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Intramural mapping of intramural septal ventricular arrhythmias

BACKGROUND: Intramural ventricular arrhythmias (VAs) can originate in patients with or without structural heart disease. Electrogram (EGM) recordings from intramural sources of VA have not been described thoroughly. OBJECTIVE: We hypothesized that the presence of scar may be linked to the site of or...

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Autores principales: Tam, Tsz‐kin, Ghannam, Michael, Liang, Jackson J., Attili, Anil, Cochet, Hubert, Jais, Pierre, Juhoor, Mehdi, Latchamsetty, Rakesh, Jongnarangsin, Krit, Morady, Fred, Bogun, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9415098/
https://www.ncbi.nlm.nih.gov/pubmed/35170146
http://dx.doi.org/10.1111/jce.15410
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author Tam, Tsz‐kin
Ghannam, Michael
Liang, Jackson J.
Attili, Anil
Cochet, Hubert
Jais, Pierre
Juhoor, Mehdi
Latchamsetty, Rakesh
Jongnarangsin, Krit
Morady, Fred
Bogun, Frank
author_facet Tam, Tsz‐kin
Ghannam, Michael
Liang, Jackson J.
Attili, Anil
Cochet, Hubert
Jais, Pierre
Juhoor, Mehdi
Latchamsetty, Rakesh
Jongnarangsin, Krit
Morady, Fred
Bogun, Frank
author_sort Tam, Tsz‐kin
collection PubMed
description BACKGROUND: Intramural ventricular arrhythmias (VAs) can originate in patients with or without structural heart disease. Electrogram (EGM) recordings from intramural sources of VA have not been described thoroughly. OBJECTIVE: We hypothesized that the presence of scar may be linked to the site of origin (SOO) of focal, intramural VAs. METHODS: In a series of 21 patients (age: 55 ± 11 years, 12 women, mean ejection fraction 43 ± 14%) in whom the SOO of intramural VAs was identified, we analyzed bipolar EGM characteristics at the SOO and compared the findings with the endocardial breakout site. The patients were from a pool of 86 patients with intramural VAs referred for ablation. RESULTS: In 16/21 patients intramural scarring was detected by cardiac magnetic resonance (CMR) imaging In patients in whom the intramural SOO was reached, intramural bipolar EGMs showed a lower voltage and had broader EGMs compared to the endocardial breakout sites (0.97 ± 0.56 vs. 2.28 ± 0.15 mV, p = .001; and 122.3 ± 31.6 vs. 96.5 ± 26.3 ms, p < .01). All intramural sampled sites at the SOO had either low voltage or broad abnormal EGMs. The activation time was significantly earlier at the intramural SOO than at breakout sites (−36.2 ± 11.8 vs. −23.2 ± 9.1 ms, p < .0001). CONCLUSIONS: Sites of origin of intramural VAs with scar by CMR display EGM characteristics of scarring, supporting that scar tissue localizes to the SOO of intramural outflow tract arrhythmias in some patients. Scarring identified by CMR may be helpful in planning ablation procedures in patients with suspected intramural VAs.
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spelling pubmed-94150982022-08-31 Intramural mapping of intramural septal ventricular arrhythmias Tam, Tsz‐kin Ghannam, Michael Liang, Jackson J. Attili, Anil Cochet, Hubert Jais, Pierre Juhoor, Mehdi Latchamsetty, Rakesh Jongnarangsin, Krit Morady, Fred Bogun, Frank J Cardiovasc Electrophysiol Original Articles BACKGROUND: Intramural ventricular arrhythmias (VAs) can originate in patients with or without structural heart disease. Electrogram (EGM) recordings from intramural sources of VA have not been described thoroughly. OBJECTIVE: We hypothesized that the presence of scar may be linked to the site of origin (SOO) of focal, intramural VAs. METHODS: In a series of 21 patients (age: 55 ± 11 years, 12 women, mean ejection fraction 43 ± 14%) in whom the SOO of intramural VAs was identified, we analyzed bipolar EGM characteristics at the SOO and compared the findings with the endocardial breakout site. The patients were from a pool of 86 patients with intramural VAs referred for ablation. RESULTS: In 16/21 patients intramural scarring was detected by cardiac magnetic resonance (CMR) imaging In patients in whom the intramural SOO was reached, intramural bipolar EGMs showed a lower voltage and had broader EGMs compared to the endocardial breakout sites (0.97 ± 0.56 vs. 2.28 ± 0.15 mV, p = .001; and 122.3 ± 31.6 vs. 96.5 ± 26.3 ms, p < .01). All intramural sampled sites at the SOO had either low voltage or broad abnormal EGMs. The activation time was significantly earlier at the intramural SOO than at breakout sites (−36.2 ± 11.8 vs. −23.2 ± 9.1 ms, p < .0001). CONCLUSIONS: Sites of origin of intramural VAs with scar by CMR display EGM characteristics of scarring, supporting that scar tissue localizes to the SOO of intramural outflow tract arrhythmias in some patients. Scarring identified by CMR may be helpful in planning ablation procedures in patients with suspected intramural VAs. John Wiley and Sons Inc. 2022-03-05 2022-05 /pmc/articles/PMC9415098/ /pubmed/35170146 http://dx.doi.org/10.1111/jce.15410 Text en © 2022 The Authors. Journal of Cardiovascular Electrophysiology published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Tam, Tsz‐kin
Ghannam, Michael
Liang, Jackson J.
Attili, Anil
Cochet, Hubert
Jais, Pierre
Juhoor, Mehdi
Latchamsetty, Rakesh
Jongnarangsin, Krit
Morady, Fred
Bogun, Frank
Intramural mapping of intramural septal ventricular arrhythmias
title Intramural mapping of intramural septal ventricular arrhythmias
title_full Intramural mapping of intramural septal ventricular arrhythmias
title_fullStr Intramural mapping of intramural septal ventricular arrhythmias
title_full_unstemmed Intramural mapping of intramural septal ventricular arrhythmias
title_short Intramural mapping of intramural septal ventricular arrhythmias
title_sort intramural mapping of intramural septal ventricular arrhythmias
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9415098/
https://www.ncbi.nlm.nih.gov/pubmed/35170146
http://dx.doi.org/10.1111/jce.15410
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