Argentine Cochrane Centre, Institute for Clinical Effectiveness and Health Policy (IECS), Center for Research in Epidemiology and Public Health, National Scientific and Technical Research Council (CONICET), Ravignani 2024, C1414CPV, Buenos Aires, Argentina.
Center for Studies in Genetics and Reproduction (CEGYR), Buenos Aires, Argentina.
J Assist Reprod Genet. 2020 Dec;37(12):2913-2928. doi: 10.1007/s10815-020-01966-5. Epub 2020 Nov 21.
To compare the effectiveness of starting the ovarian stimulation on the early follicular phase ("Conventional") with the newer range of non-conventional approaches starting in the luteal phase ("Luteal"), random-start, and studies implementing them in DuoStim ("Conventional"+"Luteal").
Systematic review. We searched CENTRAL, PubMed, and Embase, on March 2020. We included randomized and non-randomized controlled trials that compared "Luteal," random-start ovarian stimulation or DuoStim with "Conventional"; we analyzed them by subgroups: oocyte freezing and patients undergoing ART treatments, both, in the general infertile population and among poor responders.
The following results come from a sensitivity analysis that included only the low/moderate risk of bias studies. When comparing "Luteal" to "Conventional," clinically relevant differences in MII oocytes were ruled out in all subgroups. We found that "Luteal" probably increases the COH length both, in the general infertile population (OR 2.00 days, 95% CI 0.81 to 3.19, moderate-quality evidence) and in oocyte freezing cycles (MD 0.85 days, 95% CI 0.53 to 1.18, moderate-quality evidence). When analyzing DuoStim among poor responders, we found that it appears to generate a higher number of MII oocytes in comparison with a single "Conventional" (MD 3.35, 95%CI 2.54-4.15, moderate-quality evidence).
Overall, this systematic review of the available data demonstrates that in poor responders, general infertile population and oocyte freezing for cancer stimulation in the late follicular and luteal phases can be utilized in non-conventional approaches such as random-start and DuoStim cycles, offering similar outcomes to the conventional cycles but potentially with increased flexibility, within a reduced time frame. However, more well-designed trials are required to establish certainty.
比较在卵泡早期开始卵巢刺激(“常规”)与较新的非传统方法(“黄体期”、随机起始和在 DuoStim 中实施的方法)的有效性。
系统评价。我们于 2020 年 3 月检索了 CENTRAL、PubMed 和 Embase。我们纳入了比较黄体期、随机起始卵巢刺激或 DuoStim 与常规方法的随机和非随机对照试验;并按亚组分析:卵母细胞冷冻和接受 ART 治疗的患者,在一般不孕人群和反应不良者中。
以下结果来自仅纳入低/中偏倚风险研究的敏感性分析。在比较黄体期与常规方法时,在所有亚组中均排除了 MII 卵母细胞的临床相关差异。我们发现黄体期可能会增加 COH 长度,在一般不孕人群中(OR 2.00 天,95%CI 0.81 至 3.19,中等质量证据)和在卵母细胞冷冻周期中(MD 0.85 天,95%CI 0.53 至 1.18,中等质量证据)。在分析反应不良者中的 DuoStim 时,我们发现它似乎比单次常规方法产生更多的 MII 卵母细胞(MD 3.35,95%CI 2.54-4.15,中等质量证据)。
总体而言,对现有数据的系统评价表明,在反应不良者、一般不孕人群和为癌症刺激在卵泡晚期和黄体期进行卵母细胞冷冻时,可以在非传统方法(如随机起始和 DuoStim 周期)中使用,提供与常规周期相似的结果,但具有潜在的灵活性,在更短的时间内。然而,需要更多设计良好的试验来建立确定性。