Ulmsten U, Wingerup L
Prostaglandins. 1980 Sep;20(3):533-46. doi: 10.1016/0090-6980(80)90041-6.
A new gel for intracervical application of prostaglandin E2 (PGE2) has been elaborated and evaluated. The main component of the gel is a cross-linked starch polymer to which prostaglandins can be added and preserved for long-term storage (> 12 months). In a double blind study, 20 patients requiring legal abortion in late first trimester were given gel containing 0.25 mg PGE2 or gel without PGE2. The gel was applied within the cervical canal. In all patients receiving PGE2-gel, a rapid ripening of the cervix occurred which facilitated the subsequent dilatation and evacuation. In patients receiving gel without PGE2 cervix did not ripen. In a subsequent open study, 30 patients were treated with PGE2-gel before therapeutic abortion. The same degree of cervical ripening was registered as for the patients receiving PGE2-gel in the double blind study. In 50 patients at term, intracervical application of 3 ml gel containing 0.05 mg PGE2 induced labor in 27 cases, i.e. 54 per cent of the patients. In the remaining undelivered women, a prominent cervical ripening occurred within 24 hours. No side effects of the treatment were observed. We conclude the new PGE2-gel to be a promising future alternative in the treatment of patients with an unfavorable cervix, prior to surgical evacuation of the uterus in late first trimester abortion, as well as before induction of labor at term.
一种用于宫颈内应用前列腺素E2(PGE2)的新型凝胶已被研制并评估。该凝胶的主要成分是一种交联淀粉聚合物,前列腺素可添加到其中并能长期保存(>12个月)。在一项双盲研究中,20例孕早期晚期需要合法堕胎的患者被给予含0.25毫克PGE2的凝胶或不含PGE2的凝胶。凝胶被应用于宫颈管内。所有接受PGE2凝胶的患者宫颈迅速成熟,这便于随后的扩张和排空。接受不含PGE2凝胶的患者宫颈未成熟。在随后的一项开放性研究中,30例患者在治疗性流产前接受了PGE2凝胶治疗。宫颈成熟程度与双盲研究中接受PGE2凝胶的患者相同。在50例足月患者中,宫颈内应用3毫升含0.05毫克PGE2的凝胶使27例患者引产,即54%的患者。在其余未分娩的妇女中,24小时内宫颈显著成熟。未观察到治疗的副作用。我们得出结论,这种新型PGE2凝胶在孕早期晚期堕胎子宫手术排空之前以及足月引产之前,对于宫颈条件不佳的患者治疗是一种有前景的未来替代方法。