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High-flow nasal cannula oxygen in children with bronchiolitis: A randomized controlled trial
Aykut Eşki1, Gökçen Kartal Öztürk2, Caner Turan3
1Division of Pediatric Pulmonology, Department of Pediatrics, Gazi Yaşargil Gynecology, Child Health, and Diseases Training and Research Hospital, University of Health Sciences, Diyarbakır, Turkey.
High-flow nasal cannula oxygen (HFNCO) significantly improved respiratory support in infants with bronchiolitis compared to low-flow oxygen (LFO). HFNCO led to faster normalization of heart rate, respiratory rate, and clinical scores, reducing treatment failure.
Area of Science:
- Pediatrics
- Respiratory Medicine
- Critical Care
Background:
- Bronchiolitis is a common respiratory infection in infants, often requiring oxygen therapy.
- Current treatments include low-flow oxygen (LFO), but enhanced respiratory support options are being explored.
Purpose of the Study:
- To compare the efficacy of high-flow nasal cannula oxygen (HFNCO) versus LFO in providing respiratory support for infants with moderate-to-severe bronchiolitis.
Main Methods:
- A prospective, randomized controlled trial involving 87 children aged 1-24 months with moderate-to-severe bronchiolitis.
- Participants received either LFO (6-10 L/min) or HFNCO (2 L/kg/min).
- Primary outcomes included time to normalization of heart rate (HR), respiratory rate (RR), and clinical respiratory score (CRS).
Main Results:
- HFNCO therapy resulted in significantly shorter times for HR and RR normalization (2.0h vs. 12.0h for HR; 4.0h vs. 24.0h for RR) and CRS improvement (2.0h vs. 4.0h) compared to LFO.
- Duration of oxygen requirement and treatment failure rates were significantly lower in the HFNCO group (19.0h vs. 29.5h; 3% vs. 21%).
- No significant differences were observed in length of stay or adverse events between the groups.
Conclusions:
- HFNCO offers enhanced respiratory support for infants with bronchiolitis, leading to quicker physiological improvements and reduced treatment failure compared to LFO.
- Further comprehensive studies are warranted to fully assess the clinical efficacy of HFNCO therapy in this population.
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