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不育夫妇宫内人工授精的同步方法。

Synchronised approach for intrauterine insemination in subfertile couples.

作者信息

Cantineau Astrid E P, Janssen Mirjam J, Cohlen Ben J, Allersma Thomas

机构信息

Department of Obstetrics and Gynaecology, University Medical Centre, Groningen, Netherlands.

出版信息

Cochrane Database Syst Rev. 2014 Dec 21;2014(12):CD006942. doi: 10.1002/14651858.CD006942.pub3.

Abstract

BACKGROUND

In many countries intrauterine insemination (IUI) is the treatment of first choice for a subfertile couple when the infertility work up reveals an ovulatory cycle, at least one open Fallopian tube and sufficient spermatozoa. The final goal of this treatment is to achieve a pregnancy and deliver a healthy (singleton) live birth. The probability of conceiving with IUI depends on various factors including age of the couple, type of subfertility, ovarian stimulation and the timing of insemination. IUI should logically be performed around the moment of ovulation. Since spermatozoa and oocytes have only limited survival time correct timing of the insemination is essential. As it is not known which technique of timing for IUI results in the best treatment outcome, we compared different techniques for timing IUI and different time intervals.

OBJECTIVES

To evaluate the effectiveness of different synchronisation methods in natural and stimulated cycles for IUI in subfertile couples.

SEARCH METHODS

We searched for all publications which described randomised controlled trials of the timing of IUI. We searched the Cochrane Menstrual Disorders and Subfertility Group Specialised Register, Cochrane Central Register of Controlled Trials (CENTRAL) (1966 to October 2014), EMBASE (1974 to October 2014), MEDLINE (1966 to October 2014) and PsycINFO (inception to October 2014) electronic databases and prospective trial registers. Furthermore, we checked the reference lists of all obtained studies and performed a handsearch of conference abstracts.

SELECTION CRITERIA

Randomised controlled trials (RCTs) comparing different timing methods for IUI were included. The following interventions were evaluated: detection of luteinising hormone (LH) in urine or blood, single test; human chorionic gonadotropin (hCG) administration; combination of LH detection and hCG administration; basal body temperature chart; ultrasound detection of ovulation; gonadotropin-releasing hormone (GnRH) agonist administration; or other timing methods.

DATA COLLECTION AND ANALYSIS

Two review authors independently selected the trials, extracted the data and assessed study risk of bias. We performed statistical analyses in accordance with the guidelines for statistical analysis developed by The Cochrane Collaboration. The overall quality of the evidence was assessed using GRADE methods.

MAIN RESULTS

Eighteen RCTs were included in the review, of which 14 were included in the meta-analyses (in total 2279 couples). The evidence was current to October 2013. The quality of the evidence was low or very low for most comparisons . The main limitations in the evidence were failure to describe study methods, serious imprecision and attrition bias.Ten RCTs compared different methods of timing for IUI. We found no evidence of a difference in live birth rates between hCG injection versus LH surge (odds ratio (OR) 1.0, 95% confidence interval (CI) 0.06 to 18, 1 RCT, 24 women, very low quality evidence), urinary hCG versus recombinant hCG (OR 1.17, 95% CI 0.68 to 2.03, 1 RCT, 284 women, low quality evidence) or hCG versus GnRH agonist (OR 1.04, 95% CI 0.42 to 2.6, 3 RCTS, 104 women, I(2) = 0%, low quality evidence).Two RCTs compared the optimum time interval from hCG injection to IUI, comparing different time frames that ranged from 24 hours to 48 hours. Only one of these studies reported live birth rates, and found no difference between the groups (OR 0.52, 95% CI 0.27 to 1.00, 1 RCT, 204 couples). One study compared early versus late hCG administration and one study compared different dosages of hCG, but neither reported the primary outcome of live birth.We found no evidence of a difference between any of the groups in rates of pregnancy or adverse events (multiple pregnancy, miscarriage, ovarian hyperstimulation syndrome (OHSS)). However, most of these data were very low quality.

AUTHORS' CONCLUSIONS: There is insufficient evidence to determine whether there is any difference in safety and effectiveness between different methods of synchronization of ovulation and insemination. More research is needed.

摘要

背景

在许多国家,当不育症检查显示为排卵周期、至少一侧输卵管通畅且有足够精子时,宫腔内人工授精(IUI)是不育夫妇的首选治疗方法。该治疗的最终目标是实现妊娠并分娩出健康的(单胎)活产婴儿。IUI受孕的概率取决于多种因素,包括夫妇的年龄、不育类型、卵巢刺激以及授精时间。理论上,IUI应在排卵时刻左右进行。由于精子和卵子的存活时间有限,正确的授精时间至关重要。由于尚不清楚哪种IUI授精时间技术能带来最佳治疗效果,我们比较了不同的IUI授精时间技术和不同的时间间隔。

目的

评估不同同步方法在不育夫妇自然周期和促排卵周期中进行IUI的有效性。

检索方法

我们检索了所有描述IUI授精时间随机对照试验的出版物。我们检索了Cochrane月经紊乱与不育症专业注册库、Cochrane对照试验中心注册库(CENTRAL)(1966年至2014年10月)、EMBASE(1974年至2014年10月)、MEDLINE(1966年至2014年10月)和PsycINFO(创刊至2014年10月)电子数据库以及前瞻性试验注册库。此外,我们检查了所有纳入研究的参考文献列表,并对会议摘要进行了手工检索。

入选标准

纳入比较不同IUI授精时间方法的随机对照试验(RCT)。评估了以下干预措施:尿液或血液中促黄体生成素(LH)检测,单次检测;人绒毛膜促性腺激素(hCG)给药;LH检测与hCG给药联合使用;基础体温图表;超声监测排卵;促性腺激素释放激素(GnRH)激动剂给药;或其他授精时间方法。

数据收集与分析

两位综述作者独立选择试验、提取数据并评估研究的偏倚风险。我们按照Cochrane协作网制定的统计分析指南进行统计分析。使用GRADE方法评估证据的总体质量。

主要结果

本综述纳入了18项RCT,其中14项纳入荟萃分析(共2279对夫妇)。证据截至2013年10月。大多数比较的证据质量低或极低。证据的主要局限性在于未描述研究方法、严重不精确以及失访偏倚。10项RCT比较了不同的IUI授精时间方法。我们发现,hCG注射与LH峰之间的活产率无差异(优势比(OR)1.0,95%置信区间(CI)0.06至18,1项RCT,24名女性,极低质量证据),尿hCG与重组hCG之间无差异(OR 1.17,95%CI 0.68至2.03,1项RCT,284名女性,低质量证据),hCG与GnRH激动剂之间无差异(OR 1.04,95%CI 0.42至2.6,3项RCT,104名女性,I² = 0%,低质量证据)。两项RCT比较了从hCG注射到IUI的最佳时间间隔,比较了24小时至48小时的不同时间范围。这些研究中只有一项报告了活产率,且发现两组之间无差异(OR 0.52,95%CI 0.27至1.00,1项RCT,204对夫妇)。一项研究比较了hCG的早期给药与晚期给药,一项研究比较了不同剂量的hCG,但均未报告活产这一主要结局。我们发现,任何组之间在妊娠率或不良事件(多胎妊娠、流产、卵巢过度刺激综合征(OHSS))方面均无差异。然而,这些数据大多质量极低。

作者结论

尚无足够证据确定不同排卵与授精同步方法在安全性和有效性方面是否存在差异。需要更多研究。

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