将脂质内注射疗法作为子宫腺肌症相关不孕症妇女的辅助治疗方法。

IF 3.1 Q1 OBSTETRICS & GYNECOLOGY Therapeutic advances in reproductive health Pub Date : 2023-06-21 eCollection Date: 2023-01-01 DOI:10.1177/26334941231181258
James Henshaw, Kelton Tremellen
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摘要

背景:目前,有证据表明,子宫腺肌症患者在胚胎移植前使用促性腺激素释放激素(GnRH)激动剂长效降调(LDR)可提高体外受精(IVF)的成功率,但在没有子宫腺肌症的情况下,成功率达不到预期的基线。鉴于子宫腺肌症与子宫内膜免疫环境异常之间的关联,许多医生在使用 GnRH 促效剂治疗的同时,还使用泼尼松龙或 Intralipid 辅助治疗,尽管这两种治疗方法均未被证实有益:本研究旨在探讨在使用 GnRH 促效剂 LDR 的同时使用泼尼松龙或 Intralipid 免疫疗法是否能改善子宫腺肌症患者的生育效果:这是一项回顾性队列研究,研究对象是在2019年1月至2020年12月期间在一家私人试管婴儿诊所接受首次基因筛查优胚移植的116名连续腺肌症患者:结果:三个治疗组的产妇年龄、体重指数、胚胎移植数量、孕龄或胎次均无差异。与对比组相比,接受 Intralipid 治疗的患者预后较差,不孕时间较长(4 年),胚胎移植次数较多,前 5 次胚胎移植。对所有协变量进行调整后的逻辑回归分析表明,与单独使用LDR(LBR为40%)相比,LDR加Intralipid治疗的活产率(LBRs;60%)明显更高;然而,在使用GnRH激动剂LDR(LBR为30%)的基础上加用泼尼松龙并没有带来额外的活产效益:在这项回顾性分析中,我们发现在腺肌症患者接受体外受精时,Intralipid辅助治疗与GnRH激动剂治疗相结合,可使使用植入前基因检测筛选胚胎的无腺肌症妇女获得预期的LBR。在使用泼尼松龙作为 GnRH 激动剂 LDR 的辅助治疗时,则看不到这种益处。未来还需要进行随机临床试验,以确认Intralipid与GnRH激动剂联合治疗的疗效。
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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Intralipid infusion therapy as an adjunct treatment in women experiencing adenomyosis-related infertility.

Background: Currently, there is some evidence that adenomyosis patients using gonadotropin-releasing hormone (GnRH) agonist long downregulation (LDR) prior to embryo transfer may improve in vitro fertilization (IVF) success rate, but not to the baseline expected success where there is no adenomyosis. Given the association between adenomyosis and an aberrant endometrial immune environment, many physicians also use prednisolone or Intralipid adjuvant treatments in combination with GnRH agonist therapy, despite neither being of proven benefit.

Objective: The purpose of this study was to investigate whether the addition of prednisolone or Intralipid immune therapy to GnRH agonist LDR improves fertility outcomes in patients with adenomyosis.

Methods: This is a retrospective cohort study of 116 consecutive adenomyosis patients who underwent their first transfer of a genetically screened euploid embryo between January 2019 and December 2020 at a private IVF clinic.

Results: There was no difference in maternal age, body mass index, number of embryo's transferred and gravidity or parity among the three treatment groups. Patients who received Intralipid had a poorer prognosis with a longer duration of infertility (4 years) and a higher number of previous embryo transfers (ETs, 5 previous ETs) compared to the comparison groups. Logistic regression analysis adjustment for all covariates revealed that LDR plus Intralipid therapy produced significantly higher live birth rates (LBRs; 60%) compared to LDR alone (40% LBR); yet, the addition of prednisolone to GnRH agonist LDR (30% LBR) provided no additional live birth benefit.

Conclusion: In this retrospective analysis, we showed Intralipid adjuvant treatment in combination with GnRH agonist therapy in adenomyosis patients undergoing IVF resulted in a LBR expected in women without adenomyosis using preimplantation genetic testing screened embryos. This benefit was not seen when using prednisolone as an adjuvant to GnRH agonist LDR. Future randomized clinical trials will be required to confirm the therapeutic benefit of Intralipid in combination with GnRH agonist therapy.

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