About this trial
A multimodal educational intervention to target an oxygen saturation target range (SpO2 90-96%) will reduce ventilator length of stay and reduce occult hypoxemia by increased awareness and adherence to a designated oxygen saturation target range.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Admission to ICU and requiring invasive mechanical ventilation
Disqualifiers
Prisoners
Patients receiving mechanical ventilation for less than twelve hours
Trial design
Single group
Treatments tested in this trial
Education
Other intervention1\) Standardized materials to discuss the rationale and procedural aspects of the intervention, including details on the specific oxygen target-related modifications to the mechanical ventilation order-set prior to starting the intervention phase.
Epic notification alert
BehavioralAn education-based intervention that focuses on mitigating Occult Hypoxemia in mechanically ventilated patients and thus utilizes the same patient population. The second intervention will notify the clinical team to an abnormal laboratory result in real time. This laboratory result is already located in the patient's Epic chart under arterial blood gas (ABG), arterial oxygen saturation (Sa02) Patient level randomization will occur in Epic to as 1. alert (notification) the providers of sustained occult hypoxemia 2. silent alert
Treatment groups
Trial outcomes
Primary outcomes
Ventilator Free Days (Phase I,II)
The number of days the patient will be free of mechanical ventilation
Secondary outcomes
instances of occult hypoxemia (Phase I,II)
arterial oxygen saturation below 88% when the Sp02 is greater than 90% among all patients
ICU free days (Phase I,II)
Number of days patients are not in the ICU
Hospital free days (Phase I, II)
number of days patients are not hospitalized
90 Day in hospital mortality (Phase I, II)
Patients that die in the hospital before day 90
Other outcomes
Proportion of mechanically ventilated time on SpO₂ protocol target (Phase I, II)
Reported between index intubation and 30 days later. The SpO₂ protocol target is defined as SpO₂ 90-96% or receiving no oxygen (FiO₂ 0.21 with SpO₂\>96%) or maximal oxygen (FiO₂ 1.00, with SpO₂ below 90%) while requiring mechanical ventilation.
Proportion of participants receiving high levels of oxygen support (FiO₂ >0.80) (Phase I, II)
Defined as \>2 hours while requiring mechanical ventilation. This includes only the time the patient is in the ICU and receiving any amount of respiratory support (IMV or otherwise).
Proportion of time at high levels of oxygen support (FiO₂ >0.80) (Phase I, II)
Quantified during mechanical ventilation.
Proportion of time receiving room air oxygen (FiO₂ 0.21) (Phase I, II)
Quantified during mechanical ventilation.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.