Antenatal Corticosteroid Prophylaxis in Singleton and Multiple Pregnancies

Background The effects of antenatal corticosteroids (ANS) in multiple pregnancies are disputed. In this article, we examined whether estimated effects differ in singletons and multiples and in small for gestational age (SGA) preterm infants. Methods We studied 17 073 singletons (81% treated with ANS...

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Veröffentlicht in:Paediatric and perinatal epidemiology 2017-09, Vol.31 (5), p.394-401
Hauptverfasser: Gagliardi, Luigi, Lucchini, Renato, Bellù, Roberto, Zanini, Rinaldo
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Lucchini, Renato
Bellù, Roberto
Zanini, Rinaldo
description Background The effects of antenatal corticosteroids (ANS) in multiple pregnancies are disputed. In this article, we examined whether estimated effects differ in singletons and multiples and in small for gestational age (SGA) preterm infants. Methods We studied 17 073 singletons (81% treated with ANS) and 8274 multiples (86% treated) born at 24–33 weeks from the Italian Neonatal Network (2005–2013). We used Poisson regression models with robust variance to estimate adjusted risk ratios (RR) of in‐hospital death, severe intraventricular haemorrhage (IVH), periventricular leukomalacia (PVL), and the composite outcome of severe IVH and death. Results Mortality was lower among ANS‐treated vs. ANS‐untreated infants, both in singletons (RR 0.63, 95% confidence interval (CI) 0.58, 0.68) and in multiples (RR 0.85, 95% CI 0.73, 0.98). IVH and the composite outcome of IVH and death, but not PVL, also occurred less frequently among ANS‐treated infants. For these outcomes, the effect of ANS was stronger in singletons than in multiples (+35%, +32%, and +22% for death, IVH, and the composite outcome, respectively). Also among SGA infants, singletons, and multiples, ANS‐treated infants had lower risk of death, IVH and of composite outcome than untreated ones. Conclusions In this large cohort of preterm infants, both multiples and singletons treated with ANS had a lower risk of mortality, of severe IVH, and of composite outcome of IVH and death, both in the overall sample and in SGA infants. Although ANS effect was weaker in multiples, our results support current recommendations to administer ANS prophylaxis in multiple pregnancies at risk of preterm delivery.
doi_str_mv 10.1111/ppe.12385
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In this article, we examined whether estimated effects differ in singletons and multiples and in small for gestational age (SGA) preterm infants. Methods We studied 17 073 singletons (81% treated with ANS) and 8274 multiples (86% treated) born at 24–33 weeks from the Italian Neonatal Network (2005–2013). We used Poisson regression models with robust variance to estimate adjusted risk ratios (RR) of in‐hospital death, severe intraventricular haemorrhage (IVH), periventricular leukomalacia (PVL), and the composite outcome of severe IVH and death. Results Mortality was lower among ANS‐treated vs. ANS‐untreated infants, both in singletons (RR 0.63, 95% confidence interval (CI) 0.58, 0.68) and in multiples (RR 0.85, 95% CI 0.73, 0.98). IVH and the composite outcome of IVH and death, but not PVL, also occurred less frequently among ANS‐treated infants. For these outcomes, the effect of ANS was stronger in singletons than in multiples (+35%, +32%, and +22% for death, IVH, and the composite outcome, respectively). Also among SGA infants, singletons, and multiples, ANS‐treated infants had lower risk of death, IVH and of composite outcome than untreated ones. Conclusions In this large cohort of preterm infants, both multiples and singletons treated with ANS had a lower risk of mortality, of severe IVH, and of composite outcome of IVH and death, both in the overall sample and in SGA infants. Although ANS effect was weaker in multiples, our results support current recommendations to administer ANS prophylaxis in multiple pregnancies at risk of preterm delivery.</description><identifier>ISSN: 0269-5022</identifier><identifier>EISSN: 1365-3016</identifier><identifier>DOI: 10.1111/ppe.12385</identifier><identifier>PMID: 28767132</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adrenal Cortex Hormones - therapeutic use ; Adult ; Antenatal corticosteroids ; Cohort study ; Confidence intervals ; Corticoids ; Corticosteroids ; Death ; Dose-Response Relationship, Drug ; Female ; Gestational Age ; Health risk assessment ; Hemorrhage ; Humans ; Infant, Newborn ; Infant, Premature ; Infant, Premature, Diseases - prevention &amp; control ; Infant, Small for Gestational Age ; Infants ; Italy ; Male ; Mortality ; Multiple pregnancy ; Neonates ; Newborn babies ; Periventricular leukomalacia ; Pregnancy ; Pregnancy, Multiple ; Prenatal Care - methods ; Preterm neonate ; Prophylaxis ; Regression analysis ; Retrospective Studies ; Risk ; Robustness (mathematics) ; Small for