Eliminating Monitor Overuse Trial (EMO Trial)

Inclusion Criteria

• •Population a: Bronchiolitis patients directly observed while not receiving supplemental oxygen ("in room air," for primary trial outcome)
• •Infants and children 2 months through 23 months old
• •Hospitalized on non-ICU wards participating in the trial
• •Cared for by generalist inpatient services (e.g. general pediatrics, hospital medicine)
• •Primary diagnosis of bronchiolitis in most recent physician progress note
• •Not actively receiving supplemental oxygen ("in room air")
• •Last documented receipt of supplemental oxygen \>1 hour prior to direct observational data collection
• •Infants and children 2 months through 23 months old
• •Hospitalized on non-ICU wards participating in the trial
• •Cared for by generalist inpatient services (e.g. general pediatrics, hospital medicine)
• •Primary diagnosis of bronchiolitis in most recent physician progress note
• •Actively receiving ≥2 Liters/minute (2L/min) supplemental oxygen or 21% room air flow