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妊娠 13 至 16 周末行中期妊娠药物流产,米非司酮-米索前列醇间隔 1 或 2 日。

One- and two-day mifepristone-misoprostol intervals for second trimester termination of pregnancy between 13 and 16 weeks of gestation.

机构信息

Department of Gynecology and Obstetrics, The Sixth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Int J Gynaecol Obstet. 2010 Nov;111(2):126-30. doi: 10.1016/j.ijgo.2010.06.008. Epub 2010 Aug 11.

DOI:10.1016/j.ijgo.2010.06.008
PMID:20705290
Abstract

OBJECTIVE

To compare the efficacy of 1-day and 2-day mifepristone and misoprostol intervals for second trimester termination of pregnancy between 13 and 16 weeks.

METHODS

A prospective randomized cohort study of 100 women who underwent voluntary termination between 13 and 16 weeks of gestation. Patients were randomly assigned to receive 200mg of oral mifepristone, followed 1 day (group 1) or 2 days (group 2) later by 600 μg of vaginal misoprostol. All patients received 400 μg of oral misoprostol every 6 hours for a maximum of 2 doses. Main outcome measure was successful abortion rate at 24 hours after the start of misoprostol treatment. Secondary outcome measures were induction-to-abortion interval and frequency of adverse events.

RESULTS

The 24-hour successful abortion rate was similar between groups 1 and 2 (47 [94%] vs 50 [100%]; P = 0.241). The mean misoprostol-to-abortion interval was also similar (7.0 ± 3.0 vs 6.8 ± 4.3 hours; P = 0.744). Among the 86 patients for whom histological examination of the products of conception was performed, retained chorionic villi rates were higher in the 1-day regimen group compared with the 2-day regimen group (46.2% [18/39] vs 29.8% [14/47]; P<0.001).

CONCLUSION

A 2-day mifepristone-misoprostol interval resulted in fewer incomplete abortions than a 1-day interval for second trimester termination of pregnancy between 13 and 16 weeks.

摘要

目的

比较米非司酮和米索前列醇用于 13-16 周妊娠中期引产的 1 天和 2 天间隔的疗效。

方法

这是一项前瞻性随机队列研究,共纳入 100 名在 13-16 孕周行自愿终止妊娠的患者。患者被随机分为两组,分别在口服米非司酮 200mg 后第 1 天(第 1 组)或第 2 天(第 2 组)给予 600μg 阴道米索前列醇。所有患者均接受 400μg 米索前列醇口服,每 6 小时 1 次,最多 2 次。主要结局测量指标是米索前列醇治疗开始后 24 小时的完全流产率。次要结局测量指标是引产至流产的间隔时间和不良反应的发生频率。

结果

第 1 组和第 2 组的 24 小时完全流产率相似(47[94%]例 vs 50[100%]例;P=0.241)。米索前列醇至流产的间隔时间也相似(7.0±3.0 小时 vs 6.8±4.3 小时;P=0.744)。在 86 例行组织学检查的患者中,1 天方案组的残留绒毛组织率高于 2 天方案组(46.2%[18/39]例 vs 29.8%[14/47]例;P<0.001)。

结论

与 1 天间隔相比,米非司酮-米索前列醇 2 天间隔用于 13-16 孕周妊娠中期引产可减少不完全流产的发生。

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Int J Gynaecol Obstet. 2010 Nov;111(2):126-30. doi: 10.1016/j.ijgo.2010.06.008. Epub 2010 Aug 11.
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