Human Reproduction, Vol. 8, No. 9, pp. 1502-1505, 1993
© 1993 European Society of Human Reproduction and Embryology
research-article |
Pregnancy: The effect of dose of mifepristone and gestation on the efficacy of medical abortion with mifepristone and misoprostol
Department of Obstetrics and Gynaecology, Centre for Reproductive Biology, University of Edinburgh 37 Chalmers Street, Edinburgh EH3 9EW, UK
Although it has been demonstrated that a combination of mifepristone and a prostaglandin is an effective method of inducing abortion in early pregnancy, the optimum dose of the antigestogen is unknown. Women (n = 220) requesting abortion in early pregnancy (
63 days amenorrhoea) were randomized to receive a single dose of either 600 or 200 mg mifepristone followed 48 h later by a single dose of 600 µg misoprostol by mouth. The percentage of women who had a complete abortion (93.6% confidence interval 90.495.5%) was identical in the two groups. There was no significant difference in the number of women who passed the fetus within 4 h of receiving the prostaglandin (64 versus 74%), the days of bleeding (14.6 ± 1.1 versus 15.3 ± 0.9) nor in the onset of the next period (39.7 ± 1.3 versus 36.7 ± 1.3) respectively between the groups receiving 200 or 600 mg mifepristone. However, the complete abortion rate was significantly higher in women
49 days compared to women 5063 days amenorrhoea (97.5 versus 89.1% respectively; P < 0.02). There was no difference in any of the other parameters at different weeks of gestation. We conclude: (i) that the recommended dose of mifepristone could be reduced from 600 to 200 mg without loss of clinical efficacy, (ii) that the combination of mifepristone and 600 µg misoprostol is a highly effective alternative to vacuum aspiration for inducing abortion in women < 50 days amenorrhoea and (iii) at gestation >56 days, this combination may result in too many incomplete abortions to be clinically acceptable.
Key words: gestation/medical abortion/mifepristone/misoprostol
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