Post-placental intrauterine device insertion vs puerperal insertion in women undergoing caesarean delivery in Egypt: a 1 year randomised controlled trial

Eur J Contracept Reprod Health Care. 2020 Dec;25(6):439-444. doi: 10.1080/13625187.2020.1823366. Epub 2020 Oct 2.

Abstract

Objective: The aim of the study was to compare 6 month expulsion rates of the copper-bearing intrauterine device (IUD) inserted after delivery of the placenta or at the 6 week postpartum visit in women undergoing caesarean section.

Methods: A parallel-group randomised trial was conducted in an Egyptian university hospital between February 2016 and December 2018. Participants were randomised to either post-placental IUD insertion or IUD insertion at the 6 week postpartum visit. Participants were followed for 12 months. Primary outcomes were IUD expulsion and the proportion of women using an IUD at 6 months. A secondary outcome was the cumulative pregnancy rate at 12 months.

Results: Five hundred participants were enrolled in each group. At 6 months the total expulsions were 58/416 (13.9%) in the post-placental group and 4/214 (1.9%) in the puerperal group; IUD use at 6 months was 416/478 (87.0%) in the post-placental group and 214/232 (92.2%) in the puerperal group. Data collected by phone at 12 months showed a higher cumulative pregnancy rate in the puerperal group (84/500, 16.8%) vs the post-placental group (22/500, 4.4%). IUD continuation at 12 months was higher in the post-placental group.

Conclusion: Participants in the post-placental group had a higher expulsion rate at 6 months, but more IUDs were placed in this group and fewer pregnancies had occurred at 12 months compared with the puerperal group.

Trial registration: Clinicaltrials.gov NCT02679820.

Keywords: Delayed postpartum IUD insertion; IUD expulsion; family planning; intra-caesarean IUD insertion; intrauterine device; long-acting reversible contraception; puerperal IUD insertion; unintended pregnancy.

Publication types

  • Randomized Controlled Trial
  • Retracted Publication

MeSH terms

  • Adult
  • Cesarean Section
  • Contraception / adverse effects*
  • Contraception / methods*
  • Contraception / statistics & numerical data
  • Egypt
  • Female
  • Humans
  • Intrauterine Device Expulsion / adverse effects*
  • Intrauterine Devices, Copper / adverse effects*
  • Intrauterine Devices, Copper / statistics & numerical data*
  • Middle Aged
  • Placenta
  • Postpartum Period
  • Pregnancy
  • Pregnancy Rate*
  • Young Adult

Associated data

  • ClinicalTrials.gov/NCT02679820