首页> 外文期刊>International Journal of Reproduction, Contraception, Obstetrics and Gynecology >Comparative effectiveness of simultaneous administration of mifepristone and misoprostol versus interval regimen of mifepristone followed by misoprostol 12 hours apart in second trimester medical abortion
【24h】

Comparative effectiveness of simultaneous administration of mifepristone and misoprostol versus interval regimen of mifepristone followed by misoprostol 12 hours apart in second trimester medical abortion

机译:米非司酮和米索前列醇同时给药与米非司酮间隔方案联合米索前列醇间隔12小时在中期妊娠药物流产中的比较效果

获取原文
           

摘要

Background: In second trimester abortion, medical methods are preferred. Prostaglandins are the most widely used. Amongst them, misoprostol is the most commonly used. Thus, the study was conducted to delineate the effectiveness of simultaneous administration of mifepristone and misoprostol versus interval regimen mifepristone followed by misoprostol 12 hours apart in second trimester medical abortion. Methods: It was a prospective, single centered, comparative study conducted on 50 patients in Department of Obstetrics and Gynaecology, GMC, Amritsar coming for second trimester abortion, either elective or emergency, with gestational age between 12-20 weeks. Initially, 53 patients were enrolled in the study, 3 patients dropped out at different stages of study. Finally, 50 patients were enrolled and divided into two groups of 25 patients each by 1:1 randomization. In Group-A, mifepristone 200 mg orally along with misoprostol 600μg vaginally were given simultaneously, followed by 400 μg vaginal misoprostol every 4 hours for a maximum of five doses in 24 hours. Group-B initially received mifepristone 200 mg per oral followed by 12 hours later misoprostol 400μg vaginally and then 400μg vaginal misoprostol every 4 hours for a maximum of five doses in 24 hours. Primary outcome measure was effectiveness of regimen in complete abortion, which was confirmed on pelvic ultrasound 1-week after the last dose. Secondary outcome measure was to compare the induction abortion interval (IAI), dose of misoprostol required and adverse drug reaction (ADR) among both the regimens. P-value 0.05 was taken as statistically significant. Results: Mean age in Group-A was 25.68±3.79 years while in Group-B was 23.40±2.73 years. Both the regimens had success rate of 76% for complete abortion. However, IAI in Group-A was 5.9±4.47 hours whereas in Group-B was 9.6±5.07 hours, which was statistically significant (p= 0.009). A statistically significant difference was also observed in the mean dose of misoprostol between two groups that is, 1000±200μg and 1425±437.41μg respectively (p=0.01). Gestational age was related to IAI from 13 to 17.6 weeks in both groups (p=0.01) while no significant relation was seen between them in more than 17.6 weeks of gestation (p=0.63). Conclusions: Simultaneous administration of mifepristone and misoprostol showed better results than interval regimen in term of significant lesser induction abortion interval, lower dosages of misoprostol required with comparable success rates.
机译:背景:在妊娠中期流产中,首选医疗方法。前列腺素使用最广泛。其中,米索前列醇是最常用的。因此,该研究的目的是确定在中期妊娠流产中米非司酮和米索前列醇与间隔米非司酮同时给予米索前列醇相隔12小时的同时给药的有效性。方法:这是一项前瞻性,单中心,比较性研究,对50例在妇产科,GMC和阿姆利则的孕妇进行了妊娠中期妊娠(无论是择期还是急诊流产),其胎龄在12-20周之间。最初,有53名患者参加了研究,其中3名患者在研究的不同阶段退出。最后,招募了50位患者,并按1:1随机分为两组,每组25位。在A组中,同时口服200 mg米非司酮和600μg米索前列醇口服,然后每4小时服用400μg阴道米索前列醇,在24小时内最多服用5剂。 B组最初口服米非司酮200 mg,然后在12小时后阴道内注射米索前列醇400μg,然后每4小时服用400μg阴道米索前列醇,在24小时内最多服用5剂。主要结局指标是完全流产方案的有效性,这是在最后一次给药后1周通过骨盆超声证实的。次要结局指标是比较两种方案中的诱导流产间隔(IAI),所需米索前列醇剂量和药物不良反应(ADR)。 P值<0.05被认为具有统计学意义。结果:A组平均年龄为25.68±3.79岁,B组为23.40±2.73岁。两种方案完全流产的成功率均为76%。但是,A组的IAI为5.9±4.47小时,而B组的IAI为9.6±5.07小时,具有统计学意义(p = 0.009)。两组之间米索前列醇的平均剂量也有统计学差异,分别为1000±200μg和1425±437.41μg(p = 0.01)。两组的妊娠年龄与IAI在13至17.6周之间相关(p = 0.01),而在超过17.6周的妊娠中两者之间无显着相关性(p = 0.63)。结论:米非司酮和米索前列醇同时给药显示出比间隔方案更好的效果,这是因为诱导流产间隔明显更短,所需米索前列醇的剂量更低,成功率相当。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号