Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/28729
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dc.contributor.authorFerrando, Carlos-
dc.contributor.authorLibrero, Julian-
dc.contributor.authorTusman, Gerardo-
dc.contributor.authorSerpa Neto, Ary-
dc.contributor.authorVillar, Jesús-
dc.contributor.authorBelda, Francisco J-
dc.contributor.authorCosta, Eduardo-
dc.contributor.authorAmato, Marcelo B P-
dc.contributor.authorSuarez-Sipmann, Fernando-
dc.date2021-09-22-
dc.date.accessioned2022-02-01T04:45:00Z-
dc.date.available2022-02-01T04:45:00Z-
dc.date.issued2022-01-
dc.identifier.citationActa Anaesthesiologica Scandinavica 2022; 66(1): 30-39en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/28729-
dc.description.abstractThe preventive role of an intraoperative recruitment maneuver plus open lung approach (RM + OLA) ventilation on postoperative pulmonary complications (PPC) remains unclear. We aimed at investigating whether an intraoperative open lung condition reduces the risk of developing a composite of PPCs. Post hoc analysis of two randomized controlled trials including patients undergoing abdominal surgery. Patients were classified according to the intraoperative lung condition as "open" (OL) or "non-open" (NOL) if PaO2 /FIO2 ratio was ≥ or <400 mmHg, respectively. We used a multivariable logistic regression model that included potential confounders selected with directed acyclic graphs (DAG) using Dagitty software built with variables that were considered clinically relevant based on biological mechanism or evidence from previously published data. PPCs included severe acute respiratory failure, acute respiratory distress syndrome, and pneumonia. A total of 1480 patients were included in the final analysis, with 718 (49%) classified as OL. The rate of severe PPCs during the first seven postoperative days was 6.0% (7.9% in the NOL and 4.4% in the OL group, p = .007). OL was independently associated with a lower risk for severe PPCs during the first 7 and 30 postoperative days [odds ratio of 0.58 (95% CI 0.34-0.99, p = .04) and 0.56 (95% CI 0.34-0.94, p = .03), respectively]. An intraoperative open lung condition was associated with a reduced risk of developing severe PPCs in intermediate-to-high risk patients undergoing abdominal surgery. Registered at clinicaltrials.gov NCT02158923 (iPROVE), NCT02776046 (iPROVE-O2).en
dc.language.isoeng-
dc.subjectintraoperativeen
dc.subjectopen lungen
dc.subjectpositive end-expiratory pressureen
dc.subjectpostoperative pulmonary complicationsen
dc.subjectrecruitment maneuversen
dc.titleIntraoperative open lung condition and postoperative pulmonary complications. A secondary analysis of iPROVE and iPROVE-O2 trials.en
dc.typeJournal Articleen
dc.identifier.journaltitleActa Anaesthesiologica Scandinavicaen
dc.identifier.affiliationIntensive Careen
dc.identifier.affiliationAustralian and New Zealand Intensive Care-Research Centre (ANZIC-RC), Monash University, Melbourne, Vic., Australiaen
dc.identifier.affiliationMelbourne Medical School, University of Melbourne, Melbourne, Vic., Australiaen
dc.identifier.affiliationDepartment of Intensive Care, Hospital Universitario La Princesa, Madrid, Spainen
dc.identifier.affiliationNavarrabiomed, Complejo Hospitalario de Navarra, UPNA, REDISSEC (Red de Investigación en Servicios de Salud), La Palma de Cervelló, Spainen
dc.identifier.affiliationMultidisciplinary Organ Dysfunction Evaluation Research Network, Research Unit, Hospital Universitario Dr. Negrín, Las Palmas de Gran Canaria, Spainen
dc.identifier.affiliationKeenan Research Center for Biomedical Science at the Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canadaen
dc.identifier.affiliationCardio-Pulmonary Department, Pulmonary Division, Heart Institute (Incor), University of São Paulo, Sao Paulo, Brazilen
dc.identifier.affiliationResearch and Education Institute, Hospital Sirio-Libanês, Sao Paulo, Brazilen
dc.identifier.affiliationDepartment of Surgical Sciences, Hedenstierna Laboratory, Uppsala University Hospital, Uppsala, Swedenen
dc.identifier.affiliationDepartment of Critical Care Medicine, Hospital Israelita Albert Einstein, Sao Paulo, Brazilen
dc.identifier.affiliationDepartment of Anesthesiology and Critical Care, Hospital Clínic, Institut D'investigació August Pi i Sunyer, Barcelona, Spainen
dc.identifier.affiliationCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spainen
dc.identifier.affiliationDepartment of Anesthesiology, Hospital Privado de Comunidad, Mar de Plata, Argentinaen
dc.identifier.affiliationDepartment of Critical Care Medicine, Hospital Israelita Albert Einstein, Sao Paulo, Brazilen
dc.identifier.affiliationCardio-Pulmonary Department, Pulmonary Division, Heart Institute (Incor), University of São Paulo, Sao Paulo, Brazilen
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/34460936/en
dc.identifier.doi10.1111/aas.13979en
dc.type.contentTexten
dc.identifier.orcid0000-0002-1907-5323en
dc.identifier.orcid0000-0003-1520-9387en
dc.identifier.pubmedid34460936-
local.name.researcherSerpa Neto, Ary
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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