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https://dora.health.qld.gov.au/qldresearchjspui/handle/1/5791
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DC Field | Value | Language |
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dc.contributor.author | Franklin, Donna | - |
dc.contributor.author | Babl, Franz E. | - |
dc.contributor.author | George, Shane | - |
dc.contributor.author | Oakley, Ed | - |
dc.contributor.author | Borland, Meredith L. | - |
dc.contributor.author | Neutze, Jocelyn | - |
dc.contributor.author | Acworth, Jason | - |
dc.contributor.author | Craig, Simon | - |
dc.contributor.author | Jones, Mark | - |
dc.contributor.author | Gannon, Brenda | - |
dc.contributor.author | Shellshear, Deborah | - |
dc.contributor.author | McCay, Hamish | - |
dc.contributor.author | Wallace, Alexandra | - |
dc.contributor.author | Hoeppner, Tobias | - |
dc.contributor.author | Wildman, Mark | - |
dc.contributor.author | Mattes, Joerg | - |
dc.contributor.author | Pham, Trang M. T. | - |
dc.contributor.author | Miller, Letitia | - |
dc.contributor.author | Williams, Amanda | - |
dc.contributor.author | O'Brien, Sharon | - |
dc.contributor.author | Lawrence, Shirley | - |
dc.contributor.author | Bonisch, Megan | - |
dc.contributor.author | Gibbons, Kristen | - |
dc.contributor.author | Moloney, Susan | - |
dc.contributor.author | Waugh, John | - |
dc.contributor.author | Hobbins, Sue | - |
dc.contributor.author | Grew, Simon | - |
dc.contributor.author | Fahy, Rose | - |
dc.contributor.author | Dalziel, Stuart R. | - |
dc.contributor.author | Schibler, Andreas | - |
dc.date.accessioned | 2024-06-20T00:27:31Z | - |
dc.date.available | 2024-06-20T00:27:31Z | - |
dc.date.issued | 2023 | - |
dc.identifier.citation | JAMA, 2023 (329) 3 p.224-234 | en |
dc.identifier.uri | https://dora.health.qld.gov.au/qldresearchjspui/handle/1/5791 | - |
dc.description.abstract | Importance: Nasal high-flow oxygen therapy in infants with bronchiolitis and hypoxia has been shown to reduce the requirement to escalate care. The efficacy of high-flow oxygen therapy in children aged 1 to 4 years with acute hypoxemic respiratory failure without bronchiolitis is unknown.; Objective: To determine the effect of early high-flow oxygen therapy vs standard oxygen therapy in children with acute hypoxemic respiratory failure.; Design, Setting, and Participants: A multicenter, randomized clinical trial was conducted at 14 metropolitan and tertiary hospitals in Australia and New Zealand, including 1567 children aged 1 to 4 years (randomized between December 18, 2017, and March 18, 2020) requiring hospital admission for acute hypoxemic respiratory failure. The last participant follow-up was completed on March 22, 2020.; Interventions: Enrolled children were randomly allocated 1:1 to high-flow oxygen therapy (n = 753) or standard oxygen therapy (n = 764). The type of oxygen therapy could not be masked, but the investigators remained blinded until the outcome data were locked.; Main Outcomes and Measures: The primary outcome was length of hospital stay with the hypothesis that high-flow oxygen therapy reduces length of stay. There were 9 secondary outcomes, including length of oxygen therapy and admission to the intensive care unit. Children were analyzed according to their randomization group.; Results: Of the 1567 children who were randomized, 1517 (97%) were included in the primary analysis (median age, 1.9 years [IQR, 1.4-3.0 years]; 732 [46.7%] were female) and all children completed the trial. The length of hospital stay was significantly longer in the high-flow oxygen group with a median of 1.77 days (IQR, 1.03-2.80 days) vs 1.50 days (IQR, 0.85-2.44 days) in the standard oxygen group (adjusted hazard ratio, 0.83 [95% CI, 0.75-0.92]; P < .001). Of the 9 prespecified secondary outcomes, 4 showed no significant difference. The median length of oxygen therapy was 1.07 days (IQR, 0.50-2.06 days) in the high-flow oxygen group vs 0.75 days (IQR, 0.35-1.61 days) in the standard oxygen therapy group (adjusted hazard ratio, 0.78 [95% CI, 0.70-0.86]). In the high-flow oxygen group, there were 94 admissions (12.5%) to the intensive care unit compared with 53 admissions (6.9%) in the standard oxygen group (adjusted odds ratio, 1.93 [95% CI, 1.35-2.75]). There was only 1 death and it occurred in the high-flow oxygen group.; Conclusions and Relevance: Nasal high-flow oxygen used as the initial primary therapy in children aged 1 to 4 years with acute hypoxemic respiratory failure did not significantly reduce the length of hospital stay compared with standard oxygen therapy.; Trial Registration: anzctr.org.au Identifier: ACTRN12618000210279. | - |
dc.title | Effect of Early High-Flow Nasal Oxygen vs Standard Oxygen Therapy on Length of Hospital Stay in Hospitalized Children With Acute Hypoxemic Respiratory Failure: The PARIS-2 Randomized Clinical Trial | - |
dc.identifier.doi | 10.1001/jama.2022.21805 | - |
dc.relation.url | https://search.ebscohost.com/login.aspx?direct=true&AuthType=ip,athens&db=mdc&AN=36648469&site=ehost-live | - |
dc.identifier.journaltitle | JAMA | - |
dc.identifier.risid | 4411 | - |
dc.description.pages | 224-234 | - |
dc.description.volume | 329 | - |
dc.description.issue | 3 | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
Appears in Sites: | Children's Health Queensland Publications |
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