El-Nemr A, Bhide M, Khalifa Y, Al-Mizyen E, Gillott C, Lower A M, Al-Shawaf T, Grudzinskas J G
Fertility Centre, Royal Hospitals NHS Trust, St Bartholomew's Hospital, West Smithfield, EC1A, London, UK.
Eur J Obstet Gynecol Reprod Biol. 2002 Jul 10;103(2):140-5. doi: 10.1016/s0301-2115(01)00297-4.
The efficacy and safety of short acting buserelin and nafarelin intranasal spray were compared to long acting leuprorelin depot intramuscular or subcutaneous injection in this prospective study of 157 women undergoing controlled ovarian hyperstimulation (COH) for in-vitro fertilisation (IVF). Patients were allocated to three groups to receive buserelin 150 microg nasal spray three times daily (Group B), nafarelin nasal spray 400 microg twice daily (Group N), or leuprorelin depot 3.75 mg once by intramuscular or subcutaneous injection (Group L) for pituitary desensitisation prior to commencing COH with human menopausal gonadotrophins (hMG) according to the Centre's protocol. The mean (+/-S.D.) age (years) (32.6+/-3.8: Group B, 32.1+/-3.3: Group N versus 32.1+/-3.3: Group L); mean (+/-S.D.) total dosage of hMG (ampoules) (37.5+/-16.1: Group B, 39.8+/-14.2: Group N versus 41.9+/-12.6: Group L) and mean daily dosage of hMG (ampoules) (3.1: Group B, 2.8: Group N versus 3.0: Group L) seen were not statistically significantly different. The duration between starting the different gonadotrophin-releasing hormone (GnRHa) and the beginning of the next menstrual period was also not seen to be statistically significantly different between the three groups (Group B: 10+/-5.5, Group N: 9.1+/-4.1 versus Group L: 8.2+/-3, days). The number of abandoned cycles was higher in Group L (17% versus 11.8%: Group B and 11.3%: Group N) but this difference did not reach statistical significance. The clinical pregnancy rates per oocyte retrieval and per embryo transfer procedure were respectively, 31.1, 35% in Group B, 12.8, 14% in Group N versus 20.5, 23.7 in Group L and were not seen to be statistically significantly different even when ongoing pregnancy rates were compared. Apart from a statistically significantly greater incidence of allergic nasal reactions in the nafarelin group (P=0.001), all other side-effects were not shown to be statistically significantly different between the three groups. We conclude that a single dose of leuprorelin depot can be considered to be as an equally effective alternative to multiple doses of buserelin or nafarelin for pituitary desensitisation in women undergoing COH for IVF.
在这项前瞻性研究中,对157名接受体外受精(IVF)控制性卵巢刺激(COH)的女性,比较了短效布舍瑞林和那法瑞林鼻喷雾剂与长效亮丙瑞林长效注射剂肌肉注射或皮下注射的疗效和安全性。患者被分为三组,根据中心方案,在开始用人绝经期促性腺激素(hMG)进行COH之前,分别接受每日三次150微克布舍瑞林鼻喷雾剂(B组)、每日两次400微克那法瑞林鼻喷雾剂(N组)或一次肌肉注射或皮下注射3.75毫克亮丙瑞林长效注射剂(L组)进行垂体脱敏。平均(±标准差)年龄(岁)(B组:32.6±3.8,N组:32.1±3.3,L组:32.1±3.3);hMG总剂量(安瓿)的平均(±标准差)(B组:37.5±16.1,N组:39.8±14.2,L组:41.9±12.6)以及hMG每日平均剂量(安瓿)(B组:3.1,N组:2.8,L组:3.0)在统计学上无显著差异。三组在开始使用不同促性腺激素释放激素(GnRHa)至下一个月经周期开始之间的持续时间在统计学上也无显著差异(B组:10±5.5天,N组:9.1±4.1天,L组:8.2±3天)。L组放弃周期的数量更高(17%,而B组为11.8%,N组为11.3%),但这种差异未达到统计学显著性。每组取卵时和每次胚胎移植程序的临床妊娠率分别为,B组31.1%、35%,N组12.8%、14%,L组20.5%、23.7%,即使比较持续妊娠率,也未发现统计学上的显著差异。除那法瑞林组过敏鼻反应发生率在统计学上显著更高(P = 0.001)外,三组之间所有其他副作用在统计学上均无显著差异。我们得出结论,对于接受IVF的COH女性进行垂体脱敏时,单剂量亮丙瑞林长效注射剂可被视为与多剂量布舍瑞林或那法瑞林同样有效的替代方法。