Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/1244
DC FieldValueLanguage
dc.contributor.authorSotiriadis, Alexandros-
dc.contributor.authorMakrydimas, George V.-
dc.contributor.authorPapatheodorou, Stefania-
dc.contributor.authorIoannidis, John P. A.-
dc.date.accessioned2015-04-02T06:42:23Z-
dc.date.accessioned2015-12-02T09:04:39Z-
dc.date.available2015-04-02T06:42:23Z-
dc.date.available2015-12-02T09:04:39Z-
dc.date.issued2009-
dc.identifier.citationCochrane Database of Systematic Reviews, 2009, no. 4, article no. CD006614en_US
dc.identifier.issn14651858-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/1244-
dc.description.abstractBackground: Infants born at term by elective caesarean delivery are more likely to develop respiratory morbidity than infants born vaginally. Prophylactic corticosteroids in singleton preterm pregnancies accelerate lung maturation and reduce the incidence of respiratory complications. Objectives: The objective of this review was to assess the effect of prophylactic corticosteroid administration before elective caesarean section at term, as compared to usual management without corticosteroids, in reducing neonatal respiratory morbidity and admission to special care with respiratory complications. Search strategy: We searched the Cochrane Pregnancy and Chilbirth Group's Trials Register (30 June 2009). Selection criteria: Randomised and quasi-randomised controlled trials comparing prophylactic antenatal corticosteroid administration (betamethasone or dexamethasone) with placebo or with no treatment, given before elective caesarean section at term (at or after 37 weeks of gestation). Data collection and analysis: The co-authors assessed the results of the only available trial independently to retrieve data on perinatal outcomes. Results were expressed as risk ratio (RR) or mean differences (MD), together with their 95% confidence intervals (CI). Main results: One study comparing prophylactic administration of betamethasone (N = 467) versus usual treatment without steroids (N = 475) in term elective caesarean section was included in the review. Women randomised to treatment group received two intramuscular doses of betamethasone in the 48 hours before delivery, whereas the control group received treatment as usual. Prophylactic betamethasone appeared to significantly decrease the risk of admission to the neonatal intensive care unit for respiratory morbidity (RR 0.15; 95% CI 0.03 to 0.64). However, no statistically significant reduction was found in the incidence of neonatal respiratory distress syndrome (RR 0.32; 95% CI 0.07 to 1.58), transient tachypnoea of the newborn (RR 0.52; 95% CI 0.25 to 1.11), need for mechanical ventilation (RR 4.07; 95% CI 0.46 to 36.27) and length of stay in neonatal intensive care unit (MD) -2.14 days; 95% CI -5.58 to 1.30). There were no reported events of neonatal sepsis, perinatal deaths or maternal trauma infection, therefore results on these outcomes are non-estimable. The study did not provide data on other pre-defined outcomes. Authors' conclusions: The results from the single trial are promising, but more studies with larger samples are needed to investigate the effect of prophylactic steroids in the incidence of neonatal complications per se. Also more data and longer follow up would be needed for potential harms and complications.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofCochrane Database of Systematic Reviewsen_US
dc.rights© Wileyen_US
dc.subjectBetamethasoneen_US
dc.subjectCorticosteroiden_US
dc.subjectDexamethasoneen_US
dc.subjectPlaceboen_US
dc.subjectClinical trialen_US
dc.subjectCorticosteroid therapyen_US
dc.subjectElective surgeryen_US
dc.subjectNewborn morbidityen_US
dc.subjectProphylaxisen_US
dc.subjectRespiratory tract diseaseen_US
dc.titleCorticosteroids for preventing neonatal respiratory morbidity after elective caesarean section at termen_US
dc.typeArticleen_US
dc.collaborationUniversity of Ioanninaen_US
dc.collaborationUniversity Hospital of Ioanninaen_US
dc.subject.categoryClinical Medicineen_US
dc.journalsSubscriptionen_US
dc.reviewPeer Revieweden
dc.countryGreeceen_US
dc.subject.fieldMedical and Health Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1002/14651858.CD006614.pub2en_US
dc.dept.handle123456789/54en
dc.relation.issue4en_US
cut.common.academicyear2020-2021en_US
dc.identifier.spageCD006614en_US
dc.identifier.epageCD006614en_US
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.languageiso639-1en-
crisitem.journal.journalissn1465-1858-
crisitem.journal.publisherWiley-
crisitem.author.deptCyprus International Institute for Environmental and Public Health-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.orcid0000-0002-9451-9094-
crisitem.author.parentorgFaculty of Health Sciences-
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