High Flow Nasal Cannula With Noninvasive Ventilation
Acute Respiratory Failure
About this trial
This is an interventional treatment trial for Acute Respiratory Failure focused on measuring acute respiratory failure, mechanical ventilation
Eligibility Criteria
Inclusion Criteria:
- Adults at least 18 years of age
- Admission to an intensive care unit by the trauma surgery service
- Trauma patients receiving any respiratory therapies
- High risk patients, including intubation, post-operative, chronic cardiac or pulmonary comorbidities
- Thoracic injuries, including rib fractures, sternal fractures, spinal fractures, pulmonary contusions, pneumothorax, hemothorax, diaphragm injury
- Postoperative from thoracic surgery
- Postoperative from spine surgery in patients without spinal cord injury
- Abdominal injuries requiring open abdominal surgery
- No contraindications to using high flow nasal cannula or noninvasive ventilation
Exclusion Criteria:
- Contraindication to using high flow nasal cannula or noninvasive ventilation
- Intolerance of pulmonary therapies
- No one able to give informed consent
- Long-term treatment with noninvasive ventilation prior to hospital admission
- "Do not intubate" order at time of extubation
- Unplanned extubation (accidental or self-extubation)
- Age < 18 years of age
- Traumatic brain injury with GCS < 8
- Spinal cord injury
- Chronic neuromuscular disease
- Sinus precautions due to facial/sinus fractures
Sites / Locations
- OU Medical CenterRecruiting
- OU Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Not Intubated
Intubated Patients Undergoing Extubation
Patients admitted with a trauma injury who do not need to be intubated to receive treatment. Intubated means putting a tube down your throat to keep your airway from collapsing. Participants will be randomized to receive one of the three interventions in this arm.
Patients admitted with a trauma injury who had to be intubated for treatment of their injury. Interventions administered after the tube is extubated (removed from throat). Participants will be randomized to receive one of the three interventions in this arm.