About this trial
This is an investigator-initiated, international, multicenter, prospective, cross-sectional study that aims to 1) describe the incidence and types of postoperative pulmonary complications (PPCs), 2) describe patient demographics, baseline characteristics, and intraoperative ventilation management, 3) describe the occurrence of intraoperative adverse events (IAEs), and 4) their associations with PPCs, 5) assess the practice of intraoperative mechanical ventilation.
Patients will be eligible for participation if: 1) adult and 2) receiving intraoperative ventilation during general anesthesia for surgery. Patients receiving ventilation outside of an operating room as well as patients receiving intraoperative ventilation during extracorporeal life support will be excluded
Eligibility criteria
Qualifiers
Adults; and
Receiving intraoperative IMV (via tracheal intubation, or supraglottic device ) during general anesthesia for surgery
Disqualifiers
Receiving intraoperative IMV outside of an operating room; and
Receiving intraoperative IMV during extracorporeal life support
Trial design
Treatments tested in this trial
- Intraoperative mechanical ventilation for surgery
Treatment groups
Locations
1Sponsors and collaborators
Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo di Alessandria
Lead sponsor
University Of Perugia
Collaborator
University of Chieti
Collaborator
Medical University of Vienna
Collaborator
The Netherlands Cancer Institute
Collaborator
Monash University
Collaborator