Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/27457
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dc.contributor.authorDavis P.G.en
dc.contributor.authorManley B.J.en
dc.contributor.authorKamlin C.O.F.en
dc.contributor.authorGreen E.A.en
dc.contributor.authorBhatia R.en
dc.contributor.authorHalibullah I.en
dc.contributor.authorRoberts C.T.en
dc.date.accessioned2021-05-14T09:14:34Zen
dc.date.available2021-05-14T09:14:34Zen
dc.date.copyright2021en
dc.date.created20210204en
dc.date.issued2021-02-04en
dc.identifier.citationJournal of Pediatrics. 229 (pp 141-146), 2021. Date of Publication: February 2021.en
dc.identifier.issn0022-3476en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/27457en
dc.description.abstractObjective: To assess the procedural and clinical outcomes associated with the introduction of minimally invasive surfactant therapy (MIST) into standard care at 2 tertiary Australian neonatal intensive care units. Study design: A prospective audit was designed before the introduction of MIST in 2018, with data collected over a period of 18 months. Procedural data were completed by the clinical team performing MIST, including clinical observations, medication use, and adverse events. The audit team collected demographic data and subsequent clinical outcomes from medical records. Result(s): There were 135 MIST procedures recorded in 122 infants. For the included infants, the median gestation was 302/7 weeks (IQR, 276/7 to 322/7 weeks) and birth weight was 1439 g (IQR, 982-1958 g). During the MIST procedure, desaturation to a peripheral oxygen saturation of <80% was common, occurring in 75.2% of procedures. Other adverse events included need for positive pressure ventilation (10.6%) and bradycardia <100 beats per minute (13.3%). The use of atropine premedication was associated with a significantly lower incidence of bradycardia: 8.6% vs 52.9% (P < .01). Senior clinicians demonstrated higher rates of procedural success. The majority of infants (63.9%) treated with MIST did not require subsequent intubation and mechanical ventilation. Conclusion(s): MIST can be successfully introduced in neonatal units with limited experience of this technique. The use of atropine premedication decreases the incidence of bradycardia during the procedure. Success rates can be optimized by limiting MIST to clinicians with greater competence in endotracheal intubation.Copyright © 2020 Elsevier Inc.en
dc.languageEnglishen
dc.languageenen
dc.publisherMosby Inc.en
dc.relation.ispartofJournal of Pediatricsen
dc.titleOutcomes after Introduction of Minimally Invasive Surfactant Therapy in Two Australian Tertiary Neonatal Units.en
dc.typeArticleen
dc.type.studyortrialObservational study (cohort, case-control, cross sectional or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.jpeds.2020.10.025en
dc.publisher.placeUnited Statesen
dc.identifier.pubmedid33068569 [http://www.ncbi.nlm.nih.gov/pubmed/?term=33068569]en
dc.identifier.source2010053316en
dc.identifier.institution(Roberts, Bhatia, Green) Monash Newborn, Monash Children's Hospital, Clayton, Victoria, Australia (Roberts, Bhatia) Department of Paediatrics, Monash University, Clayton, Victoria, Australia (Roberts) The Ritchie Centre, Hudson Institute of Medical Research, Clayton, Victoria, Australia (Halibullah, Kamlin, Davis, Manley) Newborn Research Centre and Neonatal Services, The Royal Women's Hospital, Parkville, Victoria, Australia (Kamlin, Davis, Manley) Department of Obstetrics and Gynecology, The University of Melbourne, Parkville, Victoria, Australia (Kamlin, Davis, Manley) Clinical Sciences, Murdoch Children's Research Institute, Parkville, Victoria, Australiaen
dc.description.addressC.T. Roberts, Monash Children's Hospital, 246 Clayton Road, Clayton, Victoria 3168, Australia. E-mail: calum.roberts@monash.eduen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2021 Elsevier B.V., All rights reserved.en
dc.subect.keywordscontinuous positive airway pressure infant newborn premature respiratory distress syndromeen
dc.identifier.authoremailRoberts C.T.; calum.roberts@monash.eduen
dc.description.grantNo: 1175634 Organization: (NHMRC) *National Health and Medical Research Council* Organization No: 501100000925 Country: Australiaen
dc.identifier.affiliationext(Roberts, Bhatia) Department of Paediatrics, Monash University, Clayton, Victoria, Australia-
dc.identifier.affiliationext(Roberts) The Ritchie Centre, Hudson Institute of Medical Research, Clayton, Victoria, Australia-
dc.identifier.affiliationext(Halibullah, Kamlin, Davis, Manley) Newborn Research Centre and Neonatal Services, The Royal Women's Hospital, Parkville, Victoria, Australia-
dc.identifier.affiliationext(Kamlin, Davis, Manley) Department of Obstetrics and Gynecology, The University of Melbourne, Parkville, Victoria, Australia-
dc.identifier.affiliationext(Kamlin, Davis, Manley) Clinical Sciences, Murdoch Children's Research Institute, Parkville, Victoria, Australia-
dc.identifier.affiliationmh(Roberts, Bhatia, Green) Monash Newborn, Monash Children's Hospital, Clayton, Victoria, Australia-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
crisitem.author.deptPaediatric - Neonatal (Monash Newborn)-
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