Ho P C, Chan Y F, Lau W
Department of Obstetrics and Gynaecology, University of Hong Kong, Hong Kong.
Contraception. 1996 May;53(5):281-3.
A prospective randomized study was conducted to compare the efficacy of misoprostol with gemeprost when combined with mifepristone for termination of second trimester pregnancy. Patients requesting termination of second trimester pregnancy were randomized into two groups. In both groups of patients, 200 mg of mifepristone was given 36 to 48 hours before the administration of prostaglandins. In Group 1, the women were given 400 micrograms of oral misoprostol every 3 hours up to 5 doses. In Group 2, patients were given 1 mg of vaginal gemeprost every 6 hours up to 4 doses. The main outcomes measured were the induction-abortion intervals (the interval between the first dose of prostaglandin and abortion) and the incidence of side effects. Altogether, 50 subjects were recruited with 25 women in each group. The mean age and parity of the women and the mean gestational age of the two groups of women were comparable. There was no significant difference in the median induction-abortion intervals (8.7 hours in Group 1 and 10.8 hours in Group 2) or the incidence of side effects between the two groups of patients. We conclude that misoprostol is as effective as gemeprost in termination of second trimester pregnancy when combined with mifepristone.
进行了一项前瞻性随机研究,比较米索前列醇与吉美前列素联合米非司酮终止中期妊娠的疗效。要求终止中期妊娠的患者被随机分为两组。两组患者在给予前列腺素前36至48小时均服用200毫克米非司酮。第1组女性每3小时口服400微克米索前列醇,最多服用5剂。第2组患者每6小时阴道给予1毫克吉美前列素,最多服用4剂。主要测量指标为引产-流产间隔时间(第一剂前列腺素与流产之间的间隔)和副作用发生率。总共招募了50名受试者,每组25名女性。两组女性的平均年龄、产次以及平均孕周具有可比性。两组患者的中位引产-流产间隔时间(第1组为8.7小时,第2组为10.8小时)或副作用发生率无显著差异。我们得出结论,米索前列醇与吉美前列素在联合米非司酮终止中期妊娠方面疗效相当。