Authors

UK-ROX Investigators
Daniel S Martin, Peninsula Medical School
Doug W Gould, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.
Tasnin Shahid, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.
James C Doidge, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.
Alex Cowden, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.
Zia Sadique, London School of Hygiene and Tropical Medicine
Julie Camsooksai, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.
Walton N Charles, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.
Miriam Davey, Critical Care, Maidstone and Tunbridge Wells NHS Foundation Trust, Kent, United Kingdom.
Amelia Francis-Johnson, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.
Roger M Garrett, Patient and Public Representative, Bristol, United Kingdom.
Michael P W Grocott, University Hospital Southampton NHS Foundation Trust
Joanne Jones, Critical Care, Maidstone and Tunbridge Wells NHS Foundation Trust, Kent, United Kingdom.
Lamprini Lampro, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.
Diane M Mackle, Medical Research Institute of New Zealand
B Ronan O'Driscoll, Salford Royal University Hospital
Alvin Richards-Belle, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.
Anthony J Rostron, Integrated Critical Care Unit, South Tyneside and Sunderland NHS Foundation Trust, Sunderland, United Kingdom.
Tamás Szakmány, Aneurin Bevan Health Board
Alex Warren, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.
Paul J Young, Wellington Hospital
Kathryn M Rowan, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.
David A Harrison, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.
Paul R Mouncey, Clinical Trials Unit, Intensive Care National Audit & Research Centre (ICNARC), Napier House, London, United Kingdom.

ORCID

Abstract

IMPORTANCE: Supplemental oxygen is frequently given to patients in intensive care units (ICUs); however, there is insufficient evidence to guide its therapeutic use and to minimize the potential harm caused by administering too little or too much.

OBJECTIVE: To determine whether reducing exposure to supplemental oxygen through a strategy of conservative oxygen therapy by using a peripheral oxygen saturation (Spo2) target of 90% (range, 88%-92%) reduces mortality at 90 days in mechanically ventilated adult patients receiving supplemental oxygen in the ICU.

DESIGN, SETTING, AND PARTICIPANTS: Multicenter, pragmatic, randomized clinical trial conducted in 97 ICUs in the UK including 16 500 mechanically ventilated patients receiving supplemental oxygen. Participants were enrolled between May 2021 and November 2024. Follow-up was completed in February 2025.

INTERVENTIONS: Participants randomized to conservative oxygen therapy (n = 8258) received the lowest fraction of inspired oxygen possible to maintain their Spo2 at 90%. Participants randomized to usual oxygen therapy (n = 8242) received oxygen therapy at the discretion of the treating clinician.

MAIN OUTCOMES AND MEASURES: The primary outcome was all-cause mortality at 90 days. Secondary outcomes included duration of ICU and acute hospital stay among survivors, days alive and free from organ support at 30 days, and mortality at other time points.

RESULTS: Of 16 500 randomized patients, primary outcome data were available for 16 394 (8211 in the conservative and 8183 in the usual oxygen therapy group). Randomized groups were similar (median age, 60 [IQR, 48-71] years and 38.2% females in both groups [n = 5652]). Exposure to supplemental oxygen was 29% lower for participants in the conservative oxygen therapy group compared with the usual oxygen therapy group. By 90 days, 2908 participants (35.4%) in the conservative oxygen therapy group had died compared with 2858 (34.9%) in the usual oxygen therapy group. After adjustment for prespecified baseline variables, the risk difference was 0.7 percentage points (95% CI, -0.7 to 2.0; P = .28). There were no significant differences in durations in ICU or hospital stay, days alive and free from organ support at 30 days, or mortality at other time points.

CONCLUSIONS AND RELEVANCE: In adult patients receiving mechanical ventilation and supplemental oxygen in the ICU, minimizing oxygen exposure through conservative oxygen therapy did not significantly reduce all-cause mortality at 90 days.

TRIAL REGISTRATION: isrctn.org Identifier: ISRCTN13384956.

Publication Date

2025-06-12

Publication Title

JAMA - Journal of the American Medical Association

ISSN

0098-7484

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