Comparison of perinatal outcomes using oral misoprostol, vaginal misoprostol, and intracervical dinoprostone for induction of labor.

IF 0.5 Q4 OBSTETRICS & GYNECOLOGY
Petra Szekeresová, Lukáš Hruban, Anna Jouzová, Petr Janků, Romana Gerychová, Michal Huptych
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引用次数: 0

Abstract

Objective: To compare the effectiveness and safety of the methods of pharmacological induction of labor. To identify the advantages and disadvantages of oral and vaginal administration of misoprostol and intracervical administration of dinoprostone.

Materials and methods: Analysis of a group of women who gave birth at the Faculty Hospital Brno from 1st August 2019 to 31st January 2020, and one of the following labor induction schemes was used: group A: misoprostol 25 µg orally every 2 hours, group B: misoprostol 50 µg vaginally every 6 hours, group C: intracervical dinoprostone 1 mg every 2 hours. Inclusion criteria were: singleton pregnancy, completed 36th gestational week, live fetus, cephalic presentation, and cervix score ≥ 6. Exclusion criteria were uterine scars and fetal growth restriction. Time factors of induction, occurrence of acute hypoxia during labor, mode of delivery, use of tocolysis during labor, necessity of oxytocin infusion, use of epidural analgesia, blood loss, uterine rupture, umbilical artery pH, and Apgar score at the 5th min were evaluated.

Results: A total of 378 women were included (133 vs. 145 vs. 100). A statistically significantly higher success rate of vaginal delivery was demonstrated in group A compared to groups B and C (88 vs. 77.9 vs. 76%; P = 0.035). The longest time from the administration of the first dose of the preparation to delivery of the fetus was in group A (medians in minutes 700 vs. 565 vs. 375; P < 0.0001). There was no difference between the groups in the I. and II. labor stage duration. Cesarean delivery rate due to acute hypoxia was the lowest in group A (2.3 vs. 10.3 vs. 9%; P = 0.023). Uterine rupture was not recorded; there were no differences in neonatal outcome parameters.

Conclusion: The highest success rate of vaginal delivery was achieved with the use of low-dose oral misoprostol. The disadvantage of this method is a significant increase in the time from the start of induction to the delivery of the fetus. There was no difference in the occurrence of severe perinatal complications between the induction methods.

口服米索前列醇、阴道米索前列醇和宫颈内迪诺前列醇引产围产儿结局的比较
目的:比较几种药物引产方法的有效性和安全性。确定口服和阴道给药米索前列醇和宫颈内给药迪诺前列酮的优缺点。材料与方法:对2019年8月1日至2020年1月31日在布尔诺学院医院分娩的一组妇女进行分析,采用以下引产方案之一:a组:米索前列醇25µg / 2小时口服,B组:米索前列醇50µg / 6小时阴道,C组:迪诺前列醇1 mg / 2小时宫颈内。纳入标准为:单胎妊娠,孕满36周,活胎,头位表现,宫颈评分≥6。排除标准为子宫瘢痕和胎儿生长受限。评估引产时间因素、产程急性缺氧发生情况、分娩方式、产程使用缩胎剂、是否需要输注催产素、硬膜外镇痛、出血量、子宫破裂、第5 min脐带动脉pH、Apgar评分。结果:共纳入378名妇女(133对145对100)。A组阴道分娩成功率明显高于B组和C组(88比77.9比76%;P = 0.035)。A组从给药至分娩的时间最长(中位数为分钟700 vs. 565 vs. 375;P & lt;0.0001)。在i和II组之间没有差异。产程持续时间。急性缺氧剖宫产率A组最低(2.3 vs. 10.3 vs. 9%;P = 0.023)。子宫破裂未见记录;新生儿结局参数没有差异。结论:小剂量口服米索前列醇阴道分娩成功率最高。这种方法的缺点是从引产开始到胎儿娩出的时间明显增加。两种引产方式的严重围产儿并发症发生率无差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ceska Gynekologie-Czech Gynaecology
Ceska Gynekologie-Czech Gynaecology OBSTETRICS & GYNECOLOGY-
CiteScore
0.60
自引率
25.00%
发文量
57
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