Zhang Jing, Tang Liulin, Kong Linglingli, Wu Taixiang, Xu Liangzhi, Pan Xin, Liu Guan J
Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Cochrane Database Syst Rev. 2019 Jul 31;7(7):CD008583. doi: 10.1002/14651858.CD008583.pub2.
Ovulatory disturbance is a key diagnostic feature of polycystic ovarian syndrome (PCOS), leading to infertility and correspondingly heavy disease burden. Many therapeutic strategies have been used to induce ovulation for women with PCOS who are infertile. Ultrasound-guided transvaginal ovarian needle drilling (UTND) is a novel surgical method used to induce ovulation for women with clomiphene-resistant PCOS at the outpatients clinic. Nevertheless, the quality in most of the studies seemed low, and the safety and efficacy of UTND is still uncertain.
To evaluate the efficacy and safety of UTND for subfertile women with clomiphene-resistant PCOS.
We searched the Cochrane Gynaecology and Fertility Group (CGFG) Specialised Register, CENTRAL, MEDLINE, Embase, and six other databases to November 2018. We checked conference abstracts from the 2018 ESHRE, reference lists, and clinical trials registries. We contacted experts and specialists in the field.
We included randomised controlled trials (RCTs) comparing UTND to laparoscopic ovarian drilling (LOD), and UTND combined with gonadotropins to gonadotropins alone for women of reproductive age with clomiphene-resistant PCOS and infertility.
Two review authors independently screened appropriate trials for inclusion, assessed methodological quality and risk of bias, and extracted data. The primary outcomes were live birth rate and incidence of surgical complications (bleeding and infection). We included ovarian hyperstimulation syndrome (OHSS) as a secondary outcome. Meta-analyses could only be conducted for the secondary outcomes pregnancy rate and ovulation rate in the comparison of UTND versus LOD using a random-effect model. We calculated odds ratios (OR) with 95% confidence intervals (CI) for dichotomous data. We assessed the overall quality of the evidence by applying GRADE criteria.
We included five trials involving 639 clomiphene-resistant women with PCOS. Three studies compared UTND with LOD, and two compared UTND combined with gonadotropins with gonadotropins alone. The evidence was of low to very low quality. The main limitations were serious risk of bias due to poor reporting of methods, inconsistency resulting from heterogeneity, imprecision induced by limited sample size, and lack of reporting of clinically relevant outcomes such as live birth and surgical complications.UTND versus LODNo studies reported on the main outcome live birth. One study reported on surgical complications; however, the evidence for this outcome was of very low quality because it was based on one study with small sample size and there were no events in either arm. Thus, we are uncertain whether there is any difference in surgical complications between UTND and LOD.We are also uncertain whether there is any difference in pregnancy rate when comparing UTND with LOD (OR 0.54, 95% CI 0.28 to 1.03; I = 56%; 3 RCTs, n = 473; very-low quality evidence). UTND may lead to a slight decrease in ovulation rate when compared to LOD (OR 0.66, 95% CI 0.45 to 0.97; I = 0%; 3 RCTs, n = 473; low-quality evidence). This suggests that among clomiphene-resistant women with PCOS using LOD with an expected ovulation rate of 69.5%, the ovulation rate among women using UTND may be between 50.6% and 68.8%No studies reported on the outcomes OHSS and multiple pregnancy. There was also insufficient evidence to reach a conclusion regarding miscarriage as there was only one study of very low quality.UTND combined with gonadotropins versus gonadotropins aloneNo studies reported on the main outcomes live birth and incidence of surgical complications. The evidence for the outcomes OHSS, pregnancy, ovulation, miscarriage, and multiple pregnancy in this comparison was of very low quality. Thus, we are uncertain whether there is any difference in these outcomes for women with clomiphene-resistant PCOS using UTND combined with gonadotropins as compared with gonadotropins.
AUTHORS' CONCLUSIONS: Based on very low-quality evidence, It is uncertain whether there is any difference in pregnancy rate, incidence of surgical complications, and miscarriage rate between UTND and LOD in women with clomiphene-resistant PCOS. UTND may lead to a slight decrease in ovulation rate when compared to LOD. No studies reported on the outcomes live birth rate, incidence of OHSS, and multiple pregnancy rate. No studies reported on the main outcomes live birth and surgical complications for the comparison UTND combined with gonadotrophins versus gonadotrophins alone. The evidence for the outcomes OHSS, pregnancy, ovulation, miscarriage, and multiple pregnancy in this comparison was of very low quality. Thus, it is unclear if there is a difference in any of the outcomes between UTND combined with gonadotrophins versus gonadotrophins alone.
