Intraoperative Driving Pressure-Guided High PEEP vs Standard Low PEEP for Postoperative Pulmonary Complications
3
Issued Date
2025-01-01
Resource Type
ISSN
00987484
eISSN
15383598
Scopus ID
2-s2.0-105024343821
Pubmed ID
41334859
Journal Title
JAMA
Rights Holder(s)
SCOPUS
Bibliographic Citation
JAMA (2025)
Suggested Citation
Dorland G., Abreu M.G., Hemmes S.N.T., Hol L., Hollmann M.W., Van Meenen D.M.P., Nijbroek S.G.L.H., Schultz M.J., Serpa Neto A., Vermeulen T.D. Intraoperative Driving Pressure-Guided High PEEP vs Standard Low PEEP for Postoperative Pulmonary Complications. JAMA (2025). doi:10.1001/jama.2025.23373 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/113549
Title
Intraoperative Driving Pressure-Guided High PEEP vs Standard Low PEEP for Postoperative Pulmonary Complications
Author's Affiliation
Amsterdam UMC - University of Amsterdam
Medizinische Universität Wien
Radboud University Medical Center
Nuffield Department of Medicine
Universitätsklinikum Carl Gustav Carus Dresden
Hospital Israelita Albert Einstein
Austin Hospital
Antoni van Leeuwenhoek Ziekenhuis
Mahidol Oxford Tropical Medicine Research Unit
Department of Critical Care
Medizinische Universität Wien
Radboud University Medical Center
Nuffield Department of Medicine
Universitätsklinikum Carl Gustav Carus Dresden
Hospital Israelita Albert Einstein
Austin Hospital
Antoni van Leeuwenhoek Ziekenhuis
Mahidol Oxford Tropical Medicine Research Unit
Department of Critical Care
Corresponding Author(s)
Other Contributor(s)
Abstract
Importance: The effect of individualized high positive end-expiratory pressure (PEEP) and recruitment maneuvers, targeting a low driving pressure, on clinical outcomes in patients undergoing open abdominal surgery is uncertain. Objective: To compare driving pressure-guided high PEEP and recruitment maneuvers with standard low PEEP without recruitment maneuvers with respect to postoperative pulmonary complications. Design, Setting, and Participants: Randomized clinical trial of 1435 adults at increased risk for postoperative pulmonary complications who were scheduled for open abdominal surgery. The trial was conducted at 29 sites in 5 countries across Europe from April 2019 to December 2024; final follow-up was in March 2025. Statistical analysis was conducted in May 2025. Intervention: Patients were randomized to undergo intraoperative ventilation with driving pressure-guided high PEEP and recruitment maneuvers (n = 718) or to intraoperative ventilation with standard low PEEP (n = 717). All patients received low tidal volume ventilation. Main Outcomes and Measures: The primary outcome was a composite of pulmonary complications within the first 5 postoperative days, including severe respiratory failure, bronchospasm, suspected pulmonary infection, pulmonary infiltrates, aspiration pneumonitis, atelectasis, acute respiratory distress syndrome, pleural effusion, cardiopulmonary edema, and pneumothorax. Among the 16 prespecified secondary outcomes, 4 concerned intraoperative complications, including hypotension (decrease in mean arterial pressure of >20% for >3 minutes) and desaturation (Spo2 <92% for >1 minute). Results: Among 1468 adults, 1435 (98%) completed the trial (median [IQR] age, 66 [57-74] years; 52% female). In the primary analysis population, the primary outcome occurred in 142 of 718 patients (19.8%) in the driving pressure-guided high PEEP group compared with 125 of 717 patients (17.4%) in the low PEEP group (absolute difference, 2.5% [95% CI, -1.5% to 6.4%]; P =.23). The incidence of hypotension (382 [54.0%] vs 317 [45.0%]) and use of vasoactive agents (224 [32.0%] vs 130 [18.8%]) was higher in the high PEEP group; the incidence of intraoperative desaturation (6 [0.8%] vs 20 [2.8%]) was higher in the low PEEP group. Conclusions and Relevance: Among patients at increased risk for postoperative pulmonary complications undergoing open abdominal surgery under general anesthesia, intraoperative ventilation with driving pressure-guided high PEEP and recruitment maneuvers, compared with a strategy with standard low PEEP, did not reduce postoperative pulmonary complications. Trial Registration: ClinicalTrials.gov Identifier: NCT03884543