Jones Institute of Reproductive Medicine, Department of Obstetrics and Gynecology, Eastern Virginia Medical School, Norfolk, Virginia 23507, USA.
Fertil Steril. 2011 Jan;95(1):216-20. doi: 10.1016/j.fertnstert.2010.05.023. Epub 2010 Jul 1.
To evaluate the effect of the gonadotropin-releasing hormone antagonist Ganirelix on gonadotropin ovulation induction (OI) in patients with polycystic ovary syndrome (PCOS).
Prospective, randomized, controlled study.
Academic infertility center.
PATIENT(S): Ninety-eight anovulatory women with PCOS undergoing 154 gonadotropin OI cycles.
INTERVENTION(S): Patients were treated with recombinant FSH alone (group 1) or in conjunction with Ganirelix when the leading follicle was ≥13 mm (group 2) versus from the beginning of stimulation (group 3), followed by IUI.
MAIN OUTCOME MEASURE(S): Per cycle clinical pregnancy rate (CPR), live-birth rate (LBR), total gonadotropin dose, days of stimulation, serum LH and peak E2, and premature luteinization rate.
RESULT(S): Data are suggestive of improved CPR in group 2 versus group 1 (33% vs. 19%) and LBR (35% vs. 20%) but not significantly different. Premature luteinization was highest in group 1 (21% vs. 1.8% in group 2 and 2.1% in group 3). Group 3 had the highest cancellation rate and cost without improving CPR and LBR. No differences were noted in peak serum E2, total gonadotropin dose, or days of stimulation.
CONCLUSION(S): Adding Ganirelix in a flexible protocol to gonadotropin OI cycles in women with PCOS may be beneficial by decreasing premature luteinization.
评估促性腺激素释放激素拮抗剂加尼瑞克对多囊卵巢综合征(PCOS)患者促性腺激素诱发排卵(OI)的作用。
前瞻性、随机、对照研究。
学术不孕中心。
98 名患有 PCOS 的无排卵妇女,共进行了 154 个促性腺激素 OI 周期。
患者单独接受重组 FSH 治疗(第 1 组)或当主导卵泡≥13mm 时联合加尼瑞克治疗(第 2 组),或从刺激开始时联合加尼瑞克治疗(第 3 组),随后进行 IUI。
每个周期的临床妊娠率(CPR)、活产率(LBR)、总促性腺激素剂量、刺激天数、血清 LH 和峰值 E2 以及黄体过早化率。
数据表明,第 2 组的 CPR(33%比 19%)和 LBR(35%比 20%)均优于第 1 组,但差异无统计学意义。黄体过早化率在第 1 组最高(21%比第 2 组的 1.8%和第 3 组的 2.1%)。第 3 组的取消率和费用最高,但 CPR 和 LBR 没有改善。峰值血清 E2、总促性腺激素剂量或刺激天数无差异。
在 PCOS 患者的促性腺激素 OI 周期中,灵活使用加尼瑞克方案可能有益,可以减少黄体过早化。