About this trial
The goal of this randomized controlled clinical trial is to compare the pulmonary protective effects of two different positive end-expiratory pressure (PEEP) titrating methods in patients with non-injured lungs undergoing laparoscopic gynecological surgery.
Despite dynamic pulmonary compliance (Cdyn) guided lung protective ventilation has several proven advantages, the investigators hypothesize that optimizing intraoperative mechanical ventilation using electrical impedance tomography (EIT) may further improve patient outcomes, enhance postoperative recovery, shorten in-hospital stay and reduce healthcare related costs.
The main questions aim to answer are:
* May EIT-guided PEEP titration reduce the mechanical power of ventilation and improve oxygenation more significantly than the Cdyn-guided method? * What effect might a decrease in mechanical power of ventilation have on postoperative pulmonary complications?
Participants will:
* Receive an EIT-guided or a Cdyn-guided PEEP titration procedure during laparoscopic gynecological surgery. * Be assessed for mechanical power of ventilation, oxygenation, atelectasis and postoperative pulmonary complications during and 2 days after surgery. * Be followed-up for mortality until the 28th postoperative day.
Eligibility criteria
Qualifiers
Patient scheduled for elective laparoscopic gynaecological surgery
Age > 18 years
Signed consent to participate in the trial
Disqualifiers
Age < 18 years
American Society of Anesthesiologists (ASA) physical status IV
History of severe restrictive or chronic obstructive pulmonary disease (COPD, Global Initiative for Chronic Obstructive Lung Disease grades III or IV)
Uncontrolled bronchial asthma
Trial design
Treatments tested in this trial
- EIT-guided PEEP titration
- Cdyn-guided PEEP titration
Treatment groups
Sponsors and collaborators
Pest County Flór Ferenc Hospital
Lead sponsor
Kiskunhalas Semmelweis Hospital the Teaching Hospital of the University of Szeged
Collaborator
Semmelweis University
Collaborator