Optiflow® to Prevent Post-Extubation Hypoxemia afteR Abdominal Surgery (the OPERA Trial) (OPERA)
Postoperative Hypoxemia
About this trial
This is an interventional prevention trial for Postoperative Hypoxemia focused on measuring Postoperative pulmonary complications, Oxygen therapy, Nasal high flow oxygen therapy, Nasal high flow cannula
Eligibility Criteria
Inclusion Criteria:
- Planned or unplanned surgical procedures
- Abdominal or abdominal and thoracic surgery
- Expected duration ≥2 hours
- ARISCAT score ≥26 points
Exclusion Criteria:
- Age <18 years
- Body mass index >35 kg/m2
- Sleep apnea syndrome
- Patient refusal
- Pregnancy and/or lactation
Sites / Locations
- CHU Clermont-Ferrand
Arms of the Study
Arm 1
Arm 2
Experimental
Other
Standard oxygen therapy
nasal high flow oxygen therapy
Our hypothesis is that, compared with standard oxygen therapy, early application of nasal high flow oxygen therapy can reduce the need for postoperative NPPV for postoperative hypoxemia (defined as PaO2/FiO2 ratio <300).
Our hypothesis is that, compared with standard oxygen therapy, early application of nasal high flow oxygen therapy can reduce the need for postoperative NPPV for postoperative hypoxemia (defined as PaO2/FiO2 ratio <300).