Thong K J, Baird D T
Department of Obstetrics and Gynaecology, University of Edinburgh, Scotland.
Contraception. 1992 Jul;46(1):11-7. doi: 10.1016/0010-7824(92)90127-f.
It is well established that abortion can be induced successfully in midtrimester of pregnancy by gemeprost vaginal pessaries. A randomised study was carried out to determine the efficacy of mifepristone and dilapan in combination with gemeprost for second trimester termination between 12-18 weeks' gestation. A contemporary group of women treated with gemeprost alone was used as a control group. A single course of 4 x 1 mg gemeprost pessaries was administered every six hours. If abortion had not occurred after 24 hours, a further course of 5 x 1 mg pessaries was administered every three hours over the next 24 hours. In the first twenty hours after administration of gemeprost, 95%, 85% and 72% of women aborted in the mifepristone, dilapan and the control group, respectively. The median induction-abortion interval in the mifepristone group (6.6h) was significantly shorter than the other two groups and fewer pessaries were required to induce abortion. The incidence of diarrhoea and vomiting was lower in the mifepristone than the other two study groups. This study demonstrated the efficacy of mifepristone in combination with gemeprost and this regimen is associated with fewer gastrointestinal side effects.
已充分证实,妊娠中期使用吉美前列素阴道栓剂可成功引产。开展了一项随机研究,以确定米非司酮和地拉帕与吉美前列素联合用于终止妊娠12 - 18周的中期妊娠的疗效。一组同期仅接受吉美前列素治疗的女性作为对照组。每6小时给予一个疗程,共4片1毫克的吉美前列素栓剂。如果24小时后未发生流产,则在接下来的24小时内每3小时再给予一个疗程,共5片1毫克的栓剂。在给予吉美前列素后的前20小时内,米非司酮组、地拉帕组和对照组的流产女性分别为95%、85%和72%。米非司酮组的引产 - 流产间隔中位数(6.6小时)明显短于其他两组,且引产所需的栓剂数量更少。米非司酮组腹泻和呕吐的发生率低于其他两个研究组。本研究证明了米非司酮与吉美前列素联合使用的疗效,且该方案胃肠道副作用较少。