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辅助生殖中对不孕女性进行子宫内膜注射胚胎培养液上清液

Endometrial injection of embryo culture supernatant for subfertile women in assisted reproduction.

作者信息

Siristatidis Charalampos S, Sertedaki Eleni, Karageorgiou Vasilios, Vaidakis Dennis

机构信息

Assisted Reproduction Unit, 2nd Department of Obstetrics and Gynaecology, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

Alexandra General Hospital, Athens, Greece.

出版信息

Cochrane Database Syst Rev. 2020 Aug 14;8(8):CD013063. doi: 10.1002/14651858.CD013063.pub2.

Abstract

BACKGROUND

Despite substantial improvements in the success of assisted reproduction techniques (ART), live birth rates may remain consistently low, and practitioners may look for innovative treatments to improve the outcomes. The injection of embryo culture supernatant in the endometrial cavity can be undertaken at various time intervals before embryo transfer. It provides an altered endometrial environment through the secretion of factors considered to facilitate implantation. It is proposed that injection of the supernatant into the endometrial cavity prior to embryo transfer will stimulate the endometrium and provide better conditions for implantation to take place. An increased implantation rate would subsequently increase rates of clinical pregnancy and live birth, but current robust evidence on the efficacy of injected embryo culture supernatant is lacking.

OBJECTIVES

To evaluate the effectiveness and safety of endometrial injection of embryo culture supernatant before embryo transfer in women undergoing ART.

SEARCH METHODS

Our search strategies were designed with the help of the Cochrane Gynaecology and Fertility Group Information Specialist. We sought to identify all published and unpublished randomised controlled trials (RCTs) meeting inclusion criteria. Searches were performed on 2 December 2019. We searched the Cochrane Gynaecology and Fertility Group Specialised Register of controlled trials, CENTRAL, MEDLINE, Embase, CINAHL, trials registries and grey literature. We made further searches in the UK National Institute for Health and Care Excellence (NICE) fertility assessment and treatment guidelines. We handsearched reference lists of relevant systematic reviews and RCTs, together with searches of PubMed and Google for any recent trials that have not yet been indexed in the major databases. We had no language or location restrictions.

SELECTION CRITERIA

We included RCTs testing the use of endometrial injection of embryo culture supernatant before embryo transfer during an ART cycle, compared with the non-use of this intervention, the use of placebo or the use of any other similar drug.

DATA COLLECTION AND ANALYSIS

Two review authors independently selected studies, assessed risk of bias, extracted data from studies and attempted to contact the authors where data were missing. We pooled studies using a fixed-effect model. Our primary outcomes were live birth/ongoing pregnancy and miscarriage. We performed statistical analysis using Review Manager 5. We assessed evidence quality using GRADE methods.

