Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34416
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dc.contributor.authorSerpa Neto, Ary-
dc.contributor.authorTomlinson, George-
dc.contributor.authorSahetya, Sarina K-
dc.contributor.authorBall, Lorenzo-
dc.contributor.authorNichol, Alistair D-
dc.contributor.authorHodgson, Carol-
dc.contributor.authorCavalcanti, Alexandre Biasi-
dc.contributor.authorBriel, Matthias-
dc.contributor.authorde Abreu, Marcelo Gama-
dc.contributor.authorPelosi, Paolo-
dc.contributor.authorSchultz, Marcus J-
dc.contributor.authorGoligher, Ewan C-
dc.date2023-
dc.date.accessioned2023-12-13T05:24:45Z-
dc.date.available2023-12-13T05:24:45Z-
dc.date.issued2021-06-
dc.identifier.citationCritical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicine 2021-06; 23(2)en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34416-
dc.description.abstractObjective: Benefit or harm of higher positive end expiratory pressure (PEEP) for acute respiratory distress syndrome (ARDS) is controversial. We aimed to assess the impact of higher levels of PEEP in patients with ARDS under a Bayesian framework. Design: Systematic review and Bayesian meta-analysis of randomised clinical trials comparing higher to lower PEEP in adult patients with ARDS. Data sources: MEDLINE, EMBASE and Cochrane Central Register of Controlled Trials from 1996 to 1 March 2020. Review methods: We extracted data from high quality randomised clinical trials comparing higher to lower levels of PEEP in adult patients, using low tidal volume in both arms, and conducted a Bayesian meta-analysis using aggregate data from these studies. Results: Eight clinical trials including 3703 patients (n = 1833 for higher PEEP, n = 1870 for lower PEEP) were included. Under a minimally informative prior, the posterior probability of benefit with higher PEEP was 65% (relative risk, 0.97 [95% credible interval, 0.78-1.14]). In patients with moderate-to- severe ARDS, the posterior probability of benefit with higher PEEP was 77% (relative risk, 0.94 [95% credible interval, 0.77-1.13]). Down-weighting studies that employed a maximum recruitment strategy by 100% increased the posterior probability of benefit to 92% under a minimally informative prior. Conclusions: The probability of benefit or harm from routine use of higher PEEP for patients with ARDS ranges from 27% to 86%, and from 14% to 73% depending on one's prior, suggesting continued uncertainty and equipoise regarding the benefit of PEEP If data from trials using a maximum recruitment strategy is discounted to some extent because of uncertainty over the appropriateness of this approach, the available evidence suggests that higher PEEP could be beneficial for moderate-to-severe ARDS. However, well powered randomised clinical trials are needed to confirm these findings.en_US
dc.language.isoeng-
dc.titleHigher PEEP for acute respiratory distress syndrome: a Bayesian meta-analysis of randomised clinical trials.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleCritical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicineen_US
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, VIC, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, University Health Network, Toronto, Ont, Canada.;Toronto General Hospital Research Institute, University of Toronto, Toronto, Ont, Canada.;Institute for Health Policy, Management and Evaluation, University of Toronto, Toronto, Ont, Canada.en_US
dc.identifier.affiliationDivision of Pulmonary and Critical Care Medicine, School of Medicine, Johns Hopkins University, Baltimore, Md, USA.en_US
dc.identifier.affiliationDepartment of Surgical Sciences and Integrated Diagnostics, San Martino Policlinico Hospital, IRCCS for Oncology, University of Genoa, Genoa, Italy.en_US
dc.identifier.affiliationIntensive Care Unit, The Alfred Hospital, Melbourne, VIC, Australia.;University College Dublin Clinical Research Centre, St Vincent's University Hospital, Dublin, Ireland.en_US
dc.identifier.affiliationResearch Institute, Hospital do Coragäo, Säo Paulo, Brazil.en_US
dc.identifier.affiliationDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ont, Canada.;Department of Clinical Research, Basel Institute for Clinical Epidemiology and Biostatistics, University of Basel and University Hospital Basel, Basel, Switzerland.en_US
dc.identifier.affiliationPulmonary Engineering Group, Department of Anesthesiology and Intensive Care Medicine, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.en_US
dc.identifier.affiliationDepartment of Surgical Sciences and Integrated Diagnostics, San Martino Policlinico Hospital, IRCCS for Oncology, University of Genoa, Genoa, Italy.en_US
dc.identifier.affiliationDepartment of Intensive Care, Amsterdam University Medical Centers, Academic Medical Center, Amsterdam, The Netherlands.;Laboratory of Experimental Intensive Care and Anesthesiology, Amsterdam University Medical Centers, Academic Medical Center, Amsterdam, The Netherlands.;Nuffield Department of Medicine, University of Oxford, Oxford, UK.;Mahidol Oxford Research Unit, Mahidol University, Bangkok, Thailand.en_US
dc.identifier.affiliationDepartment of Medicine, University Health Network, Toronto, Ont, Canada.;Toronto General Hospital Research Institute, University of Toronto, Toronto, Ont, Canada.;Interdepartmental Division of Critical Care Medicine, University of Toronto, Toronto, Ont, Canada.en_US
dc.identifier.affiliationData Analytics Research and Evaluation (DARE) Centreen_US
dc.identifier.doi10.51893/2021.2.oa4en_US
dc.type.contentTexten_US
dc.identifier.pubmedid38045516-
dc.description.volume23-
dc.description.issue2-
dc.description.startpage171-
dc.description.endpage182-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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