Lung Diseases, Obesity, One-Lung Ventilation
Conditions
Brief summary
The aim of the prospective crossover study is to investigate the effect of individualized positive end-expiratory pressure (PEEP) on measures of tissue oxygenation, compared with low PEEP.
Detailed description
During surgery on the lung, ventilation of one lung at a time is often necessary. During thoracic surgery requiring one-lung ventilation (OLV), hypoxemia (reduced oxygen tension in blood) can present a clinical challenge. Due to multiple factors, the likelihood of hypoxemia during OLV in obese patients is increased. Atelectasis (collapse of the lung airspaces) contributes to hypoxemia and can be mitigated by application of recruitment maneuvers and positive end-expiratory pressure (PEEP). A recruitment maneuver is a breath given in a mechanically ventilated patient that helps to open up collapsed air spaces, and PEEP is application of a continuous amount of positive pressure that helps keep the air spaces open at the end of an exhaled breath. Adjusting the level of PEEP to each individual patient's optimal lung compliance (individualized PEEP) improves blood oxygen levels compared to application of standard low PEEP (5 cmH2O); however, higher levels of PEEP required to achieve optimal lung compliance could increase intrathoracic pressures to a level that impedes normal circulation. This could negatively affect blood flow (cardiac output) and delivery of oxgyen to vital organs. Evidence addressing OLV in obese patients is lacking. The purpose of this study is to compare brain oxygen levels (cerebral oxygen saturation) and measures of blood flow and gas exchange during OLV with individualized PEEP vs low standard PEEP in obese patients undergoing thoracic surgery. To our knowledge, there is no previous study that compares oxygen delivery to vital organs (such as the brain) during OLV using individualized PEEP versus standard low PEEP, in an obese patient population. In this study, subjects undergoing OLV during surgery to remove a portion of the lung (lobectomy) will undergo a process to determine their individualized PEEP and then two 20-minute experimental periods-- one period with OLV with low PEEP and one period with OLV with individualized PEEP. Measurements of cerebral oxygen saturation, blood oxygen levels, cardiac output, and blood pressure medication dose will be measuring before and after these experimental periods during surgery.
Interventions
PROCEDUREOne-lung ventilation with individualized PEEP
During one-lung ventilation for lung resection surgery, PEEP will be applied. After a subject's individualized PEEP (PEEP that corresponds to maximum lung compliance) is determined, the subject will receive one-lung ventilation with individualized PEEP.
PROCEDUREOne-lung ventilation with low PEEP
Subjects will receive one-lung ventilation with low PEEP (5 cmH2O)
Sponsors
Dionne Peacher
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Intervention model description
Mechanical ventilation with individualized PEEP will be compared to mechanical ventilating with low PEEP during lung isolation in each subject. Each subject will receive one PEEP level then will receive the second PEEP level. The order in which each subject receives the PEEP level will be randomized.
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
1. Subject undergoing elective pulmonary lobectomy requiring one-lung ventilation 2. Body-mass index ≥ 30 kg/m2 3. Age ≥ 18 years and ≤ 80 years
Exclusion criteria
1. Age ≤ 18 year or ≥ 80 years 2. Moderate or severe cardiac valvular disease 3. Left ventricular ejection fraction \< 30% 4. Moderate or severe right ventricular systolic dysfunction 5. Severe pulmonary hypertension 6. Presence of pulmonary bullae or blebs on preoperative chest imaging studies (e.g., radiograph, computed tomograph) 7. Emergency surgery 8. Previous history of lung surgery on the non-operative lung 9. Pregnancy 10. Incarceration 11. Mental incapacitation 12. Patient refusal 13. Non-English speaking
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Cerebral oximetry | Change from baseline cerebral oximetry at the end of each intraoperative 20 minute experimental period. All measurements are made during the 4-6 hour surgery. | Cerebral oximetry (a measure of oxygen levels in the brain) as measured by near-infrared spectroscopy (noninvasive monitor applied to the forehead) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Arterial blood oxygen tension (PaO2) | Measured at baseline, and then at the end of each 20 minute intraoperative experimental period. All measurements are made during the 4-6 hour surgery. | A measure of oxygen level in arterial blood |
| Venous blood oxygen tension (PvO2) | Measured at baseline, and then at the end of each 20 minute intraoperative experimental period. All measurements are made during the 4-6 hour surgery. | A measure of oxygen level in venous blood |
| Venous blood oxygen saturation (SvO2) | Measured at baseline, and then at the end of each 20 minute intraoperative experimental period. All measurements are made during the 4-6 hour surgery. | A measure of oxygen saturation in venous blood |
| Cardiac output | Measured at baseline, and then at the end of each 20 minute intraoperative experimental period. All measurements are made during the 4-6 hour surgery. | A measure of blood flow throughout the body |
| Phenylephrine dose | Total dose of phenylephrine administered during each intraoperative 20 minute experimental period. All measurements are made during the 4-6 hour surgery. | Total dose of phenylephrine (medication used to raise blood pressure) |
Countries
United States
Outcome results
None listed