Karimzadeh Atieh, Allahqoli Leila, Salehiniya Hamid, Hanjani Soheil, Namavari Ghazal, Fazel Anvari-Yazdi Abbas, Tahermanesh Kobra, Alkatout Ibrahim
Department of Obstetrics and Gynecology, School of Medicine, Iran University of Medical Sciences, Tehran 1449614535, Iran.
Ministry of Health and Medical Education, Tehran 1435713715, Iran.
J Clin Med. 2024 Sep 17;13(18):5494. doi: 10.3390/jcm13185494.
Hysteroscopy has been used as both a diagnostic and therapeutic tool for intrauterine pathologies under direct visualization. However, this procedure may be associated with an increased risk of complications during entry, which can be reduced by cervical ripening before the operation. The efficacy of misoprostol in this context is influenced by factors such as estrogen levels, parity, and the mode of previous deliveries. This study aimed to assess the efficacy and safety of misoprostol in women with a challenging cervix while mitigating the influence of confounding variables. Three electronic databases, namely PubMed, Scopus, and ISI Web of Science, were searched until 14 May 2024. Randomized controlled trials focusing on postmenopausal patients, nulliparous women, and multiparous women with no prior history of vaginal delivery, undergoing hysteroscopy were included. The cervical width, time needed for cervical dilation, and the need for additional dilatation alongside the complications and adverse effects from all included studies were collected and analyzed using R (version 4.2.3). Seven studies on premenopausal women and three on postmenopausal women were included. In premenopausal women, misoprostol significantly increased cervical width compared to placebo (SMD = 2.2, 95% CI 0.9 to 3.4) and reduced the need for additional cervical dilatation (OR = 0.36, 95% CI 0.17 to 0.74). No significant difference was found in the time required for cervical dilation between misoprostol and placebo groups. In postmenopausal women, misoprostol did not significantly affect cervical width compared to placebo (SMD = -0.55, 95% CI -1.3 to 0.21). Misoprostol is beneficial for cervical dilation in premenopausal women without a prior history of vaginal delivery but less effective in postmenopausal patients. While associated with postoperative risks, it reduces hysteroscopy-related complications. Future research should address discrepancies by controlling the confounding variables like menopausal status, parity, and mode of delivery to enhance the understanding of misoprostol's effects and pinpoint the specific patient populations that would derive the greatest benefits from its use.
宫腔镜检查已被用作在直接可视化下诊断和治疗子宫内病变的工具。然而,该手术在进入过程中可能会增加并发症的风险,术前宫颈成熟可降低这种风险。米索前列醇在这种情况下的疗效受雌激素水平、产次和既往分娩方式等因素影响。本研究旨在评估米索前列醇在宫颈条件不佳的女性中的疗效和安全性,同时减轻混杂变量的影响。检索了三个电子数据库,即PubMed、Scopus和ISI Web of Science,检索截至2024年5月14日。纳入了针对绝经后患者、未生育女性以及无阴道分娩史的经产妇进行宫腔镜检查的随机对照试验。收集了所有纳入研究的宫颈宽度、宫颈扩张所需时间以及额外扩张的需求,以及并发症和不良反应,并使用R(版本4.2.3)进行分析。纳入了七项关于绝经前女性的研究和三项关于绝经后女性的研究。在绝经前女性中,与安慰剂相比,米索前列醇显著增加了宫颈宽度(标准化均数差=2.2,95%置信区间0.9至3.4),并减少了额外宫颈扩张的需求(比值比=0.36,95%置信区间0.17至0.74)。米索前列醇组和安慰剂组在宫颈扩张所需时间上未发现显著差异。在绝经后女性中,与安慰剂相比,米索前列醇对宫颈宽度没有显著影响(标准化均数差=-0.55,95%置信区间-1.3至0.21)。米索前列醇对无阴道分娩史的绝经前女性的宫颈扩张有益,但对绝经后患者效果较差。虽然它与术后风险相关,但可减少宫腔镜相关并发症。未来的研究应通过控制绝经状态、产次和分娩方式等混杂变量来解决差异问题,以加深对米索前列醇作用的理解,并确定能从其使用中获得最大益处的特定患者群体。