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Effect of Amiodarone and Hypothermia on Arrhythmia Substrates During Resuscitation

BACKGROUND: Amiodarone is administered during resuscitation, but its antiarrhythmic effects during targeted temperature management are unknown. The purpose of this study was to determine the effect of both therapeutic hypothermia and amiodarone on arrhythmia substrates during resuscitation from card...

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Autores principales: Piktel, Joseph S., Suen, Yi, Kouk, Shalen, Maleski, Danielle, Pawlowski, Gary, Laurita, Kenneth R., Wilson, Lance D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8200710/
https://www.ncbi.nlm.nih.gov/pubmed/33938226
http://dx.doi.org/10.1161/JAHA.120.016676
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author Piktel, Joseph S.
Suen, Yi
Kouk, Shalen
Maleski, Danielle
Pawlowski, Gary
Laurita, Kenneth R.
Wilson, Lance D.
author_facet Piktel, Joseph S.
Suen, Yi
Kouk, Shalen
Maleski, Danielle
Pawlowski, Gary
Laurita, Kenneth R.
Wilson, Lance D.
author_sort Piktel, Joseph S.
collection PubMed
description BACKGROUND: Amiodarone is administered during resuscitation, but its antiarrhythmic effects during targeted temperature management are unknown. The purpose of this study was to determine the effect of both therapeutic hypothermia and amiodarone on arrhythmia substrates during resuscitation from cardiac arrest. METHODS AND RESULTS: We utilized 2 complementary models: (1) In vitro no‐flow global ischemia canine left ventricular transmural wedge preparation. Wedges at different temperatures (36°C or 32°C) were given 5 µmol/L amiodarone (36‐Amio or 32‐Amio, each n=8) and subsequently underwent ischemia and reperfusion. Results were compared with previous controls. Optical mapping was used to measure action potential duration, dispersion of repolarization (DOR), and conduction velocity (CV). (2) In vivo pig model of resuscitation. Pigs (control or targeted temperature management, 32–34°C) underwent ischemic cardiac arrest and were administered amiodarone (or not) after 8 minutes of ventricular fibrillation. In vitro: therapeutic hypothermia but not amiodarone prolonged action potential duration. During ischemia, DOR increased in the 32‐Amio group versus 32‐Alone (84±7 ms versus 40±7 ms, P<0.05) while CV slowed in the 32‐Amio group. Amiodarone did not affect CV, DOR, or action potential duration during ischemia at 36°C. Conduction block was only observed at 36°C (5/8 36‐Amio versus 6/7 36‐Alone, 0/8 32‐Amio, versus 0/7 32‐Alone). In vivo: QTc decreased upon reperfusion from ischemia that was ameliorated by targeted temperature management. Amiodarone did not worsen DOR or CV. Amiodarone suppressed rearrest caused by ventricular fibrillation (7/8 without amiodarone, 2/7 with amiodarone, P=0.041), but not pulseless electrical activity (2/8 without amiodarone, 5/7 with amiodarone, P=0.13). CONCLUSIONS: Although amiodarone abolishes a beneficial effect of therapeutic hypothermia on ischemia‐induced DOR and CV, it did not worsen susceptibility to ventricular tachycardia/ventricular fibrillation during resuscitation.
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spelling pubmed-82007102021-06-15 Effect of Amiodarone and Hypothermia on Arrhythmia Substrates During Resuscitation Piktel, Joseph S. Suen, Yi Kouk, Shalen Maleski, Danielle Pawlowski, Gary Laurita, Kenneth R. Wilson, Lance D. J Am Heart Assoc Original Research BACKGROUND: Amiodarone is administered during resuscitation, but its antiarrhythmic effects during targeted temperature management are unknown. The purpose of this study was to determine the effect of both therapeutic hypothermia and amiodarone on arrhythmia substrates during resuscitation from cardiac arrest. METHODS AND RESULTS: We utilized 2 complementary models: (1) In vitro no‐flow global ischemia canine left ventricular transmural wedge preparation. Wedges at different temperatures (36°C or 32°C) were given 5 µmol/L amiodarone (36‐Amio or 32‐Amio, each n=8) and subsequently underwent ischemia and reperfusion. Results were compared with previous controls. Optical mapping was used to measure action potential duration, dispersion of repolarization (DOR), and conduction velocity (CV). (2) In vivo pig model of resuscitation. Pigs (control or targeted temperature management, 32–34°C) underwent ischemic cardiac arrest and were administered amiodarone (or not) after 8 minutes of ventricular fibrillation. In vitro: therapeutic hypothermia but not amiodarone prolonged action potential duration. During ischemia, DOR increased in the 32‐Amio group versus 32‐Alone (84±7 ms versus 40±7 ms, P<0.05) while CV slowed in the 32‐Amio group. Amiodarone did not affect CV, DOR, or action potential duration during ischemia at 36°C. Conduction block was only observed at 36°C (5/8 36‐Amio versus 6/7 36‐Alone, 0/8 32‐Amio, versus 0/7 32‐Alone). In vivo: QTc decreased upon reperfusion from ischemia that was ameliorated by targeted temperature management. Amiodarone did not worsen DOR or CV. Amiodarone suppressed rearrest caused by ventricular fibrillation (7/8 without amiodarone, 2/7 with amiodarone, P=0.041), but not pulseless electrical activity (2/8 without amiodarone, 5/7 with amiodarone, P=0.13). CONCLUSIONS: Although amiodarone abolishes a beneficial effect of therapeutic hypothermia on ischemia‐induced DOR and CV, it did not worsen susceptibility to ventricular tachycardia/ventricular fibrillation during resuscitation. John Wiley and Sons Inc. 2021-05-03 /pmc/articles/PMC8200710/ /pubmed/33938226 http://dx.doi.org/10.1161/JAHA.120.016676 Text en © 2021 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Piktel, Joseph S.
Suen, Yi
Kouk, Shalen
Maleski, Danielle
Pawlowski, Gary
Laurita, Kenneth R.
Wilson, Lance D.
Effect of Amiodarone and Hypothermia on Arrhythmia Substrates During Resuscitation
title Effect of Amiodarone and Hypothermia on Arrhythmia Substrates During Resuscitation
title_full Effect of Amiodarone and Hypothermia on Arrhythmia Substrates During Resuscitation
title_fullStr Effect of Amiodarone and Hypothermia on Arrhythmia Substrates During Resuscitation
title_full_unstemmed Effect of Amiodarone and Hypothermia on Arrhythmia Substrates During Resuscitation
title_short Effect of Amiodarone and Hypothermia on Arrhythmia Substrates During Resuscitation
title_sort effect of amiodarone and hypothermia on arrhythmia substrates during resuscitation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8200710/
https://www.ncbi.nlm.nih.gov/pubmed/33938226
http://dx.doi.org/10.1161/JAHA.120.016676
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