The effect of conservative oxygen therapy on systemic biomarkers of oxidative stress in critically ill patients.

Diane Mackle, Anitra C Carr, Emma Spencer, Anna Hunt, Harriet Judd, Jan Mehrtens, Kim Parker, Zoe Stockwell, Caitlin Gale, Megan Beaumont, Simran Kaur, Shailesh Bihari, Paul J Young

Journal: Free radical biology & medicine 2021;160():13-18

PMID: 32768569

Abstract

BACKGROUND

Supplemental oxygen is delivered to critically ill patients who require mechanical ventilation. Oxidative stress is a potential complication of oxygen therapy, resulting in damage to essential biomolecules such as proteins, lipids, and nucleic acids. Whether plasma levels of oxidative stress biomarkers vary based on how liberally oxygen therapy is applied during mechanical ventilation is unknown.

METHODS

We carried out an oxidative stress substudy nested within a large multi-centre randomized controlled trial in which critically ill adults were randomized to receive either conservative oxygen therapy or standard oxygen therapy. Blood samples were collected at enrolment, and daily thereafter for up to three days. The antioxidant ascorbate (vitamin C) was assessed using HPLC with electrochemical detection and protein oxidation using a sensitive protein carbonyl ELISA. We also assessed whether critically ill patients with different disease states exhibited varying levels of oxidative stress biomarkers.

RESULTS

A total of 125 patients were included. Mean ascorbate concentrations decreased over time (from 25 ± 9 μmol/L to 14 ± 2 μmol/L, p < 0.001), however, there was no significant difference between the conservative oxygen group and standard care (p = 0.2), despite a significantly lower partial pressure of oxygen (PaO) in the conservative oxygen group (p = 0.03). Protein carbonyl concentrations increased over time (from 208 ± 30 μmol/L to 249 ± 29 μmol/L; p = 0.016), however, there was no significant difference between the conservative and standard oxygen groups (p = 0.3). Patients with sepsis had significantly higher protein carbonyl concentrations than the other critically ill patients (293 ± 92 μmol/L vs 184 ± 24 μmol/L, p = 0.03). Within the septic subgroup, there were no significant differences in protein carbonyl concentrations between the two interventions (p = 0.4).

CONCLUSIONS

Conservative oxygen therapy does not alter systemic markers of oxidative stress in critically ill ventilated patients compared with standard oxygen therapy. Patients with sepsis exhibited elevated protein carbonyls compared with the other critically ill patients implying increased oxidative stress in this patient subgroup.

Copyright © 2020 Elsevier Inc. All rights reserved.

Address: Department of Pathology and Biomedical Science, University of Otago, Christchurch, New Zealand. Electronic address: [email protected].; Department of Pathology and Biomedical Science, University of Otago, Christchurch, New Zealand.; Medical Research Institute of New Zealand, Wellington, New Zealand.; Medical Research Institute of New Zealand, Wellington, New Zealand; Wellington Hospital Intensive Care Unit, Wellington, New Zealand.; Wellington Hospital Intensive Care Unit, Wellington, New Zealand.; Christchurch Hospital Intensive Care Unit, Christchurch, New Zealand.; Centre for Postgraduate Nursing Studies, University of Otago, Christchurch, New Zealand.; Intensive and Critical Care Unit, Flinders Medical Centre, Adelaide, Australia; College of Medicine and Public Health, Flinders University, Adelaide, Australia.
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