A consensus of European experts on the definition of ventilator-associated pneumonia recurrences obtained by the Delphi method: the RECUVAP study
- PMID: 40163131
- DOI: 10.1007/s00134-025-07856-7
A consensus of European experts on the definition of ventilator-associated pneumonia recurrences obtained by the Delphi method: the RECUVAP study
Abstract
Background: There are recognized diagnostic criteria for a first ventilator-associated pneumonia (VAP) episode, but not for recurrences. Many randomized clinical trials (RCTs) have used the recurrence of VAP as a criterion for efficacy evaluation. Still, the different definitions used in RCTs make it difficult to compare studies. We aimed to develop a consensual definition of VAP recurrences and of the various types of VAP recurrences.
Methods: Thirty-six European experts constituting a multidisciplinary group of physicians (critical care, infectious diseases, microbiology) with special interest in the management of VAP were polled using the Delphi methodology.
Results: After the completion of four iterations of the DELPHI method, 94% of experts agreed that the diagnostic criteria for a first VAP episode could also be used for recurrences, except for the radiological criterion, which not all the experts considered to be mandatory. Consensus was also reached regarding the definition of four distinct entities: relapse, persistent VAP, superinfection, and new-pathogen VAP. For relapse and persistent VAP, bacteriological findings were identical for different VAP episodes, whereas they differed for superinfection and new-pathogen VAP. The distinction between relapse and persistent VAP, and between superinfection and new-pathogen VAP depended on the timing of antibiotic treatment (before or after 48-72 h after the end of antibiotic therapy) and the clinical course. Microbiological criteria were proposed to facilitate the diagnosis of persistent VAP.
Conclusion: This consensus by European experts proposes four different VAP recurrence entities which should facilitate the harmonization of recurrence criteria for clinical practice and future studies.
Keywords: Delphi; European; Persistent VAP; Recurrence; Relapse; Superinfection; Ventilator-associated pneumonia (VAP).
© 2025. Springer-Verlag GmbH Germany, part of Springer Nature.
Conflict of interest statement
Declarations. Conflicts of interest: C-E. L. received lecture fees from AdvanzPharma, Merck and Aerogen, grants from Merck and AdvanzPharma, and travel grants from Pfizer, all outside the submitted work. E. W. received a research grant and lecture fees from LFB, all outside the submitted work. K. R. received lecture fees from Shionogi, MSD, and a travel grant from Pfizer, all outside the submitted work. P. P. received lecture fess from Gilead, Pfizer, Mundipharma, MSD and advisory board from Biocodex, Gilead. J. J. D. W. has consulted for Roche Diagnostics, Menarini, MSD, Pfizer, ThermoFisher and Viatris (fees and honoraria paid to institution). A. C. M. is supported by a Clinician Scientist Fellowship from the Medical Research Council (MR/V006118/1). I. M. L. received grant from Grifols to my institution, consulting fees from MSD and Gilead, lectures fees from Gilead, Pfizer, Mundipharma and MSD. P. M. received consulting and lectures fees from Pfizer, Menarini, Viatris and Mundipharma, and participate to the Data Safety Monitoring Board or Advisory Board of Mundipharma and Viatris. F. B. received support from Shionogi and Pfizer, and grants from MSD. L. P. received grants from GIRCI, payment for expert testimony from Air Liquid Medical Systems, support for attending meetings from SMAAR and SRLF, participation on a Data Safety Monitoring Board or Advisory Board of BetaHypershock. K. A. received consulting fees from Edwards Life Science, honoraria for lectures from LFB, Baxter and Edwards Life Science. S. N. received consulting fees from MundiPharma, honoraria for lectures from MSD, Pfizer, Biomérieux, Fisher and Peykel, Medtronic. A. R. received European grants from Commission Horizon Europe—2024–2028, consulting fees from MSD. A. R. received payment or honoraria for lectures from Gilead, Pfizer and Mundipharma. G. P. received consulting fees from Pfizer, MSD, Menarini, GSK and GILEAD. G. D. received consulting fees from Pfizer, Viatris, Menarini, Gilead, ELPEN and InfectoPharm. S. H. received support for attending meetings from Pfizer and MSD. A. R. received payment or honoraria for lectures from MSD, Gilead and Mundipharma. S. E. received grants from Aerogen Ltd, Fisher & Paykel Healthcare and Open AI. F. D. received payment or honoraria for lectures from Biomerieux lecture and Septicyte lecture fee. D. R received grants from two institutional grants for clinical research from French ministry of health (COTRVAP and LOSTINDIAB). M. L. received consulting fees from Viatris and AOP, payment or honoraria for lectures Shionogi. S. H. received support for attending meetings from MSD and Pfizer. J-R. Z. received payment or honoraria for lectures from MSD, Shionogi, Gilead and Pfizer. J-A. P. participated to lectures and Advisory Boards for Pfizer, Merck-Sharp-Dohme, Gilead, Cepheid, AOP Orphan Pharmaceuticals. J. C. participate on a Data Safety Monitoring Board or Advisory Board Inotrem, Kenta/Aridis, PharmaMar and Aptarion DSMB. M. F. received payment or honoraria for lectures from Fisher & Paykel, BioMérieux and SOS oxygène. M. B. reports research grants and/or advisor/consultant and/or speaker/chairman for Bayer, Biomerieux, Cidara, Cipla, Gilead, Menarini, MSD, Pfzer, Shionogi and Thermo-Fisher, outside the submitted work.
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