Driving Pressure and Postoperative Pulmonary Complications in Thoracic Surgery
One-Lung Ventilation, Postoperative Complications, Driving Pressure
About this trial
This is an interventional prevention trial for One-Lung Ventilation focused on measuring Postoperative pulmonary complication, Driving pressure, Thoracic surgery, One lung ventilation, Positive end expiratory pressure
Eligibility Criteria
Inclusion Criteria:
Adults older than or equal to 19 years with American Society of Anesthesiologists physical status Ⅰ-Ⅲ Patient who undergoes one-lung ventilation (more than 60 minutes) for elective thoracic surgery
Exclusion Criteria:
- The American Society of Anesthesiologists (ASA) Physical Status classification greater than or equal to 4
- Symptoms of heart failure (hypertension, urination, pulmonary edema, left ventricular outflow rate <45%) or preoperative vasopressors
- Patient who is received oxygen therapy and ventilation care
- large emphysema and pneumothorax
- pregnancy and lactation
- patients participating in similar studies
- Joint with other operation
- Patient who rejects being enrolled in the study
- Patients with elevated intracranial pressure
- Patients with peripheral neuropathy or blood circulation disorders
- Patients with hematology disease
- Congenital heart disease with shunt
Sites / Locations
- Samsung medical center
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Driving pressure group
Protective Ventilation
Positive end expiratory pressure is adjusted to tidal volume of 5 mL/kg of ideal body weight, inspiratory:expiratory=1:2, and minimize driving pressure (plateau pressure minus end expiratory pressure) during one-lung ventilation. Other procedures are same with the control arm.
The control arm receives existing conventional protective ventilation with tidal volume of 5mL/kg of ideal body weight and positive end expiratory pressure of 5cmH2O during one-lung ventilation