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Oxygen administration in patients recovering from cardiac arrest: a narrative review
High oxygen tension in blood and/or tissue affects clinical outcomes in several diseases. Thus, the optimal target PaO(2) for patients recovering from cardiac arrest (CA) has been extensively examined. Many patients develop hypoxic brain injury after the return of spontaneous circulation (ROSC); thi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419438/ https://www.ncbi.nlm.nih.gov/pubmed/32832091 http://dx.doi.org/10.1186/s40560-020-00477-w |
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author | Yamamoto, Ryo Yoshizawa, Jo |
author_facet | Yamamoto, Ryo Yoshizawa, Jo |
author_sort | Yamamoto, Ryo |
collection | PubMed |
description | High oxygen tension in blood and/or tissue affects clinical outcomes in several diseases. Thus, the optimal target PaO(2) for patients recovering from cardiac arrest (CA) has been extensively examined. Many patients develop hypoxic brain injury after the return of spontaneous circulation (ROSC); this supports the need for oxygen administration in patients after CA. Insufficient oxygen delivery due to decreased blood flow to cerebral tissue during CA results in hypoxic brain injury. By contrast, hyperoxia may increase dissolved oxygen in the blood and, subsequently, generate reactive oxygen species that are harmful to neuronal cells. This secondary brain injury is particularly concerning. Although several clinical studies demonstrated that hyperoxia during post-CA care was associated with poor neurological outcomes, considerable debate is ongoing because of inconsistent results. Potential reasons for the conflicting results include differences in the definition of hyperoxia, the timing of exposure to hyperoxia, and PaO(2) values used in analyses. Despite the conflicts, exposure to PaO(2) > 300 mmHg through administration of unnecessary oxygen should be avoided because no obvious benefit has been demonstrated. The feasibility of titrating oxygen administration by targeting SpO(2) at approximately 94% in patients recovering from CA has been demonstrated in pilot randomized controlled trials (RCTs). Such protocols should be further examined. |
format | Online Article Text |
id | pubmed-7419438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74194382020-08-21 Oxygen administration in patients recovering from cardiac arrest: a narrative review Yamamoto, Ryo Yoshizawa, Jo J Intensive Care Review High oxygen tension in blood and/or tissue affects clinical outcomes in several diseases. Thus, the optimal target PaO(2) for patients recovering from cardiac arrest (CA) has been extensively examined. Many patients develop hypoxic brain injury after the return of spontaneous circulation (ROSC); this supports the need for oxygen administration in patients after CA. Insufficient oxygen delivery due to decreased blood flow to cerebral tissue during CA results in hypoxic brain injury. By contrast, hyperoxia may increase dissolved oxygen in the blood and, subsequently, generate reactive oxygen species that are harmful to neuronal cells. This secondary brain injury is particularly concerning. Although several clinical studies demonstrated that hyperoxia during post-CA care was associated with poor neurological outcomes, considerable debate is ongoing because of inconsistent results. Potential reasons for the conflicting results include differences in the definition of hyperoxia, the timing of exposure to hyperoxia, and PaO(2) values used in analyses. Despite the conflicts, exposure to PaO(2) > 300 mmHg through administration of unnecessary oxygen should be avoided because no obvious benefit has been demonstrated. The feasibility of titrating oxygen administration by targeting SpO(2) at approximately 94% in patients recovering from CA has been demonstrated in pilot randomized controlled trials (RCTs). Such protocols should be further examined. BioMed Central 2020-08-12 /pmc/articles/PMC7419438/ /pubmed/32832091 http://dx.doi.org/10.1186/s40560-020-00477-w Text en © The Author(s) 2020 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/. 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 in a credit line to the data. |
spellingShingle | Review Yamamoto, Ryo Yoshizawa, Jo Oxygen administration in patients recovering from cardiac arrest: a narrative review |
title | Oxygen administration in patients recovering from cardiac arrest: a narrative review |
title_full | Oxygen administration in patients recovering from cardiac arrest: a narrative review |
title_fullStr | Oxygen administration in patients recovering from cardiac arrest: a narrative review |
title_full_unstemmed | Oxygen administration in patients recovering from cardiac arrest: a narrative review |
title_short | Oxygen administration in patients recovering from cardiac arrest: a narrative review |
title_sort | oxygen administration in patients recovering from cardiac arrest: a narrative review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419438/ https://www.ncbi.nlm.nih.gov/pubmed/32832091 http://dx.doi.org/10.1186/s40560-020-00477-w |
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