首页> 外文期刊>British Journal of Obstetrics and Gynaecology >Misoprostol compared with methylergometrine for the prevention of postpartum haemorrhage: a double-blind randomised trial.
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Misoprostol compared with methylergometrine for the prevention of postpartum haemorrhage: a double-blind randomised trial.

机译:米索前列醇与甲基麦角新碱相比可预防产后出血:一项双盲随机试验。

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OBJECTIVE: To compare the efficacy and side effects of misoprostol, compared with methylergometrine, for the prevention of postpartum haemorrhage. DESIGN: A double-blind, randomised clinical trial of 200 women with apparently normal pregnancies. SETTING: University teaching hospital. PARTICIPANTS: Two hundred women with apparently normal pregnancies. METHODS: After the baby had been born, all women received two capsules by mouth and the contents of an ampule by intravenous injection. Each woman only received one active product. The capsules contained either a total of 600 microg misoprostol or placebo, and the ampule 200 microg of methylergometrine or placebo. MAIN OUTCOME MEASURES: Need for further oxytocic drugs, blood pressure, the presence of side effects, mean haemoglobin and haematocrit three days after delivery. RESULTS: Two hundred women completed the study (100 received methylergometrine and 100 misoprostol). Postpartum haemorrhage occurred in 4.3% of the methylergometrine group and 8.3% of the misoprostol group (P = 0.57). The need for further oxytocic drugs was 4.4% and 12.8% after methylergometrine and misoprostol, respectively (P = 0.065). One hour after the birth of the baby there was no difference in the mean systolic blood pressure (117 +/- 12 mmHg versus 115 +/- 11 mmHg) (P = 0.26) or the mean diastolic blood pressure (72 +/- 10 mmHg versus 71 +/- 11 mmHg for the groups receiving methylergometrine or misoprostol, respectively) (P = 0.97). The mean temperature in the misoprostol group rose to 37.4 degrees C, compared with 37 degrees C in the methylergometrine group (P < 0.0001). In the misoprostol group 34% developed fever (> 38 degrees C) compared with 3% in the methylergometrine group (P < 0.0001). Shivering (visual analogue score > or = 8) also occurred more often after misoprostol (42%) than after methylergometrine (8.5%) (P < 0.0001). The haemoglobin level (g/dL) on the third postpartum day was similar for both groups ( 11.0 and 11.2 for methylergometrine and misoprostol, respectively) (P = 0.39). CONCLUSIONS: This study suggests that although protection from postpartum haemorrhage using parenteral methylergometrine and oral misoprostol is nearly equal, misoprostol is associated with more side effects.
机译:目的:比较米索前列醇和甲基麦角新碱预防产后出血的疗效和副作用。设计:一项双盲,随机临床试验,对200名怀孕正常的妇女进行了研究。地点:大学教学医院。参加者:200名怀孕正常的妇女。方法:婴儿出生后,所有妇女均口服两粒胶囊,并通过静脉注射安瓿瓶中的内容物。每个女人只收到一个有效产品。胶囊包含总共600微克的米索前列醇或安慰剂,以及安瓿200微克的甲基麦角新碱或安慰剂。主要观察指标:分娩后三天需要进一步催产药物,血压,出现副作用,平均血红蛋白和血细胞比容。结果:200名妇女完成了研究(100名接受了麦角麦角新碱和100名米索前列醇)。甲基麦角新碱组和米索前列醇组的产后出血发生率分别为4.3%和8.3%(P = 0.57)。甲基麦角新碱和米索前列醇后对其他催产药物的需求分别为4.4%和12.8%(P = 0.065)。婴儿出生后一小时,平均收缩压(117 +/- 12 mmHg对115 +/- 11 mmHg)(P = 0.26)或平均舒张压(72 +/- 10)没有差异mmHg与接受甲基麦角新碱或米索前列醇的组分别为71 +/- 11 mmHg(P = 0.97)。米索前列醇组的平均温度升至37.4摄氏度,而甲基麦角新烯酮组的平均气温为37摄氏度(P <0.0001)。米索前列醇组有34%的人发烧(> 38摄氏度),而甲基麦角新碱组只有3%的人发烧(P <0.0001)。米索前列醇(42%)后发生颤抖(视觉模拟评分>或= 8)的发生率也比甲基麦角新碱(8.5%)后发生的颤抖发生的频率更高(P <0.0001)。两组产后第三天的血红蛋白水平(g / dL)相似(甲基麦角新碱和米索前列醇分别为11.0和11.2)(P = 0.39)。结论:这项研究表明,尽管使用肠胃外甲基麦角新碱和口服米索前列醇对产后出血的保护作用几乎相等,但米索前列醇的副作用更大。

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