Please use this identifier to cite or link to this item:
https://hdl.handle.net/11055/566
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DC Field | Value | Language |
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dc.contributor.author | Myles, PS | en_US |
dc.contributor.author | Bellomo, R | en_US |
dc.contributor.author | Corcoran, T | en_US |
dc.contributor.author | Forbes, A | en_US |
dc.contributor.author | Peyton, P | en_US |
dc.contributor.author | Story, D | en_US |
dc.contributor.author | Christophi, C | en_US |
dc.contributor.author | Leslie, K | en_US |
dc.contributor.author | McGuinness, S | en_US |
dc.contributor.author | Parke, R | en_US |
dc.contributor.author | Serpell, J | en_US |
dc.contributor.author | Chan, MTV | en_US |
dc.contributor.author | Painter, T | en_US |
dc.contributor.author | McCluskey, S | en_US |
dc.contributor.author | Minto, G | en_US |
dc.contributor.author | Wallace, S | en_US |
dc.contributor.author | ANZCA Clinical Trials Network | en_US |
dc.contributor.author | NZ Intensive Care Society Clinical Trials Group | en_US |
dc.date | 2018-05-10 | - |
dc.date.accessioned | 2018-05-10T06:04:03Z | - |
dc.date.available | 2018-05-10T06:04:03Z | - |
dc.date.issued | 2018-06-14 | en_US |
dc.identifier.citation | 2018; doi:10.1056/NEJMoa1801601 | en_US |
dc.identifier.issn | 0028-4793 | en_US |
dc.identifier.uri | http://hdl.handle.net/11055/566 | - |
dc.description.abstract | BACKGROUND Guidelines to promote the early recovery of patients undergoing major surgery recommend a restrictive intravenous-fluid strategy for abdominal surgery. However, the supporting evidence is limited, and there is concern about impaired organ perfusion. METHODS In a pragmatic, international trial, we randomly assigned 3000 patients who had an increased risk of complications while undergoing major abdominal surgery to receive a restrictive or liberal intravenous-fluid regimen during and up to 24 hours after surgery. The primary outcome was disability-free survival at 1 year. Key secondary outcomes were acute kidney injury at 30 days, renal-replacement therapy at 90 days, and a composite of septic complications, surgical-site infection, or death. RESULTS During and up to 24 hours after surgery, 1490 patients in the restrictive fluid group had a median intravenous-fluid intake of 3.7 liters (interquartile range, 2.9 to 4.9), as compared with 6.1 liters (interquartile range, 5.0 to 7.4) in 1493 patients in the liberal fluid group (P<0.001). The rate of disability-free survival at 1 year was 81.9% in the restrictive fluid group and 82.3% in the liberal fluid group (hazard ratio for death or disability, 1.05; 95% confidence interval, 0.88 to 1.24; P=0.61). The rate of acute kidney injury was 8.6% in the restrictive fluid group and 5.0% in the liberal fluid group (P<0.001). The rate of septic complications or death was 21.8% in the restrictive fluid group and 19.8% in the liberal fluid group (P=0.19); rates of surgical-site infection (16.5% vs. 13.6%, P=0.02) and renal-replacement therapy (0.9% vs. 0.3%, P=0.048) were higher in the restrictive fluid group, but the between-group difference was not significant after adjustment for multiple testing. CONCLUSIONS Among patients at increased risk for complications during major abdominal surgery, a restrictive fluid regimen was not associated with a higher rate of disability-free survival than a liberal fluid regimen and was associated with a higher rate of acute kidney injury. (Funded by the Australian National Health and Medical Research Council and others; RELIEF ClinicalTrials.gov number, NCT01424150.) | en_US |
dc.subject | major surgery | en_US |
dc.subject | perfusion | en_US |
dc.subject | restrictive fluid regimen | en_US |
dc.subject | RELIEF | en_US |
dc.title | Restrictive versus liberal fluid therapy for major abdominal surgery | en_US |
dc.type | Journal Article | en_US |
dc.type.content | Text | en_US |
dc.identifier.journaltitle | The New England Journal of Medicine | en_US |
dc.identifier.doi | 10.1056/NEJMoa1801601 | en_US |
dc.description.affiliates | Australian and New Zealand College of Anaesthetists | en_US |
dc.description.affiliates | Alfred Hospital | en_US |
dc.description.affiliates | Monash University | en_US |
dc.description.affiliates | University of Melbourne | en_US |
dc.description.affiliates | Austin Hospital, Heidelberg | en_US |
dc.description.affiliates | Royal Perth Hospital | en_US |
dc.description.affiliates | University of Western Australia, Perth | en_US |
dc.description.affiliates | Royal Melbourne Hospital | en_US |
dc.description.affiliates | Royal Adelaide Hospital | en_US |
dc.description.affiliates | Discipline of Acute Care Medicine, University of Adelaide | en_US |
dc.description.affiliates | Auckland City Hospital | en_US |
dc.description.affiliates | Medical Research Institute of New Zealand | en_US |
dc.description.affiliates | Chinese University of Hong Kong | en_US |
dc.description.affiliates | University Health Network, Toronto | en_US |
dc.description.affiliates | Derriford Hospital, Plymouth, United Kingdom | en_US |
dc.description.pubmeduri | https://www.nejm.org/doi/full/10.1056/NEJMoa1801601 | en_US |
dc.type.studyortrial | Random Allocation | en_US |
dc.identifier.studyname | NCT01424150 | en_US |
dc.ispartof.anzcaresearchfoundation | Yes | en_US |
item.openairetype | Journal Article | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
Appears in Collections: | Scholarly and Clinical |
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