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Atosiban versus fenoterol as a uterine relaxant for external cephalic version: randomised controlled trial

Objective To compare the effectiveness of the oxytocin receptor antagonist atosiban with the beta mimetic fenoterol as uterine relaxants in women undergoing external cephalic version (ECV) for breech presentation. Design Multicentre, open label, randomised controlled trial. Setting Eight hospitals i...

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Autores principales: Velzel, Joost, Vlemmix, Floortje, Opmeer, Brent C, Molkenboer, Jan F M, Verhoeven, Corine J, van Pampus, Mariëlle G, Papatsonis, Dimitri N M, Bais, Joke M J, Vollebregt, Karlijn C, van der Esch, Liesbeth, Van der Post, Joris A M, Mol, Ben Willem, Kok, Marjolein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421458/
https://www.ncbi.nlm.nih.gov/pubmed/28126898
http://dx.doi.org/10.1136/bmj.i6773
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author Velzel, Joost
Vlemmix, Floortje
Opmeer, Brent C
Molkenboer, Jan F M
Verhoeven, Corine J
van Pampus, Mariëlle G
Papatsonis, Dimitri N M
Bais, Joke M J
Vollebregt, Karlijn C
van der Esch, Liesbeth
Van der Post, Joris A M
Mol, Ben Willem
Kok, Marjolein
author_facet Velzel, Joost
Vlemmix, Floortje
Opmeer, Brent C
Molkenboer, Jan F M
Verhoeven, Corine J
van Pampus, Mariëlle G
Papatsonis, Dimitri N M
Bais, Joke M J
Vollebregt, Karlijn C
van der Esch, Liesbeth
Van der Post, Joris A M
Mol, Ben Willem
Kok, Marjolein
author_sort Velzel, Joost
collection PubMed
description Objective To compare the effectiveness of the oxytocin receptor antagonist atosiban with the beta mimetic fenoterol as uterine relaxants in women undergoing external cephalic version (ECV) for breech presentation. Design Multicentre, open label, randomised controlled trial. Setting Eight hospitals in the Netherlands, August 2009 to May 2014. Participants 830 women with a singleton fetus in breech presentation and a gestational age of more than 34 weeks were randomly allocated in a 1:1 ratio to either 6.75 mg atosiban (n=416) or 40 μg fenoterol (n=414) intravenously for uterine relaxation before ECV. Main outcome measures The primary outcome measures were a fetus in cephalic position 30 minutes after the procedure and cephalic presentation at delivery. Secondary outcome measures were mode of delivery, incidence of fetal and maternal complications, and drug related adverse events. All analyses were done on an intention-to-treat basis. Results Cephalic position 30 minutes after ECV occurred significantly less in the atosiban group than in the fenoterol group (34% v 40%, relative risk 0.73, 95% confidence interval 0.55 to 0.93). Presentation at birth was cephalic in 35% (n=139) of the atosiban group and 40% (n=166) of the fenoterol group (0.86, 0.72 to 1.03), and caesarean delivery was performed in 60% (n=240) of women in the atosiban group and 55% (n=218) in the fenoterol group (1.09, 0.96 to 1.20). No significant differences were found in neonatal outcomes or drug related adverse events. Conclusions In women undergoing ECV for breech presentation, uterine relaxation with fenoterol increases the rate of cephalic presentation 30 minutes after the procedure. No statistically significant difference was found for cephalic presentation at delivery. Trial registration Dutch Trial Register, NTR 1877.
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spelling pubmed-54214582017-05-12 Atosiban versus fenoterol as a uterine relaxant for external cephalic version: randomised controlled trial Velzel, Joost Vlemmix, Floortje Opmeer, Brent C Molkenboer, Jan F M Verhoeven, Corine J van Pampus, Mariëlle G Papatsonis, Dimitri N M Bais, Joke M J Vollebregt, Karlijn C van der Esch, Liesbeth Van der Post, Joris A M Mol, Ben Willem Kok, Marjolein BMJ Research Objective To compare the effectiveness of the oxytocin receptor antagonist atosiban with the beta mimetic fenoterol as uterine relaxants in women undergoing external cephalic version (ECV) for breech presentation. Design Multicentre, open label, randomised controlled trial. Setting Eight hospitals in the Netherlands, August 2009 to May 2014. Participants 830 women with a singleton fetus in breech presentation and a gestational age of more than 34 weeks were randomly allocated in a 1:1 ratio to either 6.75 mg atosiban (n=416) or 40 μg fenoterol (n=414) intravenously for uterine relaxation before ECV. Main outcome measures The primary outcome measures were a fetus in cephalic position 30 minutes after the procedure and cephalic presentation at delivery. Secondary outcome measures were mode of delivery, incidence of fetal and maternal complications, and drug related adverse events. All analyses were done on an intention-to-treat basis. Results Cephalic position 30 minutes after ECV occurred significantly less in the atosiban group than in the fenoterol group (34% v 40%, relative risk 0.73, 95% confidence interval 0.55 to 0.93). Presentation at birth was cephalic in 35% (n=139) of the atosiban group and 40% (n=166) of the fenoterol group (0.86, 0.72 to 1.03), and caesarean delivery was performed in 60% (n=240) of women in the atosiban group and 55% (n=218) in the fenoterol group (1.09, 0.96 to 1.20). No significant differences were found in neonatal outcomes or drug related adverse events. Conclusions In women undergoing ECV for breech presentation, uterine relaxation with fenoterol increases the rate of cephalic presentation 30 minutes after the procedure. No statistically significant difference was found for cephalic presentation at delivery. Trial registration Dutch Trial Register, NTR 1877. BMJ Publishing Group Ltd. 2017-01-26 /pmc/articles/PMC5421458/ /pubmed/28126898 http://dx.doi.org/10.1136/bmj.i6773 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/.
spellingShingle Research
Velzel, Joost
Vlemmix, Floortje
Opmeer, Brent C
Molkenboer, Jan F M
Verhoeven, Corine J
van Pampus, Mariëlle G
Papatsonis, Dimitri N M
Bais, Joke M J
Vollebregt, Karlijn C
van der Esch, Liesbeth
Van der Post, Joris A M
Mol, Ben Willem
Kok, Marjolein
Atosiban versus fenoterol as a uterine relaxant for external cephalic version: randomised controlled trial
title Atosiban versus fenoterol as a uterine relaxant for external cephalic version: randomised controlled trial
title_full Atosiban versus fenoterol as a uterine relaxant for external cephalic version: randomised controlled trial
title_fullStr Atosiban versus fenoterol as a uterine relaxant for external cephalic version: randomised controlled trial
title_full_unstemmed Atosiban versus fenoterol as a uterine relaxant for external cephalic version: randomised controlled trial
title_short Atosiban versus fenoterol as a uterine relaxant for external cephalic version: randomised controlled trial
title_sort atosiban versus fenoterol as a uterine relaxant for external cephalic version: randomised controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421458/
https://www.ncbi.nlm.nih.gov/pubmed/28126898
http://dx.doi.org/10.1136/bmj.i6773
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