gestational age ; Treatment Outcome</subject><ispartof>Paediatric and perinatal epidemiology, 2017-09, Vol.31 (5), p.394-401</ispartof><rights>2017 John Wiley &amp; Sons Ltd</rights><rights>2017 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2017 John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3535-94b9ae079336c3c0572d975184db0214089908bdde2617306c5bc2becb74cfa43</citedby><cites>FETCH-LOGICAL-c3535-94b9ae079336c3c0572d975184db0214089908bdde2617306c5bc2becb74cfa43</cites><orcidid>0000-0001-6074-8975</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fppe.12385$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fppe.12385$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28767132$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gagliardi, Luigi</creatorcontrib><creatorcontrib>Lucchini, Renato</creatorcontrib><creatorcontrib>Bellù, Roberto</creatorcontrib><creatorcontrib>Zanini, Rinaldo</creatorcontrib><title>Antenatal Corticosteroid Prophylaxis in Singleton and Multiple Pregnancies</title><title>Paediatric and perinatal epidemiology</title><addtitle>Paediatr Perinat Epidemiol</addtitle><description>Background The effects of antenatal corticosteroids (ANS) in multiple pregnancies are disputed. In this article, we examined whether estimated effects differ in singletons and multiples and in small for gestational age (SGA) preterm infants. Methods We studied 17 073 singletons (81% treated with ANS) and 8274 multiples (86% treated) born at 24–33 weeks from the Italian Neonatal Network (2005–2013). We used Poisson regression models with robust variance to estimate adjusted risk ratios (RR) of in‐hospital death, severe intraventricular haemorrhage (IVH), periventricular leukomalacia (PVL), and the composite outcome of severe IVH and death. Results Mortality was lower among ANS‐treated vs. ANS‐untreated infants, both in singletons (RR 0.63, 95% confidence interval (CI) 0.58, 0.68) and in multiples (RR 0.85, 95% CI 0.73, 0.98). IVH and the composite outcome of IVH and death, but not PVL, also occurred less frequently among ANS‐treated infants. For these outcomes, the effect of ANS was stronger in singletons than in multiples (+35%, +32%, and +22% for death, IVH, and the composite outcome, respectively). Also among SGA infants, singletons, and multiples, ANS‐treated infants had lower risk of death, IVH and of composite outcome than untreated ones. Conclusions In this large cohort of preterm infants, both multiples and singletons treated with ANS had a lower risk of mortality, of severe IVH, and of composite outcome of IVH and death, both in the overall sample and in SGA infants. Although ANS effect was weaker in multiples, our results support current recommendations to administer ANS prophylaxis in multiple pregnancies at risk of preterm delivery.</description><subject>Adrenal Cortex Hormones - therapeutic use</subject><subject>Adult</subject><subject>Antenatal corticosteroids</subject><subject>Cohort study</subject><subject>Confidence intervals</subject><subject>Corticoids</subject><subject>Corticosteroids</subject><subject>Death</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Gestational Age</subject><subject>Health risk assessment</subject><subject>Hemorrhage</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Infant, Premature</subject><subject>Infant, Premature, Diseases - prevention &amp; control</subject><subject>Infant, Small for Gestational Age</subject><subject>Infants</subject><subject>Italy</subject><subject>Male</subject><subject>Mortality</subject><subject>Multiple pregnancy</subject><subject>Neonates</subject><subject>Newborn babies</subject><subject>Periventricular leukomalacia</subject><subject>Pregnancy</subject><subject>Pregnancy, Multiple</subject><subject>Prenatal Care - methods</subject><subject>Preterm neonate</subject><subject>Prophylaxis</subject><subject>Regression analysis</subject><subject>Retrospective Studies</subject><subject>Risk</subject><subject>Robustness (mathematics)</subject><subject>Small for gestational age</subject><subject>Treatment Outcome</subject><issn>0269-5022</issn><issn>1365-3016</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10EtLxDAUhuEgio6XhX9ACm500ZlcmrRZyjDeUBxQ1yVNz2gkk9SkReffGx11IZhNNg8fhxehQ4LHJL1J18GYUFbxDTQiTPCcYSI20QhTIXOOKd1BuzG-YIwFl3Qb7dCqFCVhdISuz1wPTvXKZlMfeqN97CF402bz4LvnlVXvJmbGZffGPVnovcuUa7Pbwfams5AUPDnltIG4j7YWykY4-P730OP57GF6md_cXVxNz25yzTjjuSwaqQCXkjGhmca8pK0sOamKtsGUFLiSEldN2wIVpGRYaN5o2oBuykIvVMH20Ml6twv-dYDY10sTNVirHPgh1kRSzlOWgiV6_Ie--CG4dF1SBeZUVLxM6nStdPAxBljUXTBLFVY1wfVn4DoFrr8CJ3v0vTg0S2h_5U_RBCZr8GYsrP5fqufz2XryAyxKg5o</recordid><startdate>201709</startdate><enddate>201709</enddate><creator>Gagliardi, Luigi</creator><creator>Lucchini, Renato</creator><creator>Bellù, Roberto</creator><creator>Zanini, Rinaldo</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6074-8975</orcidid></search><sort><creationdate>201709</creationdate><title>Antenatal Corticosteroid Prophylaxis