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      The use of a novel signal analysis to identify the origin of idiopathic right ventricular outflow tract ventricular tachycardia during sinus rhythm: Simultaneous amplitude frequency electrogram transformation mapping

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          Abstract

          Introduction

          The signal characteristics of intracardiac bipolar electrograms at the origin of idiopathic RVOT-VT during sinus rhythm remain unclear.

          Objective

          The study sought to develop a novel real-time/online technique, simultaneous amplitude frequency electrogram transformation (SAFE-T), to quantify and localize the diseased ventricular substrate in idiopathic RVOT-VT.

          Methods

          We retrospectively investigated the intracardiac bipolar recordings in 70 consecutive patients (26% male, mean age 42±12 years) who underwent successful radiofrequency catheter ablation of idiopathic RVOT-VT. We quantified the extent of the frequency fraction of ventricular potentials during sinus rhythm or ventricular pacing using a novel formula, the product of instantaneous amplitude and frequency, and showed that in a 3D geometry as an online SAFE-T map.

          Results

          The characteristics of the HHT spectra of electrograms derived from VT origins demonstrated high frequency components (>70 Hz), which were independent of the rhythm. The density of the abnormal potentials at the VT origins were higher (VT origins, 7.5±2.3 sites/cm 2 vs. surrounding myocardium, 1.5±1.3 sites/cm 2, p<0.001), and were significantly decreased after ablation (0.7±0.6 sites/cm 2, p<0.001). A small region of abnormal potentials were observed in the VT origins (mean area of 1.5±0.8 cm 2). The SAFE-T maps predicted the VT origins with 92% sensitivity, 78% specificity with optimal cut-off value of >3.0 Hz·mV.

          Conclusion

          The online SAFE-T map was feasible for quantifying the diseased ventricular substrate, irrespective of the rhythm of activation, and can be used to identify the optimal ablation targets for idiopathic RVOT-VT. We found a limited region of abnormal potentials where the RVOT-VT origins were successfully ablated.

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          Most cited references25

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          The empirical mode decomposition and the Hilbert spectrum for nonlinear and non-stationary time series analysis

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            A new treatment for atrial fibrillation based on spectral analysis to guide the catheter RF-ablation.

            By studying the spectrum of atrial potentials by fast Fourier transform (FFT) we have found two types of atrial muscle: the compact (CM) and the fibrillar (FM) myocardium. The former presents normal in-phase conduction inferring a great number of cellular connections, long-lasting refractoriness and leftward FFT-shift. The latter shows anisotropic out-of-phase conduction, fewer cellular connections, short refractoriness and a segmented right-FFT-shift. The compact is the normal predominant muscle and the fibrillar is different and may be neural input, vein insertion, interatrial (1A) septum, left atrial (LA) roof, etc. or pathological tissue, being so by loss of cellular connections this is a possible mechanism for conversion of compact into fibrillar-like myocardium. During atrial fibrillation (AF), clusters of FM (AF nests) present higher frequencies than any surrounding tissue.
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              Right ventricular tachycardia: clinical and electrophysiologic characteristics.

              This report describes the clinical and electrophysiologic characteristics of 30 patients without myocardial disease who had ventricular tachycardia with the morphologic characteristics of left bundle branch block and inferior axis. The tachycardias were nonsustained in 24 patients, sustained (greater than 30 sec) in six patients, and provocable by exercise in 14 of 23 patients undergoing a standard Bruce protocol. Ventricular tachycardia was induced during electrophysiologic study in 22 of 30 patients. Programmed stimulation induced tachycardia in 10 of 30 patients, most frequently by rapid atrial or ventricular pacing. Isoproterenol infusion facilitated tachycardia induction in 13 of 23 patients. Endocardial activation mapping, performed in 10 patients, confirmed that earliest ventricular activation during tachycardia occurred at the right ventricular outflow tract on the interventricular septum. These tachycardias were unique in their responsiveness to a wide variety of antiarrhythmic drugs, including type I drugs and propranolol. During a mean follow-up of 30 months, no patient has died or experienced cardiac arrest. Two patients appear to be in spontaneous remission, and no patient has developed additional signs of cardiac disease.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                10 March 2017
                2017
                : 12
                : 3
                : e0173189
                Affiliations
                [1 ]Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan
                [2 ]Cardiac Electrophysiology and Pacing Laboratory, Division of Cardiovascular Medicine, Makiminato Central Hospital, Okinawa, Japan
                [3 ]Faculty of Medicine and Institute of Clinical Medicine, National Yang-Ming University, Taipei, Taiwan
                [4 ]Research Center for Adaptive Data Analysis and Center for Dynamical Biomarkers and Translational Medicine, National Central University, Jhongli, Taiwan
                University of Minnesota, UNITED STATES
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                • Conceptualization: SH ALDT YJL.

                • Data curation: SH ALDT CYL MTL CAL CL YCC YJL.

                • Formal analysis: SH ALDT CYL MTL CL YCC YJL.

                • Funding acquisition: YJL.

                • Investigation: SH ALDT CYL MTL CL YCC SLC LWL YFH FPC TCT TFC JNL YTC CHL YH SY KLP YJL SAC.

                • Methodology: SH ALDT CYL MTL CL YCC YJL.

                • Project administration: YJL SAC.

                • Resources: SH ALDT CYL MTL CL YCC SLC LWL YFH FPC TCT TFC JNL YTC CHL YH SY KLP YJL SAC.

                • Software: MTL CL YCC.

                • Supervision: YJL SAC.

                • Validation: SH ALDT YJL SAC.

                • Visualization: SH ALDT CYL MTL CL YCC YJL SAC.

                • Writing – original draft: SH ALDT YJL.

                • Writing – review & editing: SH ALDT YJL SAC.

                Article
                PONE-D-16-35531
                10.1371/journal.pone.0173189
                5345764
                28282453
                d79671a7-813c-4772-bb48-8b681f1df1df
                © 2017 Te et al

                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 author and source are credited.

                History
                : 4 September 2016
                : 16 February 2017
                Page count
                Figures: 5, Tables: 3, Pages: 16
                Funding
                Funded by: Ministry of Science and Technology of Taiwan
                Award ID: MOST 104-2314-B-010-063-MY2
                Award Recipient :
                Funded by: Grant of Taipei Veterans General Hospital
                Award ID: V105C-122
                Award Recipient :
                Funded by: Joint foundation of Taipei Veterans General Hospital and National Taiwan University Hospital
                Award ID: 105AC-D710
                Award Recipient :
                Funded by: Joint foundation of Taipei Veterans General Hospital and National Taiwan University Hospital
                Award ID: VGHUST105-G7-4-1
                Award Recipient :
                Funded by: Research Foundation of Cardiovascular Medicine
                Award ID: RFCM 105-01-007
                Award Recipient :
                Funded by: Research Foundation of Cardiovascular Medicine
                Award ID: RFCM 105-02-008
                Award Recipient :
                Funded by: Foundation for the Development of Internal Medicine in Okinawa
                Award ID: 26-02-004
                Award Recipient :
                Funded by: Foundation for the Development of Internal Medicine in Okinawa
                Award ID: 28-02-002
                Award Recipient :
                This work was supported by Ministry of Science and Technology of Taiwan support for National Yang-Ming University (MOST 104-2314-B-010-063-MY2); Grant of Taipei Veterans General Hospital (V105C-122); Joint foundation of Taipei Veterans General Hospital and National Taiwan University Hospital (105AC-D710, VGHUST105-G7-4-1).
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