Fanchin R, Olivennes F, Righini C, Hazout A, Schwab B, Frydman R
Department of Obstetrics and Gynecology, Hôpital Antoine Béclère, Clamart, France.
Fertil Steril. 1995 Sep;64(3):505-10. doi: 10.1016/s0015-0282(16)57784-x.
To evaluate the relative efficacy of a new system for fallopian tube sperm perfusion in comparison with standard IUI in controlled ovarian hyperstimulation (COH) cycles.
Prospective randomized trial.
Ovulation induction program of a tertiary outpatient care center, Hôpital Antoine Béclère, Clamart, France.
We studied 74 infertile women aged 20 to 38 years undergoing 100 cycles of COH from December 1993 to May 1994 only excluding cases of age > 38 years, obstructed or severely damaged fallopian tubes, E2 levels per mature follicle < 250 pg/mL (conversion factor to SI unit, 3.671) on the day of hCG administration, spontaneous LH surge, and cases of marked sperm abnormalities.
Controlled ovarian hyperstimulation was achieved using three types of ovarian stimulation protocols: clomiphene citrate (CC) and hMG (n = 35). hMG alone (n = 35) or GnRH agonist and FSH and hMG (n = 30). Thirty-six hours after hCG administration, patients were assigned randomly to either IUI (group A, n = 50) or fallopian tube sperm perfusion (group B, n = 50). Intrauterine insemination was performed with 0.2 mL of sperm suspension according to a standard technique. Fallopian tube sperm perfusion was performed using a simple and reliable system that ensures a good cervical seal and allows to a pressurized injection of 4 mL of sperm suspension.
Feasibility of the fallopian tube sperm perfusion method, clinical pregnancy (presence of gestational sac with heart beats at 6 weeks of amenorrhea), and ongoing pregnancy rates (PRs) (> 12 weeks of amenorrhea), incidence of complications (multiple pregnancies and ovarian hyperstimulation syndrome [OHSS]).
Overall, the new fallopian tube sperm perfusion system was simple to handle and well tolerated by patients. In group A, we observed 10 clinical pregnancies (20% per cycle) of which 7 were ongoing (14%). In group B, 20 clinical pregnancies (40% per cycle) of which 17 ongoing pregnancies (34%) were obtained. These differences were statistically significant. The prevalence of twin and three or more sac pregnancies was similar in the two groups (3/10 and 0/10, respectively, in group A, and 5/20 and 2/20, respectively, in group B). No case of moderate or severe OHSS was observed in this series.
Our results indicate that the new system for fallopian tube sperm perfusion is not only simple and reliable but also may lead to PRs twice as high as standard IUI in COH cycles.
评估在控制性卵巢刺激(COH)周期中,一种新的输卵管精子灌注系统与标准宫腔内人工授精(IUI)相比的相对疗效。
前瞻性随机试验。
法国克拉马尔安托万·贝克莱尔医院三级门诊护理中心的排卵诱导项目。
我们研究了1993年12月至1994年5月期间74名年龄在20至38岁的不孕女性,她们接受了100个COH周期的治疗,仅排除年龄>38岁、输卵管阻塞或严重受损、注射人绒毛膜促性腺激素(hCG)当天每个成熟卵泡的雌二醇(E2)水平<250 pg/mL(换算为国际单位制的转换因子为3.671)、促黄体生成素(LH)自发峰值以及精子明显异常的病例。
采用三种卵巢刺激方案实现控制性卵巢刺激:枸橼酸氯米芬(CC)和人绝经期促性腺激素(hMG)(n = 35);单独使用hMG(n = 35);促性腺激素释放激素(GnRH)激动剂、促卵泡生成素(FSH)和hMG(n = 30)。注射hCG 36小时后,患者被随机分配至IUI组(A组,n = 50)或输卵管精子灌注组(B组,n = 50)。按照标准技术,用0.2 mL精子悬液进行宫腔内人工授精。使用一种简单可靠的系统进行输卵管精子灌注,该系统可确保良好的宫颈封闭,并允许加压注射4 mL精子悬液。
输卵管精子灌注方法的可行性、临床妊娠(闭经6周时出现有心跳的妊娠囊)和持续妊娠率(PRs)(闭经>12周)、并发症发生率(多胎妊娠和卵巢过度刺激综合征[OHSS])。
总体而言,新的输卵管精子灌注系统操作简单,患者耐受性良好。A组中,我们观察到10例临床妊娠(每个周期20%),其中7例为持续妊娠(14%)。B组中,获得了20例临床妊娠(每个周期40%),其中17例为持续妊娠(34%)。这些差异具有统计学意义。两组中双胎及三胎或更多孕囊妊娠的发生率相似(A组分别为3/10和0/10,B组分别为5/20和2/20)。本系列中未观察到中度或重度OHSS病例。
我们的结果表明,新的输卵管精子灌注系统不仅简单可靠,而且在COH周期中可能使持续妊娠率比标准IUI高出两倍。