TY - JOUR
T1 - Effect of Early High-Flow Nasal Oxygen vs Standard Oxygen Therapy on Length of Hospital Stay in Hospitalized Children with Acute Hypoxemic Respiratory Failure
T2 - The PARIS-2 Randomized Clinical Trial
AU - Franklin, Donna
AU - Babl, Franz E.
AU - George, Shane
AU - Oakley, Ed
AU - Borland, Meredith L.
AU - Neutze, Jocelyn
AU - Acworth, Jason
AU - Craig, Simon
AU - Jones, Mark
AU - Gannon, Brenda
AU - Shellshear, Deborah
AU - McCay, Hamish
AU - Wallace, Alexandra
AU - Hoeppner, Tobias
AU - Wildman, Mark
AU - Mattes, Joerg
AU - Pham, Trang M.T.
AU - Miller, Letitia
AU - Williams, Amanda
AU - O'Brien, Sharon
AU - Lawrence, Shirley
AU - Bonisch, Megan
AU - Gibbons, Kristen
AU - Moloney, Susan
AU - Waugh, John
AU - Hobbins, Sue
AU - Grew, Simon
AU - Fahy, Rose
AU - Dalziel, Stuart R.
AU - Schibler, Andreas
N1 - Funding Information:
Funding/Support: This research was supported by grant 1139903 from the National Health and Medical Research Council in Australia and funding from the Thrasher Research Fund in the US , the Children’s Hospital Foundation in Australia , the Perth Children’s Hospital Foundation in Australia , and the Emergency Medicine Foundation in Australia . The OptiFlow equipment and consumables were supplied free of charge for this study by Fisher & Paykel Healthcare .
Funding Information:
Conflict of Interest Disclosures: Dr Franklin reported receiving grants from the National Health and Medical Research Council (NHMRC) in Australia, the Thrasher Research Fund, the Children’s Health Foundation, and the Emergency Medicine Foundation; receiving travel reimbursement from Fisher & Paykel Healthcare; and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Babl reported receiving grants from the NHMRC. Dr George reported receiving grants from the NHMRC, the Thrasher Research Fund, and the Emergency Medicine Foundation and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Oakley reported receiving grants from the NHMRC and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Neutze reported receiving grants from the NHMRC and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Acworth reported receiving grants from the NHMRC and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Craig reported receiving grants from the NHMRC. Dr McCay reported receiving grants from the NHMRC, the Thrasher Research Fund, the Children’s Health Foundation, and the Emergency Medicine Foundation and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Wallace reported receiving grants from the NHMRC and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Hoeppner reported receiving grants from the Children’s Hospital Foundation and the NHMRC and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Wildman reported receiving grants from the NHMRC and the Education and Research Trust Account and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Mattes reported receiving grants from the NHMRC. Ms Pham reported receiving grants from the NHMRC and receiving nonfinancial support from Fisher & Paykel Healthcare Equipment. Ms O’Brien reported receiving grants from the NHMRC and Children’s Hospital Foundation and receiving nonfinancial support from Fisher & Paykel Healthcare. Ms Lawrence reported receiving grants from the NHMRC and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Gibbons reported receiving grants from the NHMRC and the Thrasher Research Fund and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Moloney reported receiving grants from the NHMRC and Fisher & Paykel Healthcare. Dr Waugh reported receiving grants from the NHMRC, the Thrasher Research Fund, the Children’s Health Foundation, and the Emergency Medicine Foundation and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Grew reported receiving grants from the NHMRC and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Fahy reported receiving grants from the NHMRC and receiving nonfinancial support from Fisher & Paykel Healthcare. Dr Dalziel reported receiving grants from the NHMRC and Cure Kids New Zealand; receiving nonfinancial support from Fisher & Paykel Healthcare; and receiving travel reimbursement from Fisher & Paykel Healthcare. Dr Schibler reported receiving grants from the NHMRC, the Children’s Health Foundation, the Thrasher Research Fund, and the Emergency Medicine Foundation; receiving nonfinancial support from Fisher & Paykel Healthcare; receiving travel reimbursement from Fisher & Paykel Healthcare; and receiving consulting fees from Fisher & Paykel Healthcare. No other disclosures were reported.
Publisher Copyright:
© 2023 American Medical Association. All rights reserved.
PY - 2023/1/17
Y1 - 2023/1/17
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85146484286&partnerID=8YFLogxK
U2 - 10.1001/jama.2022.21805
DO - 10.1001/jama.2022.21805
M3 - Article
C2 - 36648469
AN - SCOPUS:85146484286
SN - 0098-7484
VL - 329
SP - 224
EP - 234
JO - JAMA: Journal of the American Medical Association
JF - JAMA: Journal of the American Medical Association
IS - 3
ER -