Univ Tsukuba, Fac Med, Dept Cardiol, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan
关键词
apical aneurysm; hypertrophic cardiomyopathy; outcome radiofrequency catheter ablation; ventricular tachycardia;
D O I
10.1016/j.jacep.2017.12.020
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES This study evaluated the characteristics and results of radiofrequency catheter ablation (RFCA) of ventricular tachycardia (VT) in patients with hypertrophic cardiomyopathy (HCM) and left ventricular apical aneurysm (AA). BACKGROUND Monomorphic VT in patients with HCM and left ventricular AA has been reported. However, outcome data of RFCA are insufficient. METHODS Fifteen patients with HCM and AA who underwent RFCA for VT at 5 different institutions were included in this study. The data were evaluated retrospectively. RESULTS Endocardial voltage mapping showed a low-voltage area (LVA), and late potential in the AA was recorded in 12 patients (80%). Although epicardial or intramural origin of VT was suspected in 7 patients, endocardial RFCA successfully suppressed the VT at the LVA border (n = 10) or within the LVA (n = 2). In 2 of 3 patients without LVA at the endocardial site, linear RFCA at the anterior wall of the aneurysmal neck side was successful. In the remaining patient, endocardial RFCA of AA was not effective, and epicardial RFCA site was needed. In all patients, clinical VT became noninducible after RFCA. VT recurrence was observed in 2 patients (13.3%) during the 12-month follow-up period. One patient underwent a second endocardial RFCA, and no VT recurrence was noted. In the other patient, VT recurred 3 months after RFCA and was successfully terminated by antitachycardia pacing of the implantable cardioverter-defibrillator. CONCLUSIONS In patients with HCM and AA, endocardial RFCA of AA effectively suppressed monomorphic VT which was related to AA and resulted in satisfactory outcomes. (C) 2018 by the American College of Cardiology Foundation.
引用
收藏
页码:340 / 350
页数:11
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