Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30214
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dc.contributor.authorCampos, Niklas S-
dc.contributor.authorBluth, Thomas-
dc.contributor.authorHemmes, Sabrine N T-
dc.contributor.authorLibrero, Julian-
dc.contributor.authorPozo, Natividad-
dc.contributor.authorFerrando, Carlos-
dc.contributor.authorBall, Lorenzo-
dc.contributor.authorMazzinari, Guido-
dc.contributor.authorPelosi, Paolo-
dc.contributor.authorGama de Abreu, Marcelo-
dc.contributor.authorSchultz, Marcus J-
dc.contributor.authorSerpa Neto, Ary-
dc.date2022-04-15-
dc.date.accessioned2022-06-23T00:29:29Z-
dc.date.available2022-06-23T00:29:29Z-
dc.date.issued2022-06-
dc.identifier.citationBritish Journal of Anaesthesia 2022; 128(6): 1040-1051en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/30214-
dc.description.abstractHigh intraoperative PEEP with recruitment manoeuvres may improve perioperative outcomes. We re-examined this question by conducting a patient-level meta-analysis of three clinical trials in adult patients at increased risk for postoperative pulmonary complications who underwent non-cardiothoracic and non-neurological surgery. The three trials enrolled patients at 128 hospitals in 24 countries from February 2011 to February 2018. All patients received volume-controlled ventilation with low tidal volume. Analyses were performed using one-stage, two-level, mixed modelling (site as a random effect; trial as a fixed effect). The primary outcome was a composite of postoperative pulmonary complications within the first week, analysed using mixed-effect logistic regression. Pre-specified subgroup analyses of nine patient characteristics and seven procedure and care-delivery characteristics were also performed. Complete datasets were available for 1913 participants ventilated with high PEEP and recruitment manoeuvres, compared with 1924 participants who received low PEEP. The primary outcome occurred in 562/1913 (29.4%) participants randomised to high PEEP, compared with 620/1924 (32.2%) participants randomised to low PEEP (unadjusted odds ratio [OR]=0.87; 95% confidence interval [95% CI], 0.75-1.01; P=0.06). Higher PEEP resulted in 87/1913 (4.5%) participants requiring interventions for desaturation, compared with 216/1924 (11.2%) participants randomised to low PEEP (OR=0.34; 95% CI, 0.26-0.45). Intraoperative hypotension was associated more frequently (784/1913 [41.0%]) with high PEEP, compared with low PEEP (579/1924 [30.1%]; OR=1.87; 95% CI, 1.60-2.17). High PEEP combined with recruitment manoeuvres during low tidal volume ventilation in patients undergoing major surgery did not reduce postoperative pulmonary complications. NCT03937375 (Clinicaltrials.gov).en
dc.language.isoeng
dc.subjectPEEPen
dc.subjectmechanical ventilationen
dc.subjectpostoperative pulmonary complicationsen
dc.subjectsurgeryen
dc.titleIntraoperative positive end-expiratory pressure and postoperative pulmonary complications: a patient-level meta-analysis of three randomised clinical trials.en
dc.typeJournal Articleen
dc.identifier.journaltitleBritish Journal of Anaesthesiaen
dc.identifier.affiliationMedicine (University of Melbourne)en
dc.identifier.affiliationDepartment of Critical Care, Melbourne Medical School, University of Melbourne, Melbourne, Australiaen
dc.identifier.affiliationDepartment of Critical Care Medicine, Hospital Israelita Albert Einstein, Sao Paulo, Brazilen
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre (ANZIC-RC), Monash University, Melbourne, Australiaen
dc.identifier.affiliationCoração, Hospital das Clinicas HCFMUSP, Universidade de Sao Paulo, Sao Paulo, Brazilen
dc.identifier.affiliationMahidol Oxford Research Unit (MORU), Mahidol University, Bangkok, Thailanden
dc.identifier.affiliationDepartment of Intensive Care, Amsterdam University Medical Centers, location 'AMC', Amsterdam, the Netherlands;en
dc.identifier.affiliationPulmonary Engineering Group, Department of Anesthesiology and Intensive Care Medicine, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germanyen
dc.identifier.affiliationDepartment of Anesthesiology, Amsterdam University Medical Centers, location 'AMC', Amsterdam, the Netherlandsen
dc.identifier.affiliationNavarrabiomed-Fundación Miguel Servet, Red de Investigación en Servicios de Salud en Enfermedades Crónicas (REDISSEC), Pamplona, Spainen
dc.identifier.affiliationINCLIVA Clinical Research Institute, Hospital Clinico Universitario de Valencia, Valencia, Spainen
dc.identifier.affiliationDepartment of Anesthesiology & Critical Care, Hospital Clinico Universitario de Valencia, Valencia, Spainen
dc.identifier.affiliationDepartment of Surgical Sciences and Integrated Diagnostics, San Martino Policlinico Hospital - IRCCS for Oncology, University of Genoa, Genoa, Italyen
dc.identifier.affiliationResearch Group in Perioperative Medicine, Hospital Universitario y Politécnico la Fe, Valencia, Spainen
dc.identifier.affiliationLaboratory of Experimental Intensive Care and Anesthesiology (LEICA), Amsterdam University Medical Centers, location 'AMC', Amsterdam, the Netherlandsen
dc.identifier.affiliationNuffield Department of Medicine, University of Oxford, Oxford, UKen
dc.identifier.affiliationCardio-Pulmonary Department, Pulmonary Division, Faculdade de Medicina, Instituto doen
dc.identifier.affiliationCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spainen
dc.identifier.affiliationDepartment of Anesthesiology, Hospital Universitario y Politécnico la Fe, Valencia, Spainen
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35431038/en
dc.identifier.doi10.1016/j.bja.2022.02.039en
dc.type.contentTexten
dc.identifier.orcid0000-0003-1520-9387en
dc.identifier.pubmedid35431038
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
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