口服米索前列醇与阴道米索前列醇用于足月引产的比较,在Zaria的Ahmadu Bello大学教学医院

S. Hauwa, S. Shittu, H. Umar-Sulayman, B. Audu
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引用次数: 3

摘要

背景:通过口服和阴道途径对相同、相等和低剂量的米索前列醇进行足月引产的比较需要进一步阐明。目的:比较25微克口服米索前列醇和25微克阴道米索前列用于足月引产的疗效和安全性。方法:一项随机对照试验,涉及169名同意引产的女性。共有85名妇女口服米索前列醇,84名妇女阴道服用米索前列。口服米索前列醇剂量(25μg)每2小时重复一次,而阴道剂量(25µg)每6小时重复一一次,最长持续时间为24小时或需要干预时。使用SPSS版本20对数据进行分析。结果:与阴道组相比,口服组的平均引产间隔显著缩短(18.48+/-2.01 vs.22.82+/-2.50,P=0.00),阴道分娩次数分别增加(88.2%vs.85.7%,P=0.000)。阴道组的心分娩异常明显高于口服组(8.3%对1.2%,P=0.03)。阴道组的胎儿窘迫和胎粪染色液较多,但无统计学意义。
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A comparison of oral versus vaginal misoprostol for induction of labor at term, at the Ahmadu Bello University Teaching Hospital, Zaria
Background: The comparison of same,equal and low dose of misoprostol by the oral and vaginal routes for induction of labour at term requires further elucidation. Objective: To compare the efficacy and safety of 25 micrograms (ug) of oral misoprostol with 25ug vaginal misoprostol for induction of labor at term. Methods: A randomised control trial that involved 169 consented women with indication for induction of labor. A total of 85 women had oral misoprostol while 84 women had vaginal misoprostol. The oral misoprostol dose (25ug) was repeated every 2 hours, while the vaginal dose (25ug) was repeated every 6 hours for a maximum duration of 24 hours or when need arose for intervention. Data was analysed using SPSS version 20. Results: The mean induction-delivery interval was significantly shorter (18.48 +/- 2.01 vs. 22.82 +/- 2.50, P = 0.00), with more vaginal deliveries (88.2% vs. 85.7%, P = 0.00) in the oral group compared to the vaginal group respectively. The cardiotocographic abnormalities in the vaginal group were significantly higher than the oral group (8.3% vs. 1.2%, P = 0.03). There were more foetal distress and meconium stained liquor in the vaginal group but not statistically significant.
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