Cargando…

Hyperoxia is associated with a greater risk for mortality in critically ill traumatic brain injury patients than in critically ill trauma patients without brain injury

OBJECTIVE: The role of hyperoxia in patients with traumatic brain injury (TBI) remains controversial. The objective of this study was to determine the association between hyperoxia and mortality in critically ill TBI patients compared to critically ill trauma patients without TBI. DESIGN: Secondary...

Descripción completa

Detalles Bibliográficos
Autores principales: Douin, David J, Dylla, Layne, Anderson, Erin L, Rice, John D, Jackson, Conner L, Bebarta, Vikhyat S, Neumann, Robert T, Schauer, Steven G, Ginde, Adit A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450323/
https://www.ncbi.nlm.nih.gov/pubmed/36879502
http://dx.doi.org/10.1177/00368504231160416
_version_ 1785095172016570368
author Douin, David J
Dylla, Layne
Anderson, Erin L
Rice, John D
Jackson, Conner L
Bebarta, Vikhyat S
Neumann, Robert T
Schauer, Steven G
Ginde, Adit A
author_facet Douin, David J
Dylla, Layne
Anderson, Erin L
Rice, John D
Jackson, Conner L
Bebarta, Vikhyat S
Neumann, Robert T
Schauer, Steven G
Ginde, Adit A
author_sort Douin, David J
collection PubMed
description OBJECTIVE: The role of hyperoxia in patients with traumatic brain injury (TBI) remains controversial. The objective of this study was to determine the association between hyperoxia and mortality in critically ill TBI patients compared to critically ill trauma patients without TBI. DESIGN: Secondary analysis of a multicenter retrospective cohort study. SETTING: Three regional trauma centers in Colorado, USA, between October 1, 2015, and June 30, 2018. PATIENTS: We included 3464 critically injured adults who were admitted to an intensive care unit (ICU) within 24 h of arrival and qualified for inclusion into the state trauma registry. We analyzed all available SpO2 values during the first seven ICU days. The primary outcome was in-hospital mortality. Secondary outcomes included the proportion of time spent in hyperoxia (defined as SpO(2) > 96%) and ventilator-free days. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: In-hospital mortality occurred in 163 patients (10.7%) in the TBI group and 101 patients (5.2%) in the non-TBI group. After adjusting for ICU length of stay, TBI patients spent a significantly greater amount of time in hyperoxia versus non-TBI patients (p = 0.024). TBI status significantly modified the effect of hyperoxia on mortality. At each specific SpO(2) level, the risk of mortality increases with increasing FiO(2) for both patients with and without TBI. This trend was more pronounced at lower FiO(2) and higher SpO(2) values, where a greater number of patient observations were obtained. Among patients who required invasive mechanical ventilation, TBI patients required significantly more days of ventilation to day 28 than non-TBI patients. CONCLUSIONS: Critically ill trauma patients with a TBI spend a greater proportion of time in hyperoxia compared to those without a TBI. TBI status significantly modified the effect of hyperoxia on mortality. Prospective clinical trials are needed to better assess a possible causal relationship.
format Online
Article
Text
id pubmed-10450323
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-104503232023-08-26 Hyperoxia is associated with a greater risk for mortality in critically ill traumatic brain injury patients than in critically ill trauma patients without brain injury Douin, David J Dylla, Layne Anderson, Erin L Rice, John D Jackson, Conner L Bebarta, Vikhyat S Neumann, Robert T Schauer, Steven G Ginde, Adit A Sci Prog Original Manuscript OBJECTIVE: The role of hyperoxia in patients with traumatic brain injury (TBI) remains controversial. The objective of this study was to determine the association between hyperoxia and mortality in critically ill TBI patients compared to critically ill trauma patients without TBI. DESIGN: Secondary analysis of a multicenter retrospective cohort study. SETTING: Three regional trauma centers in Colorado, USA, between October 1, 2015, and June 30, 2018. PATIENTS: We included 3464 critically injured adults who were admitted to an intensive care unit (ICU) within 24 h of arrival and qualified for inclusion into the state trauma registry. We analyzed all available SpO2 values during the first seven ICU days. The primary outcome was in-hospital mortality. Secondary outcomes included the proportion of time spent in hyperoxia (defined as SpO(2) > 96%) and ventilator-free days. