Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, Wayne State University School of Medicine/Detroit Medical Center, 275 E. Hancock Street, Detroit, MI, 48201, USA.
Division of Genetic and Metabolic Disorders, Department of Pediatrics and Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI, USA.
J Assist Reprod Genet. 2018 Feb;35(2):289-295. doi: 10.1007/s10815-017-1056-6. Epub 2017 Sep 30.
The purpose of the study is to determine whether continued stimulation of mature follicles to allow "catch up" growth of medium-sized follicles in assisted reproductive technology compromises the clinical pregnancy (CPR) and live birth (LBR) rates in IVF/ICSI cycles.
This retrospective cohort study reviewed 200 first IVF ± ICSI cycles out of a total of 340 cycles with complete data. Women underwent stimulation protocols with gonadotropins (Gn) and GnRH antagonist. Treatment cycles were divided into two groups (Gp): hCG administration delayed despite the presence of two mature follicles, defined as ≥ 18 mm [Gp1, n = 79] and hCG administration given when there were two mature follicles [Gp2, n = 121].
The patients in Gp1 were significantly younger than those in Gp2 [32.9 (4.5) vs. 34.3 (4.8), p = 0.04] and needed a median of one more day of superovulation before ovulation was triggered with hCG. The extra days was associated with the use of 450 [75-2025] more Gn, such that at the time the hCG was administered, patient's in group 1 had developed significantly greater number of follicles ≥ 18 mm [mean (SD), 4.9 (1.8) vs. 3.4 (1.7), p < 0.0001]. The clinical pregnancy (48.1 vs. 38.0%, [OR (95% CI)] [1.6 (1.0-2.5), p = 0.09]) and live birth (43.0 vs. 35.5%, [1.4 (0.9-2.3), p = 0.21]) rates per cycle started were not significantly different between the two groups. Forward stepwise logistic regression showed that only maternal age (p = 0.04) influenced clinical pregnancy rates (OR = 0.88, CI 0.78-0.99) and only the number of days for superovulation influenced live birth rates (OR = 0.65, CI 0.486-0.869).
This study demonstrated that delaying hCG administration to allow further growth of the medium-sized follicles added further days of superovulation and cost without improvement in CPR and LBR.
本研究旨在确定在辅助生殖技术中继续刺激成熟卵泡以允许中等大小卵泡“追赶”生长是否会影响体外受精/卵胞浆内单精子注射(IVF/ICSI)周期中的临床妊娠(CPR)和活产(LBR)率。
本回顾性队列研究分析了 340 个周期中 200 个完整数据的首次 IVF ± ICSI 周期。女性接受促性腺激素(Gn)和 GnRH 拮抗剂刺激方案。治疗周期分为两组(Gp):尽管存在两个成熟卵泡(定义为≥18mm),但仍延迟给予人绒毛膜促性腺激素(hCG)[Gp1,n=79];当有两个成熟卵泡时给予 hCG[Gp2,n=121]。
Gp1 组的患者明显比 Gp2 组年轻[32.9(4.5)岁 vs. 34.3(4.8)岁,p=0.04],并且在 hCG 触发排卵前需要多一天的超排卵。额外的天数与使用 450[75-2025]更多的 Gn 相关,因此在给予 hCG 时,Gp1 组的患者发育出了显著更多的≥18mm 的卵泡[平均(SD),4.9(1.8)vs. 3.4(1.7),p<0.0001]。每个周期开始时的临床妊娠(48.1% vs. 38.0%,[OR(95%CI)] [1.6(1.0-2.5),p=0.09])和活产(43.0% vs. 35.5%,[1.4(0.9-2.3),p=0.21])率无显著差异。向前逐步逻辑回归显示,只有母亲年龄(p=0.04)影响临床妊娠率(OR=0.88,CI 0.78-0.99),只有超排卵天数影响活产率(OR=0.65,CI 0.486-0.869)。
本研究表明,延迟 hCG 给药以允许中等大小卵泡进一步生长会增加额外的超排卵天数和成本,但不会提高 CPR 和 LBR。