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Meta-analysis of targeted temperature management in animal models of cardiac arrest

BACKGROUND: Targeted temperature management (TTM) of 32 to 34 °C has been the standard treatment for out-of-hospital cardiac arrest since clinical trials in 2002 indicated benefit on survival and neurological outcome. In 2013, a clinical trial showed no difference in outcome between TTM of 33 °C and...

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Autores principales: Olai, Hilmer, Thornéus, Gustav, Watson, Hannah, Macleod, Malcolm, Rhodes, Jonathan, Friberg, Hans, Nielsen, Niklas, Cronberg, Tobias, Deierborg, Tomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6969098/
https://www.ncbi.nlm.nih.gov/pubmed/31953652
http://dx.doi.org/10.1186/s40635-019-0291-9
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author Olai, Hilmer
Thornéus, Gustav
Watson, Hannah
Macleod, Malcolm
Rhodes, Jonathan
Friberg, Hans
Nielsen, Niklas
Cronberg, Tobias
Deierborg, Tomas
author_facet Olai, Hilmer
Thornéus, Gustav
Watson, Hannah
Macleod, Malcolm
Rhodes, Jonathan
Friberg, Hans
Nielsen, Niklas
Cronberg, Tobias
Deierborg, Tomas
author_sort Olai, Hilmer
collection PubMed
description BACKGROUND: Targeted temperature management (TTM) of 32 to 34 °C has been the standard treatment for out-of-hospital cardiac arrest since clinical trials in 2002 indicated benefit on survival and neurological outcome. In 2013, a clinical trial showed no difference in outcome between TTM of 33 °C and TTM of 36 °C. In this meta-analysis, we investigate the evidence for TTM in animal models of cardiac arrest. METHODS: We searched PubMed and EMBASE for adult animal studies using TTM as a treatment in different models of cardiac arrest or global brain ischemia which reported neurobehavioural outcome, brain histology or mortality. We used a random effects model to calculate estimates of efficacy and assessed risk of bias using an adapted eight-item version of the Collaborative Approach to Meta-Analysis and Review of Animal Data from Experimental Studies (CAMARADES) quality checklist. We also used a scoring system based on the recommendations of the Stroke Treatment Academic Industry Roundtable (STAIR), to assess the scope of testing in the field. Included studies which investigated a post-ischemic induction of TTM had their treatment regimens characterized with regard to depth, duration and time to treatment and scored against the modified STAIR criteria. RESULTS: The initial and updated search generated 17809 studies after duplicate removal. One hundred eighty-one studies met the inclusion criteria, including data from 1,787, 6,495 and 2,945 animals for neurobehavioural, histological and mortality outcomes, respectively. TTM was favoured compared to control for all outcomes. TTM was beneficial using short and prolonged cooling, deep and moderate temperature reduction, and early and delayed time to treatment. Median [IQR] study quality was 4 [3 to 6]. Eighteen studies checked seven or more of the eight CAMARADES quality items. There was no clear correlation between study quality and efficacy for any outcome. STAIR analysis identified 102 studies investigating post-ischemic induction of TTM, comprising 147 different treatment regimens of TTM. Only 2 and 8 out of 147 regimens investigated comorbid and gyrencephalic animals, respectively. CONCLUSIONS: TTM is beneficial under most experimental conditions in animal models of cardiac arrest or global brain ischemia. However, research on gyrencephalic species and especially comorbid animals is uncommon and a possible translational gap. Also, low study quality suggests risk of bias within studies. Future animal research should focus on mimicking the clinical scenario and employ similar rigour in trial design to that of modern clinical trials.
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spelling pubmed-69690982020-01-30 Meta-analysis of targeted temperature management in animal models of cardiac arrest Olai, Hilmer Thornéus, Gustav Watson, Hannah Macleod, Malcolm Rhodes, Jonathan Friberg, Hans Nielsen, Niklas Cronberg, Tobias Deierborg, Tomas Intensive Care Med Exp Research BACKGROUND: Targeted temperature management (TTM) of 32 to 34 °C has been the standard treatment for out-of-hospital cardiac arrest since clinical trials in 2002 indicated benefit on survival and neurological outcome. In 2013, a clinical trial showed no difference in outcome between TTM of 33 °C and TTM of 36 °C. In this meta-analysis, we investigate the evidence for TTM in animal models of cardiac arrest. METHODS: We searched PubMed and EMBASE for adult animal studies using TTM as a treatment in different models of cardiac arrest or global brain ischemia which reported neurobehavioural outcome, brain histology or mortality. We used a random effects model to calculate estimates of efficacy and assessed risk of bias using an adapted eight-item version of the Collaborative Approach to Meta-Analysis and Review of Animal Data from Experimental Studies (CAMARADES) quality checklist. We also used a scoring system based on the recommendations of the Stroke Treatment Academic Industry Roundtable (STAIR), to assess the scope of testing in the field. Included studies which investigated a post-ischemic induction of TTM had their treatment regimens characterized with regard to depth, duration and time to treatment and scored against the modified STAIR criteria. RESULTS: The initial and updated search generated 17809 studies after duplicate removal. One hundred eighty-one studies met the inclusion criteria, including data from 1,787, 6,495 and 2,945 animals for neurobehavioural, histological and mortality outcomes, respectively. TTM was favoured compared to control for all outcomes. TTM was beneficial using short and prolonged cooling, deep and moderate temperature reduction, and early and delayed time to treatment. Median [IQR] study quality was 4 [3 to 6]. Eighteen studies checked seven or more of the eight CAMARADES quality items. There was no clear correlation between study quality and efficacy for any outcome. STAIR analysis identified 102 studies investigating post-ischemic induction of TTM, comprising 147 different treatment regimens of TTM. Only 2 and 8 out of 147 regimens investigated comorbid and gyrencephalic animals, respectively. CONCLUSIONS: TTM is beneficial under most experimental conditions in animal models of cardiac arrest or global brain ischemia. However, research on gyrencephalic species and especially comorbid animals is uncommon and a possible translational gap. Also, low study quality suggests risk of bias within studies. Future animal research should focus on mimicking the clinical scenario and employ similar rigour in trial design to that of modern clinical trials. Springer International Publishing 2020-01-17 /pmc/articles/PMC6969098/ /pubmed/31953652 http://dx.doi.org/10.1186/s40635-019-0291-9 Text en © The Author(s). 2020 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.
spellingShingle Research
Olai, Hilmer
Thornéus, Gustav
Watson, Hannah
Macleod, Malcolm
Rhodes, Jonathan
Friberg, Hans
Nielsen, Niklas
Cronberg, Tobias
Deierborg, Tomas
Meta-analysis of targeted temperature management in animal models of cardiac arrest
title Meta-analysis of targeted temperature management in animal models of cardiac arrest
title_full Meta-analysis of targeted temperature management in animal models of cardiac arrest
title_fullStr Meta-analysis of targeted temperature management in animal models of cardiac arrest
title_full_unstemmed Meta-analysis of targeted temperature management in animal models of cardiac arrest
title_short Meta-analysis of targeted temperature management in animal models of cardiac arrest
title_sort meta-analysis of targeted temperature management in animal models of cardiac arrest
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6969098/
https://www.ncbi.nlm.nih.gov/pubmed/31953652
http://dx.doi.org/10.1186/s40635-019-0291-9
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