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Πεδίο DCΤιμήΓλώσσα
dc.contributor.authorDaly, Déirdre-
dc.contributor.authorMinnie, Karin C.S.-
dc.contributor.authorBlignaut, Alwiena J.-
dc.contributor.authorBlix, Ellen Störe-
dc.contributor.authorVika Nilsen, Anne Britt-
dc.contributor.authorDencker, Anna-
dc.contributor.authorBeeckman, Katrien-
dc.contributor.authorGroß, Mechthild M.-
dc.contributor.authorPehlke-Milde, Jessica-
dc.contributor.authorGrylka-Baeschlin, Susanne-
dc.contributor.authorKoenig-Bachmann, Martina-
dc.contributor.authorClausen, Jette Aaroe-
dc.contributor.authorHadjigeorgiou, Eleni-
dc.contributor.authorMorano, Sandra-
dc.contributor.authorIannuzzi, Laura-
dc.contributor.authorBaranowska, Barbara-
dc.contributor.authorKiersnowska, Iwona-
dc.contributor.authorUvnäs-Moberg, Kerstin-
dc.date.accessioned2020-10-31T09:48:05Z-
dc.date.available2020-10-31T09:48:05Z-
dc.date.issued2020-07-07-
dc.identifier.citationPLoS ONE, 2020, vol. 15, no. 7 July, articl. no. e0227941en_US
dc.identifier.issn19326203-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/19316-
dc.description.abstractObjective To compare synthetic oxytocin infusion regimens used during labour, calculate the International Units (IU) escalation rate and total amount of IU infused over eight hours. Design Observational study Setting Twelve countries, eleven European and South Africa. Sample National, regional or institutional-level regimens on oxytocin for induction and augmentation labour Methods Data on oxytocin IU dose, infusion fluid amount, start dose, escalation rate and maximum dose were collected. Values for each regimen were converted to IU in 1000ml diluent. One IU corresponded to 1.67μg for doses provided in grams/micrograms. IU hourly dose increase rates were based on escalation frequency. Cumulative doses and total IU amount infused were calculated by adding the dose administered for each previous hour. Main Outcome Measures Oxytocin IU dose infused Results Data were obtained on 21 regimens used in 12 countries. Details on the start dose, escalation interval, escalation rate and maximum dose infused were available from 16 regimens. Starting rates varied from 0.06 IU/hour to 0.90 IU/hour, and the maximum dose rate varied from 0.90 IU/hour to 3.60 IU/hour. The total amount of IU oxytocin infused, estimated over eight hours, ranged from 2.38 IU to 27.00 IU, a variation of 24.62 IU and an 11-fold difference. Conclusion Current variations in oxytocin regimens for induction and augmentation of labour are inexplicable. It is crucial that the appropriate minimum infusion regimen is administered because synthetic oxytocin is a potentially harmful medication with serious consequences for women and babies when inappropriately used. Estimating the total amount of oxytocin IU received by labouring women, alongside the institution’s mode of birth and neonatal outcomes, may deepen our understanding and be the way forward to identifying the optimal infusion regimen.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofPLoS ONEen_US
dc.rights© 2020 Daly et al.en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectOxytocin infusion regimensen_US
dc.subjectInternational Unitsen_US
dc.subjectDrug dose escalationen_US
dc.subjectDrug dose regimenen_US
dc.subjectDrug infusionen_US
dc.subjectDrug administrationen_US
dc.titleHow much synthetic oxytocin is infused during labour? A review and analysis of regimens used in 12 countriesen_US
dc.typeArticleen_US
dc.collaborationTrinity College Dublinen_US
dc.collaborationNorth-West Universityen_US
dc.collaborationOslo Metropolitan Universityen_US
dc.collaborationWestern Norway University of Applied Sciencesen_US
dc.collaborationUniversity of Gothenburgen_US
dc.collaborationVrije Universiteit Brusselen_US
dc.collaborationUniversity of Antwerpen_US
dc.collaborationHannover Medical Schoolen_US
dc.collaborationZurich University of Applied Sciencesen_US
dc.collaborationHealth University of Applied Sciences Tyrolen_US
dc.collaborationCopenhagen University Collegeen_US
dc.collaborationCyprus University of Technologyen_US
dc.collaborationUniversity of Genoaen_US
dc.collaborationBournemouth Universityen_US
dc.collaborationCentre of Postgraduate Medical Educationen_US
dc.collaborationMedical University of Warsawen_US
dc.collaborationSwedish University of Agricultural Sciencesen_US
dc.subject.categoryClinical Medicineen_US
dc.journalsOpen Accessen_US
dc.countryIrelanden_US
dc.countrySouth Africaen_US
dc.countryNorwayen_US
dc.countrySwedenen_US
dc.countryBelgiumen_US
dc.countryGermanyen_US
dc.countrySwitzerlanden_US
dc.countryAustriaen_US
dc.countryDenmarken_US
dc.countryCyprusen_US
dc.countryItalyen_US
dc.countryUnited Kingdomen_US
dc.countryPolanden_US
dc.subject.fieldMedical and Health Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1371/journal.pone.0227941en_US
dc.identifier.pmid32722667-
dc.relation.issue7en_US
dc.relation.volume15en_US
cut.common.academicyear2019-2020en_US
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.languageiso639-1en-
item.fulltextWith Fulltext-
crisitem.journal.journalissn1932-6203-
crisitem.journal.publisherPloS-
crisitem.author.deptDepartment of Nursing-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.orcid0000-0002-5834-4207-
crisitem.author.parentorgFaculty of Health Sciences-
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