Robot Assisted Laparoscopic Surgery Robot Assisted Laparoscopic Surgery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients meeting all of the following criteria will be eligible for inclusion in this study. 1. Patients scheduled to undergo robot-assisted laparoscopic abdominal surgery (intra-pelvic or lower abdominal surgery) under general anesthesia. 2. Patients aged 18 years or older but under 80 years at the time of informed consent acquisition. 3. Patients with a moderate or higher risk of postoperative pulmonary complications. 4.Patients classified as ASA Physical Status I to III 5. Patients from whom written informed consent has been obtained
Exclusion criteria
Exclusion criteria: Patients meeting any of the following criteria will be excluded. 1. Patients with severe chronic respiratory disease (e.g., severe COPD, receiving home oxygen therapy) 2. Patients with severe obesity (BMI >= 35kg/m2) 3.Pregnant patients 4. Patients with heart failure (NYHA class 3 or higher) or severe arrhythmia 5. Patients with implanted electronic devices such as pacemakers, defibrillators, or neurostimulators 6. Cases where EIT belt application is difficult due to torso deformities 7. Patients with a tracheostomy 8. Cases deemed inappropriate by the principal investigator or sub-investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| P/F ratio prior to extubation (T3) T0: After induction of anesthesia T1: After positioning and initiation of pneumoperitoneum, following recruitment maneuver (RM) PEEP set via DFV, 5 minutes later T2: Immediately before pneumoperitoneum release T3: Prior to extubation | — |
Secondary
| Measure | Time frame |
|---|---|
| Efficacy Evaluation Items T1-T2 P/F ratio The following measurements from T1-T3 Intraoperative respiratory dynamics indicators: Driving Pressure (Plateau Pressure - PEEP), Peak Airway Pressure, Mean Airway Pressure, Lung Compliance Arterial Blood Gas Analysis Values: SaO2, PaO2, PaCO2 Postoperative pulmonary complications (PPC) within 7 days Safety Evaluation Items Incidence rate of device-related adverse events occurring from the day of surgery through the observation period in study subjects who received protocol treatment among all enrolled patients | — |
Contacts
Kobe university hospital