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Near-infrared spectroscopy after out-of-hospital cardiac arrest
BACKGROUND: Cerebral hypoperfusion may aggravate neurological damage after cardiac arrest. Near-infrared spectroscopy (NIRS) provides information on cerebral oxygenation but its relevance during post-resuscitation care is undefined. We investigated whether cerebral oxygen saturation (rSO(2)) measure...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518726/ https://www.ncbi.nlm.nih.gov/pubmed/31088512 http://dx.doi.org/10.1186/s13054-019-2428-3 |
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author | Jakkula, Pekka Hästbacka, Johanna Reinikainen, Matti Pettilä, Ville Loisa, Pekka Tiainen, Marjaana Wilkman, Erika Bendel, Stepani Birkelund, Thomas Pulkkinen, Anni Bäcklund, Minna Heino, Sirkku Karlsson, Sari Kopponen, Hiski Skrifvars, Markus B. |
author_facet | Jakkula, Pekka Hästbacka, Johanna Reinikainen, Matti Pettilä, Ville Loisa, Pekka Tiainen, Marjaana Wilkman, Erika Bendel, Stepani Birkelund, Thomas Pulkkinen, Anni Bäcklund, Minna Heino, Sirkku Karlsson, Sari Kopponen, Hiski Skrifvars, Markus B. |
author_sort | Jakkula, Pekka |
collection | PubMed |
description | BACKGROUND: Cerebral hypoperfusion may aggravate neurological damage after cardiac arrest. Near-infrared spectroscopy (NIRS) provides information on cerebral oxygenation but its relevance during post-resuscitation care is undefined. We investigated whether cerebral oxygen saturation (rSO(2)) measured with NIRS correlates with the serum concentration of neuron-specific enolase (NSE), a marker of neurological injury, and with clinical outcome in out-of-hospital cardiac arrest (OHCA) patients. METHODS: We performed a post hoc analysis of a randomised clinical trial (COMACARE, NCT02698917) comparing two different levels of carbon dioxide, oxygen and arterial pressure after resuscitation from OHCA with ventricular fibrillation as the initial rhythm. We measured rSO(2) in 118 OHCA patients with NIRS during the first 36 h of intensive care. We determined the NSE concentrations from serum samples at 48 h after cardiac arrest and assessed neurological outcome with the Cerebral Performance Category (CPC) scale at 6 months. We evaluated the association between rSO(2) and serum NSE concentrations and the association between rSO(2) and good (CPC 1–2) and poor (CPC 3–5) neurological outcome. RESULTS: The median (inter-quartile range (IQR)) NSE concentration at 48 h was 17.5 (13.4–25.0) μg/l in patients with good neurological outcome and 35.2 (22.6–95.8) μg/l in those with poor outcome, p < 0.001. We found no significant correlation between median rSO(2) and NSE at 48 h, r(s) = − 0.08, p = 0.392. The median (IQR) rSO(2) during the first 36 h of intensive care was 70.0% (63.5–77.0%) in patients with good outcome and 71.8% (63.3–74.0%) in patients with poor outcome, p = 0.943. There was no significant association between rSO(2) over time and neurological outcome. In a binary logistic regression model, rSO(2) was not a statistically significant predictor of good neurological outcome (odds ratio 0.99, 95% confidence interval 0.94–1.04, p = 0.635). CONCLUSIONS: We found no association between cerebral oxygenation measured with NIRS and NSE concentrations or outcome in patients resuscitated from OHCA. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02698917. Registered on 26 January 2016. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-019-2428-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6518726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65187262019-05-21 Near-infrared spectroscopy after out-of-hospital cardiac arrest Jakkula, Pekka Hästbacka, Johanna Reinikainen, Matti Pettilä, Ville Loisa, Pekka Tiainen, Marjaana Wilkman, Erika Bendel, Stepani Birkelund, Thomas Pulkkinen, Anni Bäcklund, Minna Heino, Sirkku Karlsson, Sari Kopponen, Hiski Skrifvars, Markus B. Crit Care Research BACKGROUND: Cerebral hypoperfusion may aggravate neurological damage after cardiac arrest. Near-infrared spectroscopy (NIRS) provides information on cerebral oxygenation but its relevance during post-resuscitation care is undefined. We investigated whether cerebral oxygen saturation (rSO(2)) measured with NIRS correlates with the serum concentration of neuron-specific enolase (NSE), a marker of neurological injury, and with clinical outcome in out-of-hospital cardiac arrest (OHCA) patients. METHODS: We performed a post hoc analysis of a randomised clinical trial (COMACARE, NCT02698917) comparing two different levels of carbon dioxide, oxygen and arterial pressure after resuscitation from OHCA with ventricular fibrillation as the initial rhythm. We measured rSO(2) in 118 OHCA patients with NIRS during the first 36 h of intensive care. We determined the NSE concentrations from serum samples at 48 h after cardiac arrest and assessed neurological outcome with the Cerebral Performance Category (CPC) scale at 6 months. We evaluated the association between rSO(2) and serum NSE concentrations and the association between rSO(2) and good (CPC 1–2) and poor (CPC 3–5) neurological outcome. RESULTS: The median (inter-quartile range (IQR)) NSE concentration at 48 h was 17.5 (13.4–25.0) μg/l in patients with good neurological outcome and 35.2 (22.6–95.8) μg/l in those with poor outcome, p < 0.001. We found no significant correlation between median rSO(2) and NSE at 48 h, r(s) = − 0.08, p = 0.392. The median (IQR) rSO(2) during the first 36 h of intensive care was 70.0% (63.5–77.0%) in patients with good outcome and 71.8% (63.3–74.0%) in patients with poor outcome, p = 0.943. There was no significant association between rSO(2) over time and neurological outcome. In a binary logistic regression model, rSO(2) was not a statistically significant predictor of good neurological outcome (odds ratio 0.99, 95% confidence interval 0.94–1.04, p = 0.635). CONCLUSIONS: We found no association between cerebral oxygenation measured with NIRS and NSE concentrations or outcome in patients resuscitated from OHCA. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02698917. Registered on 26 January 2016. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-019-2428-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-14 /pmc/articles/PMC6518726/ /pubmed/31088512 http://dx.doi.org/10.1186/s13054-019-2428-3 Text en © The Author(s). 2019 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 Jakkula, Pekka Hästbacka, Johanna Reinikainen, Matti Pettilä, Ville Loisa, Pekka Tiainen, Marjaana Wilkman, Erika Bendel, Stepani Birkelund, Thomas Pulkkinen, Anni Bäcklund, Minna Heino, Sirkku Karlsson, Sari Kopponen, Hiski Skrifvars, Markus B. Near-infrared spectroscopy after out-of-hospital cardiac arrest |
title | Near-infrared spectroscopy after out-of-hospital cardiac arrest |
title_full | Near-infrared spectroscopy after out-of-hospital cardiac arrest |
title_fullStr | Near-infrared spectroscopy after out-of-hospital cardiac arrest |
title_full_unstemmed | Near-infrared spectroscopy after out-of-hospital cardiac arrest |
title_short | Near-infrared spectroscopy after out-of-hospital cardiac arrest |
title_sort | near-infrared spectroscopy after out-of-hospital cardiac arrest |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518726/ https://www.ncbi.nlm.nih.gov/pubmed/31088512 http://dx.doi.org/10.1186/s13054-019-2428-3 |
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