in Singleton and Multiple Pregnancies</title><author>Gagliardi, Luigi ; Lucchini, Renato ; Bellù, Roberto ; Zanini, Rinaldo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3535-94b9ae079336c3c0572d975184db0214089908bdde2617306c5bc2becb74cfa43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adrenal Cortex Hormones - therapeutic use</topic><topic>Adult</topic><topic>Antenatal corticosteroids</topic><topic>Cohort study</topic><topic>Confidence intervals</topic><topic>Corticoids</topic><topic>Corticosteroids</topic><topic>Death</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Gestational Age</topic><topic>Health risk assessment</topic><topic>Hemorrhage</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Infant, Premature</topic><topic>Infant, Premature, Diseases - prevention &amp; control</topic><topic>Infant, Small for Gestational Age</topic><topic>Infants</topic><topic>Italy</topic><topic>Male</topic><topic>Mortality</topic><topic>Multiple pregnancy</topic><topic>Neonates</topic><topic>Newborn babies</topic><topic>Periventricular leukomalacia</topic><topic>Pregnancy</topic><topic>Pregnancy, Multiple</topic><topic>Prenatal Care - methods</topic><topic>Preterm neonate</topic><topic>Prophylaxis</topic><topic>Regression analysis</topic><topic>Retrospective Studies</topic><topic>Risk</topic><topic>Robustness (mathematics)</topic><topic>Small for gestational age</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gagliardi, Luigi</creatorcontrib><creatorcontrib>Lucchini, Renato</creatorcontrib><creatorcontrib>Bellù, Roberto</creatorcontrib><creatorcontrib>Zanini, Rinaldo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Paediatric and perinatal epidemiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gagliardi, Luigi</au><au>Lucchini, Renato</au><au>Bellù, Roberto</au><au>Zanini, Rinaldo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antenatal Corticosteroid Prophylaxis in Singleton and Multiple Pregnancies</atitle><jtitle>Paediatric and perinatal epidemiology</jtitle><addtitle>Paediatr Perinat Epidemiol</addtitle><date>2017-09</date><risdate>2017</risdate><volume>31</volume><issue>5</issue><spage>394</spage><epage>401</epage><pages>394-401</pages><issn>0269-5022</issn><eissn>1365-3016</eissn><abstract>Background The effects of antenatal corticosteroids (ANS) in multiple pregnancies are disputed. In this article, we examined whether estimated effects differ in singletons and multiples and in small for gestational age (SGA) preterm infants. Methods We studied 17 073 singletons (81% treated with ANS) and 8274 multiples (86% treated) born at 24–33 weeks from the Italian Neonatal Network (2005–2013). We used Poisson regression models with robust variance to estimate adjusted risk ratios (RR) of in‐hospital death, severe intraventricular haemorrhage (IVH), periventricular leukomalacia (PVL), and the composite outcome of severe IVH and death. Results Mortality was lower among ANS‐treated vs. ANS‐untreated infants, both in singletons (RR 0.63, 95% confidence interval (CI) 0.58, 0.68) and in multiples (RR 0.85, 95% CI 0.73, 0.98). IVH and the composite outcome of IVH and death, but not PVL, also occurred less frequently among ANS‐treated infants. For these outcomes, the effect of ANS was stronger in singletons than in multiples (+35%, +32%, and +22% for death, IVH, and the composite outcome, respectively). Also among SGA infants, singletons, and multiples, ANS‐treated infants had lower risk of death, IVH and of composite outcome than untreated ones. Conclusions In this large cohort of preterm infants, both multiples and singletons treated with ANS had a lower risk of mortality, of severe IVH, and of composite outcome of IVH and death, both in the overall sample and in SGA infants. Although ANS effect was weaker in multiples, our results support current recommendations to administer ANS prophylaxis in multiple pregnancies at risk of preterm delivery.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28767132</pmid><doi>10.1111/ppe.12385</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-6074-8975</orcidid></addata></record>
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subjects Adrenal Cortex Hormones - therapeutic use
Adult
Antenatal corticosteroids
Cohort study
Confidence intervals
Corticoids
Corticosteroids
Death
Dose-Response Relationship, Drug
Female
Gestational Age
Health risk assessment
Hemorrhage
Humans
Infant, Newborn
Infant, Premature
Infant, Premature, Diseases - prevention & control
Infant, Small for Gestational Age
Infants
Italy
Male
Mortality
Multiple pregnancy
Neonates
Newborn babies
Periventricular leukomalacia
Pregnancy
Pregnancy, Multiple
Prenatal Care - methods
Preterm neonate
Prophylaxis
Regression analysis
Retrospective Studies
Risk
Robustness (mathematics)
Small for gestational age
Treatment Outcome
title Antenatal Corticosteroid Prophylaxis in Singleton and Multiple Pregnancies
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