Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/46949
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dc.contributor.authorLo S.C.-Y.-
dc.contributor.authorBhatia R.-
dc.contributor.authorRoberts C.T.-
dc.date.accessioned2022-04-06T01:57:46Z-
dc.date.available2022-04-06T01:57:46Z-
dc.date.copyright2021-
dc.date.issued2022-02-12en
dc.identifier.citationNeonatology. 118(5) (pp 578-585), 2021. Date of Publication: 01 Oct 2021.-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/46949-
dc.description.abstractIntroduction: Exposure to mechanical ventilation (MV) is a risk factor for bronchopulmonary dysplasia (BPD) in very preterm infants (VPTIs). We assessed the impact of a quality improvement (QI) bundle in VPTIs (<32 week gestation) on exposure to MV. Method(s): We introduced a QI bundle consisting of deferred cord clamping (DCC), nasal bubble continuous positive airway pressure (bCPAP) in the delivery room (DR), and minimally invasive surfactant therapy (MIST). We compared respiratory outcomes and neonatal morbidity in historical pre-QI (July-December 2017) and prospective post-QI (February-July 2019) cohorts (QICs) of VPTIs. We pre-specified an adjusted analysis to account for the effects of gestational age, sex, antenatal steroids, and any demographic data that significantly differed between cohorts. Result(s): The pre-QI and post-QICs included 87 and 98 VPTIs, respectively. The post-QIC had decreased rates of MV in the DR (adjusted odds ratio [aOR] 0.26, 95% confidence interval [CI] 0.09-0.71), in the first 72 h of life (aOR 0.27, 95% CI 0.11-0.62) and during admission (aOR 0.28, 95% CI 0.12-0.66). Rates of BPD, combined BPD/death, and BPD severity were similar. The post-QIC was less likely to be discharged with home oxygen (aOR 0.27, 95% CI 0.08-0.91). Necrotising enterocolitis grade >=2 increased (aOR 19.01, 95% CI 1.93-188.6) in the post-QIC. Conclusion(s): In this rapid-cycle QI study, implementation of a QI bundle consisting of DCC, early nasal bCPAP, and MIST in VPTIs was associated with reduced rates of MV in the DR, in the first 72 h of life and during admission, and reduced need for home oxygen.Copyright © 2021-
dc.publisherS. Karger AG-
dc.relation.ispartofNeonatology-
dc.subject.meshartificial ventilation-
dc.subject.meshassisted ventilation-
dc.subject.meshbubble continuous positive airway pressure-
dc.subject.meshdelayed cord clamping-
dc.subject.meshdelivery room-
dc.subject.meshdemographics-
dc.subject.meshgestational age-
dc.subject.meshhome care-
dc.subject.meshhospital admission-
dc.subject.meshhospital discharge-
dc.subject.meshhyperthermia-
dc.subject.meshhypothermia-
dc.subject.meshlung dysplasia-
dc.subject.meshminimally invasive procedure-
dc.subject.meshnecrotizing enterocolitis-
dc.subject.meshnewborn noninvasive ventilation-
dc.subject.meshoxygen consumption-
dc.subject.meshoxygen therapy-
dc.subject.meshpositive pressure ventilation-
dc.subject.meshprematurity-
dc.subject.meshprenatal care-
dc.subject.meshquality improvement study-
dc.subject.meshrespiration control-
dc.subject.meshresuscitation-
dc.subject.meshtotal quality management-
dc.subject.meshcaffeine-
dc.subject.meshepinephrine/pv [Special Situation for Pharmacovigilance]-
dc.subject.meshlung surfactant/pv [Special Situation for Pharmacovigilance]-
dc.subject.meshmagnesium sulfate-
dc.subject.meshoxygen-
dc.subject.meshsteroid/pv [Special Situation for Pharmacovigilance]-
dc.subject.meshsurfactant-
dc.subject.meshendotracheal tube-
dc.subject.meshface mask-
dc.subject.meshresuscitator-
dc.subject.meshtransport ventilator-
dc.subject.meshminimally invasive surfactant therapy-
dc.titleIntroduction of a quality improvement bundle is associated with reduced exposure to mechanical ventilation in very preterm infants.-
dc.typeArticle-
dc.identifier.affiliationPaediatric - Neonatal (Monash Newborn)-
dc.identifier.affiliationMonash University - School of Clinical Sciences at Monash Health-
dc.type.studyortrialObservational study (cohort, case-control, cross sectional, or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=https://dx.doi.org/10.1159/000518392-
dc.publisher.placeSwitzerland-
dc.identifier.pubmedid34515183 [https://www.ncbi.nlm.nih.gov/pubmed/?term=34515183]-
dc.identifier.institution(Lo, Bhatia, Roberts) Department of Paediatrics, School of Clinical Sciences at Monash Health, Monash University, Melbourne, VIC, Australia-
dc.identifier.institution(Bhatia, Roberts) Monash Newborn, Monash Children's Hospital, Melbourne, VIC, Australia-
dc.identifier.institution(Roberts) The Ritchie Centre, Hudson Institute of Medical Research, Melbourne, VIC, Australia-
dc.identifier.affiliationmh(Lo, Bhatia, Roberts) Department of Paediatrics, School of Clinical Sciences at Monash Health, Monash University, Melbourne, VIC, Australia-
dc.identifier.affiliationmh(Bhatia, Roberts) Monash Newborn, Monash Children's Hospital, Melbourne, VIC, Australia-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptPaediatric - Neonatal (Monash Newborn)-
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