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      Substrate Mapping and Ablation for Ventricular Tachycardia in Patients with Structural Heart Disease: How to Identify Ventricular Tachycardia Substrate

      review-article
      , MD 1 , 2 , 3 , 7 , , MD, PhD 1 , 2 , 3 , 4 , , MD, PhD 1 , 2 , 3 , , MD 1 , 2 , 3 , 5 , , MD, PhD 1 , 2 , 3 , 6 , , MD, PhD 1 , 2 , 3 , , MD 1 , 2 , 3 , , MD 1 , 2 , 3 , , MD 1 , 2 , 3 , , MD 1 , 2 , 3 , , MD 1 , 2 , 3 , , MD 1 , 2 , 3 , , MD 1 , 2 , 3 , , MD 1 , 2 , 3 , , MD 1 , 2 , 3 , , MD 1 , 2 , 3 , , MD, PhD 1 , 2 , 3 , , MD, PhD 1 , 2 , 3 , , MD, PhD 1 , 2 , 3 , , MD, PhD 1 , 2 , 3
      The Journal of Innovations in Cardiac Rhythm Management
      MediaSphere Medical
      Ablation, cardiac imaging, substrate, three-dimensional mapping system, ventricular tachycardia

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          Abstract

          Catheter ablation for ventricular tachycardia (VT) has been increasingly used over the past two decades in patients with structural heart disease (SHD). In these individuals, a substrate mapping strategy is being more commonly applied to identify targets for VT ablation, which has been shown to be more effective versus targeting mappable VTs alone. There are a number of substrate mapping methods in existence that aim to explore potential VT isthmuses, although their success rates vary. Most of the reported electrogram-based mapping studies have been performed with ablation catheters; meanwhile, the use of multipolar mapping catheters with smaller electrodes and closer interelectrode spacing has emerged, which allows for an assessment of detailed near-field abnormal electrograms at a higher resolution. Another recent advancement has occurred in the use of imaging techniques in VT ablation, particularly in refining the substrate. The goal of this paper is to review the key developments and limitations of current mapping strategies of substrate-based VT ablation and their outcomes. In addition, we briefly summarize the role of cardiac imaging in delineating VT substrate.

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          Prophylactic catheter ablation for the prevention of defibrillator therapy.

          For patients who have a ventricular tachyarrhythmic event, implantable cardioverter-defibrillators (ICDs) are a mainstay of therapy to prevent sudden death. However, ICD shocks are painful, can result in clinical depression, and do not offer complete protection against death from arrhythmia. We designed this randomized trial to examine whether prophylactic radiofrequency catheter ablation of arrhythmogenic ventricular tissue would reduce the incidence of ICD therapy. Eligible patients with a history of a myocardial infarction underwent defibrillator implantation for spontaneous ventricular tachycardia or fibrillation. The patients did not receive antiarrhythmic drugs. Patients were randomly assigned to defibrillator implantation alone or defibrillator implantation with adjunctive catheter ablation (64 patients in each group). Ablation was performed with the use of a substrate-based approach in which the myocardial scar is mapped and ablated while the heart remains predominantly in sinus rhythm. The primary end point was survival free from any appropriate ICD therapy. The mortality rate 30 days after ablation was zero, and there were no significant changes in ventricular function or functional class during the mean (+/-SD) follow-up period of 22.5+/-5.5 months. Twenty-one patients assigned to defibrillator implantation alone (33%) and eight patients assigned to defibrillator implantation plus ablation (12%) received appropriate ICD therapy (antitachycardia pacing or shocks) (hazard ratio in the ablation group, 0.35; 95% confidence interval, 0.15 to 0.78, P=0.007). Among these patients, 20 in the control group (31%) and 6 in the ablation group (9%) received shocks (P=0.003). Mortality was not increased in the group assigned to ablation as compared with the control group (9% vs. 17%, P=0.29). In this randomized trial, prophylactic substrate-based catheter ablation reduced the incidence of ICD therapy in patients with a history of myocardial infarction who received ICDs for the secondary prevention of sudden death. (Current Controlled Trials number, ISRCTN62488166 [controlled-trials.com].). Copyright 2007 Massachusetts Medical Society.
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            Slow conduction in the infarcted human heart. 'Zigzag' course of activation.

