High-flow nasal cannula for stabilisation of very premature infants: A prospective observational study
Jazyk angličtina Země Norsko Médium print-electronic
Typ dokumentu časopisecké články, pozorovací studie
Grantová podpora
RVO-VFN64165
Všeobecná Fakultní Nemocnice v Praze
PubMed
39584601
PubMed Central
PMC11976121
DOI
10.1111/apa.17519
Knihovny.cz E-zdroje
- Klíčová slova
- continuous positive airway pressure, delivery room, high‐flow nasal cannula, positive pressure ventilation, very premature infant,
- MeSH
- kanyla * MeSH
- lidé MeSH
- novorozenci extrémně nezralí * MeSH
- novorozenec nedonošený MeSH
- novorozenec MeSH
- oxygenoterapie * přístrojové vybavení metody MeSH
- prospektivní studie MeSH
- studie proveditelnosti MeSH
- trvalý přetlak v dýchacích cestách MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- novorozenec MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- pozorovací studie MeSH
AIM: To assess the feasibility, safety and efficacy of using a high-flow nasal cannula (HFNC) for stabilising very preterm infants after birth. METHODS: A prospective observational study included preterm infants born at 28 + 0 to 31 + 6 weeks' gestation between February 2021 and December 2022 at the General University Hospital in Prague. Following delayed cord clamping, HFNC was administered at a flow rate of 8 L/min through the infants' nostrils. Criteria for switching to continuous positive airway pressure (CPAP) or positive pressure ventilation (PPV) included persistent bradycardia in the first few minutes or low saturation of oxygen (SpO2) after 5 min, respectively. RESULTS: Of the 65 infants enrolled in the study, 56 (86%) were successfully stabilised exclusively using HFNC while 7 (11%) required PPV. Additionally, 52 (80%) infants achieved SpO2 > 80% at 5 min, and 54 (83%) infants were successfully treated with HFNC within the first 3 h of life. CONCLUSION: The primary use of HFNC seems to be an appropriate alternative to CPAP for the stabilisation of very premature infants after birth and subsequent transfer to the NICU. A randomised trial comparing HFNC and CPAP in the delivery room will enable to answer the questions raised in this study.
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