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首页> 外文期刊>The journal of maternal-fetal & neonatal medicine >A novel protocol for postpartum magnesium sulphate in severe pre-eclampsia: a randomized controlled pilot trial
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A novel protocol for postpartum magnesium sulphate in severe pre-eclampsia: a randomized controlled pilot trial

机译:重度先兆子痫产后硫酸镁的新方案:随机对照试验

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Objective: Magnesium sulphate is the preferred anticonvulsant used to prevent the development of fits in severe pre-eclampsia; we aim to compare between three different protocols of postpartum magnesium sulphate in the effectiveness of preventing the development of fits in severe pre-eclampsia.Methods: Double-blind randomized controlled pilot trial, done in Cairo university hospital, Cairo, Egypt during 2013-2014, on 240 women with severe pre-eclampsia. Magnesium sulphate intravenous infusion was given in the postpartum period to all the patients, women were randomly allocated to group I (Single loading dose only), group II (12h abbreviated protocol) or group III (24h standard protocol) (n=80 in each group).Results: There were no significant difference between the three groups as regards the incidence of eclampsia, elevated liver enzymes and low platelets syndrome, maternal ICU admission and; however The incidence of flushing was significantly higher in group III than group II and I (24 [30%] versus 12 [15%] versus 4 [5%]; p<0.001) respectively.Conclusion: The pilot study demonstrates that the single-loading dose of postpartum magnesium sulphate is a promising alternative to the standard and the abbreviated protocol in preventing eclampsia; however, a large clinical trial is necessary to prove this.
机译:目的:硫酸镁是预防严重先兆子痫发作时首选的抗惊厥药。我们旨在比较三种不同的产后硫酸镁治疗方案在预防严重先兆子痫发作中的有效性。方法:双盲随机对照试验,于2013-2014年在埃及开罗的开罗大学医院进行,针对240名患有严重先兆子痫的女性。所有患者在产后均接受硫酸镁静脉输液,将妇女随机分配至I组(仅单剂量),II组(缩写为12h方案)或III组(24h标准方案)(每组n = 80)结果:在子痫的发生率,肝酶升高和低血小板综合征,孕产妇加护病房和三组之间,三组之间无显着差异。但是,第三组的潮红发生率显着高于第二组和第二组(分别为24 [30%]对12 [15%]对4 [5%]; p <0.001)。结论:初步研究表明负荷剂量的产后硫酸镁是该标准和缩写方案预防子痫的有希望的替代方法;但是,必须进行大规模的临床试验才能证明这一点。

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