RANDOMIZED TRIAL OF MISOPROSTOL AND CERVAGEM IN COMBINATION WITH A REDUCED DOSE OF MIFEPRISTONE FOR INDUCTION OF ABORTION

Citation
Dt. Baird et al., RANDOMIZED TRIAL OF MISOPROSTOL AND CERVAGEM IN COMBINATION WITH A REDUCED DOSE OF MIFEPRISTONE FOR INDUCTION OF ABORTION, Human reproduction, 10(6), 1995, pp. 1521-1527
Citations number
20
Categorie Soggetti
Reproductive Biology
Journal title
ISSN journal
02681161
Volume
10
Issue
6
Year of publication
1995
Pages
1521 - 1527
Database
ISI
SICI code
0268-1161(1995)10:6<1521:RTOMAC>2.0.ZU;2-R
Abstract
Mifepristone (600 mg) in combination with a prostaglandin has been dem onstrated to be a safe, acceptable alternative to vacuum aspiration fo r induction of abortion in the first 9 weeks of pregnancy. However, th e efficacy and side-effects of different prostaglandins used in combin ation vith mifepristone have not been assessed in a randomized trial. In this study, 800 women seeking an abortion at gestational age less t han or equal to 63 days amenorrhoea were randomized to receive either 0.5 mg gemeprost by vaginal pessary (group I) or 600 mu g misoprostol (group II) by mouth similar to 48 h after taking 200 mg mifepristone b y mouth. The side-effects and number of complete abortions were used a s measures of efficacy. There was no significant difference in the rat e of complete abortion between group I [96.7%; 95% confidence interval (CI) 94.9-98.5%, n = 391] and group II (94.6%; 95% CI 92.3-96,9, n = 386). It was not possible to assess the outcome with certainty in the remaining 23 women. However, there were significantly more ongoing pre gnancies in the women who received misoprostol than in those who recei ved gemeprost (nine versus one, P < 0.01) and in eight of these 10 wom en the gestation was > 49 days, Fewer women in group II required analg esia than in group I (48 versus 60% P < 0.001) although the number req uesting opiate was similar in each group (6.9 versus 5.2%, P > 0.4). T he incidence of nausea and vomiting after misoprostol (47.8 and 21.9% respectively) was higher (P < 0.001) than after gemeprost (33.9 and 12 % respectively). The incidence of infection and heavy bleeding was low in both groups (< 2%) and only one woman required blood transfusion. We conclude that the recommended dose of mifepristone and gemeprost ca n be reduced without impairing clinical efficacy in pregnancies up to 63 days amenorrhoea. Misoprostol is a safe alternative prostaglandin b ut has a higher incidence of ongoing pregnancies especially at gestati on after 49 days amenorrhoea.