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dc.rights.licenseopenen_US
dc.contributor.authorRENESME, L.
dc.contributor.authorDUMAS DE LA ROQUE, E.
dc.contributor.authorGERMAIN, C.
dc.contributor.authorCHEVRIER, A.
dc.contributor.authorREBOLA, M.
dc.contributor.authorCRAMAREGEAS, S.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBENARD, Antoine
dc.contributor.authorELLEAU, C.
dc.contributor.authorTANDONNET, O.
dc.date.accessioned2021-03-18T08:28:51Z
dc.date.available2021-03-18T08:28:51Z
dc.date.issued2020-10
dc.identifier.issn1099-0496en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/26713
dc.description.abstractEnOBJECTIVE: To determine if nasal high-frequency percussive ventilation (nHFPV) to manage neonatal respiratory distress decreases the regional cerebral oxygen saturation (rScO(2) ) compared to nasal CPAP. STUDY DESIGN: A prospective, randomized, monocentric, open-label, non-inferiority crossover trial. Newborns of gestational age (GA) ≥ 33 weeks exhibiting persistent respiratory distress after 10 min of life were treated with nHFPV and nCPAP, in succession and in random order. The primary endpoint was the mean rScO(2) , as revealed by near-infrared spectroscopy (NIRS). RESULTS: Forty-nine newborns were randomized; the mean GA and birth weight were 36.4 ± 1.9 weeks and 2,718 ± 497 g. The mean rScO(2) difference during the last 5 min of each ventilation mode (nHFPV minus nCPAP) was -0.7 ± 5.4% (95% CI -2.25; 0.95%). CONCLUSION: In our study on newborns of GA ≥ 33 weeks treated for respiratory distress, cerebral oxygenation via nHFPV was not inferior to nCPAP. This article is protected by copyright. All rights reserved.
dc.language.isoENen_US
dc.title.enNasal high-frequency percussive ventilation vs nasal continuous positive airway pressure in newborn infants respiratory distress: A cross over clinical trial
dc.title.alternativePediatr Pulmonolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1002/ppul.24935en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed32609946en_US
bordeaux.journalPediatric Pulmonologyen_US
bordeaux.page2617-2623en_US
bordeaux.volume55en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - U1219en_US
bordeaux.issue10en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.teamPharmacoEpi-Drugsen_US
bordeaux.teamEMOSen_US
bordeaux.teamUSMRen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03172879
hal.version1
hal.date.transferred2021-03-18T08:28:54Z
hal.exporttrue
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