经阴道灌注G-CSF治疗子宫内膜薄的不孕妇女冷冻ET:一项非随机临床试验。

Maryam Eftekhar, Mozhgan Sayadi, Farideh Arabjahvani
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引用次数: 0

摘要

背景:尽管接受了标准和辅助治疗,但在ART周期中我们经常看到子宫内膜薄的患者。改善子宫内膜薄的患者的子宫内膜生长是非常困难的。如果没有足够的子宫内膜厚度,这些患者很可能无法进行胚胎移植。目的:探讨子宫内粒细胞集落刺激因子(G-CSF)灌注对冻融胚胎移植周期子宫内膜及妊娠率的改善作用。材料与方法:这是一项非随机干预临床试验。68例子宫内膜薄(-7 mm)的不孕症患者,在第12 -13个周期天,34例患者接受G-CSF治疗。G-CSF(300微克/1mL)用于改善子宫内膜厚度,经宫内输注IUI导管直接缓慢输注。如果子宫内膜在48-72小时内未达到至少7mm,则给予第二次输注。在子宫内膜条纹扩张最广的区域用连续阴道超声评估子宫内膜厚度。结果:子宫内膜薄(子宫内膜厚度小于7mm)的患者最终周期取消至第19个周期日,G-CSF组因子宫内膜薄导致周期取消率相似(15.20%),对照组为15.20% (p=1.00)。子宫内膜生长在两组内无差异,对照组和G-CSF共处理组之间有所改善,化学(39.30% vs. 14.30%)和临床妊娠率(32.10% vs. 12.00%)尽管无显著性差异。结论:本研究未能证明G-CSF有改善子宫内膜厚度的潜力,但有可能提高冻融胚胎移植周期中子宫内膜薄的不孕症妇女的化学和临床妊娠率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Transvaginal perfusion of G-CSF for infertile women with thin endometrium in frozen ET program: A non-randomized clinical trial.

Background: We often see patients with a thin endometrium in ART cycles, in spite of standard and adjuvant treatments. Improving endometrial growth in patients with a thin endometrium is very difficult. Without adequate endometrial thickness these patients, likely, would not have reached embryo transfer.

Objective: We planned this study to investigate the efficacy of intrauterine granulocyte colony-stimulating factor (G-CSF) perfusion in improving endometrium, and possibly pregnancy rates in frozen-thawed embryo transfer cycles.

Materials and methods: This is a non-randomized intervention clinical trial. Among 68 infertile patients with thin endometrium (-7 mm) at the 12(th)-13(th) cycle day, 34 patients received G-CSF. G-CSF (300 microgram/1mL) to improve endometrial thickness was direct administered by slow intrauterine infusion using IUI catheter. If the endometrium had not reached at least a 7-mm within 48-72 h, a second infusion was given. Endometrial thickness was assessed by serial vaginal ultrasound at the most expanded area of the endometrial stripe.

Results: The cycle was cancelled in the patients with thin endometrium (endometrial thickness below 7mm) until 19(th) cycle day ultimately The cycle cancelation rate owing to thin endometrium was similar in G-CSF group (15.20%), followed by (15.20%) in the control group (p=1.00). The endometrial growth was not different within 2 groups, an improvement was shown between controlled and G-CSF cotreated groups, with chemical (39.30% vs. 14.30%) and clinical pregnancy rates (32.10% vs. 12.00%) although were not significant.

Conclusion: Our study fails to demonstrate that G-CSF has the potential to improve endometrial thickness but has the potential to improve chemical and clinical pregnancy rate of the infertile women with thin endometrium in frozen-thawed embryo transfer cycle.

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