Use of Intravenous Dexamethasone for Cervical Ripening and Labor Induction in Term Pregnancies with Pre-labour Rupture of Membranes: Randomized control trial

S. Safwat
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Abstract

Abstract Background: During the first 36 to 38 weeks of normal gestation, the myometrium is in a preparatory yet unresponsive state. Concurrently, the cervix begins an early stage of remodeling yet maintains structural integrity. Induction of labour is a complex process involving cervical ripening which undergo extensive remodeling and dynamic changes controlled by hormonal, inflammatory changes, and other biological processes. Aim of the Work: to assess the effect of intravenous administration of dexamethasone on the induction delivery interval in term patients with prelabour rupture of membranes undergoing induction of labor. Patients and Methods: This randomized control trial was conducted at department of Obstetrics and Gynecology at Ain Shams University Maternity Hospital (ASUMH) in the period between August 2020 and January 2021. Participants of this study were 80 full term pregnant women with pre-labor rupture of membranes attended the labor ward in El Demerdash Maternity Hospital and scheduled for induction of labor by 8 mg dexamethasone IV before starting induction by PGE1, after 4 hours oxytocin was added by 1 IU/hr with the dose increasing by 1 IU every 30 minutes till optimal contractions were reached which were three uterine contractions in 10 minutes and each lasting for 40-50 seconds. Results: Fetal distress, arrest of delivery and indications of CS delivery were non-significantly less frequent among Dexamethasone group. Induction-active phase and active phase durations were significantly shorter among dexamethasone group than among control group. Second and third stages durations were non-significantly shorter among dexamethasone group than among control group. Total induction-delivery duration was significantly shorter and rate of vaginal delivery was significantly higher among dexamethasone group than among control group. Postpartum hemorrhage (PPH), postpartum endometritis, chorioamnionitis were not reported among the studied groups. No significant difference between Dexamaethasone and Control groups regarding neonatal condition Conclusion: Intravenous administration of dexamethasone in addition to labor induction protocol shortened the induction - active phase and active phase durations. It shortened the total induction-delivery duration and increased the rate of successful vaginal delivery. It has no effect on second and third stages durations with no increase in incidence of intrapartum, postpartum nor neonatal complications.
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静脉注射地塞米松用于足月妊娠合并胎膜破裂的宫颈成熟和引产:随机对照试验
摘要背景:在正常妊娠的前36至38周,子宫肌层处于准备状态,但没有反应。与此同时,子宫颈开始了早期的重塑,但仍保持着结构的完整性。引产是一个复杂的过程,涉及宫颈成熟,经历广泛的重塑和受激素、炎症变化和其他生物过程控制的动态变化。本工作的目的:评估静脉注射地塞米松对足月产前膜破裂引产患者引产间隔的影响。患者和方法:这项随机对照试验于2020年8月至2021年1月在艾因沙姆斯大学妇产医院妇产科进行。本研究的参与者是80名产前胎膜破裂的足月孕妇,她们在El Demerdash妇产医院的产房接受了8 mg地塞米松IV的引产,4小时后以1IU/hr的剂量加入催产素,剂量每30分钟增加1IU,直到达到最佳宫缩,即10分钟内三次宫缩,每次持续40-50秒。结果:地塞米松组的胎儿窘迫、分娩停止和CS分娩指征的发生率没有显著降低。地塞米松组诱导活动期和活动期持续时间明显短于对照组。地塞米松组的第二阶段和第三阶段持续时间与对照组相比无显著性缩短。地塞米松组的总诱导分娩时间明显短于对照组,阴道分娩率明显高于对照组。研究组中未报告产后出血(PPH)、产后子宫内膜炎、绒毛膜羊膜炎。地塞米松组和对照组在新生儿状况方面没有显著差异。结论:除引产方案外,静脉注射地塞米松缩短了引产活动期和活动期的持续时间。它缩短了诱导分娩的总持续时间,并提高了阴道分娩的成功率。它对第二和第三阶段的持续时间没有影响,产时、产后和新生儿并发症的发生率没有增加。
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