The Effects of Flow Settings During High Flow Nasal Cannula for Adult Hypoxemia Patients
Hypoxemia
About this trial
This is an interventional treatment trial for Hypoxemia focused on measuring High flow nasal cannula, Hypoxemia, Flow setting
Eligibility Criteria
Inclusion Criteria:
Adult patients (Age > 18yrs and < 90yrs) who need nasal cannula oxygen flow ≥ 5 L/min to maintain SpO2 at 90-97%.
Exclusion Criteria (Common): - Unable to use resuscitation mask, such as facial trauma, claustrophobia
- Inability to verbally communicate;
- Pregnant
- Inability to breathe via nose, such as nasosinusitis, stuffy nose or nasal obstruction, etc.
- Ordered SpO2 goal is above 97%
- FIO2 needs ≤ 0.4
- Using inhaled pulmonary vasodilator via HFNC
Sites / Locations
- Rush University Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Oxygenation on hypoxemia patients
Lung expansion on healthy volunteer
Adult patients with hypoxemia will be recruited, their own breathing profiles (inspiratory flow, respiratory rates and tidal volume) will be measured. Then patients will be placed on high flow nasal cannula (HFNC), HFNC flow will be titrated based on the hospital's policy or protocol and patient's comfort, patient's clinical effects on oxygenation will be monitored and recorded during the titration process.
Adult healthy volunteers will be recruited, their own breathing profiles (inspiratory flow, respiratory rates and tidal volume) will be measured. Then they will be placed on HFNC, HFNC flow will be increased sequentially by research protocol and their comfort, subjects' lung expansion effects in different flow will be quantified by Electrical impedance tomography (EIT), a noninvasive assessment tool. Their comfort will also be assessed using a visual scale.