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      Association between antenatal corticosteroids use and perinatal mortality among preterm singletons and twins in Mwanza, Tanzania: an observational study

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          Abstract

          Objectives

          To examine the association between antenatal corticosteroids (ACS) use and perinatal mortality in singletons and twins delivered before 35 weeks of gestation.

          Design

          Secondary analysis of data from an observational prospective chart review study that investigated if exposure to ACS was associated with lower rates of perinatal mortality in preterm infants.

          Setting

          This study was conducted in four hospitals located in Mwanza region, Tanzania.

          Participants

          The study population included all preterm singletons and twins delivered at these hospitals between 24 weeks 0 days and 34 weeks 6 days of gestation from July 2019 to February 2020.

          Outcome measures

          The primary outcome was perinatal mortality; the secondary outcome was respiratory distress syndrome (RDS).

          Results

          The study included 844 singletons and 210 twin infants. Three hundred and fourteen singletons (37.2%) and 52 twins (24.8%) were exposed to at least one dose of ACS. Adjusted multivariate analyses revealed that among singletons’ exposure to ACS was significantly associated with a lower likelihood of perinatal mortality, adjusted relative risk (aRR) 0.30 (95% CI 0.22 to 0.40) and RDS, aRR 0.92 (95% CI 0.87 to 0.97). In twin infants, exposure to ACS was associated with a reduced risk of RDS only, aRR 0.87 (95% CI 0.78 to 0.98).

          Conclusion

          The use of ACS between 24 weeks 0 days and 34 weeks 6 days of gestation in both singletons and twins in low-resource settings is associated with positive infant outcomes. No adverse effects were noted. Further research that examines the benefits of ACS for twin infants is needed.

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          Most cited references33

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          A controlled trial of antepartum glucocorticoid treatment for prevention of the respiratory distress syndrome in premature infants.

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            Antenatal corticosteroids for accelerating fetal lung maturation for women at risk of preterm birth

            Respiratory morbidity including respiratory distress syndrome (RDS) is a serious complication of preterm birth and the primary cause of early neonatal mortality and disability. Despite early evidence indicating a beneficial effect of antenatal corticosteroids on fetal lung maturation and widespread recommendations to use this treatment in women at risk of preterm delivery, some uncertainty remains about their effectiveness particularly with regard to their use in lower-resource settings, different gestational ages and high-risk obstetric groups such as women with hypertension or multiple pregnancies. This updated review (which supersedes an earlier review Crowley 1996) was first published in 2006 and subsequently updated in 2017.
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              Committee Opinion No. 713: Antenatal Corticosteroid Therapy for Fetal Maturation.

              (2017)
              Corticosteroid administration before anticipated preterm birth is one of the most important antenatal therapies available to improve newborn outcomes. A single course of corticosteroids is recommended for pregnant women between 24 0/7 weeks and 33 6/7 weeks of gestation who are at risk of preterm delivery within 7 days, including for those with ruptured membranes and multiple gestations. It also may be considered for pregnant women starting at 23 0/7 weeks of gestation who are at risk of preterm delivery within 7 days, based on a family's decision regarding resuscitation, irrespective of membrane rupture status and regardless of fetal number. Administration of betamethasone may be considered in pregnant women between 34 0/7 weeks and 36 6/7 weeks of gestation who are at risk of preterm birth within 7 days, and who have not received a previous course of antenatal corticosteroids. A single repeat course of antenatal corticosteroids should be considered in women who are less than 34 0/7 weeks of gestation who are at risk of preterm delivery within 7 days, and whose prior course of antenatal corticosteroids was administered more than 14 days previously. Rescue course corticosteroids could be provided as early as 7 days from the prior dose, if indicated by the clinical scenario. Continued surveillance of long-term outcomes after in utero corticosteroid exposure should be supported. Quality improvement strategies to optimize appropriate and timely antenatal corticosteroid administration are encouraged.
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                Author and article information

                Journal
                BMJ Open
                BMJ Open
                bmjopen
                bmjopen
                BMJ Open
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                2044-6055
                2022
                6 April 2022
                : 12
                : 4
                : e059030
                Affiliations
                [1 ]departmentSchool of Pharmacy , Catholic University of Health and Allied Sciences , Mwanza, United Republic of Tanzania
                [2 ]departmentDepartment of Research , Haydom Lutheran Hospital , Mbulu, Manyara, United Republic of Tanzania
                [3 ]departmentDepartment of Epidemiology and Biostatistics , Muhimbili University of Health and Allied Sciences , Dar es Salaam, United Republic of Tanzania
                [4 ]departmentDepartment of Epidemiology and Biostatistics , Catholic University of Health and Allied , Mwanza, United Republic of Tanzania
                [5 ]departmentDepartment of Peadiatrics and Child Health , Bugando Medical Centre , Mwanza, United Republic of Tanzania
                [6 ]departmentDepartment of Radiology , Bugando Medical Centre , Mwanza, United Republic of Tanzania
                [7 ]departmentDepartment of Obstetrics and Gynaecology , Catholic University of Health and Allied Sciences , Mwanza, United Republic of Tanzania
                [8 ]departmentDepartment of Pharmacology , Catholic University of Health and Allied Sciences , Mwanza, United Republic of Tanzania
                [9 ]departmentOwerko Centre at the Alberta Children's Hospital Research Institute and Departments of Pediatrics and Community Health Sciences , The University of Calgary , Calgary, Alberta, Canada
                Author notes
                [Correspondence to ] Stanley Mwita; stanleymwita@ 123456gmail.com
                Author information
                http://orcid.org/0000-0003-0563-6705
                Article
                bmjopen-2021-059030
                10.1136/bmjopen-2021-059030
                8991063
                35393329
                c9487f5a-2ddf-4f72-b181-f284459d5be1
                © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See:  http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 08 November 2021
                : 18 March 2022
                Categories
                Obstetrics and Gynaecology
                1506
                Original research
                Custom metadata
                unlocked

                Medicine
                neonatology,fetal medicine,maternal medicine,perinatology,respiratory infections
                Medicine
                neonatology, fetal medicine, maternal medicine, perinatology, respiratory infections

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