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A comprehensive neuromonitoring approach in a large animal model of cardiac arrest

BACKGROUND: Anoxic brain injuries represent the main determinant of poor outcome after cardiac arrest (CA). Large animal models have been described to investigate new treatments during CA and post‐resuscitation phase, but a detailed model that includes extensive neuromonitoring is lacking. METHOD: B...

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Autores principales: Annoni, Filippo, Peluso, Lorenzo, Hirai, Lucas Akira, Babini, Giovanni, Khaldi, Amina, Herpain, Antoine, Pitisci, Lorenzo, Ferlini, Lorenzo, Garcia, Bruno, Taccone, Fabio Silvio, Creteur, Jacques, Su, Fuhong
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/PMC8879632/
https://www.ncbi.nlm.nih.gov/pubmed/35229991
http://dx.doi.org/10.1002/ame2.12200
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author Annoni, Filippo
Peluso, Lorenzo
Hirai, Lucas Akira
Babini, Giovanni
Khaldi, Amina
Herpain, Antoine
Pitisci, Lorenzo
Ferlini, Lorenzo
Garcia, Bruno
Taccone, Fabio Silvio
Creteur, Jacques
Su, Fuhong
author_facet Annoni, Filippo
Peluso, Lorenzo
Hirai, Lucas Akira
Babini, Giovanni
Khaldi, Amina
Herpain, Antoine
Pitisci, Lorenzo
Ferlini, Lorenzo
Garcia, Bruno
Taccone, Fabio Silvio
Creteur, Jacques
Su, Fuhong
author_sort Annoni, Filippo
collection PubMed
description BACKGROUND: Anoxic brain injuries represent the main determinant of poor outcome after cardiac arrest (CA). Large animal models have been described to investigate new treatments during CA and post‐resuscitation phase, but a detailed model that includes extensive neuromonitoring is lacking. METHOD: Before an electrically‐induced 10‐minute CA and resuscitation, 46 adult pigs underwent neurosurgery for placement of a multifunctional probe (intracranial pressure or ICP, tissue oxygen tension or PbtO(2) and cerebral temperature) and a bolt‐based technique for the placement and securing of a regional blood flow probe and two sEEG electrodes; two modified cerebral microdialysis (CMD) probes were also inserted in the frontal lobes and accidental misplacement was prevented using a perforated head support. RESULT: 42 animals underwent the CA procedure and 41 achieved the return of spontaneous circulation (ROSC). In 4 cases (8.6%) an adverse event took place during preparation, but only in two cases (4.3%) this was related to the neurosurgery. In 6 animals (13.3%) the minor complications that occurred resolved after probe repositioning. CONCLUSION: Herein we provide a detailed comprehensive neuromonitoring approach in a large animal model of CA that might help future research.
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spelling pubmed-88796322022-03-01 A comprehensive neuromonitoring approach in a large animal model of cardiac arrest Annoni, Filippo Peluso, Lorenzo Hirai, Lucas Akira Babini, Giovanni Khaldi, Amina Herpain, Antoine Pitisci, Lorenzo Ferlini, Lorenzo Garcia, Bruno Taccone, Fabio Silvio Creteur, Jacques Su, Fuhong Animal Model Exp Med Regular Articles BACKGROUND: Anoxic brain injuries represent the main determinant of poor outcome after cardiac arrest (CA). Large animal models have been described to investigate new treatments during CA and post‐resuscitation phase, but a detailed model that includes extensive neuromonitoring is lacking. METHOD: Before an electrically‐induced 10‐minute CA and resuscitation, 46 adult pigs underwent neurosurgery for placement of a multifunctional probe (intracranial pressure or ICP, tissue oxygen tension or PbtO(2) and cerebral temperature) and a bolt‐based technique for the placement and securing of a regional blood flow probe and two sEEG electrodes; two modified cerebral microdialysis (CMD) probes were also inserted in the frontal lobes and accidental misplacement was prevented using a perforated head support. RESULT: 42 animals underwent the CA procedure and 41 achieved the return of spontaneous circulation (ROSC). In 4 cases (8.6%) an adverse event took place during preparation, but only in two cases (4.3%) this was related to the neurosurgery. In 6 animals (13.3%) the minor complications that occurred resolved after probe repositioning. CONCLUSION: Herein we provide a detailed comprehensive neuromonitoring approach in a large animal model of CA that might help future research. John Wiley and Sons Inc. 2022-01-28 /pmc/articles/PMC8879632/ /pubmed/35229991 http://dx.doi.org/10.1002/ame2.12200 Text en © 2022 The Authors. Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences 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 Regular Articles
Annoni, Filippo
Peluso, Lorenzo
Hirai, Lucas Akira
Babini, Giovanni
Khaldi, Amina
Herpain, Antoine
Pitisci, Lorenzo
Ferlini, Lorenzo
Garcia, Bruno
Taccone, Fabio Silvio
Creteur, Jacques
Su, Fuhong
A comprehensive neuromonitoring approach in a large animal model of cardiac arrest
title A comprehensive neuromonitoring approach in a large animal model of cardiac arrest
title_full A comprehensive neuromonitoring approach in a large animal model of cardiac arrest
title_fullStr A comprehensive neuromonitoring approach in a large animal model of cardiac arrest
title_full_unstemmed A comprehensive neuromonitoring approach in a large animal model of cardiac arrest
title_short A comprehensive neuromonitoring approach in a large animal model of cardiac arrest
title_sort comprehensive neuromonitoring approach in a large animal model of cardiac arrest
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879632/
https://www.ncbi.nlm.nih.gov/pubmed/35229991
http://dx.doi.org/10.1002/ame2.12200
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