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Reversible Pulsed Electrical Fields as an In Vivo Tool to Study Cardiac Electrophysiology: The Advent of Pulsed Field Mapping
BACKGROUND: During electrophysiological mapping of tachycardias, putative target sites are often only truly confirmed to be vital after observing the effect of ablation. This lack of mapping specificity potentiates inadvertent ablation of innocent cardiac tissue not relevant to the arrhythmia. But i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578517/ https://www.ncbi.nlm.nih.gov/pubmed/37727989 http://dx.doi.org/10.1161/CIRCEP.123.012018 |
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author | Koruth, Jacob S. Neuzil, Petr Kawamura, Iwanari Kuroki, Kenji Petru, Jan Rackauskas, Gediminas Funasako, Moritoshi Aidietis, Audrius Reddy, Vivek Y. |
author_facet | Koruth, Jacob S. Neuzil, Petr Kawamura, Iwanari Kuroki, Kenji Petru, Jan Rackauskas, Gediminas Funasako, Moritoshi Aidietis, Audrius Reddy, Vivek Y. |
author_sort | Koruth, Jacob S. |
collection | PubMed |
description | BACKGROUND: During electrophysiological mapping of tachycardias, putative target sites are often only truly confirmed to be vital after observing the effect of ablation. This lack of mapping specificity potentiates inadvertent ablation of innocent cardiac tissue not relevant to the arrhythmia. But if myocardial excitability could be transiently suppressed at critical regions, their suitability as targets could be conclusively determined before delivering tissue-destructive ablation lesions. We studied whether reversible pulsed electric fields (PF(REV)) could transiently suppress electrical conduction, thereby providing a means to dissect tachycardia circuits in vivo. METHODS: PF(REV) energy was delivered from a 9-mm lattice-tip catheter to the atria of 12 swine and 9 patients, followed by serial electrogram assessments. The effects on electrical conduction were explored in 5 additional animals by applying PF(REV) to the atrioventricular node: 17 low-dose (PF(REV-LOW)) and 10 high-dose (PF(REV-HIGH)) applications. Finally, in 3 patients manifesting spontaneous tachycardias, PF(REV) was applied at putative critical sites. RESULTS: In animals, the immediate post-PF(REV) electrogram amplitudes diminished by 74%, followed by 78% recovery by 5 minutes. Similarly, in patients, a 69.9% amplitude reduction was followed by 84% recovery by 3 minutes. Histology revealed only minimal to no focal, superficial fibrosis. PF(REV-LOW) at the atrioventricular node resulted in transient PR prolongation and transient AV block in 59% and 6%, while PF(REV-HIGH) caused transient PR prolongation and transient AV block in 30% and 50%, respectively. The 3 tachycardia patients had atypical atrial flutters (n=2) and atrioventricular nodal reentrant tachycardia. PF(REV) at putative critical sites reproducibly terminated the tachycardias; ablation rendered the tachycardias noninducible and without recurrence during 1-year follow-up. CONCLUSIONS: Reversible electroporation pulses can be applied to myocardial tissue to transiently block electrical conduction. This technique of pulsed field mapping may represent a novel electrophysiological tool to help identify the critical isthmus of tachycardia circuits. |
format | Online Article Text |
id | pubmed-10578517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-105785172023-10-17 Reversible Pulsed Electrical Fields as an In Vivo Tool to Study Cardiac Electrophysiology: The Advent of Pulsed Field Mapping Koruth, Jacob S. Neuzil, Petr Kawamura, Iwanari Kuroki, Kenji Petru, Jan Rackauskas, Gediminas Funasako, Moritoshi Aidietis, Audrius Reddy, Vivek Y. Circ Arrhythm Electrophysiol Original Articles BACKGROUND: During electrophysiological mapping of tachycardias, putative target sites are often only truly confirmed to be vital after observing the effect of ablation. This lack of mapping specificity potentiates inadvertent ablation of innocent cardiac tissue not relevant to the arrhythmia. But if myocardial excitability could be transiently suppressed at critical regions, their suitability as targets could be conclusively determined before delivering tissue-destructive ablation lesions. We studied whether reversible pulsed electric fields (PF(REV)) could transiently suppress electrical conduction, thereby providing a means to dissect tachycardia circuits in vivo. METHODS: PF(REV) energy was delivered from a 9-mm lattice-tip catheter to the atria of 12 swine and 9 patients, followed by serial electrogram assessments. The effects on electrical conduction were explored in 5 additional animals by applying PF(REV) to the atrioventricular node: 17 low-dose (PF(REV-LOW)) and 10 high-dose (PF(REV-HIGH)) applications. Finally, in 3 patients manifesting spontaneous tachycardias, PF(REV) was applied at putative critical sites. RESULTS: In animals, the immediate post-PF(REV) electrogram amplitudes diminished by 74%, followed by 78% recovery by 5 minutes. Similarly, in patients, a 69.9% amplitude reduction was followed by 84% recovery by 3 minutes. Histology revealed only minimal to no focal, superficial fibrosis. PF(REV-LOW) at the atrioventricular node resulted in transient PR prolongation and transient AV block in 59% and 6%, while PF(REV-HIGH) caused transient PR prolongation and transient AV block in 30% and 50%, respectively. The 3 tachycardia patients had atypical atrial flutters (n=2) and atrioventricular nodal reentrant tachycardia. PF(REV) at putative critical sites reproducibly terminated the tachycardias; ablation rendered the tachycardias noninducible and without recurrence during 1-year follow-up. CONCLUSIONS: Reversible electroporation pulses can be applied to myocardial tissue to transiently block electrical conduction. This technique of pulsed field mapping may represent a novel electrophysiological tool to help identify the critical isthmus of tachycardia circuits. Lippincott Williams & Wilkins 2023-09-20 /pmc/articles/PMC10578517/ /pubmed/37727989 http://dx.doi.org/10.1161/CIRCEP.123.012018 Text en © 2023 The Authors. https://creativecommons.org/licenses/by-nc-nd/4.0/Circulation: Arrhythmia and Electrophysiology is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDerivs (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made. |
spellingShingle | Original Articles Koruth, Jacob S. Neuzil, Petr Kawamura, Iwanari Kuroki, Kenji Petru, Jan Rackauskas, Gediminas Funasako, Moritoshi Aidietis, Audrius Reddy, Vivek Y. Reversible Pulsed Electrical Fields as an In Vivo Tool to Study Cardiac Electrophysiology: The Advent of Pulsed Field Mapping |
title | Reversible Pulsed Electrical Fields as an In Vivo Tool to Study Cardiac Electrophysiology: The Advent of Pulsed Field Mapping |
title_full | Reversible Pulsed Electrical Fields as an In Vivo Tool to Study Cardiac Electrophysiology: The Advent of Pulsed Field Mapping |
title_fullStr | Reversible Pulsed Electrical Fields as an In Vivo Tool to Study Cardiac Electrophysiology: The Advent of Pulsed Field Mapping |
title_full_unstemmed | Reversible Pulsed Electrical Fields as an In Vivo Tool to Study Cardiac Electrophysiology: The Advent of Pulsed Field Mapping |
title_short | Reversible Pulsed Electrical Fields as an In Vivo Tool to Study Cardiac Electrophysiology: The Advent of Pulsed Field Mapping |
title_sort | reversible pulsed electrical fields as an in vivo tool to study cardiac electrophysiology: the advent of pulsed field mapping |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578517/ https://www.ncbi.nlm.nih.gov/pubmed/37727989 http://dx.doi.org/10.1161/CIRCEP.123.012018 |
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