Singh Aparna, Bhandari Shilpa, Agrawal Pallavi, Gupta Nitika, Munaganuru Niharika
Department of Reproductive Medicine, Sri Aurobindo Medical College and Post Graduate Institute, Indore, Madhya Pradesh, India.
J Hum Reprod Sci. 2016 Jul-Sep;9(3):159-163. doi: 10.4103/0974-1208.192054.
This study was undertaken to compare between clomiphene citrate (CC) and gonadotropin-releasing hormone antagonist-based protocols in donor-recipient cycles in terms of parameters of ovarian stimulation and obstetric outcome.
Two hundred and three fertile oocyte donors were stimulated using two different protocols: Clomiphene based ( = 103) and antagonist based ( = 100). Donors in the one group were stimulated from day 1 or 2 of spontaneous or withdrawal bleeds with CC (50 mg/day) and recombinant follicle-stimulating hormone (FSH) till the day of trigger while donors in the other group were stimulated using recombinant FSH from day 1 or 2, and the antagonist was added as per flexible antagonist protocol. When >3 follicles were >17 mm in diameter, trigger was given with 2 mg leuprolide intramuscular. Transvaginal oocyte retrieval was done after 34 h of trigger.
There was no significant difference in between the two groups in terms of age, antral follicle count, starting dose of gonadotropins, total dose required, duration of stimulation, number of follicles retrieved, mature follicles, and fertilization rate. The serum estradiol levels were significantly raised in the clomiphene group ( < 0.001). Pregnancy rate was similar in both the groups. The clinical pregnancy rate was 65.94% in the clomiphene group and 57.46% in the antagonist group. The live birth rate per cycle started was 47.8% in the clomiphene group and 39.55% in the antagonist group. There was one case of ectopic pregnancy in the antagonist group.
Controlled ovarian stimulation using clomiphene and gonadotropin is a viable option for donor oocyte cycles. The cost and number of injections used per cycle can be reduced by using the clomiphene-based protocols.
本研究旨在比较枸橼酸氯米芬(CC)方案和促性腺激素释放激素拮抗剂方案在供体 - 受体周期中的卵巢刺激参数和产科结局。
203名可育卵母细胞供体采用两种不同方案进行刺激:氯米芬方案(n = 103)和拮抗剂方案(n = 100)。一组供体从自然月经周期第1天或第2天或撤退性出血后开始,使用CC(50mg/天)和重组促卵泡激素(FSH)刺激至扳机日,而另一组供体从第1天或第2天开始使用重组FSH刺激,并根据灵活拮抗剂方案添加拮抗剂。当3个以上卵泡直径>17mm时,给予2mg亮丙瑞林肌肉注射扳机。扳机后34小时行经阴道取卵。
两组在年龄、窦卵泡计数、促性腺激素起始剂量、所需总剂量、刺激持续时间、取卵卵泡数、成熟卵泡数和受精率方面无显著差异。氯米芬组血清雌二醇水平显著升高(P < 0.001)。两组妊娠率相似。氯米芬组临床妊娠率为65.94%,拮抗剂组为57.46%。氯米芬组每个启动周期的活产率为47.8%,拮抗剂组为39.55%。拮抗剂组有1例宫外孕。
使用氯米芬和促性腺激素进行控制性卵巢刺激是供体卵母细胞周期的可行选择。使用基于氯米芬的方案可降低每个周期的成本和注射次数。