首页> 外文期刊>International Journal of Reproduction, Contraception, Obstetrics and Gynecology >A randomized study to compare the efficacy and side effects of misoprostol given either orally or vaginally for first trimester medical termination of pregnancy
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A randomized study to compare the efficacy and side effects of misoprostol given either orally or vaginally for first trimester medical termination of pregnancy

机译:一项随机研究,比较口服或阴道给予米索前列醇对妊娠早期妊娠终止的功效和副作用

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Background: Medical abortion represents an alternative to first trimester aspiration abortion and has been used by millions of women throughout the world. A numerous study has demonstrated that combination of mifepristone and misporostol is highly efficacious with success rate of approximately 97%. Methods: In the present randomized study 100 women who were requesting for first trimester medical abortion were included in the study. This randomized study was conducted for a period of one year in a tertiary health care centre. All these women were randomly assigned to receive either oral misoprostol (n=52) (group 1) or vaginal misoprostol (n=48) (group 2). We found that after the administration of mifepristone, vaginal misoprostol for the induction of abortion upto 49 days was more effective than oral misoprostol. Results: In present study maximum number of patients were in the age group of 26-30 years. Multiparous women comprised of maximum number of patients in both 70% in group 1 and 83% in group 2. The gestational age at the time of inclusion in study was maximum upto 7 weeks or 49 days gestation in both groups. Acceptability of medical abortion is more in urban locality i.e. 73% in group 1 and 81% in group 2. 73% in group 1 and 79% in group 2 chose to have misoprostol at home. 92% patients in group 1 and 95% patients in group 2 initiated bleeding per vaginum within 4 hours. Side effects like nausea, vomiting and diarrhea were compared. 92.4% patients in group 1 and 97% patients in group 2 who had expulsion of conception without need of surgical intervention was comparable. Only 2 patients in group 1 had incomplete abortion and needed surgical aspiration. Conclusions: This study showed UA-S/D ratio and UA-RI2SD are significant predictors of perinatal deaths and immediate neonatal resuscitation in preeclampsia. Acute fetal distress in labour or neonatal nursery admission could not be predicted.
机译:背景:药物流产是孕早期人工流产的一种替代方法,已被全世界数百万妇女使用。大量研究表明,米非司酮和米泊甾醇的组合非常有效,成功率约为97%。方法:在本随机研究中,包括100名要求进行早孕药物流产的妇女。这项随机研究是在三级医疗中心进行的,为期一年。所有这些妇女被随机分配接受口服米索前列醇(n = 52)(第1组)或阴道米索前列醇(n = 48)(第2组)。我们发现,在服用米非司酮后,阴道米索前列醇诱导流产长达49天比口服米索前列醇更有效。结果:在本研究中,最大患者数在26-30岁之间。第1组的70%和第2组的83%的患者中,多胎女性最多。两组中纳入研究时的胎龄最大为妊娠7周或49天。药物流产的可接受性在城市地区较高,即第1组为73%,第2组为81%,第1组的73%和第2组的79%选择在家中接受米索前列醇。组1中的92%患者和组2中的95%患者在4小时内开始每个阴道出血。比较了恶心,呕吐和腹泻等副作用。在第1组中有92.4%的患者和在第2组中有97%的患者在无需手术干预的情况下被排除了妊娠。第一组中只有2例患者流产不完全,需要手术抽吸。结论:这项研究表明,UA-S / D比和UA-RI> 2SD是先兆子痫围产期死亡和新生儿立即复苏的重要预测指标。无法预测分娩或新生儿保育期中的急性胎儿窘迫。

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