Normoxemia
Cross-source consensus on Normoxemia from 1 sources and 5 claims.
1 sources · 5 claims
Uses
How it works
Dosage & preparation
Comparisons
Highlighted claims
- The primary outcome is the proportion of patient-time spent in the normoxemia range (SpO₂ 90–96%) during the first 72 hours after randomization. — Statistical analysis plan for the Strategy to Avoid Excessive Oxygen using Autonomous Oxygen Titration Intervention (SAVE-O2 AI) trial: protocol
- All patients in both groups share a target SpO₂ of 93% with an acceptable range of 90–96%. — Statistical analysis plan for the Strategy to Avoid Excessive Oxygen using Autonomous Oxygen Titration Intervention (SAVE-O2 AI) trial: protocol
- Observation time for the primary outcome is censored at discharge, escalation to high-flow or mechanical ventilation, sustained room-air breathing for 12 hours, or death. — Statistical analysis plan for the Strategy to Avoid Excessive Oxygen using Autonomous Oxygen Titration Intervention (SAVE-O2 AI) trial: protocol
- Based on prior SAVE-O2 trials, the expected proportion of time in normoxemia under usual care is 60%. — Statistical analysis plan for the Strategy to Avoid Excessive Oxygen using Autonomous Oxygen Titration Intervention (SAVE-O2 AI) trial: protocol
- A previous autonomous titration trial observed a 32 percentage point improvement (95% CI 26–37) in normoxemia proportion. — Statistical analysis plan for the Strategy to Avoid Excessive Oxygen using Autonomous Oxygen Titration Intervention (SAVE-O2 AI) trial: protocol