Tobias Arleth, Josefine Baekgaard, Felicia Dinesen, Andreas Creutzburg, Helene Dalsten, Carl Johan Queitsch, Sarah Sofie Wadland, Oscar Rosenkrantz, Volkert Siersma, Claus Moser, Peter Østrup Jensen, Lars S Rasmussen, Jacob Steinmetz
{"title":"Oxidative stress in trauma patients receiving a restrictive or liberal oxygen strategy - A sub-study of the TRAUMOX2 trial.","authors":"Tobias Arleth, Josefine Baekgaard, Felicia Dinesen, Andreas Creutzburg, Helene Dalsten, Carl Johan Queitsch, Sarah Sofie Wadland, Oscar Rosenkrantz, Volkert Siersma, Claus Moser, Peter Østrup Jensen, Lars S Rasmussen, Jacob Steinmetz","doi":"10.1016/j.freeradbiomed.2025.02.016","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>A liberal supplemental oxygen approach is recommended for all severely injured trauma patients despite limited evidence. Liberal oxygen administration may cause oxidative stress. The aim of this study was to investigate the effect of an early restrictive oxygen strategy versus a liberal oxygen strategy in adult trauma patients on biomarkers of oxidative stress within 48 hours of hospital admission.</p><p><strong>Materials and methods: </strong>This was a single-centre, sub-study of an international, randomised controlled trial TRAUMOX2. In TRAUMOX2, patients were randomised shortly after trauma to a restrictive oxygen strategy (arterial oxygen saturation target of 94%) or a liberal oxygen strategy (12-15 litres of oxygen per minute or fraction of inspired oxygen of 0.6-1.0) for eight hours. Blood samplings were performed at four time points within 48 hours after randomisation: upon arrival at the trauma centre, and at eight, 24, and 48 hours post-randomisation. The primary outcome was the plasma level of malondialdehyde (MDA) 24 hours post-randomisation. Secondary outcomes were numerous, and included the level of MDA at other time points, superoxide dismutase (SOD) at all time points, 30-day mortality, and major respiratory complications.</p><p><strong>Results: </strong>The sub-study included 90 adult trauma patients. The median MDA levels at 24 hours post-randomisation was 60.9 μM (95% CI 49.5 to 73.4) in the restrictive oxygen group and 56.7 μM (95% CI 46.9 to 68.2) in the liberal oxygen group, corresponding to a difference of -4.2 μM (95% CI -19.8 to 10.5; P = 0.35). No significant differences were found in MDA or SOD at the other time points either. Neither did we find a significant difference in 30-day mortality or major respiratory complications.</p><p><strong>Conclusions: </strong>In this sub-study of the TRAUMOX2 trial, no significant differences were found in biomarkers of oxidative stress between a restrictive oxygen strategy and liberal oxygen strategy in adult trauma patients.</p>","PeriodicalId":12407,"journal":{"name":"Free Radical Biology and Medicine","volume":" ","pages":""},"PeriodicalIF":7.1000,"publicationDate":"2025-02-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Free Radical Biology and Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.freeradbiomed.2025.02.016","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: A liberal supplemental oxygen approach is recommended for all severely injured trauma patients despite limited evidence. Liberal oxygen administration may cause oxidative stress. The aim of this study was to investigate the effect of an early restrictive oxygen strategy versus a liberal oxygen strategy in adult trauma patients on biomarkers of oxidative stress within 48 hours of hospital admission.
Materials and methods: This was a single-centre, sub-study of an international, randomised controlled trial TRAUMOX2. In TRAUMOX2, patients were randomised shortly after trauma to a restrictive oxygen strategy (arterial oxygen saturation target of 94%) or a liberal oxygen strategy (12-15 litres of oxygen per minute or fraction of inspired oxygen of 0.6-1.0) for eight hours. Blood samplings were performed at four time points within 48 hours after randomisation: upon arrival at the trauma centre, and at eight, 24, and 48 hours post-randomisation. The primary outcome was the plasma level of malondialdehyde (MDA) 24 hours post-randomisation. Secondary outcomes were numerous, and included the level of MDA at other time points, superoxide dismutase (SOD) at all time points, 30-day mortality, and major respiratory complications.
Results: The sub-study included 90 adult trauma patients. The median MDA levels at 24 hours post-randomisation was 60.9 μM (95% CI 49.5 to 73.4) in the restrictive oxygen group and 56.7 μM (95% CI 46.9 to 68.2) in the liberal oxygen group, corresponding to a difference of -4.2 μM (95% CI -19.8 to 10.5; P = 0.35). No significant differences were found in MDA or SOD at the other time points either. Neither did we find a significant difference in 30-day mortality or major respiratory complications.
Conclusions: In this sub-study of the TRAUMOX2 trial, no significant differences were found in biomarkers of oxidative stress between a restrictive oxygen strategy and liberal oxygen strategy in adult trauma patients.
期刊介绍:
Free Radical Biology and Medicine is a leading journal in the field of redox biology, which is the study of the role of reactive oxygen species (ROS) and other oxidizing agents in biological systems. The journal serves as a premier forum for publishing innovative and groundbreaking research that explores the redox biology of health and disease, covering a wide range of topics and disciplines. Free Radical Biology and Medicine also commissions Special Issues that highlight recent advances in both basic and clinical research, with a particular emphasis on the mechanisms underlying altered metabolism and redox signaling. These Special Issues aim to provide a focused platform for the latest research in the field, fostering collaboration and knowledge exchange among researchers and clinicians.