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First-trimester medical abortion with mifepristone 200 mg and misoprostol: A systematic review

机译:米非司酮200 mg和米索前列醇的孕早期药物流产:系统评价

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Background: The dose of mifepristone approved by most government agencies for medical abortion is 600 mg. Our aim was to summarize extant data on the effectiveness and safety of regimens using the widely recommended lower mifepristone dose, 200 mg, followed by misoprostol in early pregnancy and to explore potential correlates of abortion failure. Study Design: To identify eligible reports, we searched Medline, reviewed reference lists of published reports, and contacted experts to identify all prospective trials of any design of medical abortion using 200 mg mifepristone followed by misoprostol in women with viable pregnancies up to 63 days' gestation. Two authors independently extracted data from each study. We used logistic regression models to explore associations between 15 characteristics of the trial groups and, separately, the rates of medical abortion failure and of ongoing pregnancy. Results: We identified 87 trials that collectively included 120 groups of women treated with a regimen of interest. Of the 47,283 treated subjects in these groups, abortion outcome data were reported for 45,528 (96%). Treatment failure occurred in 2,192 (4.8%) of these evaluable subjects. Ongoing pregnancy was reported in 1.1% (499/45,150) of the evaluable subjects in the 117 trial groups reporting this outcome. The risk of medical abortion failure was higher among trial groups in which at least 25% of subjects had gestational age > 8 weeks, the specified interval between mifepristone and misoprostol was less than 24 h, the total misoprostol dose was 400 mcg (rather than higher), or the misoprostol was administered by the oral route (rather than by vaginal, buccal, or sublingual routes). Across all trials, 119 evaluable subjects (0.3%) were hospitalized, and 45 (0.1%) received blood transfusions. Conclusions: Early medical abortion with mifepristone 200 mg followed by misoprostol is highly effective and safe. ? 2013 Elsevier Inc.
机译:背景:大多数政府机构批准的米非司酮用于药物流产的剂量为600毫克。我们的目的是总结使用广泛推荐的米非司酮低剂量200 mg,米索前列醇在妊娠早期使用该药的有效性和安全性的现有数据,并探讨流产失败的潜在相关性。研究设计:为确定合格的报告,我们检索了Medline,审查了已发表报告的参考文献清单,并与专家联系,以确定在200天以下可存活妊娠妇女中使用200 mg米非司酮联合米索前列醇进行任何药物流产设计的所有前瞻性试验。妊娠。两位作者分别从每个研究中提取数据。我们使用逻辑回归模型探讨了试验组的15个特征之间的关联,并分别探讨了药物流产失败率和持续妊娠率。结果:我们确定了87个试验,这些试验总共包括120组受关注的方案治疗的女性。在这些组中的47,283名接受治疗的受试者中,据报有45,528名(96%)流产结果数据。这些可评估受试者中有2,192名(4.8%)发生了治疗失败。在117个报告此结果的试验组中,有1.1%(499 / 45,150)的可评估受试者报告了持续妊娠。试验组中至少有25%的受试者的胎龄> 8周,米非司酮与米索前列醇之间的指定间隔小于24小时,米索前列醇总剂量为400 mcg(而非更高)的试验组中,药物流产失败的风险较高。 ),或者通过口服途径(而不是通过阴道,颊或舌下途径)施用米索前列醇。在所有试验中,有119名可评估的受试者(0.3%)入院,有45名(0.1%)接受了输血。结论:米非司酮200毫克米索前列醇然后米索前列醇的早期药物流产是高度安全的。 ? 2013爱思唯尔公司

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