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Cerebral monitoring in a pig model of cardiac arrest with 48 h of intensive care

BACKGROUND: Neurological injury is the primary cause of death after out-of-hospital cardiac arrest. There is a lack of studies investigating cerebral injury beyond the immediate post-resuscitation phase in a controlled cardiac arrest experimental setting. METHODS: The aim of this study was to invest...

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Autores principales: Vammen, Lauge, Johannsen, Cecilie Munch, Magnussen, Andreas, Povlsen, Amalie, Petersen, Søren Riis, Azizi, Arezo, Pedersen, Michael, Korshøj, Anders Rosendal, Ringgaard, Steffen, Løfgren, Bo, Andersen, Lars W., Granfeldt, Asger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596181/
https://www.ncbi.nlm.nih.gov/pubmed/36284020
http://dx.doi.org/10.1186/s40635-022-00475-2
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author Vammen, Lauge
Johannsen, Cecilie Munch
Magnussen, Andreas
Povlsen, Amalie
Petersen, Søren Riis
Azizi, Arezo
Pedersen, Michael
Korshøj, Anders Rosendal
Ringgaard, Steffen
Løfgren, Bo
Andersen, Lars W.
Granfeldt, Asger
author_facet Vammen, Lauge
Johannsen, Cecilie Munch
Magnussen, Andreas
Povlsen, Amalie
Petersen, Søren Riis
Azizi, Arezo
Pedersen, Michael
Korshøj, Anders Rosendal
Ringgaard, Steffen
Løfgren, Bo
Andersen, Lars W.
Granfeldt, Asger
author_sort Vammen, Lauge
collection PubMed
description BACKGROUND: Neurological injury is the primary cause of death after out-of-hospital cardiac arrest. There is a lack of studies investigating cerebral injury beyond the immediate post-resuscitation phase in a controlled cardiac arrest experimental setting. METHODS: The aim of this study was to investigate temporal changes in measures of cerebral injury and metabolism in a cardiac arrest pig model with clinically relevant post-cardiac arrest intensive care. A cardiac arrest group (n = 11) underwent 7 min of no-flow and was compared with a sham group (n = 6). Pigs underwent intensive care with 24 h of hypothermia at 33 °C. Blood markers of cerebral injury, cerebral microdialysis, and intracranial pressure (ICP) were measured. After 48 h, pigs underwent a cerebral MRI scan. Data are presented as median [25th; 75th percentiles]. RESULTS: Return of spontaneous circulation was achieved in 7/11 pigs. Time to ROSC was 4.4 min [4.2; 10.9]. Both NSE and NfL increased over time (p < 0.001), and were higher in the cardiac arrest group at 48 h (NSE 4.2 µg/L [2.4; 6.1] vs 0.9 [0.7; 0.9], p < 0.001; NfL 63 ng/L [35; 232] vs 29 [21; 34], p = 0.02). There was no difference in ICP at 48 h (17 mmHg [14; 24] vs 18 [13; 20], p = 0.44). The cerebral lactate/pyruvate ratio had secondary surges in 3/7 cardiac arrest pigs after successful resuscitation. Apparent diffusion coefficient was lower in the cardiac arrest group in white matter cortex (689 × 10(–6) mm(2)/s [524; 765] vs 800 [799; 815], p = 0.04) and hippocampus (854 [834; 910] vs 1049 [964; 1180], p = 0.03). N-Acetylaspartate was lower on MR spectroscopy in the cardiac arrest group (− 17.2 log [− 17.4; − 17.0] vs − 16.9 [− 16.9; − 16.9], p = 0.03). CONCLUSIONS: We have developed a clinically relevant cardiac arrest pig model that displays cerebral injury as marked by NSE and NfL elevations, signs of cerebral oedema, and reduced neuron viability. Overall, the burden of elevated ICP was low in the cardiac arrest group. A subset of pigs undergoing cardiac arrest had persisting metabolic disturbances after successful resuscitation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40635-022-00475-2.
