Effects of atosiban on uterine peristalsis following frozen embryo transfer: A randomized controlled trial
Nattapong Buddhabunyakan, เจน โสธรวิทย์, กนก สีจร, ประนอม บุพศิริ, Lingling Salang*Department of Obstetrics and Gynecology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
บทคัดย่อ
Objectives: To compare the effects of atosiban (oxytocin antagonist) on uterine peristalsis and pregnancy outcomes in the frozen embryo transfer (FET) cycle.
Setting: Srinagarind Hospital, a university hospital, Khon Kaen, Thailand.
Design: A randomized, double-blinded, controlled trial.
Methods: Fifty infertile women were randomized into the atosiban (n = 25) and placebo group (n = 25). Women in the study group received intravenous atosiban 6.75 mg, 30 min before embryo transfer, and continued infusion at 18 mg/h for 1 h. The dose was reduced to 6 mg/h for another 2 h. Saline solution was applied in the placebo group. The uterine peristalsis frequency was measured by transvaginal ultrasound 30 min before and 3 h after the embryo transfer.
Results: The respective mean baseline uterine peristalsis frequency (time) in the atosiban and placebo group was 10.3 ± 2.4 and 9.2 ± 3.4. The respective duration of uterine peristalsis in the atosiban and placebo group after receiving the intervention was reduced to 7.9 ± 2.1 and 6.9 ± 2.7. The implantation rate and clinical pregnancy rate were not statistically significant different between atosiban group and placebo group (37.5% versus 31.0%, RR 1.21, 95%CI: 0.60–2.44 and 44% versus 36%, RR 1.22, 95%CI: 0.62–2.42, respectively). Subgroup analysis indicated that the clinical pregnancy rate in those >35 years of age was not significantly different between both groups (31.6% and 18.8 %, RR 1.68, 95%CI: 0.50–5.68).
Conclusion: Adding atosiban in FET did not reduce uterine peristalsis but may benefit the advanced age group.
ที่มา
European Journal Obstetrics Gynecology and Reproductive Biology ปี 2564, October
ปีที่: 265 ฉบับที่ หน้า 96-101
คำสำคัญ
Uterine peristalsis, Frozen embryo transfer, Oxytocin-antagonist