Human Reproduction, Vol. 15, No. 10, 2205-2208,
October 2000
© 2000 European Society of Human Reproduction and Embryology
Randomized comparison of vaginal (200 µg every 3 h) and oral (400 µg every 3 h) misoprostol when combined with mifepristone in termination of second trimester pregnancy
Department of Obstetrics and Gynaecology, University of Hong Kong, Queen Mary Hospital, Hong Kong, People's Republic of China
It is known that when misoprostol is given at 200 µg every 3 h after mifepristone pretreatment, the vaginal route is more effective than the oral route. However, women prefer the oral route. This randomized study was to test our hypothesis that oral misoprostol 400 µg is as effective as vaginal misoprostol 200 µg when given every 3 h in termination of second trimester pregnancy after priming with mifepristone. A total of 142 patients was randomly assigned to group 1 (200 mg mifepristone + 400 µg oral misoprostol every 3 h up to five doses) or group 2 (200 mg mifepristone + 200 µg vaginal misoprostol every 3 h up to five doses). The incidence of side-effects and the preference study were assessed through a standardized questionnaire during and after the abortion. For the oral group, both the incidence of diarrhoea (40.0 versus 23.2%, P = 0.03) and the amount of drug used (1734 compared with 812 µg, P < 0.0001) were significantly higher than that of the vaginal group but the incidence of fever appeared to be lower (not significant). There was no significant difference in complete abortion rate: 81.4% in the oral group and 75.4% in the vaginal group. The median inductionabortion interval was similar in the two groups (10.4 versus 10.0 h). The percentage of women who aborted in 24 h was also similar: 57/70 (81.4%) in the oral group and 58/69 (87.0%) in the vaginal group. Overall, 82.0% of women preferred the oral route. Oral misoprostol (400 µg) given every 3 h up to five doses, when combined with mifepristone, was as effective as the vaginal (200 µg) route in second trimester termination of pregnancy. This regimen could also be offered to those women who found repeated vaginal administration unacceptable.
Key words: mifepristone/misoprostol/second trimester abortion
1 To whom correspondence should be addressed at: Department of Obstetrics and Gynaecology, Queen Mary Hospital, Pokfulam Road, Hong Kong SAR, People's Republic of China.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
I. Saav, A. Aronsson, L. Marions, O. Stephansson, and K. Gemzell-Danielsson Cervical priming with sublingual misoprostol prior to insertion of an intrauterine device in nulliparous women: a randomized controlled trial Hum. Reprod., October 1, 2007; 22(10): 2647 - 2652. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Lalitkumar, M. Bygdeman, and K. Gemzell-Danielsson Mid-trimester induced abortion: a review Hum. Reprod. Update, January 1, 2007; 13(1): 37 - 52. [Abstract] [Full Text] [PDF] |
||||
![]() |
O. S. Tang, C. C.W. Chan, A. S.Y. Kan, and P. C. Ho A prospective randomized comparison of sublingual and oral misoprostol when combined with mifepristone for medical abortion at 12-20 weeks gestation Hum. Reprod., November 1, 2005; 20(11): 3062 - 3066. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Yilmaz, S. Kelekci, I. E. Ertas, S. Kahyaoglu, M. Ozel, N. Sut, and N. Danisman Misoprostol moistened with acetic acid or saline for second trimester pregnancy termination: a randomized prospective double-blind trial Hum. Reprod., November 1, 2005; 20(11): 3067 - 3071. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Hamoda, P. W. Ashok, G. M.M. Flett, and A. Templeton A randomized trial of mifepristone in combination with misoprostol administered sublingually or vaginally for medical abortion at 13-20 weeks gestation Hum. Reprod., August 1, 2005; 20(8): 2348 - 2354. [Abstract] [Full Text] [PDF] |
||||

