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Oxygen Supplementation in Pediatric Sedation: Prospective, Multicenter, Randomized Controlled Trial.

Anesthesiology2025-04-11PubMed
Total: 79.5Innovation: 7Impact: 8Rigor: 9Citation: 7

Summary

In a multicenter RCT of 250 children undergoing moderate-to-deep sedation, both low-flow nasal cannula and high-flow nasal cannula drastically reduced hypoxemia versus no oxygen, with fewer rescue interventions and complications. High-flow was not significantly superior to low-flow, supporting low-flow oxygen as a pragmatic standard.

Key Findings

  • Hypoxemia incidence: control 27.6% vs low-flow 7.2% vs high-flow 1.2% (P<0.001).
  • Odds of hypoxemia vs control: low-flow OR 0.184 (95% CI 0.067–0.503); high-flow OR 0.026 (95% CI 0.003–0.207).
  • Rescue interventions: control 52.9% vs low-flow 10.8% vs high-flow 3.6% (P<0.001).
  • High-flow was not statistically superior to low-flow (OR 0.143; 95% CI 0.017–1.245; P=0.078).

Clinical Implications

Adopt routine low-flow oxygen supplementation during moderate-to-deep pediatric sedation to prevent hypoxemia and reduce rescue interventions; reserve high-flow for selected higher-risk cases or when low-flow is insufficient.

Why It Matters

This trial directly informs procedural sedation safety in children and is likely to change routine oxygen supplementation practices globally.

Limitations

  • High-flow vs low-flow comparison may be underpowered for detecting small differences.
  • Generalisability may be influenced by sedation protocols and monitoring practices at participating centers.

Future Directions

Define risk strata to target high-flow nasal cannula; assess cost-effectiveness and implementation outcomes across diverse procedural settings.

Study Information

Study Type
RCT
Research Domain
Prevention
Evidence Level
I - High-quality multicenter randomized controlled trial.
Study Design
OTHER