Franco J G, Baruffi R L R, Mauri A L, Petersen C G, Felipe V, Cornicelli J, Cavagna M, Oliveira J B A
Centre for Human Reproduction Prof. Franco Junior, Av. Prof. João Fiusa, 689-CEP 14025-310, Ribeirão Preto, SP, Brazil.
Reprod Biomed Online. 2006 Nov;13(5):618-27. doi: 10.1016/s1472-6483(10)60651-7.
The aim of this meta-analysis was to compare the efficacy of gonadotrophin antagonist (GnRH-ant) versus GnRH agonist (GnRHa) as coadjuvant therapy for ovarian stimulation in poor ovarian responders in IVF/intracytoplasmic sperm injection cycles. Search strategies included on-line surveys of databases such as MEDLINE , EMBASE and others. A fixed effects model was used for odds ratio (OR) and effect size (weighted mean difference, WMD). Six trials fulfilled the inclusion criteria (randomized controlled trials). There was no difference between GnRH-ant and GnRHa (long and flare-up protocols) with respect to cycle cancellation rate, number of mature oocytes and clinical pregnancy rate per cycle initiated, per oocyte retrieval and per embryo transfer. When the meta-analysis was applied to the two trials that had used GnRH-ant versus long protocols of GnRHa, a significantly higher number of retrieved oocytes was observed in the GnRH-ant protocols [P=0.018; WMD: 1.12 (0.18, 2.05)]. However, when the meta-analysis was applied to the four trials that had used GnRH-ant versus flare-up protocols, a significantly higher number of retrieved oocytes (P=0.032; WMD: -0.51, 95% CI -0.99, -0.04) was observed in the GnRHa protocols. Nevertheless, additional randomized controlled trials with better planning are needed to confirm these results.
本荟萃分析的目的是比较促性腺激素拮抗剂(GnRH-ant)与促性腺激素释放激素激动剂(GnRHa)作为辅助治疗在体外受精/卵胞浆内单精子注射周期中对卵巢反应不良者进行卵巢刺激的疗效。检索策略包括对MEDLINE、EMBASE等数据库进行在线检索。采用固定效应模型计算比值比(OR)和效应量(加权平均差,WMD)。六项试验符合纳入标准(随机对照试验)。在取消周期率、每个启动周期、每次取卵和每次胚胎移植的成熟卵母细胞数量及临床妊娠率方面,GnRH-ant与GnRHa(长效和激发方案)之间无差异。当对两项使用GnRH-ant与GnRHa长效方案的试验进行荟萃分析时,GnRH-ant方案中观察到的回收卵母细胞数量显著更多[P = 0.018;WMD:1.12(0.18,2.05)]。然而,当对四项使用GnRH-ant与激发方案的试验进行荟萃分析时,GnRHa方案中观察到的回收卵母细胞数量显著更多(P = 0.032;WMD:-0.51,95%CI -0.99,-0.04)。尽管如此,仍需要进行更多规划更好的随机对照试验来证实这些结果。