黄体期
胚胎移植
医学
活产
怀孕
体外受精
卵胞浆内精子注射
妇科
优势比
妊娠率
产科
回顾性队列研究
男科
低温保存
卵泡期
胚胎
内科学
生物
细胞生物学
遗传学
作者
Daniel J. Kaser,Elizabeth S. Ginsburg,Stacey A. Missmer,Katharine F. Correia,Catherine Racowsky
标识
DOI:10.1016/j.fertnstert.2012.08.007
摘要
ObjectiveTo compare outcomes after intramuscular progesterone (IMP) or 8% Crinone vaginal gel for luteal support for day 3 cryopreserved embryo transfer (CET).DesignRetrospective cohort study with multivariable analysis.SettingAcademic medical center.Patient(s)All autologous and donor egg in vitro fertilization and intracytoplasmic sperm injection patients who had a day 3 CET from January 1, 2008, to April 30, 2011, with luteal support using 25–50 mg/d IMP or 8% Crinone twice daily, initiated 3 days before the CET.Intervention(s)None.Main Outcome Measure(s)Implantation rate, clinical pregnancy, and live birth rates per CET.Result(s)IMP (n = 440) and Crinone (n = 298) recipients were similar for all demographic characteristics and cycle parameters assessed. Although implantation rates did not differ significantly between the two groups (Crinone vs. IMP: 19.6% vs. 30.4%), women supplemented with Crinone had significantly lower rates of clinical pregnancy (36.9% vs. 51.1%) and live birth (24.4% vs. 39.1%) compared with those on IMP.Conclusion(s)We observed that day 3 CET cycles with 8% Crinone luteal support had a 44% and 49% lower odds of clinical pregnancy and live birth, respectively, compared with those with IMP support. Further studies are required to identify the optimal timing and dose of 8% Crinone vaginal gel for use in CET cycles. To compare outcomes after intramuscular progesterone (IMP) or 8% Crinone vaginal gel for luteal support for day 3 cryopreserved embryo transfer (CET). Retrospective cohort study with multivariable analysis. Academic medical center. All autologous and donor egg in vitro fertilization and intracytoplasmic sperm injection patients who had a day 3 CET from January 1, 2008, to April 30, 2011, with luteal support using 25–50 mg/d IMP or 8% Crinone twice daily, initiated 3 days before the CET. None. Implantation rate, clinical pregnancy, and live birth rates per CET. IMP (n = 440) and Crinone (n = 298) recipients were similar for all demographic characteristics and cycle parameters assessed. Although implantation rates did not differ significantly between the two groups (Crinone vs. IMP: 19.6% vs. 30.4%), women supplemented with Crinone had significantly lower rates of clinical pregnancy (36.9% vs. 51.1%) and live birth (24.4% vs. 39.1%) compared with those on IMP. We observed that day 3 CET cycles with 8% Crinone luteal support had a 44% and 49% lower odds of clinical pregnancy and live birth, respectively, compared with those with IMP support. Further studies are required to identify the optimal timing and dose of 8% Crinone vaginal gel for use in CET cycles.
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