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米非司酮(RU 486)联合前列腺素类似物(硫前列酮)用于早期妊娠终止。

Termination of early pregnancy with RU 486 (mifepristone) in combination with a prostaglandin analogue (sulprostone).

作者信息

Swahn M L, Bygdeman M

机构信息

Department of Obstetrics and Gynecology, Karolinska Sjukhuset, Stockholm, Sweden.

出版信息

Acta Obstet Gynecol Scand. 1989;68(4):293-300. doi: 10.3109/00016348909028661.

Abstract

The antiprogestin RU 486 (mifepristone) has been shown to induce abortion when administered in early pregnancy, but the rate of incomplete abortion is high, around 40%. As blockage of the progesterone receptor increases the myometrial sensitivity to prostaglandins, a combination of RU 486 and a prostaglandin E2-analogue was tested for termination of pregnancy. One hundred and sixteen women, with a gestational length of less than 49 days from the first day of the last menstrual period, were treated with a daily dose of 50 or 100 mg RU 486 for 3 to 6 days, complemented with an intramuscular dose of 0.25 mg sulprostone (16-phenoxy-PGE2-sulfonylamide) on the last day of RU 486 treatment. The results confirmed that a reduction of treatment duration to 3 days is just as effective for inducing abortion (91% complete abortion) as a 4-6-day treatment regimen (95% complete abortion). Six patients had an incomplete abortion and in one the pregnancy continued unaffected. Side effects included intense uterine pain after the prostaglandin administration (16%), vomiting associated with the antiprogestin intake (9%) and after the prostaglandin administration (9%). One woman needed emergency curettage due to heavy bleeding. Six percent of the treated patients had a decrease in hemoglobin exceeding 20 g/l during the first week but no patient needed blood transfusion. No serious side effects were recorded.

摘要

抗孕激素RU 486(米非司酮)已被证明在孕早期使用时可诱导流产,但不完全流产率很高,约为40%。由于孕酮受体的阻断会增加子宫肌层对前列腺素的敏感性,因此对RU 486与前列腺素E2类似物的联合用药进行了终止妊娠的测试。116名妇女,自末次月经第一天起妊娠时长小于49天,每天服用50或100毫克RU 486,持续3至6天,并在RU 486治疗的最后一天补充一剂0.25毫克的磺前列酮(16-苯氧基-PGE2-磺酰胺)肌肉注射。结果证实,将治疗时间缩短至3天诱导流产的效果(完全流产率91%)与4至6天的治疗方案(完全流产率95%)相同。6名患者发生不完全流产,1名患者妊娠继续未受影响。副作用包括前列腺素给药后剧烈的子宫疼痛(16%)、与抗孕激素摄入相关的呕吐(9%)以及前列腺素给药后(9%)。1名妇女因大出血需要紧急刮宫。6%的治疗患者在第一周血红蛋白下降超过20克/升,但没有患者需要输血。未记录到严重的副作用。

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