Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, Center for Advanced Reproductive Services, University of Connecticut Health Center, Farmington, Connecticut.
Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, Center for Advanced Reproductive Services, University of Connecticut Health Center, Farmington, Connecticut.
Fertil Steril. 2014 Sep;102(3):753-8. doi: 10.1016/j.fertnstert.2014.05.030. Epub 2014 Jun 19.
To compare the rate of congenital anomalies, obstetrical complications, and neonatal complications in antagonist cycles where either GnRH agonist (GnRHa) or hCG was used for final oocyte maturation.
Retrospective cohort study.
University-based tertiary fertility center.
PATIENT(S): Three hundred ninety-two women under 40 years of age who underwent controlled ovarian stimulation using a GnRH antagonist protocol and who had final oocyte maturation triggered with either a GnRHa or hCG that resulted in pregnancy and delivery after 16 weeks' gestation.
INTERVENTION(S): GnRHa versus hCG trigger of final oocyte maturation.
MAIN OUTCOME MEASURE(S): Congenital anomaly rates, obstetrical complications, and neonatal complications.
RESULT(S): There were no significant differences in the rate of congenital anomalies between GnRHa and hCG trigger (6.6 vs. 9.2%). There were also no differences in the maternal complications (27.6 vs. 20.8%) or neonatal complications (19.7 vs. 20.0%) between the GnRHa trigger and hCG trigger groups.
CONCLUSION(S): GnRHa trigger does not affect the rate of congenital anomalies or obstetrical or neonatal complications and remains a viable option in the prevention of ovarian hyperstimulation syndrome.
比较使用 GnRH 激动剂(GnRHa)或 hCG 进行最终卵母细胞成熟时拮抗剂周期中先天性异常、产科并发症和新生儿并发症的发生率。
回顾性队列研究。
大学附属三级生育中心。
392 名年龄在 40 岁以下的妇女,她们接受了 GnRH 拮抗剂方案的控制性卵巢刺激,最终卵母细胞成熟的触发使用 GnRHa 或 hCG,导致妊娠,并在 16 周妊娠后分娩。
GnRHa 与 hCG 触发最终卵母细胞成熟。
先天性异常发生率、产科并发症和新生儿并发症。
GnRHa 与 hCG 触发的先天性异常发生率无显著差异(6.6%比 9.2%)。GnRHa 触发组和 hCG 触发组的母体并发症(27.6%比 20.8%)或新生儿并发症(19.7%比 20.0%)也无差异。
GnRHa 触发不会影响先天性异常或产科或新生儿并发症的发生率,仍然是预防卵巢过度刺激综合征的可行选择。