Esophageal Balloon Guided Weaning of the Morbidly Obese Patient
Morbid Obesity
About this trial
This is an interventional treatment trial for Morbid Obesity focused on measuring Transpulmonary pressure, Esophageal balloon, Esophageal pressure monitoring device, Cstat, Static effective compliance, Ventilator weaning, Morbidly Obese Ventilator Dependent Tracheotomized Patients
Eligibility Criteria
Inclusion Criteria:
- Morbidly obese patients with BMI of 40 or greater
- Ventilator dependent patients (defined as at least one prior failure at weaning)
- Tracheotomized
- No active underlying lung disease that would preclude ventilator weaning
- Stable hemodynamics
- Patient/ family able to give consent
- No naso-facial abnormalities that would interfere with placement of an esophageal balloon
- Fio2 <= 60%
- Patient able to tolerate Pressure Support ventilation
Exclusion Criteria:
- Lack of consent
- Patient deemed not weanable from mechanical ventilation as per the clinical judgement of the pulmonary physician
- Significant lung, heart or neuromuscular disease that would interfere with or preclude ventilator weaning, including an active ongoing lung infection.
- Contraindications to placement of an esophageal pressure monitoring device - such as ulcerations, tumors, diverticulitis, uncontrolled bleeding varices, sinusitis, epistaxis or recent nasopharyngeal surgery
Sites / Locations
- Vidant Medical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
No Intervention
Esophageal balloon Arm
Cstat Arm
Historic Controls
Patients in this arm were randomly assigned to have their PEEP adjusted to maintain a positive transpulmonary pressure (0 to 10 cm H20).
Patients in this arm had their PEEP adjusted to achieve the best static effective compliance (CStat).
These were historic controls with similar patient characteristics weaned by traditional methods in the 2-year period prior to the start of the study.