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低剂量阴道米索前列醇用于引产是否比地诺前列酮凝胶更有效:一项随机对照试验

Is low dose vaginal misoprostol better than dinoprostone gel for induction of labor: a randomized controlled trial.

作者信息

Madaan Monika, Agrawal Swati, Puri Manju, Nigam Aruna, Kaur Harvinder, Trivedi Shubha Sagar

机构信息

Ex Assistant Professor, Department of Obstetrics and Gynecology, LHMC & SSKH (Lady Hardinge Medical College and Smt Sucheta Kriplani Hospital) , New Delhi, India .

Assistant Professor, Department of Obstetrics and Gynecology, LHMC & SSKH , New Delhi, India .

出版信息

J Clin Diagn Res. 2014 Sep;8(9):OC31-4. doi: 10.7860/JCDR/2014/8101.4906. Epub 2014 Sep 20.

Abstract

OBJECTIVE

To compare the efficacy and safety profile of low dose vaginal misoprostol with dinoprostone gel for induction of labor in term pregnancies.

METHODS

The study was conducted at Lady Hardinge Medical College and Smt Sucheta Kriplani Hospital on 100 pregnant women with term pregnancy after application of inclusion and exclusion criteria. The women were randomized in 2 groups of 50 women each. Group I received misoprostol 25μg at every six hour vaginally for a maximum of five doses for induction of labor; while group II received dinoprostone gel 0.5 mg every six hourly for a maximum of three doses. Maternal outcomes such as mode of delivery and induction delivery interval; and fetal outcomes such as APGAR score and incidence of NICU admission were assessed in both the groups. Statistical analysis was done using student t-test and chi-square test.

RESULTS

There was no significant difference in the mean induction to delivery interval in both the groups (14.32±0.13 hours in Group I and 14.92±0.18 hours in Group II, p=0.75), mode of delivery, indication of cesarean section and perinatal outcome. However, significant difference was observed in requirement of oxytocin augmentation in both the groups (32% in Group I and 68% in Group II, p=0.005).

CONCLUSION

Vaginal misoprostol in low doses is similar in efficacy and safety to dinoprostone gel for cervical ripening and labor induction in term pregnancy.

摘要

目的

比较低剂量阴道米索前列醇与地诺前列酮凝胶用于足月妊娠引产的疗效和安全性。

方法

在哈丁夫人医学院和苏切塔·克里普拉尼夫人医院对100名符合纳入和排除标准的足月妊娠孕妇进行了研究。将这些妇女随机分为两组,每组50名。第一组每6小时阴道给予25μg米索前列醇,最多5剂用于引产;而第二组每6小时给予0.5mg地诺前列酮凝胶,最多3剂。评估两组的产妇结局,如分娩方式和引产至分娩间隔;以及胎儿结局,如阿氏评分和新生儿重症监护病房(NICU)入住率。使用学生t检验和卡方检验进行统计分析。

结果

两组的平均引产至分娩间隔(第一组为14.32±0.13小时,第二组为14.92±0.18小时,p = 0.75)、分娩方式、剖宫产指征和围产期结局均无显著差异。然而,两组在催产素增强需求方面存在显著差异(第一组为32%,第二组为68%,p = 0.005)。

结论

低剂量阴道米索前列醇在足月妊娠宫颈成熟和引产方面的疗效和安全性与地诺前列酮凝胶相似。

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