MAIN RESULTS

We found five RCTs suitable for inclusion in the review (526 women analysed). We made two comparisons: embryo culture supernatant use versus standard care or no intervention; and embryo culture supernatant use versus culture medium. All studies were published as full-text articles. Data derived from the reports or through direct communication with investigators were available for the final meta-analysis performed. The GRADE evidence quality of studies ranged from very low-quality to moderate-quality. Factors reducing evidence quality included high risk of bias due to lack of blinding, unclear risk of publication bias and selective outcome reporting, serious inconsistency among study outcomes, and serious imprecision due to wide confidence intervals (CIs) and low numbers of events. Comparison 1. Endometrial injection of embryo culture supernatant before embryo transfer versus standard care or no intervention: One study reported live birth only and two reported the composite outcome live birth and ongoing pregnancy. We are uncertain whether endometrial injection of embryo culture supernatant before embryo transfer during an ART cycle improves live birth/ongoing pregnancy rates compared to no intervention (odds ratio (OR) 1.11, 95% CI 0.73 to 1.70; 3 RCTs; n = 340, I = 84%; very low-quality evidence). Results suggest that if the chance of live birth/ongoing pregnancy following placebo or no treatment is assumed to be 42%, the chance following the endometrial injection of embryo culture supernatant before embryo transfer would vary between 22% and 81%. We are also uncertain whether the endometrial injection of embryo culture supernatant could decrease miscarriage rates, compared to no intervention (OR 0.89, 95% CI 0.44 to 1.78, 4 RCTs, n = 430, I = 58%, very low-quality evidence). Results suggest that if the chance of miscarriage following placebo or no treatment is assumed to be 9%, the chance following injection of embryo culture supernatant would vary between 3% and 30%. Concerning the secondary outcomes, we are uncertain whether the injection of embryo culture supernatant prior to embryo transfer could increase clinical pregnancy rates (OR 1.13, 95% CI 0.80 to 1.61; 5 RCTs; n = 526, I = 0%; very low-quality evidence), decrease ectopic pregnancy rates (OR 0.32, 95% CI 0.01 to 8.24; n = 250; 2 RCTs; I = 41%; very low-quality evidence), decrease multiple pregnancy rates (OR 0.70, 95% CI 0.26 to 1.83; 2 RCTs; n = 150; I = 63%; very low-quality evidence), or decrease preterm delivery rates (OR 0.63, 95% CI 0.17 to 2.42; 1 RCT; n = 90; I = 0%; very low-quality evidence), compared to no intervention. Finally, there may have been little or no difference in foetal abnormality rates between the two groups (OR 3.10, 95% CI 0.12 to 79.23; 1 RCT; n = 60; I = 0%; low-quality evidence). Comparison 2. Endometrial injection of embryo culture supernatant versus endometrial injection of culture medium before embryo transfer We are uncertain whether the use of embryo culture supernatant improves clinical pregnancy rates, compared to the use of culture medium (OR 1.09, 95% CI 0.48 to 2.46; n = 96; 1 RCT; very low-quality evidence). No study reported live birth/ongoing pregnancy, miscarriage, ectopic or multiple pregnancy, preterm delivery or foetal abnormalities.

AUTHORS' CONCLUSIONS: We are uncertain whether the addition of endometrial injection of embryo culture supernatant before embryo transfer as a routine method for the treatment of women undergoing ART can improve pregnancy outcomes. This conclusion is based on current available data from five RCTs, with evidence quality ranging from very low to moderate across studies. Further large well-designed RCTs reporting on live births and adverse clinical outcomes are still required to clarify the exact role of endometrial injection of embryo culture supernatant before embryo transfer.

摘要

背景

尽管辅助生殖技术(ART)的成功率有了显著提高,但活产率可能仍持续较低,从业者可能会寻求创新治疗方法来改善治疗结果。在胚胎移植前的不同时间间隔,可将胚胎培养液上清液注入子宫内膜腔。它通过分泌被认为有助于着床的因子,营造一个改变了的子宫内膜环境。有人提出,在胚胎移植前将上清液注入子宫内膜腔会刺激子宫内膜,并为着床创造更好的条件。着床率的提高随后会增加临床妊娠率和活产率,但目前缺乏关于注入胚胎培养液上清液疗效的确凿证据。

目的

评估在接受ART的女性中,胚胎移植前子宫内膜注射胚胎培养液上清液的有效性和安全性。

检索方法

我们的检索策略是在Cochrane妇科与生育组信息专家的帮助下设计的。我们试图识别所有符合纳入标准的已发表和未发表的随机对照试验(RCT)。检索于2019年12月2日进行。我们检索了Cochrane妇科与生育组专业对照试验注册库、CENTRAL、MEDLINE、Embase、CINAHL、试验注册库和灰色文献。我们还在英国国家卫生与临床优化研究所(NICE)的生育评估和治疗指南中进行了进一步检索。我们手工检索了相关系统评价和RCT的参考文献列表,并在PubMed和谷歌上搜索了主要数据库中尚未索引的任何近期试验。我们没有语言或地域限制。

