Respiratory Distress Syndrome, Newborn Clinical Trial
Official title:
Patient Comfort During High Flow Nasal Cannula (HFNC)Versus Nasal Continuous Airway Pressure (CPAP): a Cross Over Randomised Trial
Preterm children are at increased risk for developing lung disease due to immature lungs.
Non-invasive ventilation (NIV) support is increasingly used as treatment. Nasal continuous
positive airway pressure (nCPAP) is the most common NIV-mode. Recently, high flow nasal
cannulas (HFNC) have become an alternative NIV-mode. Both nCPAP and HFNC provide increased
pressure in the airways aiming to keep the lungs open. With nCPAP it is common to use short
binasal prongs that fill the nostrils completely and are pressed tightly over the nose. With
HFNC oxygen/air is administered via two small, thin cannulas located just inside the
nostrils, but the nostrils are not blocked.
The aim of this study is to compare patient comfort in premature infants treated with nCPAP
and HFNC. The investigators hypothesis is that HFNC increases patient comfort.
The study is a randomized cross over study (2 x 24 hours). Children eligible for inclusion
should be born before 34 weeks of gestation and have moderate respiratory distress, thus be
"in need" of nCPAP. During the study period (48 hours) the investigators will consider how
the child tolerates treatment with nCPAP versus HFNC. Primary outcome is patient comfort
assessed with the EDIN-score (Neonatal pain and comfort score). Secondary outcomes are
stress hormone response (cortisol in saliva), surrounding noise and parental satisfaction.
The child's breathing pattern will be carefully monitored. The study involves no extra
painful investigations.
The investigators plan to recruit 20 patients.
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