Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/24866
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dc.contributor.authorKaralapillai, Dharshi-
dc.contributor.authorWeinberg, Laurence-
dc.contributor.authorPeyton, Philip-
dc.contributor.authorEllard, Louise-
dc.contributor.authorHu, Raymond-
dc.contributor.authorPearce, Brett-
dc.contributor.authorTan, Chong O-
dc.contributor.authorStory, David-
dc.contributor.authorO'Donnell, Mark-
dc.contributor.authorHamilton, Patrick-
dc.contributor.authorOughton, Chad-
dc.contributor.authorGaltieri, Jonathan-
dc.contributor.authorWilson, Anthony-
dc.contributor.authorSerpa Neto, Ary-
dc.contributor.authorEastwood, Glenn-
dc.contributor.authorBellomo, Rinaldo-
dc.contributor.authorJones, Daryl A-
dc.date2020-09-01-
dc.date.accessioned2020-09-28T23:22:21Z-
dc.date.available2020-09-28T23:22:21Z-
dc.date.issued2020-09-01-
dc.identifier.citationJAMA 2020; 324(9): 848-858en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/24866-
dc.description.abstractIn patients who undergo mechanical ventilation during surgery, the ideal tidal volume is unclear. To determine whether low-tidal-volume ventilation compared with conventional ventilation during major surgery decreases postoperative pulmonary complications. Single-center, assessor-blinded, randomized clinical trial of 1236 patients older than 40 years undergoing major noncardiothoracic, nonintracranial surgery under general anesthesia lasting more than 2 hours in a tertiary hospital in Melbourne, Australia, from February 2015 to February 2019. The last date of follow-up was February 17, 2019. Patients were randomized to receive a tidal volume of 6 mL/kg predicted body weight (n = 614; low tidal volume group) or a tidal volume of 10 mL/kg predicted body weight (n = 592; conventional tidal volume group). All patients received positive end-expiratory pressure (PEEP) at 5 cm H2O. The primary outcome was a composite of postoperative pulmonary complications within the first 7 postoperative days, including pneumonia, bronchospasm, atelectasis, pulmonary congestion, respiratory failure, pleural effusion, pneumothorax, or unplanned requirement for postoperative invasive or noninvasive ventilation. Secondary outcomes were postoperative pulmonary complications including development of pulmonary embolism, acute respiratory distress syndrome, systemic inflammatory response syndrome, sepsis, acute kidney injury, wound infection (superficial and deep), rate of intraoperative need for vasopressor, incidence of unplanned intensive care unit admission, rate of need for rapid response team call, intensive care unit length of stay, hospital length of stay, and in-hospital mortality. Among 1236 patients who were randomized, 1206 (98.9%) completed the trial (mean age, 63.5 years; 494 [40.9%] women; 681 [56.4%] undergoing abdominal surgery). The primary outcome occurred in 231 of 608 patients (38%) in the low tidal volume group compared with 232 of 590 patients (39%) in the conventional tidal volume group (difference, -1.3% [95% CI, -6.8% to 4.2%]; risk ratio, 0.97 [95% CI, 0.84-1.11]; P = .64). There were no significant differences in any of the secondary outcomes. Among adult patients undergoing major surgery, intraoperative ventilation with low tidal volume compared with conventional tidal volume, with PEEP applied equally between groups, did not significantly reduce pulmonary complications within the first 7 postoperative days. ANZCTR Identifier: ACTRN12614000790640.en
dc.language.isoeng
dc.titleEffect of Intraoperative Low Tidal Volume vs Conventional Tidal Volume on Postoperative Pulmonary Complications in Patients Undergoing Major Surgery: A Randomized Clinical Trial.en
dc.typeJournal Articleen
dc.identifier.journaltitleJAMAen
dc.identifier.affiliationAnaesthesiaen
dc.identifier.affiliationIntensive Careen
dc.identifier.affiliationAustralian and New Zealand Intensive Care Research Centre, School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationData Analytics Research and Evaluation (DARE) Centreen
dc.identifier.affiliationDepartment of Anesthesia, The University of Melbourne, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Critical Care Medicine, Hospital Israelita Albert Einstein, São Paulo, Brazilen
dc.identifier.affiliationDepartment of Intensive Care, Amsterdam University Medical Centres, Location AMC, Amsterdam, the Netherlandsen
dc.identifier.doi10.1001/jama.2020.12866en
dc.type.contentTexten
dc.identifier.pubmedid32870298
local.name.researcherBellomo, Rinaldo
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.deptAnaesthesia-
crisitem.author.deptAnaesthesia-
crisitem.author.deptAnaesthesia-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptAnaesthesia-
crisitem.author.deptAnaesthesia-
crisitem.author.deptAnaesthesia-
crisitem.author.deptAnaesthesia-
crisitem.author.deptAnaesthesia-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptIntensive Care-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptIntensive Care-
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