A systematic review of more than one dose of misoprostol after mifepristone for abortion up to 10 weeks of gestation

被引:8
作者
Gallo, MF [1 ]
Cahill, S
Castleman, L
Mitchell, EMH
机构
[1] Ipas, Res & Evaluat Unit, Chapel Hill, NC 27516 USA
[2] Choice Family Hlth Care, Kalispell, MT USA
[3] Ipas, Training & Serv Delivery Improvement Unit, Chapel Hill, NC 27516 USA
关键词
mifepristone; misoprostol; abortion; induced; review;
D O I
10.1016/j.contraception.2006.02.011
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
Objectives: This review aimed to assess the effectiveness, acceptability and safety of regimens that include mifepristone and multiple misoprostol doses for abortion up to 10 weeks of gestation. Methods: We searched MEDLINE and reference lists for English-language reports (published between January 1990 and September 2005) of trials evaluating a medication abortion regimen consisting of mifepristone and multiple doses of misoprostol. Eligible trials had to either be restricted to women with less than 10 weeks' gestation or report stratified results that allowed the extraction of data for this subset. Results: Although we identified 26 eligible studies, only 3 were randomized controlled trials (RCTs), comparing regimens that differed in the repeat-dose misoprostol component. These trials did not detect differences in effectiveness between the randomized groups. One RCT found evidence of higher effectiveness from repeat misoprostol doses among a subgroup of women with more advanced gestations. Conclusions: Although clinicians often prescribe a repeat dose of misoprostol to increase effectiveness in medication abortion, the effect of the repeat dose has not been established. Because mifepristone followed by a single misoprostol dose is highly effective in inducing abortion, determining the effect of a repeat misoprostol dose would require a large sample size. The resource expenditure on such large trials might not be warranted. Any future studies should use induction-to-completion time to measure effectiveness and should assess acceptability and side effects. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:36 / 41
页数:6
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