Nuffield Department of Women's and Reproductive Health, University of Oxford , Oxford, UK.
Department of Obstetrics and Gynaecology, Royal Berkshire Hospital, Reading, UK.
Cochrane Database Syst Rev. 2023 Sep 15;9(9):CD011345. doi: 10.1002/14651858.CD011345.pub3.
Many factors influence fertility, one being the timing of intercourse. The 'fertile window' describes a stage in the cycle when conception can occur and is approximately five days before to several hours after ovulation. 'Timed intercourse' is the practice of prospectively identifying ovulation and, thus, the fertile window to increase the likelihood of conception. Methods of predicting ovulation include urinary hormone measurement (luteinising hormone (LH) and oestrogen), fertility awareness-based methods (FABM) (including tracking basal body temperatures, cervical mucus monitoring, calendar charting/tracking apps), and ultrasonography. However, there are potentially negative aspects associated with ovulation prediction, including stress, time consumption, and cost implications of purchasing ovulation kits and app subscriptions. This review considered the evidence from randomised controlled trials (RCTs) evaluating the use of timed intercourse (using ovulation prediction) on pregnancy outcomes.
To evaluate the benefits and risks of ovulation prediction methods for timing intercourse on conception in couples trying to conceive.
We searched the Cochrane Gynaecology and Fertility (CGF) Group Specialised Register, CENTRAL, MEDLINE, and Embase in January 2023. We also checked the reference lists of relevant studies and searched trial registries for any additional trials.
We included RCTs that compared methods of timed intercourse using ovulation prediction to other forms of ovulation prediction or intercourse without ovulation prediction in couples trying to conceive.
We used standard methodological procedures recommended by Cochrane to select and analyse studies in this review. The primary review outcomes were live birth and adverse events (such as depression and stress). Secondary outcomes were clinical pregnancy, pregnancy (clinical or positive urinary pregnancy test not yet confirmed by ultrasound), time to pregnancy, and quality of life. We assessed the overall quality of the evidence for the main comparisons using GRADE methods.
This review update included seven RCTs involving 2464 women or couples. Four of the five studies from the previous review were included in this update, and three new studies were added. We assessed the quality of the evidence as moderate to very low, the main limitations being imprecision, indirectness, and risk of bias. Urinary ovulation tests versus intercourse without ovulation prediction Compared to intercourse without ovulation prediction, urinary ovulation detection probably increases the chance of live birth in couples trying to conceive (risk ratio (RR) 1.36, 95% confidence interval (CI) 1.02 to 1.81, 1 RCT, n = 