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

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          Abstract

          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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          Most cited references48

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          Meta-analysis of data from animal studies: a practical guide.

          Meta-analyses of data from human studies are invaluable resources in the life sciences and the methods to conduct these are well documented. Similarly there are a number of benefits in conducting meta-analyses on data from animal studies; they can be used to inform clinical trial design, or to try and explain discrepancies between preclinical and clinical trial results. However there are inherit differences between animal and human studies and so applying the same techniques for the meta-analysis of preclinical data is not straightforward. For example preclinical studies are frequently small and there is often substantial heterogeneity between studies. This may have an impact on both the method of calculating an effect size and the method of pooling data. Here we describe a practical guide for the meta-analysis of data from animal studies including methods used to explore sources of heterogeneity. Copyright © 2013 The Authors. Published by Elsevier B.V. All rights reserved.
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            Small differences in intraischemic brain temperature critically determine the extent of ischemic neuronal injury.

            We have tested whether small intraischemic variations in brain temperature influence the outcome of transient ischemia. To measure brain temperature, a thermocouple probe was placed stereotaxically into the left dorsolateral striatum of rats prior to 20 min of four-vessel occlusion. Rectal temperature was maintained at 36-37 degrees C by a heating lamp, and striatal temperature prior to ischemia was 36 degrees C in all animals. Six animal subgroups were investigated, including rats whose intraischemic striatal brain temperature was not regulated, or was maintained at 33, 34, 36, or 39 degrees C. Postischemic brain temperature was regulated at 36 degrees C, except for one group in which brain temperature was lowered from 36 degrees C to 33 degrees C during the first hour of recirculation. Energy metabolites were measured at the end of the ischemic insult, and histopathological evaluation was carried out at 3 days after ischemia. Intraischemic variations in brain temperature had no significant influence on energy metabolite levels measured at the conclusion of ischemia: Severe depletion of brain ATP, phosphocreatine, glucose, and glycogen and elevation of lactate were observed to a similar degree in all experimental groups. The histopathological consequences of ischemia, however, were markedly influenced by variations in intraischemic brain temperature. In the hippocampus, CA1 neurons were consistently damaged at 36 degrees C, but not at 34 degrees C. Within the dorsolateral striatum, ischemic cell change was present in 100% of the hemispheres at 36 degrees C, but in only 50% at 34 degrees C. Ischemic neurons within the central zone of striatum were not observed in any rats at 34 degrees C, but in all rats at 36 degrees C. In rats whose striatal temperature was not controlled, brain temperature fell from 36 to 30-31 degrees C during the ischemic insult. In this group, no ischemic cell change was seen within striatal areas and was only inconsistently documented within the CA1 hippocampal region. These results demonstrate that (a) rectal temperature unreliably reflects brain temperature during ischemia; (b) despite severe depletion of brain energy metabolites during ischemia at all temperatures, small increments of intraischemic brain temperature markedly accentuate histopathological changes following 3-day survival; and (c) brain temperature must be controlled above 33 degrees C in order to ensure a consistent histopathological outcome. Lowering of the brain temperature by only a few degrees during ischemia confers a marked protective effect.
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              Empirical evidence of bias in the design of experimental stroke studies: a metaepidemiologic approach.

              At least part of the failure in the transition from experimental to clinical studies in stroke has been attributed to the imprecision introduced by problems in the design of experimental stroke studies. Using a metaepidemiologic approach, we addressed the effect of randomization, blinding, and use of comorbid animals on the estimate of how effectively therapeutic interventions reduce infarct size. Electronic and manual searches were performed to identify meta-analyses that described interventions in experimental stroke. For each meta-analysis thus identified, a reanalysis was conducted to estimate the impact of various quality items on the estimate of efficacy, and these estimates were combined in a meta-meta-analysis to obtain a summary measure of the impact of the various design characteristics. Thirteen meta-analyses that described outcomes in 15,635 animals were included. Studies that included unblinded induction of ischemia reported effect sizes 13.1% (95% CI, 26.4% to 0.2%) greater than studies that included blinding, and studies that included healthy animals instead of animals with comorbidities overstated the effect size by 11.5% (95% CI, 21.2% to 1.8%). No significant effect was found for randomization, blinded outcome assessment, or high aggregate CAMARADES quality score. We provide empirical evidence of bias in the design of studies, with studies that included unblinded induction of ischemia or healthy animals overestimating the effectiveness of the intervention. This bias could account for the failure in the transition from bench to bedside of stroke therapies.
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                Author and article information