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: In-hospital mortality occurred in 163 patients (10.7%) in the TBI group and 101 patients (5.2%) in the non-TBI group. After adjusting for ICU length of stay, TBI patients spent a significantly greater amount of time in hyperoxia versus non-TBI patients (p = 0.024). TBI status significantly modified the effect of hyperoxia on mortality. At each specific SpO(2) level, the risk of mortality increases with increasing FiO(2) for both patients with and without TBI. This trend was more pronounced at lower FiO(2) and higher SpO(2) values, where a greater number of patient observations were obtained. Among patients who required invasive mechanical ventilation, TBI patients required significantly more days of ventilation to day 28 than non-TBI patients. CONCLUSIONS: Critically ill trauma patients with a TBI spend a greater proportion of time in hyperoxia compared to those without a TBI. TBI status significantly modified the effect of hyperoxia on mortality. Prospective clinical trials are needed to better assess a possible causal relationship. SAGE Publications 2023-03-06 /pmc/articles/PMC10450323/ /pubmed/36879502 http://dx.doi.org/10.1177/00368504231160416 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Manuscript
Douin, David J
Dylla, Layne
Anderson, Erin L
Rice, John D
Jackson, Conner L
Bebarta, Vikhyat S
Neumann, Robert T
Schauer, Steven G
Ginde, Adit A
Hyperoxia is associated with a greater risk for mortality in critically ill traumatic brain injury patients than in critically ill trauma patients without brain injury
title Hyperoxia is associated with a greater risk for mortality in critically ill traumatic brain injury patients than in critically ill trauma patients without brain injury
title_full Hyperoxia is associated with a greater risk for mortality in critically ill traumatic brain injury patients than in critically ill trauma patients without brain injury
title_fullStr Hyperoxia is associated with a greater risk for mortality in critically ill traumatic brain injury patients than in critically ill trauma patients without brain injury
title_full_unstemmed Hyperoxia is associated with a greater risk for mortality in critically ill traumatic brain injury patients than in critically ill trauma patients without brain injury
title_short Hyperoxia is associated with a greater risk for mortality in critically ill traumatic brain injury patients than in critically ill trauma patients without brain injury
title_sort hyperoxia is associated with a greater risk for mortality in critically ill traumatic brain injury patients than in critically ill trauma patients without brain injury
topic Original Manuscript
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450323/
https://www.ncbi.nlm.nih.gov/pubmed/36879502
http://dx.doi.org/10.1177/00368504231160416
work_keys_str_mv AT douindavidj hyperoxiaisassociatedwithagreaterriskformortalityincriticallyilltraumaticbraininjurypatientsthanincriticallyilltraumapatientswithoutbraininjury
AT dyllalayne hyperoxiaisassociatedwithagreaterriskformortalityincriticallyilltraumaticbraininjurypatientsthanincriticallyilltraumapatientswithoutbraininjury
AT andersonerinl hyperoxiaisassociatedwithagreaterriskformortalityincriticallyilltraumaticbraininjurypatientsthanincriticallyilltraumapatientswithoutbraininjury
AT ricejohnd hyperoxiaisassociatedwithagreaterriskformortalityincriticallyilltraumaticbraininjurypatientsthanincriticallyilltraumapatientswithoutbraininjury
AT jacksonconnerl hyperoxiaisassociatedwithagreaterriskformortalityincriticallyilltraumaticbraininjurypatientsthanincriticallyilltraumapatientswithoutbraininjury
AT bebartavikhyats hyperoxiaisassociatedwithagreaterriskformortalityincriticallyilltraumaticbraininjurypatientsthanincriticallyilltraumapatientswithoutbraininjury
AT neumannrobertt hyperoxiaisassociatedwithagreaterriskformortalityincriticallyilltraumaticbraininjurypatientsthanincriticallyilltraumapatientswithoutbraininjury
AT schauersteveng hyperoxiaisassociatedwithagreaterriskformortalityincriticallyilltraumaticbraininjurypatientsthanincriticallyilltraumapatientswithoutbraininjury
AT gindeadita hyperoxiaisassociatedwithagreaterriskformortalityincriticallyilltraumaticbraininjurypatientsthanincriticallyilltraumapatientswithoutbraininjury