844, moderate-quality evidence). This suggests that if the chance of a live birth without urine ovulation prediction is 16%, the chance of a live birth with urine ovulation prediction is 16% to 28%. However, we are uncertain whether timed intercourse using urinary ovulation detection resulted in a difference in stress (mean difference (MD) 1.98, 95% CI -0.87 to 4.83, I² = 0%, P = 0.17, 1 RCT, n = 77, very low-quality evidence) or clinical pregnancy (RR 1.09, 95% CI 0.51 to 2.31, I² = 0%, 1 RCT, n = 148, low-quality evidence). Similar to the live birth result, timed intercourse using urinary ovulation detection probably increases the chances of clinical pregnancy or positive urine pregnancy test (RR 1.28, 95% CI 1.09 to 1.50, I² = 0, 4 RCTs, n = 2202, moderate-quality evidence). This suggests that if the chance of a clinical pregnancy or positive urine pregnancy test without ovulation prediction is assumed to be 18%, the chance following timed intercourse with urinary ovulation detection would be 20% to 28%. Evidence was insufficient to determine the effect of urine ovulation tests on time to pregnancy or quality of life. Fertility awareness-based methods (FABM) versus intercourse without ovulation prediction Due to insufficient evidence, we are uncertain whether timed intercourse using FABM resulted in a difference in live birth rate compared to intercourse without ovulation prediction (RR 0.95, 95% CI 0.76 to 1.20, I² = 0%, 2 RCTs, n = 157, low-quality evidence). We are also uncertain whether FABM affects stress (MD -1.10, 95% CI -3.88 to 1.68, 1 RCT, n = 183, very low-quality evidence). Similarly, we are uncertain of the effect of timed intercourse using FABM on anxiety (MD 0.5, 95% CI -0.52 to 1.52, P = 0.33, 1 RCT, n = 183, very low-quality evidence); depression (MD 0.4, 95% CI -0.28 to 1.08, P = 0.25, 1 RCT, n = 183, very low-quality evidence); or erectile dysfunction (MD 1.2, 95% CI -0.38 to 2.78, P = 0.14, 1 RCT, n = 183, very low-quality evidence). Evidence was insufficient to detect a benefit of timed intercourse using FABM on clinical pregnancy (RR 1.13, 95% CI 0.31 to 4.07, 1 RCT, n = 17, very low-quality evidence) or clinical or positive pregnancy test rates (RR 1.08, 95% CI 0.89 to 1.30, 3 RCTs, n = 262, very low-quality evidence). Finally, we are uncertain whether timed intercourse using FABM affects the time to pregnancy (hazard ratio 0.86, 95% CI 0.53 to 1.38, 1 RCT, n = 140, low-quality evidence) or quality of life. No studies assessed the use of timed intercourse with pelvic ultrasonography.