选择标准

我们纳入了在ART周期中,测试胚胎移植前子宫内膜注射胚胎培养液上清液的使用情况的RCT,与不使用该干预措施、使用安慰剂或使用任何其他类似药物进行比较。

数据收集与分析

两位综述作者独立选择研究、评估偏倚风险、从研究中提取数据,并在数据缺失时尝试联系作者。我们使用固定效应模型汇总研究。我们的主要结局是活产/持续妊娠和流产。我们使用Review Manager 5进行统计分析。我们使用GRADE方法评估证据质量。

主要结果

我们发现五项RCT适合纳入本综述(共分析526名女性)。我们进行了两项比较:使用胚胎培养液上清液与标准治疗或不干预;使用胚胎培养液上清液与培养基。所有研究均以全文文章形式发表。可从报告中获取或通过与研究者直接沟通获得的数据,用于最终的荟萃分析。研究的GRADE证据质量从极低质量到中等质量不等。降低证据质量的因素包括:由于缺乏盲法导致的高偏倚风险、出版偏倚和选择性结局报告的风险不明确、研究结局之间存在严重不一致,以及由于置信区间(CI)宽和事件数量少导致的严重不精确性。比较1.胚胎移植前子宫内膜注射胚胎培养液上清液与标准治疗或不干预:一项研究仅报告了活产情况,两项研究报告了活产和持续妊娠的综合结局。我们不确定在ART周期中,胚胎移植前子宫内膜注射胚胎培养液上清液与不干预相比,是否能提高活产/持续妊娠率(优势比(OR)1.11,95%CI 0.73至1.70;3项RCT;n = 340,I² = 84%;极低质量证据)。结果表明,如果假设安慰剂或不治疗后活产/持续妊娠的概率为42%,那么胚胎移植前子宫内膜注射胚胎培养液上清液后的概率在22%至81%之间。我们也不确定与不干预相比,胚胎移植前子宫内膜注射胚胎培养液上清液是否能降低流产率(OR 0.89,95%CI 0.44至1.78,4项RCT,n = 430,I² = 58%,极低质量证据)。结果表明,如果假设安慰剂或不治疗后流产的概率为9%,那么注射胚胎培养液上清液后的概率在3%至30%之间。关于次要结局,我们不确定胚胎移植前注射胚胎培养液上清液与不干预相比,是否能提高临床妊娠率(OR 1.13,95%CI 0.80至1.61;5项RCT;n = 526,I² = 0%;极低质量证据),降低异位妊娠率(OR 0.32,95%CI 0.01至8.24;n = 250;2项RCT;I² = 41%;极低质量证据),降低多胎妊娠率(OR 0.70,95%CI 0.26至1.83;2项RCT;n = 150;I² = 63%;极低质量证据),或降低早产率(OR 0.63,95%CI 0.17至2.42;1项RCT;n = 90;I² = 0%;极低质量证据)。最后可能两组之间胎儿异常率几乎没有差异(OR 3.10,95%CI 0.12至79.23;1项RCT;n = 60;I² = 0%;低质量证据)。比较2.胚胎移植前子宫内膜注射胚胎培养液上清液与注射培养基相比:与使用培养基相比,我们不确定使用胚胎培养液上清液是否能提高临床妊娠率(OR 1.09,95%CI 0.48至2.46;n = 96;1项RCT;极低质量证据)。没有研究报告活产/持续妊娠、流产、异位或多胎妊娠、早产或胎儿异常情况。

作者结论

我们不确定在接受ART的女性中,胚胎移植前常规添加子宫内膜注射胚胎培养液上清液是否能改善妊娠结局。这一结论基于目前五项RCT的现有数据,各研究的证据质量从极低到中等不等。仍需要进一步的大型设计良好的RCT报告活产情况和不良临床结局,以明确胚胎移植前子宫内膜注射胚胎培养液上清液的确切作用。

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