A randomized trial of levonorgestrel intrauterine system insertion 6 to 48 h compared to 6 weeks after vaginal delivery; lessons learned

Abstract The objective of this randomized trial was to compare breastfeeding among women who received a levonorgestrel-releasing intrauterine system within 6–48 h (early) or 4–6 weeks (standard) after an uncomplicated vaginal birth. Analysis groups of 86 women in each arm were needed to demonstrate...

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Veröffentlicht in:Contraception (Stoneham) 2015-04, Vol.91 (4), p.284-288
Hauptverfasser: Stuart, Gretchen S, Lesko, Catherine R, Stuebe, Alison M, Bryant, Amy G, Levi, Erika E, Danvers, Antoinette I
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Sprache:eng
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Zusammenfassung:Abstract The objective of this randomized trial was to compare breastfeeding among women who received a levonorgestrel-releasing intrauterine system within 6–48 h (early) or 4–6 weeks (standard) after an uncomplicated vaginal birth. Analysis groups of 86 women in each arm were needed to demonstrate a 20% difference in any breastfeeding. Thirty-five women were randomized to the early ( N = 17) and standard ( N = 18) arms. The combination of unsuccessful placement (2/17; 12%), expulsions (7/17; 41%) and removals (3/17; 18%) reached 71% (12/17) in the early arm, so the study was stopped. In our small study cohort, levonorgestrel-releasing intrauterine system insertion between 6 and 48 h after vaginal birth was associated with a high rate of expulsion or removal soon after insertion.
ISSN:0010-7824
1879-0518
DOI:10.1016/j.contraception.2014.12.009