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Efficacy of Misoprostol Alone for First-Trimester Medical Abortion A Systematic Review

机译:仅为孕孕前孕孕医生医疗堕胎的疗效效果系统审查

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OBJECTIVE: To summarize available data on the effectiveness and safety of single-agent misoprostol for medical abortion in the first trimester. DATA SOURCES: We searched MEDLINE, CABI, Cochrane, EMBASE, LILACS, the Web of Science, and ClinicalTrials. gov for English-language studies that evaluated misoprostol alone for abortion of a viable pregnancy in the first trimester. METHODS OF STUDY SELECTION: Our search yielded 1,562 citations, of which 38 included data from 53 trial groups that met our inclusion and exclusion criteria. TABULATION, INTEGRATION, AND RESULTS: We abstracted data about each trial group, including study characteristics, treatment regimen, clinical protocol, number of women treated and followed, and numbers with outcomes of interest. We used meta-analytic methods and logistic regression to examine factors associated with surgical intervention after treatment. Among all 12,829 evaluable women, 2,536 (meta-analytic estimate 22.0%, 95% CI 18.8-25.5%) had surgical uterine evacuation. Multiple factors were significantly associated with this proportion, including misoprostol amount per dose and route of administration, loss to follow-up rate, publication date, geographic region, number of misoprostol doses, duration of dosing, and time between dosing and evaluation. Of 6,359 evaluable women, 384 (metaanalytic estimate 6.8%, 95% CI 5.3-8.5%) had ongoing pregnancies. At most 26 of 12,184 evaluable women (meta-analytic estimate 0.7%, 95% CI 0.4-1.0%) were transfused or hospitalized for abortion-related reasons. In trials that provided satisfaction data, most women were satisfied or very satisfied with the treatment (meta-analytic estimate 78%, 95% CI 71-85%). CONCLUSIONS: Misoprostol alone is effective and safe and is a reasonable option for women seeking abortion in the first trimester. Research is indicated to further refine the regimen and to establish efficacy in the late first trimester.
机译:目的:总结上在第一季度的有效性和单药米索前列醇的安全药物流产的数据。资料来源:检索了MEDLINE,CABI,科克伦,文摘,紫丁香,科学的Web和ClinicalTrials。 GOV为评估米索前列醇单独用于在第一季度可行妊娠流产英语学习。研究选择方法:我们的研究发现了1562个引文,从能够满足我们入选和排除标准53个试验组38个包含的数据。 TABULATION,集成和结果:我们抽象的关于每个治疗组数据,包括研究的特点,治疗方案,临床治疗方案,治疗和随后的妇女人数和数字与感兴趣的结果。我们使用荟萃分析方法和逻辑回归到检查与治疗后外科手术相关的因素。在所有12,829评估妇女,2,536(荟萃分析估计22.0%,95%CI 18.8-25.5%)有手术刮宫。多种因素与此比例进行显著相关联,包括每剂量米索前列醇量和给药途径,损失随访率,出版日期,地理区域,米索前列醇剂量数,剂量的持续时间,和给药和评估之间的时间。 6,359评估妇女,384(metaanalytic估计为6.8%,95%CI 5.3-8.5%)有继续妊娠。最多26的12184名妇女评估(荟萃分析估计为0.7%,95%CI 0.4-1.0%)的输血或住院堕胎有关的原因。在试验中,所提供满意度数据,大多数女性都表示满意或非常满意的治疗(荟萃分析估计为78%,95%CI 71-85%)。结论:单纯米索前列醇是有效和安全的,是求败在孕早期的女性一个合理的选择。研究表示,进一步细化方案,并在早孕晚期建立功效。

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