            Ventricular tachycardias occurring in the chronic phase of myocardial infarction are caused by reentry. Areas of slow conduction, facilitating reentry, are often found in the infarcted zone. The purpose of this study was to elucidate the mechanism of slow conduction in the chronic infarcted human heart. Spread of activation was studied in infarcted papillary muscles from hearts of patients who underwent heart transplantation because of infarction. Recordings were carried out on 10 papillary muscles that were superfused in a tissue bath. High-resolution mapping was performed in areas revealing slow conduction. Activation delay between sites perpendicular to the fiber direction and 1.4 mm apart could be as long as 45 milliseconds. Analysis of activation times revealed that activation spread in tracts parallel to the fiber direction. Conduction velocity in the tracts was between 0.6 and 1 m/s. Although tracts were separated from each other over distances up to 8 mm, they often connected with each other at one or more sites, forming a complex network of connected tracts. In this network, wave fronts could travel perpendicular to the fiber direction. Separation of tracts was due to collagenous septa. At sites where tracts were interconnected, the collagenous barriers were interrupted. Slow conduction perpendicular to the fiber direction in infarcted myocardial tissue is caused by a "zigzag" course of activation at high speed. Activation proceeds along pathways lengthened by branching and merging bundles of surviving myocytes ensheathed by collagenous septa.
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              EHRA/HRS Expert Consensus on Catheter Ablation of Ventricular Arrhythmias: developed in a partnership with the European Heart Rhythm Association (EHRA), a Registered Branch of the European Society of Cardiology (ESC), and the Heart Rhythm Society (HRS); in collaboration with the American College of Cardiology (ACC) and the American Heart Association (AHA).

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                Author and article information

                Journal
                J Innov Card Rhythm Manag
                J Innov Card Rhythm Manag
                JICRM
                The Journal of Innovations in Cardiac Rhythm Management
                MediaSphere Medical (United States )
                2156-3977
                2156-3993
                15 March 2019
                March 2019
                : 10
                : 3
                : 3565-3580
                Affiliations
                [1] 1IHU Liryc, Electrophysiology and Heart Modeling Institute, Fondation Bordeaux Université, Pessac-Bordeaux, France
                [2] 2Electrophysiology and Ablation Unit, Bordeaux University Hospital (CHU), Pessac, France
                [3] 3Centre de recherche Cardio-Thoracique de Bordeaux, University of Bordeaux, Bordeaux, France
                [4] 4Royal Papworth Hospital NHS Foundation Trust, Cambridge, UK
                [5] 5Newcastle University, Newcastle-upon-Tyne, UK
                [6] 6San Raffaele Hospital, Milan, Italy
                [7] 7Tokyo Metropolitan Hiroo Hospital, Tokyo, Japan
                Author notes
                Address correspondence to: Takeshi Kitamura, MD, Department of Electrophysiology, Hôpital Cardiologique du Haut-Lévêque (Centre Hospitalier Universitaire de Bordeaux), Avenue de Magellan, 33604 Bordeaux-Pessac, France. Email: takektmr@ 123456gmail.com .

                Dr. Denis and Dr. Derval have received speaking honoraria and consulting fees from Boston Scientific. Dr. Hocini, Dr. Haïssaguerre, and Dr. Jaïs have received lecture fees from Abbott and Biosense Webster. Dr. Sacher has received consulting fees and speaking honorarium from Abbott, Boston Scientific, Medtronic, and Biosense Webster. The other authors report no conflicts of interest for the published content. This research was supported by an ANR grant (IHU LIRYC grant no. ANR-10-IAHU-04).

                Article
                icrm.2019.100302
                10.19102/icrm.2019.100302
                7252795
                32477720
                5a96f8b6-f033-4e9e-a500-dc2c674646a9
                Copyright: © 2019 Innovations in Cardiac Rhythm Management

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 16 July 2018
                : 20 August 2018
                Categories
                Research Review

                ablation,cardiac imaging,substrate,three-dimensional mapping system,ventricular tachycardia

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