Table 2.
Variable | Odds Ratio | 95% CI | p-value |
---|---|---|---|
Implementation of apneic oxygenation | |||
Pre-intervention | Reference | ||
Post-intervention | 0.55 | 0.34–0.88 | 0.013 |
Patient | |||
Respiratory indication | 1.37 | 0.91–2.06 | 0.130 |
Procedural indication | 0.55 | 0.35–0.87 | 0.010 |
Device | |||
Direct laryngoscopy | Reference | ||
Video laryngoscopy | 1.45 | 0.89–2.35 | 0.132 |
Other* | 4.32 | 1.57–11.85 | 0.004 |
Total N=1,368. Five Encounters are missing device data.
Goodness-of-fit test Chi(2)=18.07, p=0.259.
Covariates were selected based on the change in patient and practice between pre- and post-intervention phases.
Other device includes laryngeal mask airway, fiberoptic bronchoscope or combination of two devices.