Lelaidier C, Saint-Mleux C B, Fernandez H, Bourget P, Frydman R
Service de gynécologie-Obstétrique, Hôpital Antoine Béclère, Clamart.
Contracept Fertil Sex. 1993 Jun;21(6):505-8.
We investigated the use of oral mifepristone (RU486) for the induction of natural expulsion in women with spontaneously interrupted pregnancy in the first trimester in a double blind placebo controlled study against placebo. 46 women consulting for interrupted pregnancy diagnosed at ultrasound with no clinical sign of miscarriage were included in the trial. Main outcome measures were occurrence of natural expulsion, frequency of complete expulsion need for subsequent surgical evacuation, analgesia and need for transfusion. Natural expulsion occurred within 5 days in 82% patients receiving treatment versus 8% placebo treated patients (p < 0.001). All patients experienced bleeding after RU486 and 2 needed emergency aspiration for haemorrhagic expulsion. The treatment failed in 4 patients who underwent evacuation under local anesthesia. In the control group 19 patients underwent evacuation under local (n = 9) or general (n = 11) anesthesia.
A standard oral pilot dose of 600 mg of Mifepristone induces natural expulsion in 82% women with non developing first trimester intra-uterine pregnancies.
在一项针对安慰剂的双盲安慰剂对照研究中,我们调查了口服米非司酮(RU486)用于诱导孕早期自然流产妇女自然排出妊娠物的情况。46名因妊娠中断前来咨询且经超声诊断无流产临床体征的妇女被纳入试验。主要观察指标为自然排出的发生率、完全排出的频率、后续手术清宫的必要性、镇痛情况及输血需求。接受治疗的患者中有82%在5天内自然排出,而接受安慰剂治疗的患者中这一比例为8%(p<0.001)。所有接受米非司酮治疗的患者均出现出血,2例因出血性排出需要紧急清宫。4例患者治疗失败,需在局部麻醉下清宫。在对照组中,19例患者在局部麻醉(n=9)或全身麻醉(n=11)下清宫。
标准口服试验剂量600mg米非司酮可使82%孕早期宫内妊娠未发育的妇女自然排出妊娠物。