Melody Adesina, Astrid Ep Cantineau, Marian G Showell, Andy Vail, Jack Wilkinson
{"title":"同步方法在不孕夫妇的宫内人工授精。","authors":"Melody Adesina, Astrid Ep Cantineau, Marian G Showell, Andy Vail, Jack Wilkinson","doi":"10.1002/14651858.CD006942.pub4","DOIUrl":null,"url":null,"abstract":"<p><strong>Rationale: </strong>Intrauterine insemination (IUI) is widely used as a first-line treatment for subfertile couples with favourable prognostic factors, yet pregnancy rates vary considerably. The optimal method for timing IUI - whether through different monitoring strategies or ovulation triggering techniques in natural or stimulated cycles - remains uncertain. This review explores which timing approaches and methods of ovulation monitoring and triggering lead to the best outcomes, including live birth and clinical pregnancy. It updates a Cochrane review last published in 2014.</p><p><strong>Objectives: </strong>To evaluate the effectiveness of different methods of synchronisation of insemination with ovulation on live birth or ongoing pregnancy, in natural and stimulated cycles for IUI in subfertile couples.</p><p><strong>Search methods: </strong>We used the Cochrane Gynaecology and Fertility Group specialised register, CENTRAL, MEDLINE, and two other databases, along with reference checking, citation searching, handsearching of conference abstracts, and contact with study authors to identify the studies included in the review. The latest search date was October 2023.</p><p><strong>Eligibility criteria: </strong>We included randomised controlled trials (RCTs) comparing timing methods in natural or stimulated cycles, and different ovulation triggering methods. These included: varying the time interval between ovulation triggering and insemination, luteinising hormone (LH) detection in urine, LH detection in blood, basal body temperature charts, ultrasound detection of ovulation, human chorionic gonadotropin (hCG) administration, a combination of LH detection and hCG administration, gonadotropin-releasing hormone (GnRH) agonist administration, and other trigger administrations.</p><p><strong>Outcomes: </strong>Critical outcome: live birth or ongoing pregnancy rate per couple. Important outcomes (all are rate per couple): clinical pregnancy; multiple pregnancy; miscarriage; ovarian hyperstimulation syndrome; tubal pregnancy.</p><p><strong>Risk of bias: </strong>We used the Cochrane Collaboration's original tool to assess the risk of bias in the included RCTs.</p><p><strong>Synthesis methods: </strong>After the search, we screened the trials, extracted the data, and assessed the risk of bias and trustworthiness of the included studies. We synthesised results for each outcome using meta-analysis where possible. We expressed results for each included study as Mantel-Haenszel odds ratios (OR) with 95% confidence intervals (CI). We used GRADE to assess the certainty of the evidence for each outcome.</p><p><strong>Included studies: </strong>This review update includes 42 studies: 18 from the 2014 version, plus 24 studies newly identified in the updated search.</p><p><strong>Synthesis of results: </strong>Of the 42 included studies (a total of 6603 couples), we included seven in the primary meta-analyses (1917 couples) and 12 in the sensitivity meta-analyses (2143 couples). The certainty of the evidence was low for most comparisons. The main limitation of the evidence was serious imprecision. Of the seven studies included in the primary analyses, two compared the optimum time interval from hCG injection to IUI for live birth or ongoing pregnancy rate, comparing different time frames ranging from 0 to 48 hours. We categorised the time frames into three groups: (i) 0 to 33 hours; (ii) 34 to 40 hours; and (iii) more than 40 hours. We compared 0 to 33 hours versus 34 to 40 hours, and 34 to 40 hours versus more than 40 hours. Results were too imprecise to be informative in both comparisons (0 to 33 hours versus 34 to 40 hours: OR 1.42, 95% CI 