Longitudinal Respiratory Subphenotypes and Differences in Response to Positive End-Expiratory Pressure and FIO2 Ventilation Strategy in COVID-19 ARDS

dc.contributor.authorGoossen R.L.
dc.contributor.authorFilippini D.F.L.
dc.contributor.authorvan Vliet R.
dc.contributor.authorBuiteman-Kruizinga L.A.
dc.contributor.authorHollmann M.W.
dc.contributor.authorMyatra S.N.
dc.contributor.authorNeto A.S.
dc.contributor.authorSpronk P.E.
dc.contributor.authorvan der Woude M.C.E.
dc.contributor.authorSchultz M.J.
dc.contributor.authorvan Meenen D.M.P.
dc.contributor.authorPaulus F.
dc.contributor.authorBos L.D.J.
dc.contributor.correspondenceGoossen R.L.
dc.contributor.otherMahidol University
dc.date.accessioned2025-06-05T18:15:00Z
dc.date.available2025-06-05T18:15:00Z
dc.date.issued2025-06-01
dc.description.abstractBackground: In patients with ARDS, positive end-expiratory pressure (PEEP) titration remains a challenge and recommendations are not in agreement. In mechanically ventilated patients with COVID-19, subphenotypes based on different respiratory trajectories have been identified, but their heterogeneity in response to PEEP/FIO<inf>2</inf> strategy remains understudied. Research Question: Can these previously determined subphenotypes be detected early in the course of mechanical ventilation, and do these subphenotypes moderate the association between PEEP and FIO<inf>2</inf> ventilation strategy and mortality? Study Design and Methods: Retrospective analysis of invasively ventilated patients with COVID-19. Patients were categorized into 2 treatment groups: high PEEP/low FIO<inf>2</inf> strategy and low PEEP/high FIO<inf>2</inf> strategy. To replicate previously described longitudinal respiratory subphenotypes, hereafter named the low-power or high-power subphenotype, a prediction model was created. The primary outcome was the interaction between PEEP/FIO<inf>2</inf> strategy and subphenotype, with mortality as the dependent variable. Results: Of the 1,464 patients included in this analysis, 361 patients (25%) were allocated into the high PEEP/low FIO<inf>2</inf> strategy and 1,103 patients (75%) were allocated into the low PEEP/high FIO<inf>2</inf> strategy. A prediction model consisting of respiratory data of the first 2 days of invasive ventilation (area under the receiver operating characteristics curve, 0.88) assigned 908 patients (62%) to the low-power subphenotype and 556 patients (38%) to the high-power subphenotype. The high-power subphenotype was characterized by higher minute volume, mechanical power, ventilatory ratio, and driving pressure. The association between PEEP/FIO<inf>2</inf> ventilation strategy and ICU mortality was moderated by the subphenotype (P = .03), with high PEEP/low FIO<inf>2</inf> ventilation being associated with lower mortality in the low-power subphenotype (OR, 0.46; 95% CI, 0.31-0.67; P < .001) and not in the high-power subphenotype (OR, 0.85; 95% CI, 0.57-1.28; P = .44). Interpretation: In this study, high PEEP/low FIO<inf>2</inf> ventilation was associated with improved mortality only in one of the subphenotypes, suggesting that such subphenotypes influence heterogeneity of PEEP and FIO<inf>2</inf> effect and should be considered in personalized ventilation strategies. Clinical Trial Registry: ClinicalTrials.gov; No.: NCT05954351; URL: www.clinicaltrials.gov
dc.identifier.citationChest Critical Care Vol.3 No.2 (2025)
dc.identifier.doi10.1016/j.chstcc.2025.100145
dc.identifier.eissn29497884
dc.identifier.scopus2-s2.0-105006506497
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/110468
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleLongitudinal Respiratory Subphenotypes and Differences in Response to Positive End-Expiratory Pressure and FIO2 Ventilation Strategy in COVID-19 ARDS
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105006506497&origin=inward
oaire.citation.issue2
oaire.citation.titleChest Critical Care
oaire.citation.volume3
oairecerif.author.affiliationMelbourne Medical School
oairecerif.author.affiliationNuffield Department of Medicine
oairecerif.author.affiliationReinier de Graaf Hospital - SSDZ
oairecerif.author.affiliationHogeschool van Amsterdam, University of Applied Sciences
oairecerif.author.affiliationZuyderland
oairecerif.author.affiliationMahidol Oxford Tropical Medicine Research Unit
oairecerif.author.affiliationMedizinische Universität Wien
oairecerif.author.affiliationMonash University
oairecerif.author.affiliationTata Memorial Hospital
oairecerif.author.affiliationGelre Ziekenhuizen
oairecerif.author.affiliationAustin Hospital
oairecerif.author.affiliationHospital Israelita Albert Einstein
oairecerif.author.affiliationUniversiteit van Amsterdam

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