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Tocolysis compared with no tocolysis in women with threatened preterm birth and ruptured membranes: A propensity score analysis.
van Winden, T M S; Roos, C; Nijman, T A J; Kleinrouweler, C E; Olaru, Adriana; Mol, B W; McAuliffe, F M; Pajkrt, E; Oudijk, M A.
Afiliação
  • van Winden TMS; Amsterdam UMC, University of Amsterdam, Obstetrics, Amsterdam Reproduction and Development Research Institute, Amsterdam, the Netherlands.
  • Roos C; Amsterdam UMC, University of Amsterdam, Obstetrics, Amsterdam Reproduction and Development Research Institute, Amsterdam, the Netherlands.
  • Nijman TAJ; Leiden University Medical Centre, Department of Obstetrics and Gynecology, Leiden, the Netherlands.
  • Kleinrouweler CE; Amsterdam UMC, University of Amsterdam, Obstetrics, Amsterdam Reproduction and Development Research Institute, Amsterdam, the Netherlands.
  • Olaru A; UCD Perinatal Research Centre, School of Medicine, University College Dublin, National Maternity Hospital, Ireland.
  • Mol BW; Department of Obstetrics and Gynaecology, Monash University, Clayton, Victoria, Australia.
  • McAuliffe FM; UCD Perinatal Research Centre, School of Medicine, University College Dublin, National Maternity Hospital, Ireland.
  • Pajkrt E; Amsterdam UMC, University of Amsterdam, Obstetrics, Amsterdam Reproduction and Development Research Institute, Amsterdam, the Netherlands.
  • Oudijk MA; Amsterdam UMC, University of Amsterdam, Obstetrics, Amsterdam Reproduction and Development Research Institute, Amsterdam, the Netherlands. Electronic address: m.a.oudijk@amsterdamumc.nl.
Eur J Obstet Gynecol Reprod Biol ; 255: 67-73, 2020 Dec.
Article em En | MEDLINE | ID: mdl-33096392
INTRODUCTION: In women with preterm ruptured membranes and contractions, the administration of tocolysis is controversial. This study compares tocolysis with no tocolysis in women with threatened preterm birth and ruptured membranes. OBJECTIVE: To compare tocolysis with no tocolysis in women with threatened preterm birth and ruptured membranes. STUDY DESIGN: Data from the APOSTEL III RCT was combined with data from the National Maternity Hospital, Dublin. In the APOSTEL III trial, women with threatened preterm birth were randomized to atosiban or nifedipine. Patient data from Ireland were obtained from a cohort of women with threatened preterm birth with ruptured membranes. The Irish women received no tocolytic treatment. Only women with ruptured membranes and contractions were selected. We studied women with singleton or twin pregnancies and a gestational age between 25+0 and 33+6 weeks. Propensity score matching was performed to create comparable groups. Primary outcome was a composite adverse neonatal outcome. Secondary outcomes were individual components of the primary outcome, as well as neonatal intensive care unit (NICU) admission, gestational age at delivery, prolongation of pregnancy and mode of delivery. RESULTS: 153 women from the Apostel III trial were compared with 51 eligible women of the Irish cohort. We could match 46 women who received tocolysis and 46 women who received no tocolysis. All women had ruptured membranes. Maternal age, BMI, parity and gestational age at study entry were comparable between the groups after matching. There were no statistically significant differences in neonatal composite outcome (9.6 % in the tocolysis group versus 18 % in the control group, OR 0.46, 95 % CI 0.13-1.63). We found a lower incidence of NICU admission in the tocolysis group (63 %) than in the control group (94 %; OR 0.11, 95 % CI 0.03-0.41), which could be explained by differences in national admission policies. There were no statistically significant differences between tocolysis and no tocolysis in any of the other outcomes including sepsis, gestational age at delivery and time to delivery. CONCLUSION: In this propensity score analysis of women with threatened preterm birth and ruptured membranes, tocolytic therapy did not alter composite adverse neonatal outcome or time to delivery.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tocolíticos / Nascimento Prematuro Tipo de estudo: Clinical_trials Limite: Female / Humans / Infant / Newborn / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Eur J Obstet Gynecol Reprod Biol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tocolíticos / Nascimento Prematuro Tipo de estudo: Clinical_trials Limite: Female / Humans / Infant / Newborn / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Eur J Obstet Gynecol Reprod Biol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Holanda