0.90 to 2.23; 1 study, 374 couples; 34 to 40 hours versus more than 40 hours: OR 0.45, 95% CI 0.15 to 1.33; 1 study, 107 couples). We included one study in the primary analysis for each of the following comparisons: hCG versus LH surge; recombinant hCG versus urinary hCG; and hCG alone versus hCG plus follicle-stimulating hormone (FSH). It is unclear whether there might be a difference in live birth or ongoing pregnancy rates in the first two comparisons: hCG versus LH surge: OR 1.08, 95% CI 0.50 to 2.37; 1 study, 392 couples; low-certainty evidence; recombinant hCG versus urinary hCG: OR 1.13, 95% CI 0.49 to 2.63; 1 study, 125 couples; low-certainty evidence. However, live birth or ongoing pregnancy rates may be lower with hCG alone compared to hCG plus FSH (OR 0.35, 95% CI 0.13 to 0.95; 1 study, 108 couples; low-certainty evidence). We found no clear evidence of a difference between any of the groups in clinical pregnancy rate or adverse events (multiple pregnancy rate, miscarriage rate, tubal pregnancy rate). However, all results were of low-certainty evidence. None of the studies included in the primary analyses reported on ovarian hyperstimulation syndrome.</p><p><strong>Authors' conclusions: </strong>There is insufficient evidence to determine whether there is any difference in effectiveness between different methods of synchronisation of ovulation and insemination.</p><p><strong>Funding: </strong>This Cochrane review had no dedicated funding.</p><p><strong>Registration: </strong>First review update (2014): doi.org/10.1002/14651858.CD006942.pub3 Review (2010): doi.org/10.1002/14651858.CD006942.pub2 Protocol (2008): doi.org/10.1002/14651858.CD006942.</p>","PeriodicalId":10473,"journal":{"name":"Cochrane Database of Systematic Reviews","volume":"9 ","pages":"CD006942"},"PeriodicalIF":8.8000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12455694/pdf/","citationCount":"0","resultStr":"{\"title\":\"Synchronised approach for intrauterine insemination in subfertile couples.\",\"authors\":\"Melody Adesina, Astrid Ep Cantineau, Marian G Showell, Andy Vail, Jack Wilkinson\",\"doi\":\"10.1002/14651858.CD006942.pub4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Rationale: </strong>Intrauterine insemination (IUI) is widely used as a first-line treatment for subfertile couples with favourable prognostic factors, yet pregnancy rates vary considerably. The optimal method for timing IUI - whether through different monitoring strategies or ovulation triggering techniques in natural or stimulated cycles - remains uncertain. This review explores which timing approaches and methods of ovulation monitoring and triggering lead to the best outcomes, including live birth and clinical pregnancy. It updates a Cochrane review last published in 2014.</p><p><strong>Objectives: </strong>To evaluate the effectiveness of different methods of synchronisation of insemination with ovulation on live birth or ongoing pregnancy, in natural and stimulated cycles for IUI in subfertile couples.</p><p><strong>Search methods: </strong>We used the Cochrane Gynaecology and Fertility Group specialised register, CENTRAL, MEDLINE, and two other databases, along with reference checking, citation searching, handsearching of conference abstracts, and contact with study authors to identify the studies included in the review. The latest search date was October 2023.</p><p><strong>Eligibility criteria: </strong>We included randomised controlled trials (RCTs) comparing timing methods in natural or stimulated cycles, and different ovulation triggering methods. These included: varying the time interval between ovulation triggering and insemination, luteinising hormone (LH) detection in urine, LH detection in blood, basal body temperature charts, ultrasound detection of ovulation, human chorionic gonadotropin (hCG) administration, a combination of LH detection and hCG administration, gonadotropin-releasing hormone (GnRH) agonist administration, and other trigger administrations.