Effect of Boussignac CPAP Ventilation on PaO2 and PaO2/FiO2 Ratio in Morbidly Obese Patients Undergoing Bariatric Surgery
Morbid Obesity
About this trial
This is an interventional treatment trial for Morbid Obesity
Eligibility Criteria
Inclusion Criteria:
- Patients age between 18 and 65 years of age
- Morbidly obese with a body mass index > 35 kg/m2
- Laparoscopic gastric bypass
Exclusion Criteria:
- Patient refusal
- American Society of Anesthesiologists' (ASA) class IV
- Lung parenchyma disease
- Chronic Obstructive Pulmonary Disease
- Moderate to severe asthma
- Pre-existing cardiac failure (above class II in the New York Heart Association (NYHA) classification)
- Estimated pulmonary artery pressure ≥35mmHg
- Hemoglobin concentration ([Hgb]) less than 7 g / dL
- Need for invasive ventilation during preoperative immediate post-extubation defined in the preoperative period
- Patients with obstructive sleep apnea previously treated with CPAP
- Severe psychiatric disorder
- Language barrier
Sites / Locations
- Centro Hospitalar Porto
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Boussignac CPAP
Ventury face mask
Boussignac CPAP with a 50% FiO2 (adjusted in a piece adapted to the system) and a pressure of 5cmH2O (measured with a manometer) is applied immediately after extubation and mantained for two hours after extubation in the post anesthesia care unit (PACU). Arterial blood samples to measure PaO2 and PaO2/FiO2 ratio are collected before surgery and at 1, 2 and 24 hours after extubation. Spirometry is performed at the same intervals measuring FEV1 and FVC.
Venturi mask with a 50% FiO2 is used immediately after extubation and mantained for two hours in the post anesthesia care unit (PACU). Arterial blood samples to measure PaO2 and PaO2/FiO2 ratio are collected before surgery and at 1, 2 and 24 hours after extubation. Spirometry is performed at the same intervals measuring FEV1 and FVC.