2021
DOI: 10.1136/bmjopen-2020-045897
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Protocol for a randomised controlled trial comparing two CPAP levels to prevent extubation failure in extremely preterm infants

Abstract: IntroductionRespiratory distress syndrome is a complication of prematurity and extremely preterm infants born before 28 weeks’ gestation often require endotracheal intubation and mechanical ventilation. In this high-risk population, mechanical ventilation is associated with lung injury and contributes to bronchopulmonary dysplasia. Therefore, clinicians attempt to extubate infants as quickly and use non-invasive respiratory support such as nasal continuous positive airway pressure (CPAP) to facilitate the tran… Show more

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Cited by 7 publications
(2 citation statements)
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“…CPAP and early initiation of noninvasive ventilation should be explored in well-designed clinical trials given their promising results in preventing extubation failure. (38)(39)(40) This study provides important data on the use of RSS and OSI for early identification of moderate preterm infants at risk of NRS failure. However, there are several notable limitations.…”
Section: Manuscriptmentioning
confidence: 98%
“…CPAP and early initiation of noninvasive ventilation should be explored in well-designed clinical trials given their promising results in preventing extubation failure. (38)(39)(40) This study provides important data on the use of RSS and OSI for early identification of moderate preterm infants at risk of NRS failure. However, there are several notable limitations.…”
Section: Manuscriptmentioning
confidence: 98%
“…14 Further studies on the choice of initial postextubation pressures and settings on noninvasive modes, especially in relation to preextubation settings, are warranted such as the ongoing trial comparing postextubation CPAP levels of 10 vs. 7 cm H 2 O. 15…”
Section: Comparison To Previous Literaturementioning
confidence: 99%