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spelling pubmed-95961812022-10-26 Cerebral monitoring in a pig model of cardiac arrest with 48 h of intensive care Vammen, Lauge Johannsen, Cecilie Munch Magnussen, Andreas Povlsen, Amalie Petersen, Søren Riis Azizi, Arezo Pedersen, Michael Korshøj, Anders Rosendal Ringgaard, Steffen Løfgren, Bo Andersen, Lars W. Granfeldt, Asger Intensive Care Med Exp Research Articles BACKGROUND: Neurological injury is the primary cause of death after out-of-hospital cardiac arrest. There is a lack of studies investigating cerebral injury beyond the immediate post-resuscitation phase in a controlled cardiac arrest experimental setting. METHODS: The aim of this study was to investigate temporal changes in measures of cerebral injury and metabolism in a cardiac arrest pig model with clinically relevant post-cardiac arrest intensive care. A cardiac arrest group (n = 11) underwent 7 min of no-flow and was compared with a sham group (n = 6). Pigs underwent intensive care with 24 h of hypothermia at 33 °C. Blood markers of cerebral injury, cerebral microdialysis, and intracranial pressure (ICP) were measured. After 48 h, pigs underwent a cerebral MRI scan. Data are presented as median [25th; 75th percentiles]. RESULTS: Return of spontaneous circulation was achieved in 7/11 pigs. Time to ROSC was 4.4 min [4.2; 10.9]. Both NSE and NfL increased over time (p < 0.001), and were higher in the cardiac arrest group at 48 h (NSE 4.2 µg/L [2.4; 6.1] vs 0.9 [0.7; 0.9], p < 0.001; NfL 63 ng/L [35; 232] vs 29 [21; 34], p = 0.02). There was no difference in ICP at 48 h (17 mmHg [14; 24] vs 18 [13; 20], p = 0.44). The cerebral lactate/pyruvate ratio had secondary surges in 3/7 cardiac arrest pigs after successful resuscitation. Apparent diffusion coefficient was lower in the cardiac arrest group in white matter cortex (689 × 10(–6) mm(2)/s [524; 765] vs 800 [799; 815], p = 0.04) and hippocampus (854 [834; 910] vs 1049 [964; 1180], p = 0.03). N-Acetylaspartate was lower on MR spectroscopy in the cardiac arrest group (− 17.2 log [− 17.4; − 17.0] vs − 16.9 [− 16.9; − 16.9], p = 0.03). CONCLUSIONS: We have developed a clinically relevant cardiac arrest pig model that displays cerebral injury as marked by NSE and NfL elevations, signs of cerebral oedema, and reduced neuron viability. Overall, the burden of elevated ICP was low in the cardiac arrest group. A subset of pigs undergoing cardiac arrest had persisting metabolic disturbances after successful resuscitation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40635-022-00475-2. Springer International Publishing 2022-10-26 /pmc/articles/PMC9596181/ /pubmed/36284020 http://dx.doi.org/10.1186/s40635-022-00475-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Vammen, Lauge
Johannsen, Cecilie Munch
Magnussen, Andreas
Povlsen, Amalie
Petersen, Søren Riis
Azizi, Arezo
Pedersen, Michael
Korshøj, Anders Rosendal
Ringgaard, Steffen
Løfgren, Bo
Andersen, Lars W.
Granfeldt, Asger
Cerebral monitoring in a pig model of cardiac arrest with 48 h of intensive care
title Cerebral monitoring in a pig model of cardiac arrest with 48 h of intensive care
title_full Cerebral monitoring in a pig model of cardiac arrest with 48 h of intensive care
title_fullStr Cerebral monitoring in a pig model of cardiac arrest with 48 h of intensive care
title_full_unstemmed Cerebral monitoring in a pig model of cardiac arrest with 48 h of intensive care
title_short Cerebral monitoring in a pig model of cardiac arrest with 48 h of intensive care
title_sort cerebral monitoring in a pig model of cardiac arrest with 48 h of intensive care
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9596181/
https://www.ncbi.nlm.nih.gov/pubmed/36284020
http://dx.doi.org/10.1186/s40635-022-00475-2
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