</p><p><strong>Outcomes: </strong>Critical outcome: live birth or ongoing pregnancy rate per couple. 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We compared 0 to 33 hours versus 34 to 40 hours, and 34 to 40 hours versus more than 40 hours. Results were too imprecise to be informative in both comparisons (0 to 33 hours versus 34 to 40 hours: OR 1.42, 95% CI 0.90 to 2.23; 1 study, 374 couples; 34 to 40 hours versus more than 40 hours: OR 0.45, 95% CI 0.15 to 1.33; 1 study, 107 couples). We included one study in the primary analysis for each of the following comparisons: hCG versus LH surge; recombinant hCG versus urinary hCG; and hCG alone versus hCG plus follicle-stimulating hormone (FSH). It is unclear whether there might be a difference in live birth or ongoing pregnancy rates in the first two comparisons: hCG versus LH surge: OR 1.08, 95% CI 0.50 to 2.37; 1 study, 392 couples; low-certainty evidence; recombinant hCG versus urinary hCG: OR 1.13, 95% CI 0.49 to 2.63; 1 study, 125 couples; low-certainty evidence. However, live birth or ongoing pregnancy rates may be lower with hCG alone compared to hCG plus FSH (OR 0.35, 95% CI 0.13 to 0.95; 1 study, 108 couples; low-certainty evidence). We found no clear evidence of a difference between any of the groups in clinical pregnancy rate or adverse events (multiple pregnancy rate, miscarriage rate, tubal pregnancy rate). However, all results were of low-certainty evidence. 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引用次数: 0
摘要
理由:宫内人工授精(IUI)被广泛应用于具有良好预后因素的不孕夫妇的一线治疗,但妊娠率差异很大。人工授精的最佳方法-无论是通过不同的监测策略还是在自然周期或刺激周期中触发排卵技术-仍然不确定。这篇综述探讨了排卵监测和触发的时机途径和方法导致最好的结果,包括活产和临床妊娠。它更新了上一次发表于2014年的Cochrane综述。目的:评价在自然周期和人工授精周期中,人工授精与活产或妊娠期排卵同步的不同方法对低生育能力夫妇人工授精的效果。检索方法:我们使用Cochrane妇科与生育组专业注册、CENTRAL、MEDLINE和其他两个数据库,同时进行参考文献检查、引文检索、手工检索会议摘要,并与研究作者联系,以确定纳入综述的研究。最近一次搜索日期是2023年10月。入选标准:我们纳入了随机对照试验(rct),比较自然周期或刺激周期中的定时方法,以及不同的排卵触发方法。这些包括:改变排卵触发和授精之间的时间间隔,尿液中黄体生成素(LH)检测,血液中黄体生成素检测,基础体温图,排卵超声检测,人绒毛膜促性腺激素(hCG)给药,LH检测和hCG给药的组合,促性腺激素释放激素(GnRH)激动剂给药,和其他触发给药。结局:关键结局:每对夫妇的活产率或持续妊娠率。重要结果(均为每对夫妇的比率):临床妊娠;多个怀孕;流产;卵巢过度刺激综合征;输卵管妊娠。偏倚风险:我们使用Cochrane协作的原始工具来评估纳入的随机对照试验的偏倚风险。综合方法:检索后,我们筛选试验,提取数据,并评估纳入研究的偏倚风险和可信度。在可能的情况下,我们使用荟萃分析综合了每个结果的结果。我们将每个纳入研究的结果表示为Mantel-Haenszel优势比(OR), 95%置信区间(CI)。我们使用GRADE来评估每个结果证据的确定性。纳入的研究:本次综述更新包括42项研究:18项来自2014年版本,加上24项在更新后的检索中新发现的研究。结果综合:在纳入的42项研究(共6603对夫妇)中,我们纳入了7项主要荟萃分析(1917对夫妇)和12项敏感性荟萃分析(2143对夫妇)。在大多数比较中,证据的确定性很低。证据的主要限制是严重不精确。在初步分析中纳入的7项研究中,有2项比较了从注射hCG到IUI对活产或妊娠率的最佳时间间隔,比较了从0到48小时的不同时间范围。我们将时间框架分为三组:(i) 0至33小时;(ii) 34至40小时;(三)40小时以上。我们比较了0到33小时和34到40小时,34到40小时和超过40小时。两项比较的结果都太不精确,不能提供信息(0至33小时vs . 34至40小时:OR 1.42, 95% CI 0.90至2.23;1项研究,374对夫妇;34至40小时vs . 40小时以上:OR 0.45, 95% CI 0.15至1.33;1项研究,107对夫妇)。我们在主要分析中分别纳入了一项研究:hCG与LH激增;重组hCG与尿hCG;hCG单独与hCG加促卵泡激素(FSH)比较。目前尚不清楚前两组比较在活产率或持续妊娠率方面是否存在差异:hCG与LH激增:or 1.08, 95% CI 0.50至2.37;1项研究,392对夫妇;确定性的证据;重组hCG与尿hCG: OR 1.13, 95% CI 0.49 - 2.63;1项研究,125对夫妇;确定性的证据。然而,与hCG + FSH相比,单独使用hCG的活产率或持续妊娠率可能更低(or 0.35, 95% CI 0.13至0.95;1项研究,108对夫妇;低确定性证据)。我们没有发现任何一组在临床妊娠率或不良事件(多胎妊娠率、流产率、输卵管妊娠率)方面有明显差异的证据。然而,所有结果都是低确定性证据。初步分析中没有一项研究报告卵巢过度刺激综合征。作者的结论:没有足够的证据来确定不同的同步排卵和授精方法之间是否存在有效性差异。资金来源:Cochrane综述没有专门的资金来源。注册:第一次审查更新(2014年):doi.org/10.1002/14651858.CD006942。 pub3 Review (2010): doi.org/10.1002/14651858.CD006942.pub2 Protocol (2008): doi.org/10.1002/14651858.CD006942。
Synchronised approach for intrauterine insemination in subfertile couples.
Rationale: Intrauterine insemination (IUI) is widely used as a first-line treatment for subfertile couples with favourable prognostic factors, yet pregnancy rates vary considerably. The optimal method for timing IUI - whether through different monitoring strategies or ovulation triggering techniques in natural or stimulated cycles - remains uncertain. This review explores which timing approaches and methods of ovulation monitoring and triggering lead to the best outcomes, including live birth and clinical pregnancy. It updates a Cochrane review last published in 2014.
