Early noninvasive ventilation in general wards for acute respiratory failure: an international, multicentre, open-label, randomised trial.
Summary
In a multinational open-label RCT of 524 adults with mild acute respiratory failure on general wards, early NIV reduced progression to severe respiratory failure (18.5% vs 28.3%; RR 0.65) without differences in 28-day mortality, respiratory complications, or adverse events. Length of stay was similar.
Key Findings
- Early NIV reduced progression to severe acute respiratory failure (18.5% vs 28.3%; RR 0.65, 95% CI 0.48-0.90, P=0.008).
- No differences in 28-day mortality, respiratory complications, or adverse events between groups.
- Hospital length of stay was similar (median 10 vs 9 days; P=0.30).
Clinical Implications
Hospitals can implement protocolized, monitored early NIV on general wards for mild acute respiratory failure to reduce deterioration, with appropriate staff training and escalation pathways.
Why It Matters
This pragmatic RCT provides high-level evidence that ward-based early NIV prevents deterioration, informing resource-appropriate respiratory support strategies beyond ICUs.
Limitations
- Open-label design may introduce performance bias.
- Study powered for progression outcome; mortality effects remain uncertain.
Future Directions
Evaluate implementation strategies, cost-effectiveness, and patient selection criteria for ward-based NIV; assess impacts on ICU admission and long-term outcomes.
Study Information
- Study Type
- RCT
- Research Domain
- Treatment
- Evidence Level
- I - Randomized controlled trial providing highest level clinical evidence.
- Study Design
- OTHER