Contemporary Tools and Techniques for Substrate Ablation of Ventricular Tachycardia in Structural Heart Disease

被引:3
作者
Hutchinson M.D. [1 ,2 ]
Garza H.-H.K. [1 ]
机构
[1] Division of Cardiovascular Medicine, Department of Medicine, University of Arizona College of Medicine, Tucson, AZ
[2] Sarver Heart Center, University of Arizona, 1501 N. Campbell Avenue, 4142B, Tucson, 85724, AZ
关键词
Arrhythmia; Epicardial; Intramural; Intraseptal; Nonischemic; VT ablation;
D O I
10.1007/s11936-018-0610-6
中图分类号
学科分类号
摘要
As we have witnessed in other arenas of catheter-based therapeutics, ventricular tachycardia (VT) ablation has become increasingly anatomical in its execution. Multi-modality imaging provides anatomical detail in substrate characterization, which is often complex in nonischemic cardiomyopathy patients. Patients with intramural, intraseptal, and epicardial substrates provide challenges in delivering effective ablation to the critical arrhythmia substrate due to the depth of origin or the presence of adjacent critical structures. Novel ablation techniques such as simultaneous unipolar or bipolar ablation can be useful to achieve greater lesion depth, though at the expense of increasing collateral damage. Disruptive technologies like stereotactic radioablation may provide a tailored approach to these complex patients while minimizing procedural risk. Substrate ablation is a cornerstone of the contemporary VT ablation procedure, and recent data suggest that it is as effective and more efficient that conventional activation guided ablation. A number of specific targets and techniques for substrate ablation have been described, and all have shown a fairly high success in achieving their acute procedural endpoint. Substrate ablation also provides a novel and reproducible procedural endpoint, which may add predictive value for VT recurrence beyond conventional programmed stimulation. Extrapolation of outcome data to nonischemic phenotypes requires caution given both the variability in substrate nonischemic distribution and the underrepresentation of these patients in previous trials. © 2018, Springer Science+Business Media, LLC, part of Springer Nature.
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