Interruption of early pregnancy with mifepristone in combination with gemeprost

被引:9
作者
Sandstrom, O
Brooks, L
Schantz, A
Grinsted, J
Grinsted, L
Jacobsen, JD
Nielsen, SP
机构
[1] Hillerod Sygehus, Dept Gynecol & Obstet, DK-3400 Hillerod, Denmark
[2] Hillerod Sygehus, Dept Radiol, DK-3400 Hillerod, Denmark
关键词
abortion; gemeprost; mifepristone;
D O I
10.1034/j.1600-0412.1999.780913.x
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background. Mifepristone in combination with prostaglandin has been used since 1988 for induction of early abortion. The aim of the present investigation was to assess the tolerance and efficacy of 600 mg. mifepristone orally followed by gemeprost 1 mg. vaginally either 24 hours (group one) or 48 hours (group two) later. Methods. Sixty-Four healthy women applying for abortion within the first 8 weeks of pregnancy were randomly allocated to one of the two treatment groups. Intrauterine pregnancy and gestational age were verified by ultrasonography. Symptoms after administration of mifepristone and gemeprost were recorded, and the patients observed at the hospital for at least three hours after prostaglandin-insertion. Blood samples for blood group, hemoglobin, beta-chorion-gonadotrophin, aspartate-aminotransferase and creatinine were drawn. Results. Outcome was established by gynecological examination, the level of beta-hCG and ultrasonography, at visits one, two and if necessary three to four weeks later. Surgical curettage was performed in case of incomplete abortion, of which there were four in the 24-hour interval group and five in the 48-hour interval group with a success rate (complete abortion) of 55 out of 64 patients (86%). Conclusions. There was no difference in efficacy or side effects whether the prostaglandin was administered 24 or 48 hours after mifepristone intake, which suggests that the treatment period can be reduced from the conventional 48 hours.
引用
收藏
页码:806 / 809
页数:4
相关论文
共 21 条
[1]   CONTRAGESTION AND OTHER CLINICAL-APPLICATIONS OF RU-486, AN ANTIPROGESTERONE AT THE RECEPTOR [J].
BAULIEU, EE .
SCIENCE, 1989, 245 (4924) :1351-1357
[2]   CERVICAL-MUCUS CONCENTRATION OF PROSTAGLANDINS E(2) AND F2-ALPHA AFTER PRETREATMENT WITH MIFEPRISTONE IN THE FIRST TRIMESTER OF PREGNANCY [J].
BOKSTROM, H ;
NORSTROM, A ;
WIQVIST, N .
PROSTAGLANDINS & OTHER LIPID MEDIATORS, 1995, 49 (01) :41-48
[3]   PROGESTERONE-RECEPTOR BLOCKAGE - EFFECT ON UTERINE CONTRACTILITY AND EARLY-PREGNANCY [J].
BYGDEMAN, M ;
SWAHN, ML .
CONTRACEPTION, 1985, 32 (01) :45-51
[4]   PROGESTERONE-RECEPTOR AND THE MECHANISM OF ACTION OF PROGESTERONE ANTAGONISTS [J].
EDWARDS, DP ;
ALTMANN, M ;
DEMARZO, A ;
ZHANG, YX ;
WEIGEL, NL ;
BECK, CA .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 53 (1-6) :449-458
[5]   EARLY INDUCTION OF ABORTION BY A COMBINATION OF ORAL MIFEPRISTONE AND MISOPROSTOL ADMINISTERED BY THE VAGINAL ROUTE [J].
ELREFAEY, H ;
TEMPLETON, A .
CONTRACEPTION, 1994, 49 (02) :111-114
[6]   EARLY COMPLICATIONS AFTER INDUCED 1ST-TRIMESTER ABORTION [J].
HEISTERBERG, L ;
KRINGELBACH, M .
ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA, 1987, 66 (03) :201-204
[7]  
HERRMANN W, 1982, CR ACAD SCI III-VIE, V294, P933
[8]  
HILL NCW, 1997, CONTRACEPTION, V55, P1
[9]   TERMINATION OF VERY EARLY-PREGNANCY BY RU-486 - AN ANTIPROGESTATIONAL COMPOUND [J].
KOVACS, L ;
SAS, M ;
RESCH, BA ;
UGOCSAI, G ;
SWAHN, ML ;
BYGDEMAN, M ;
ROWE, PJ .
CONTRACEPTION, 1984, 29 (05) :399-410
[10]   THE EFFECT OF DOSE OF MIFEPRISTONE AND GESTATION ON THE EFFICACY OF MEDICAL ABORTION WITH MIFEPRISTONE AND MISOPROSTOL [J].
MCKINLEY, C ;
THONG, KJ ;
BAIRD, DT .
HUMAN REPRODUCTION, 1993, 8 (09) :1502-1505