                Contributors
                tomas.deierborg@med.lu.se
                Journal
                Intensive Care Med Exp
                Intensive Care Med Exp
                Intensive Care Medicine Experimental
                Springer International Publishing (Cham )
                2197-425X
                17 January 2020
                17 January 2020
                December 2020
                : 8
                : 3
                Affiliations
                [1 ]ISNI 0000 0001 0930 2361, GRID grid.4514.4, Department of Experimental Medical Science, Experimental Neuroinflammation Laboratory, , Lund University, ; Lund, Sweden
                [2 ]ISNI 0000 0001 0388 0742, GRID grid.39489.3f, Department of Anaesthesia, Western General Hospital, , NHS Lothian, ; Edinburgh, UK
                [3 ]ISNI 0000 0001 0388 0742, GRID grid.39489.3f, Department of Critical Care, Western General Hospital, , NHS Lothian, ; Edinburgh, UK
                [4 ]ISNI 0000 0004 1936 7988, GRID grid.4305.2, Centre for Clinical Brain Sciences, , University of Edinburgh, ; Edinburgh, UK
                [5 ]ISNI 0000 0004 1936 7988, GRID grid.4305.2, Department of Anaesthesia, Critical care and Pain Medicine/NHS Lothian, , University of Edinburgh, ; Edinburgh, UK
                [6 ]ISNI 0000 0001 0930 2361, GRID grid.4514.4, Department of Clinical Sciences, Anesthesia & Intensive care, Skåne University Hospital, , Lund University, ; Lund, Sweden
                [7 ]ISNI 0000 0001 0930 2361, GRID grid.4514.4, Department of Clinical Sciences Lund, Anesthesia & Intensive care, Helsingborg Hospital, , Lund University, ; Lund, Sweden
                [8 ]ISNI 0000 0001 0930 2361, GRID grid.4514.4, Department of Clinical Sciences Lund, Neurology, Skåne University Hospital, , Lund University, ; Lund, Sweden
                Author information
                http://orcid.org/0000-0002-3651-3444
                Article
                291
                10.1186/s40635-019-0291-9
                6969098
                31953652
                706fb307-e6b3-48d1-b66a-452f7363557e
                © 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.

                History
                : 23 September 2019
                : 29 December 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100004359, Vetenskapsrådet;
                Award ID: 2018-03033
                Award ID: MultiPark
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100004200, Stiftelsen Olle Engkvist Byggmästare;
                Funded by: FundRef http://dx.doi.org/10.13039/501100009738, Anna och Edwin Bergers Stiftelse;
                Funded by: FundRef http://dx.doi.org/10.13039/501100003173, Crafoordska Stiftelsen;
                Funded by: FundRef http://dx.doi.org/10.13039/501100003792, Hjärnfonden;
                Funded by: FundRef http://dx.doi.org/10.13039/501100006075, Greta och Johan Kocks stiftelser;
                Funded by: FundRef http://dx.doi.org/10.13039/100010773, Demensförbundet;
                Funded by: FundRef http://dx.doi.org/10.13039/501100008590, STROKE-Riksförbundet;
                Funded by: FundRef http://dx.doi.org/10.13039/100008443, ParkinsonFörbundet;
                Funded by: FundRef http://dx.doi.org/10.13039/501100005753, Kungliga Fysiografiska Sällskapet i Lund;
                Funded by: FundRef http://dx.doi.org/10.13039/501100004102, Laerdal Foundation for Acute Medicine;
                Funded by: FundRef http://dx.doi.org/10.13039/501100000849, National Centre for the Replacement, Refinement and Reduction of Animals in Research;
                Award ID: ivSyRMAF–the CAMARADES–NC3Rs in vivo systematic review and meta‐analysis facility, grant number NC/L000970/1
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2020

                targeted temperature management,hypothermia,cardiac arrest,global ischemia,animals,meta-analysis

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