Objectives: To evaluate the effectiveness of different methods of synchronisation of insemination with ovulation on live birth or ongoing pregnancy, in natural and stimulated cycles for IUI in subfertile couples.
Search methods: We used the Cochrane Gynaecology and Fertility Group specialised register, CENTRAL, MEDLINE, and two other databases, along with reference checking, citation searching, handsearching of conference abstracts, and contact with study authors to identify the studies included in the review. The latest search date was October 2023.
Eligibility criteria: We included randomised controlled trials (RCTs) comparing timing methods in natural or stimulated cycles, and different ovulation triggering methods. These included: varying the time interval between ovulation triggering and insemination, luteinising hormone (LH) detection in urine, LH detection in blood, basal body temperature charts, ultrasound detection of ovulation, human chorionic gonadotropin (hCG) administration, a combination of LH detection and hCG administration, gonadotropin-releasing hormone (GnRH) agonist administration, and other trigger administrations.
Outcomes: Critical outcome: live birth or ongoing pregnancy rate per couple. Important outcomes (all are rate per couple): clinical pregnancy; multiple pregnancy; miscarriage; ovarian hyperstimulation syndrome; tubal pregnancy.
Risk of bias: We used the Cochrane Collaboration's original tool to assess the risk of bias in the included RCTs.
Synthesis methods: After the search, we screened the trials, extracted the data, and assessed the risk of bias and trustworthiness of the included studies. We synthesised results for each outcome using meta-analysis where possible. We expressed results for each included study as Mantel-Haenszel odds ratios (OR) with 95% confidence intervals (CI). We used GRADE to assess the certainty of the evidence for each outcome.
Included studies: This review update includes 42 studies: 18 from the 2014 version, plus 24 studies newly identified in the updated search.
Synthesis of results: Of the 42 included studies (a total of 6603 couples), we included seven in the primary meta-analyses (1917 couples) and 12 in the sensitivity meta-analyses (2143 couples). The certainty of the evidence was low for most comparisons. The main limitation of the evidence was serious imprecision. Of the seven studies included in the primary analyses, two compared the optimum time interval from hCG injection to IUI for live birth or ongoing pregnancy rate, comparing different time frames ranging from 0 to 48 hours. We categorised the time frames into three groups: (i) 0 to 33 hours; (ii) 34 to 40 hours; and (iii) more than 40 hours. We compared 0 to 33 hours versus 34 to 40 hours, and 34 to 40 hours versus more than 40 hours. Results were too imprecise to be informative in both comparisons (0 to 33 hours versus 34 to 40 hours: OR 1.42, 95% CI 0.90 to 2.23; 1 study, 374 couples; 34 to 40 hours versus more than 40 hours: OR 0.45, 95% CI 0.15 to 1.33; 1 study, 107 couples). We included one study in the primary analysis for each of the following comparisons: hCG versus LH surge; recombinant hCG versus urinary hCG; and hCG alone versus hCG plus follicle-stimulating hormone (FSH). It is unclear whether there might be a difference in live birth or ongoing pregnancy rates in the first two comparisons: hCG versus LH surge: OR 1.08, 95% CI 0.50 to 2.37; 1 study, 392 couples; low-certainty evidence; recombinant hCG versus urinary hCG: OR 1.13, 95% CI 0.49 to 2.63; 1 study, 125 couples; low-certainty evidence. However, live birth or ongoing pregnancy rates may be lower with hCG alone compared to hCG plus FSH (OR 0.35, 95% CI 0.13 to 0.95; 1 study, 108 couples; low-certainty evidence). We found no clear evidence of a difference between any of the groups in clinical pregnancy rate or adverse events (multiple pregnancy rate, miscarriage rate, tubal pregnancy rate). However, all results were of low-certainty evidence. None of the studies included in the primary analyses reported on ovarian hyperstimulation syndrome.
Authors' conclusions: There is insufficient evidence to determine whether there is any difference in effectiveness between different methods of synchronisation of ovulation and insemination.
Funding: This Cochrane review had no dedicated funding.
期刊介绍:
The Cochrane Database of Systematic Reviews (CDSR) stands as the premier database for systematic reviews in healthcare. It comprises Cochrane Reviews, along with protocols for these reviews, editorials, and supplements. Owned and operated by Cochrane, a worldwide independent network of healthcare stakeholders, the CDSR (ISSN 1469-493X) encompasses a broad spectrum of health-related topics, including health services.