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Does therapeutic hypothermia during extracorporeal cardiopulmonary resuscitation preserve cardiac function?

BACKGROUND: Extracorporeal cardiopulmonary resuscitation (E-CPR) is increasingly used as a rescue method in the management of cardiac arrest and provides the opportunity to rapidly induce therapeutic hypothermia. The survival after a cardiac arrest is related to post-arrest cardiac function, and the...

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Autores principales: Bergan, Harald A., Halvorsen, Per S., Skulstad, Helge, Fosse, Erik, Bugge, Jan F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5175383/
https://www.ncbi.nlm.nih.gov/pubmed/27998282
http://dx.doi.org/10.1186/s12967-016-1099-y
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author Bergan, Harald A.
Halvorsen, Per S.
Skulstad, Helge
Fosse, Erik
Bugge, Jan F.
author_facet Bergan, Harald A.
Halvorsen, Per S.
Skulstad, Helge
Fosse, Erik
Bugge, Jan F.
author_sort Bergan, Harald A.
collection PubMed
description BACKGROUND: Extracorporeal cardiopulmonary resuscitation (E-CPR) is increasingly used as a rescue method in the management of cardiac arrest and provides the opportunity to rapidly induce therapeutic hypothermia. The survival after a cardiac arrest is related to post-arrest cardiac function, and the application of therapeutic hypothermia post-arrest is hypothesized to improve cardiac outcome. The present animal study compares normothermic and hypothermic E-CPR considering resuscitation success, post-arrest left ventricular function and magnitude of myocardial injury. METHODS: After a 15-min untreated ventricular fibrillation, the pigs (n = 20) were randomized to either normothermic (38 °C) or hypothermic (32–33 °C) E-CPR. Defibrillation terminated ventricular fibrillation after 5 min of E-CPR, and extracorporeal support continued for 2 h, followed by warming, weaning and a stabilization period. Magnetic resonance imaging and left ventricle pressure measurements were used to assess left ventricular function pre-arrest and 5 h post-arrest. Myocardial injury was estimated by serum concentrations of cardiac TroponinT and Aspartate transaminase (ASAT). RESULTS: E-CPR resuscitated all animals and the hypothermic strategy induced therapeutic hypothermia within minutes without impairment of the resuscitation success rate. All animals suffered a severe global systolic left ventricular dysfunction post-arrest with 50–70% reductions in stroke volume, ejection fraction, wall thickening, strain and mitral annular plane systolic excursion. Serum concentrations of cardiac TroponinT and ASAT increased considerably post-arrest. No significant differences were found between the two groups. CONCLUSIONS: Two-hour therapeutic hypothermia during E-CPR offers an equal resuscitation success rate, but does not preserve the post-arrest cardiac function nor reduce the magnitude of myocardial injury, compared to normothermic E-CPR. Trial registration FOTS 4611/13 registered 25 October 2012 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12967-016-1099-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-51753832016-12-28 Does therapeutic hypothermia during extracorporeal cardiopulmonary resuscitation preserve cardiac function? Bergan, Harald A. Halvorsen, Per S. Skulstad, Helge Fosse, Erik Bugge, Jan F. J Transl Med Research BACKGROUND: Extracorporeal cardiopulmonary resuscitation (E-CPR) is increasingly used as a rescue method in the management of cardiac arrest and provides the opportunity to rapidly induce therapeutic hypothermia. The survival after a cardiac arrest is related to post-arrest cardiac function, and the application of therapeutic hypothermia post-arrest is hypothesized to improve cardiac outcome. The present animal study compares normothermic and hypothermic E-CPR considering resuscitation success, post-arrest left ventricular function and magnitude of myocardial injury. METHODS: After a 15-min untreated ventricular fibrillation, the pigs (n = 20) were randomized to either normothermic (38 °C) or hypothermic (32–33 °C) E-CPR. Defibrillation terminated ventricular fibrillation after 5 min of E-CPR, and extracorporeal support continued for 2 h, followed by warming, weaning and a stabilization period. Magnetic resonance imaging and left ventricle pressure measurements were used to assess left ventricular function pre-arrest and 5 h post-arrest. Myocardial injury was estimated by serum concentrations of cardiac TroponinT and Aspartate transaminase (ASAT). RESULTS: E-CPR resuscitated all animals and the hypothermic strategy induced therapeutic hypothermia within minutes without impairment of the resuscitation success rate. All animals suffered a severe global systolic left ventricular dysfunction post-arrest with 50–70% reductions in stroke volume, ejection fraction, wall thickening, strain and mitral annular plane systolic excursion. Serum concentrations of cardiac TroponinT and ASAT increased considerably post-arrest. No significant differences were found between the two groups. CONCLUSIONS: Two-hour therapeutic hypothermia during E-CPR offers an equal resuscitation success rate, but does not preserve the post-arrest cardiac function nor reduce the magnitude of myocardial injury, compared to normothermic E-CPR. Trial registration FOTS 4611/13 registered 25 October 2012 ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12967-016-1099-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-12-20 /pmc/articles/PMC5175383/ /pubmed/27998282 http://dx.doi.org/10.1186/s12967-016-1099-y Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Bergan, Harald A.
Halvorsen, Per S.
Skulstad, Helge
Fosse, Erik
Bugge, Jan F.
Does therapeutic hypothermia during extracorporeal cardiopulmonary resuscitation preserve cardiac function?
title Does therapeutic hypothermia during extracorporeal cardiopulmonary resuscitation preserve cardiac function?
title_full Does therapeutic hypothermia during extracorporeal cardiopulmonary resuscitation preserve cardiac function?
title_fullStr Does therapeutic hypothermia during extracorporeal cardiopulmonary resuscitation preserve cardiac function?
title_full_unstemmed Does therapeutic hypothermia during extracorporeal cardiopulmonary resuscitation preserve cardiac function?
title_short Does therapeutic hypothermia during extracorporeal cardiopulmonary resuscitation preserve cardiac function?
title_sort does therapeutic hypothermia during extracorporeal cardiopulmonary resuscitation preserve cardiac function?
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5175383/
https://www.ncbi.nlm.nih.gov/pubmed/27998282
http://dx.doi.org/10.1186/s12967-016-1099-y
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