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      Evaluation of the reentry vulnerability index to predict ventricular tachycardia circuits using high-density contact mapping

      research-article
      , PhD , , , , MD , , MD, PhD , , PhD § , , PhD , , MD, FRCP , , MD , , MD, FRCP , , MD, PhD , , , MD, MRCP , , MD, FRCP , , MD , , MD, FRCP , , MD , , MD , , MD, FRCP , , MD, FRCP , , PhD § , , MD, DSci , , MD, FHRS , ,
      Heart Rhythm
      Elsevier
      Ablation, Activation time, Reentry vulnerability index, Repolarization time, Substrate mapping, Ventricular tachycardia

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          Abstract

          Background

          Identifying arrhythmogenic sites to improve ventricular tachycardia (VT) ablation outcomes remains unresolved. The reentry vulnerability index (RVI) combines activation and repolarization timings to identify sites critical for reentrant arrhythmia initiation without inducing VT.

          Objective

          The purpose of this study was to provide the first assessment of RVI’s capability to identify VT sites of origin using high-density contact mapping and comparison with other activation-repolarization markers of functional substrate.

          Methods

          Eighteen VT ablation patients (16 male; 72% ischemic) were studied. Unipolar electrograms were recorded during ventricular pacing and analyzed offline. Activation time (AT), activation–recovery interval (ARI), and repolarization time (RT) were measured. Vulnerability to reentry was mapped based on RVI and spatial distribution of AT, ARI, and RT. The distance from sites identified as vulnerable to reentry to the VT site of origin was measured, with distances <10 mm and >20 mm indicating accurate and inaccurate localization, respectively.

          Results

          The origins of 18 VTs (6 entrainment, 12 pace-mapping) were identified. RVI maps included 1012 (408–2098) (median, 1st–3rd quartiles) points per patient. RVI accurately localized 72.2% VT sites of origin, with median distance of 5.1 (3.2–10.1) mm. Inaccurate localization was significantly less frequent for RVI than AT (5.6% vs 33.3%; odds ratio 0.12; P = .035). Compared to RVI, distance to VT sites of origin was significantly larger for sites showing prolonged RT and ARI and were nonsignificantly larger for sites showing highest AT and ARI gradients.

          Conclusion

          RVI identifies vulnerable regions closest to VT sites of origin. Activation-repolarization metrics may improve VT substrate delineation and inform novel ablation strategies.

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          Most cited references20

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          Late potentials abolition as an additional technique for reduction of arrhythmia recurrence in scar related ventricular tachycardia ablation.

          To evaluate the efficacy of radiofrequency ventricular tachycardia (VT) ablation targeting complete late potential (LP) activity.
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            Substrate Mapping for Ventricular Tachycardia

            Substrate mapping was developed to treat poorly tolerated infarct-related ventricular tachycardias (VTs). This concept was based on 30-year-old data derived from surgical and percutaneous mapping during sinus rhythm and VT that demonstrated specific electrograms (EGMs) that characterized the "arrhythmogenic substrate" of VT. Electrogram characteristics of the arrhythmogenic VT substrate during sinus rhythm included low-voltage, fractionation, long duration, split signals, and isolated late potentials as well as EGMs demonstrating adjacent early and late activation. Introduction of electroanatomical mapping (EAM) systems during the mid-1990s has allowed investigators to record electrograms in 3 dimensions and to identify sites assumed to represent the central common pathway ("isthmus") during re-entrant VTs. However, several important assumptions and misconceptions make currently used "substrate mapping" techniques inaccurate. These include: 1) re-entrant circuits are produced by fixed barriers of immutable "inexcitable" scar; 2) low voltage amplitude (≤0.5 mV) implies dense "inexcitable" scar; 3) isthmuses identified in patients with tolerated VTs using entrainment mapping are both valid and provide an accurate depiction of isthmuses in less hemodynamically tolerated VTs; and 4) current mapping tools and methods can delineate specific electrophysiologic features that will determine the barriers forming channels during re-entrant VTs. None of these assumptions has been validated and recent experimental and human data using higher resolution mapping with very small electrodes cast doubt on their validity. These data call for re-evaluation of substrate-mapping techniques to characterize the arrhythmogenic substrate of post-infarction VT. Standardization of recording techniques including electrode size, interelectrode spacing, tissue contact, catheter orientation, and wavefront activation must be taken into consideration.
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              Dispersion of repolarization and arrhythmogenesis.

              The relation between induction of arrhythmias and dispersion of repolarization is not completely understood. The purpose of this study was to study the relation between heterogeneity in repolarization and arrhythmogenesis under conditions of selective regional action potential prolongation and shortening. Pig hearts were perfused in a Langendorff setup. The left anterior descending artery (LAD) was cannulated and perfused. Sotalol (220 microM) was infused in the aortic cannula, and pinacidil (20 microM) was infused through the LAD, causing a gradient in repolarization time between the two myocardial regions. Premature stimulation was performed from the LAD region. No transmural repolarization gradients developed after infusion of the drugs. High-density epicardial activation/repolarization mapping (176 unipolar electrodes, 2-mm interelectrode spacing) revealed a maximum repolarization gradient of approximately 120 ms over 14 mm. The critical parameter for differentiating between the occurrence of reentry and the mere occurrence of a line of activation block between the two myocardial regions (and no reentry) was not the magnitude of the repolarization gradient but the timing of arrival of the premature activation wave at the distal side of the line of activation block relative to the repolarization time of the premature beat proximal to the line of block. No spontaneous arrhythmias were observed despite the presence of the repolarization gradient. It is not the repolarization gradient but the restitution characteristics of the tissue with the shorter action potential, in combination with the time of arrival of the premature wavefront at the distal side of the line of block, that determines the occurrence of reentry.
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                Author and article information

                Contributors
                Journal
                Heart Rhythm
                Heart Rhythm
                Heart Rhythm
                Elsevier
                1547-5271
                1556-3871
                1 April 2020
                April 2020
                : 17
                : 4
                : 576-583
                Affiliations
                []Institute of Cardiovascular Science, University College London, London, United Kingdom
                []The William Harvey Research Institute, Queen Mary University of London, London, United Kingdom
                []Electrophysiology Department, Barts Heart Centre, St Bartholomew's Hospital, London, United Kingdom
                [§ ]School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom
                []Department of Mechanical Engineering, University College London, London, United Kingdom
                []Department of Cardiology, Guys and St Thomas' NHS Trust, London, United Kingdom
                Author notes
                [] Address reprint requests and correspondence: Dr Pier Lambiase and Dr Michele Orini, University College London, 5 University St, London WC1E 6JF, United Kingdom. m.orini@ 123456ucl.ac.uk p.lambiase@ 123456ucl.ac.uk
                Article
                S1547-5271(19)31025-2
                10.1016/j.hrthm.2019.11.013
                7105818
                31751771
                9baa472a-2eb5-4d9c-bb8b-0481f2bf96cf
                © 2019 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                Categories
                Article

                Cardiovascular Medicine
                ablation,activation time,reentry vulnerability index,repolarization time,substrate mapping,ventricular tachycardia

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