Oxidative stress, redox status and surfactant metabolism in mechanically ventilated patients receiving different approaches to oxygen therapy (MecROX): An observational study protocol for mechanistic evaluation.

Hyperoxia Mechanical ventilation Oxidative stress Oxygen Redox Surfactant

Journal

NIHR open research
ISSN: 2633-4402
Titre abrégé: NIHR Open Res
Pays: England
ID NLM: 9918333281906676

Informations de publication

Date de publication:
2024
Historique:
accepted: 02 07 2024
medline: 15 8 2024
pubmed: 15 8 2024
entrez: 15 8 2024
Statut: epublish

Résumé

MecROX is a mechanistic sub-study of the UK-ROX trial which was designed to evaluate the clinical and cost-effectiveness of a conservative approach to oxygen therapy for invasively ventilated adults in intensive care. This is based on the scientific rationale that excess oxygen is harmful. Epithelial cell damage with alveolar surfactant deficiency is characteristic of hyperoxic acute lung injury. Additionally, hyperoxaemia (excess blood oxygen levels) may exacerbate whole-body oxidative stress leading to cell death, autophagy, mitochondrial dysfunction, bioenergetic failure and multi-organ failure resulting in poor clinical outcomes. However, there is a lack of The aim of the MecROX mechanistic sub-study is to assess lung surfactant composition and global systemic redox status to provide a mechanistic and complementary scientific rationale to the UK-ROX trial findings. The objectives are to quantify After randomisation into the UK-ROX trial, 100 adult participants (50 in the conservative and 50 in usual care group) will be recruited at two trial sites. Blood and endotracheal samples will be taken at 0, 48 and 72 hours following an infusion of 3 mg/kg

Sections du résumé

Background UNASSIGNED
MecROX is a mechanistic sub-study of the UK-ROX trial which was designed to evaluate the clinical and cost-effectiveness of a conservative approach to oxygen therapy for invasively ventilated adults in intensive care. This is based on the scientific rationale that excess oxygen is harmful. Epithelial cell damage with alveolar surfactant deficiency is characteristic of hyperoxic acute lung injury. Additionally, hyperoxaemia (excess blood oxygen levels) may exacerbate whole-body oxidative stress leading to cell death, autophagy, mitochondrial dysfunction, bioenergetic failure and multi-organ failure resulting in poor clinical outcomes. However, there is a lack of
Aim UNASSIGNED
The aim of the MecROX mechanistic sub-study is to assess lung surfactant composition and global systemic redox status to provide a mechanistic and complementary scientific rationale to the UK-ROX trial findings. The objectives are to quantify
Methods and design UNASSIGNED
After randomisation into the UK-ROX trial, 100 adult participants (50 in the conservative and 50 in usual care group) will be recruited at two trial sites. Blood and endotracheal samples will be taken at 0, 48 and 72 hours following an infusion of 3 mg/kg

Identifiants

pubmed: 39145107
doi: 10.3310/nihropenres.13567.2
pmc: PMC11320187
doi:

Types de publication

Journal Article

Langues

eng

Pagination

23

Informations de copyright

Copyright: © 2024 Dushianthan A et al.

Déclaration de conflit d'intérêts

No competing interests were disclosed.

Auteurs

Ahilanandan Dushianthan (A)

General Intensive Care Unit, University Hospital Southampton, Southamnpton, Hampshire, SO16 6YD, UK.
NIHR Biomedical Research Centre, University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.
Faculty of Medicine, University of Southampton, Southampton, England, SO16 6YD, UK.

Daniel Martin (D)

Peninsula Medical School, University of Plymouth, Plymouth, England, PL6 8BT, UK.
Department of Intensive Care, University Hospital Plymouth, Plymouth, Devon, PL6 8DH, UK.

Paul Mouncey (P)

Intensive Care National Audit and Research Centre, London, England, UK.

Tasnin Shahid (T)

Intensive Care National Audit and Research Centre, London, England, UK.

Lamprini Lampro (L)

Intensive Care National Audit and Research Centre, London, England, UK.

Amelia Francis Johnson (AF)

Intensive Care National Audit and Research Centre, London, England, UK.

Victoria Goss (V)

Clinical Trials Unit (CTU), University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.

Angelica Cazley (A)

Clinical Trials Unit (CTU), University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.

William Herbert (W)

Clinical Trials Unit (CTU), University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.

William Jones (W)

Patient and Public Involvement Team, University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.

Mark Lamond (M)

Patient and Public Involvement Team, University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.

Florence Neyroud (F)

General Intensive Care Unit, University Hospital Southampton, Southamnpton, Hampshire, SO16 6YD, UK.

Karen Salmon (K)

General Intensive Care Unit, University Hospital Southampton, Southamnpton, Hampshire, SO16 6YD, UK.

Julian Lentaigne (J)

Department of Intensive Care, University Hospital Plymouth, Plymouth, Devon, PL6 8DH, UK.

Magdalena Minnion (M)

NIHR Biomedical Research Centre, University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.

Madhuri Panchal (M)

NIHR Biomedical Research Centre, University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.

Grielof Koster (G)

NIHR Biomedical Research Centre, University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.

Helen Moyses (H)

NIHR Biomedical Research Centre, University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.

Anthony D Postle (AD)

NIHR Biomedical Research Centre, University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.
Faculty of Medicine, University of Southampton, Southampton, England, SO16 6YD, UK.

Martin Feelisch (M)

NIHR Biomedical Research Centre, University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.
Faculty of Medicine, University of Southampton, Southampton, England, SO16 6YD, UK.

Michael P W Grocott (MPW)

General Intensive Care Unit, University Hospital Southampton, Southamnpton, Hampshire, SO16 6YD, UK.
NIHR Biomedical Research Centre, University Hospital Southampton, Southampton, Hampshire, SO16 6YD, UK.
Faculty of Medicine, University of Southampton, Southampton, England, SO16 6YD, UK.

Classifications MeSH