Optimizing flow rate of high-flow nasal cannula using peak inspiratory flow during spontaneous breathing trial for post-extubation pediatric populations
Not Applicable
- Conditions
- pediatric patient
- Registration Number
- JPRN-UMIN000053260
- Lead Sponsor
- Tokushima University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 32
Inclusion Criteria
Not provided
Exclusion Criteria
Difficulty fitting HFNC (nasal congestion, facial trauma, intolerance) Difficulty fitting transducer (trunk trauma, burns, intolerance) Combination of HFNC with NO inhalation therapy Hemodynamic instability (mean blood pressure: <40 mmHg in neonates, <50 mmHg in infants) Severe hypoxemia (PaO2: Partial pressure of arterial oxygen/FiO2 ratio <150 in non-cyanotic heart disease) Severe acidemia (pH < 7.20)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Phase angle We collect data during SBT before extubation and during HFNC at different flow settings after extubation.
- Secondary Outcome Measures
Name Time Method