Intrauterine Extra-amniotic Misoprostol Solution is Effective for Termination of Second Trimester Missed Abortion: A clinical pilot descriptive study

Q4 Medicine
A. B. A. Mitwaly, A. Abbas
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引用次数: 2

Abstract

Objectives: The purpose of this study was to determine the efficacy and safety of intrauterine extra-amniotic misoprostol solution for termination of the second trimester missed abortion. Methods: A clinical pilot descriptive study that was done in Women Health Hospital, Assiut University, Egypt between March 2015 and June 2015. Fifty patients having missed abortion of gestational age between 13 to 24 weeks were included in the study. Insertion of an intrauterine Foley’s catheter followed by infusion of sterile misoprostol solution through a sterile infusion set at a constant drip rate. The primary outcome was successful expulsion of the fetus in 12 hours after starting misoprostol infusion. Results: The mean age of the study group was 27.25±4.08, the mean BMI was 26.35±3.6, the mean gestational age was 22.85±3.4 and the mean parity was 2.5±1.5. The mean induction expulsion interval was 5.27±2.66 hours. Six cases (12%) needed analgesic. Surgical evacuation of retained contents was needed in 3 cases (6%). Side effects in the form of rigors, fever and diarrhea were recorded in 4 cases (8%). No serious maternal events were recorded. Conclusion: Our results showed that intrauterine extra-amniotic misoprostol solution instillation appear to be effective and safe for termination of a second trimester missed abortions.
宫内羊水外米索前列醇溶液对终止中期流产有效:一项临床初步描述性研究
目的:本研究的目的是确定米索前列醇子宫内羊膜外溶液终止妊娠中期漏产的有效性和安全性。方法:2015年3月至2015年6月在埃及Assiut大学妇女健康医院进行临床试点描述性研究。50例胎龄在13 - 24周之间的流产患者被纳入研究。通过无菌输液器以恒定滴速输注无菌米索前列醇溶液后插入宫内Foley氏导管。主要结果是开始米索前列醇输注后12小时内胎儿成功排出。结果:研究组平均年龄27.25±4.08,平均BMI 26.35±3.6,平均胎龄22.85±3.4,平均胎次2.5±1.5。平均诱导排出时间为5.27±2.66小时。6例(12%)需要镇痛。3例(6%)需要手术清除残留内容物。不良反应4例(8%)出现僵硬、发热、腹泻。没有严重的产妇事件记录。结论:子宫内羊膜外滴注米索前列醇溶液对终止妊娠中期流产是安全有效的。
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来源期刊
Thai Journal of Obstetrics and Gynaecology
Thai Journal of Obstetrics and Gynaecology Medicine-Obstetrics and Gynecology
CiteScore
0.40
自引率
0.00%
发文量
3
审稿时长
24 weeks
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