排卵障碍是多囊卵巢综合征(PCOS)的关键诊断特征,会导致不孕并相应带来沉重的疾病负担。许多治疗策略已被用于为患有PCOS的不孕女性诱导排卵。超声引导下经阴道卵巢穿刺打孔术(UTND)是一种新型手术方法,用于在门诊为对克罗米芬耐药的PCOS女性诱导排卵。然而,大多数研究的质量似乎较低,UTND的安全性和有效性仍不确定。
评估UTND对克罗米芬耐药的PCOS不孕女性的有效性和安全性。
我们检索了Cochrane妇科与生育组(CGFG)专业注册库、CENTRAL、MEDLINE、Embase以及其他六个数据库,检索截至2018年11月的数据。我们查阅了2018年欧洲人类生殖与胚胎学会(ESHRE)的会议摘要、参考文献列表以及临床试验注册库。我们还联系了该领域的专家。
我们纳入了随机对照试验(RCT),这些试验比较了UTND与腹腔镜卵巢打孔术(LOD),以及UTND联合促性腺激素与单纯促性腺激素,受试对象为有克罗米芬耐药性PCOS且不孕的育龄女性。
两位综述作者独立筛选合适的试验以纳入研究,评估方法学质量和偏倚风险,并提取数据。主要结局为活产率和手术并发症(出血和感染)的发生率。我们将卵巢过度刺激综合征(OHSS)作为次要结局纳入。仅能对UTND与LOD比较中的次要结局妊娠率和排卵率采用随机效应模型进行Meta分析。对于二分数据,我们计算了比值比(OR)及95%置信区间(CI)。我们应用GRADE标准评估证据的整体质量。
我们纳入了五项试验共639例对克罗米芬耐药的PCOS女性。三项研究比较了UTND与LOD,两项研究比较了UTND联合促性腺激素与单纯促性腺激素。证据质量低至极低。主要局限性包括:由于方法报告不佳导致严重的偏倚风险、异质性导致的不一致性、样本量有限引起的不精确性,以及缺乏对活产和手术并发症等临床相关结局的报告。
UTND与LOD的比较:没有研究报告主要结局活产情况。一项研究报告了手术并发症;然而,该结局的证据质量极低,因为它基于一项样本量小的研究,且两组均无事件发生。因此,我们不确定UTND与LOD在手术并发症方面是否存在差异。
我们也不确定UTND与LOD在妊娠率方面是否存在差异(OR 0.54,95%CI 0.28至1.03;I² = 56%;3项RCT,n = 473;极低质量证据)。与LOD相比,UTND可能导致排卵率略有下降(OR 0.66,95%CI 0.45至0.97;I² = 0%;3项RCT,n = 473;低质量证据)。这表明,在预期排卵率为69.5%的使用LOD的对克罗米芬耐药的PCOS女性中,使用UTND的女性排卵率可能在50.6%至68.8%之间。
没有研究报告OHSS和多胎妊娠结局。关于流产也没有足够的证据得出结论,因为仅有一项质量极低的研究。
UTND联合促性腺激素与单纯促性腺激素的比较:没有研究报告主要结局活产和手术并发症发生率。此比较中OHSS、妊娠、排卵、流产和多胎妊娠结局的证据质量极低。因此,我们不确定对于使用UTND联合促性腺激素的对克罗米芬耐药的PCOS女性与使用单纯促性腺激素的女性在这些结局方面是否存在差异。
基于极低质量的证据,对于对克罗米芬耐药的PCOS女性,不确定UTND与LOD在妊娠率、手术并发症发生率和流产率方面是否存在差异。与LOD相比,UTND可能导致排卵率略有下降。没有研究报告活产率结局、OHSS发生率和多胎妊娠率。没有研究报告UTND联合促性腺激素与单纯促性腺激素比较的主要结局活产和手术并发症。此比较中OHSS、妊娠、排卵、流产和多胎妊娠结局的证据质量极低。因此,不清楚UTND联合促性腺激素与单纯促性腺激素在任何结局方面是否存在差异。