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醋酸那法瑞林与D-色氨酸6-促黄体生成素释放激素在体外受精(IVF)患者中进行垂体暂时抑制的比较:一项前瞻性交叉研究。

Comparison between nafarelin acetate and D-Trp6-LHRH for temporary pituitary suppression in in vitro fertilization (IVF) patients: a prospective crossover study.

作者信息

Tanos V, Friedler S, Shushan A, Strauss N, Hetsroni I, Lewin A

机构信息

Department of Obstetrics and Gynecology, Hadassah University Hospital, Ein-Kerem, Jerusalem, Israel.

出版信息

J Assist Reprod Genet. 1995 Nov;12(10):715-9. doi: 10.1007/BF02212899.

Abstract

PURPOSE

Nafarelin acetate is a new gonadotropin releasing (GnRH) agonist analogue with unique potency, intranasal administration, and convenient storage. Hence, nafarelin was considered as an alternative for temporary pituitary suppression in patients undergoing ovulation induction in IVF. A crossover treatment in a prospective study was performed including 40 women with bilateral obstructed tubes and normal ovarian function, treated in 80 ovulation induction cycles using the long protocol. Twenty patients used nafarelin acetate 600 micrograms/daily in their first cycle and received D-Trp6-LHRH, 0.5 mg/daily, in their following cycle. The other 20 women used decapeptyl in their cycle and received nafarelin in the second.

RESULTS

Estradiol suppression was achieved by both D-Trp6-LHRH and nafarelin at equal time intervals. The average total number of ampoules (P = 0.0005) and the length of administration of hMG required for ovarian stimulation (P = 0.0002) and the time interval between GnRHa initiation to oocyte retrieval (P = 0.04) was significantly lower in nafarelin cycles. The number and the distribution between large and small follicles as well as the average number of oocytes retrieved did not differ between the two GnRH analogues.

CONCLUSION

Our results demonstrate that nafarelin acetate is comparable to D-Trp6-LHRH for temporary pituitary suppression used for controlled ovarian stimulation in IVF patients. However, using nafarelin ovarian stimulation was achieved with few ampoules of hMG, administered for a shorter period of time, thus with a lesser cost.

摘要

目的

醋酸那法瑞林是一种新型促性腺激素释放(GnRH)激动剂类似物,具有独特的效力、鼻内给药方式和便于储存的特点。因此,那法瑞林被视为体外受精(IVF)中接受促排卵治疗患者临时垂体抑制的替代药物。在一项前瞻性研究中进行了交叉治疗,纳入了40名双侧输卵管阻塞但卵巢功能正常的女性,她们在80个促排卵周期中采用长方案进行治疗。20名患者在第一个周期每天使用600微克醋酸那法瑞林,并在随后的周期中每天接受0.5毫克D-色氨酸6-促黄体生成素释放激素(D-Trp6-LHRH)治疗。另外20名女性在第一个周期使用曲普瑞林,并在第二个周期接受那法瑞林治疗。

结果

D-Trp6-LHRH和那法瑞林在相同时间间隔内均实现了雌二醇抑制。在使用那法瑞林的周期中,促性腺激素(hMG)刺激卵巢所需的安瓿平均总数(P = 0.0005)、hMG给药时长(P = 0.0002)以及从启动GnRHa到取卵的时间间隔(P = 0.04)均显著更低。两种GnRH类似物之间,大小卵泡的数量及分布以及平均取卵数均无差异。

结论

我们的结果表明,在IVF患者中用于控制性卵巢刺激的临时垂体抑制方面,醋酸那法瑞林与D-Trp6-LHRH相当。然而,使用那法瑞林时,只需较少安瓿的hMG就能实现卵巢刺激,给药时间更短,因此成本更低。

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