AUTHORS' CONCLUSIONS: The new evidence presented in this review update shows that timed intercourse using urine ovulation tests probably improves live birth and pregnancy rates (clinical or positive urine pregnancy tests but not yet confirmed by ultrasound) in women under 40, trying to conceive for less than 12 months, compared to intercourse without ovulation prediction. However, there are insufficient data to determine the effects of urine ovulation tests on adverse events, clinical pregnancy, time to pregnancy, and quality of life. Similarly, due to limited data, we are uncertain of the effect of FABM on pregnancy outcomes, adverse effects, and quality of life. Further research is therefore required to fully understand the safety and effectiveness of timed intercourse for couples trying to conceive. This research should include studies reporting clinically relevant outcomes such as live birth and adverse effects in fertile and infertile couples and utilise various methods to determine ovulation. Only with a comprehensive understanding of the risks and benefits of timed intercourse can recommendations be made for all couples trying to conceive.
许多因素会影响生育能力,其中一个因素是性交的时机。“生育窗口”描述了一个可以发生受孕的阶段,大约在排卵前 5 天到排卵后数小时。“定时性交”是指前瞻性地识别排卵,从而确定生育窗口,以增加受孕的可能性。预测排卵的方法包括尿液激素测量(黄体生成素 (LH) 和雌激素)、生育意识为基础的方法(FABM)(包括跟踪基础体温、宫颈粘液监测、日历图表/跟踪应用程序)和超声检查。然而,排卵预测可能存在一些潜在的负面影响,包括压力、时间消耗以及购买排卵试剂盒和应用程序订阅的成本问题。本综述考虑了来自随机对照试验 (RCT) 的证据,这些试验评估了在尝试怀孕的夫妇中使用定时性交(使用排卵预测)对妊娠结局的影响。
评估在尝试怀孕的夫妇中使用排卵预测方法进行定时性交对受孕的益处和风险。
我们于 2023 年 1 月检索了 Cochrane 妇科和生育组专业注册库 (CGF)、CENTRAL、MEDLINE 和 Embase,并检查了相关研究的参考文献列表以及检索了试验注册库,以查找任何其他试验。
我们纳入了比较使用排卵预测的定时性交与其他形式的排卵预测或无排卵预测的性交的 RCT。
我们使用 Cochrane 推荐的标准方法学程序来选择和分析本综述中的研究。主要的综述结局是活产和不良事件(如抑郁和压力)。次要结局是临床妊娠、妊娠(临床或阳性尿妊娠试验但尚未通过超声确认)、妊娠时间和生活质量。我们使用 GRADE 方法评估主要比较的总体证据质量。
本次综述更新包括了 7 项 RCT,涉及 2464 名女性或夫妇。之前综述中的 5 项研究中的 4 项被纳入本次更新,另有 3 项新研究被添加。我们评估了证据的质量为中度至非常低,主要限制因素为不精确性、间接性和偏倚风险。
尿液排卵检测与无排卵预测的性交
与无排卵预测的性交相比,尿液排卵检测可能会增加尝试怀孕的夫妇的活产几率(风险比 (RR) 1.36,95%置信区间 (CI) 1.02 至 1.81,1 项 RCT,n = 844,中等质量证据)。这表明,如果没有尿液排卵预测的活产机会为 16%,那么使用尿液排卵预测的活产机会为 16%至 28%。然而,我们不确定使用尿液排卵检测的定时性交是否会导致压力(平均差值 (MD) 1.98,95%置信区间 (CI) -0.87 至 4.83,I² = 0%,P = 0.17,1 项 RCT,n = 77,非常低质量证据)或临床妊娠(RR 1.09,95%置信区间 0.51 至 2.31,I² = 0%,1 项 RCT,n = 148,低质量证据)的差异。与活产结果相似,使用尿液排卵检测的定时性交可能会增加临床妊娠或阳性尿妊娠试验的几率(RR 1.28,95%置信区间 1.09 至 1.50,I² = 0,4 项 RCT,n = 2202,中等质量证据)。这表明,如果没有排卵预测的临床妊娠或阳性尿妊娠试验的机会假设为 18%,那么使用尿液排卵检测的机会将为 20%至 28%。
证据不足,我们不确定使用基于生育意识的方法(FABM)的定时性交是否会导致与无排卵预测的性交相比,活产率有所不同(RR 0.95,95%置信区间 0.76 至 1.20,I² = 0%,2 项 RCT,n = 157,低质量证据)。我们也不确定 FABM 是否会影响压力(MD-1.10,95%置信区间-3.88 至 1.68,1 项 RCT,n = 183,非常低质量证据)。同样,我们也不确定使用 FABM 的定时性交对焦虑(MD 0.5,95%置信区间 0.52 至 1.52,P = 0.33,1 项 RCT,n = 183,非常低质量证据)、抑郁(MD 0.4,95%置信区间 0.28 至 1.08,P = 0.25,1 项 RCT,n = 183,非常低质量证据)或勃起功能障碍(MD 1.2,95%置信区间 0.38 至 2.78,P = 0.14,1 项 RCT,n = 183,非常低质量证据)有影响。证据不足,无法确定使用 FABM 的定时性交对临床妊娠(RR 1.13,95%置信区间 0.31 至 4.07,1 项 RCT,n = 17,非常低质量证据)或临床或阳性妊娠试验率(RR 1.08,95%置信区间 0.89 至 1.30,3 项 RCT,n = 262,非常低质量证据)有好处。最后,我们不确定使用 FABM 的定时性交是否会影响妊娠时间(风险比 0.86,95%置信区间 0.53 至 1.38,1 项 RCT,n = 140,低质量证据)或生活质量。没有研究评估使用盆腔超声的定时性交。
本综述更新提供的新证据表明,与无排卵预测的性交相比,在尝试怀孕不到 12 个月、年龄在 40 岁以下的女性中,使用尿液排卵检测的定时性交可能会提高活产率和妊娠率(临床或阳性尿妊娠试验但尚未通过超声确认)。然而,由于数据有限,我们不确定尿液排卵检测对不良事件、临床妊娠、妊娠时间和生活质量的影响。同样,由于数据有限,我们不确定 FABM 对妊娠结局、不良影响和生活质量的影响。因此,需要进一步的研究来充分了解定时性交对尝试怀孕的夫妇的安全性和有效性。这项研究应该包括报告在有生育能力和无生育能力的夫妇中,临床相关结局(如活产和不良影响)的研究,并利用各种方法来确定排卵。只有全面了解定时性交的风险和益处,才能为所有尝试怀孕的夫妇提出建议。