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Misoprostol Alone Is Associated with a High Rate of Successful First-Trimester Abortion

机译:单独的米索前列醇与高孕孕率堕胎的高率有关

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This is an updated meta-analysis of misoprostol alone for abortion in the first trimester of pregnancy. Selected studies included women with viable pregnancies of variable gestational age limit, ranging from 42 to 98 days, nearly universally determined by ultrasonography. The meta analysis included 42 studies with 53 study groups and 13,573 women. A total of 12,829 women were included in the analysis after the exclusion of 744 who were lost before outcomes were known (5%). There were multiple regimens, with dosing from 200 mg to 800 mg. The most common dose was 800 mg (n = 40 groups, 92% of women); the most common route of administration was vaginal (n = 38 groups, 81% of women). Most women were instructed to take no more than three doses within 48 hours. After one or more required doses, women in 35 groups (38% of women) could use additional doses, up to a maximum of six doses over 14 days. Across all studies, the meta-analytic estimate of the rate of women who underwent subsequent surgical evacuation was 22.0% (95% CI, 18.8% to 25.5%). The authors analyzed heterogeneity across studies and identified several factors associated with higher risk of surgical evacuation. They demonstrated a linear trend (P <.001) with the 800-mg dosing being approximately one-fourth the risk of the 200-mg dosing. Oral administration was associated with a threefold higher risk compared with vaginal, buccal, or sublingual administration. Surgery was less common when tablets were moistened before vaginal insertion (odds ratio = 0.46; 0.35 to 0.60). Surgery also declined with allowed number of doses, duration of dosing (linear trend P 5._.01 in each case). It was also less frequent when the decision to perform surgery was delayed three to seven days after treatment (odds ratio = 0.55; 0.31 to 0.96). Safety was demonstrated by the rare need for hospitalization (n = 14 women) or transfusion (n = 12). The meta-analytic estimate for either was 0.7% (0.4% to 1.0%). No women died.
机译:这是单独的乳房司司醇的更新荟萃分析,妊娠第一个三个月的堕胎。所选研究包括可变性妊娠年龄限制可行性妊娠的妇女,从42〜98天内,几乎通过超声检查普遍确定。 Meta分析包括42项研究,其中53项研究组和13,573名女性。在分析中,分析中共有12,829名妇女排除在已知成果之前丢失744人(5%)。有多种方案,给药从200mg到800毫克。最常见的剂量为800毫克(n = 40组,女性92%);最常见的给药途径是阴道(n = 38组,81%的女性)。大多数女性被指示在48小时内不超过三剂量。在一种或多种所需剂量之后,35次妇女(38%的女性)可以使用额外的剂量,最多六剂量超过14天。在所有研究中,接受后续外科疏散的妇女速度的荟萃分析估计为22.0%(95%CI,18.8%至25.5%)。作者分析了研究的异质性,并确定了与手术疏散风险更高的几个因素。它们展示了线性趋势(P <.001),800mg给药大约是200mg给药的风险。与阴道,口腔或舌下给药相比,口服给药与三倍的风险相关。当在阴道插入之前润湿片剂时,手术较差(差距= 0.46; 0.35至0.60)。手术也随着允许的剂量次数,给药持续时间(线性趋势P 5._。在每种情况下01)。当治疗后三到七天进行手术延迟三至七天时,它也缺少频率(差价率= 0.55; 0.31至0.96)。通过罕见的住院治疗(n = 14个女性)或输血(n = 12),证明了安全性。荟萃分析估计为0.7%(0.4%至1.0%)。没有女人死了。

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