在印度北方邦东部的一家三级医疗中心进行的一项关于固定剂量与滴定剂量的米索前列醇口服溶液用于足月妊娠引产的比较干预研究

Amrita Saxena, Swati Kumari, V. Aditya, Najma Malik, H. Tiwari
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引用次数: 0

摘要

引产是指在自然分娩开始前,无论羊膜是否破裂,故意启动子宫收缩。改良毕晓普评分为 6 分或更高,表示宫颈成熟或 "有利"--此时自然分娩的可能性很高,或对旨在引产的干预措施有反应。米索前列醇成本低廉、易于获得且在室温下稳定,如果胎儿和产妇的安全问题有证据证明,它将成为一种很有前途的引产药物。我们的研究旨在比较滴定剂量与固定剂量米索前列醇口服溶液作为引产药物的疗效,以及对胎儿和产妇结局的影响。总样本量为 150 人,每组 75 人。固定剂量组(F 组)的引产成功率(80%)高于滴定剂量组(T 组)的 65.53%,差异有统计学意义(P=0.0439)。F 组(30.67%)的增量需求低于 T 组(56%)。从统计学角度看,这一差异具有显著性(P=0.0017)。子宫过度刺激和无张力产后出血在 T 组较多,但差异不显著(p = 0.1461;p = 0.3108)。与 F 组[16(21.33%)]相比,T 组[34(45.34%)]需要进行新生儿复苏。从统计学角度看,这一差异显著[P=0.0081]。本研究得出结论,固定剂量和滴定剂量的米索前列醇口服溶液方案都能有效引产,但固定剂量方案的优势在于米索前列醇的平均总剂量较少、引产到分娩的间隔时间缩短、子宫过度刺激较少、无张力产后出血以及更好的胎儿-产妇和新生儿安全性。
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A comparative interventional study on fixed-dose versus titrated- dose oral misoprostol solution for induction of labour at term gestation in a tertiary care centre of Eastern Uttar Pradesh
Induction of labor entails the deliberate initiation of uterine contractions before the spontaneous onset of labor, irrespective of whether the amniotic membranes have ruptured or not. The Modified Bishop’s score of six or higher indicates that the cervix is ripe, or “favorable” – when there is a high likelihood of spontaneous labor or responsiveness to interventions designed to induce labor. Misoprostol being cost-effective, easily available and stable at room temperature makes itself a promising agent in future for induction of labour if the feto-maternal safety concerns are proved with evidence. The aim of our study was to compare the efficacy of titrated versus fixed dose oral misoprostol solution regimen as inducing agents and the effects on fetomaternal outcome.A comparative interventional study was conducted for one year and study population consisted of term pregnant women admitted to the labour room of the hospital. A total sample size of 150 was deemed necessary, with 75 participants required per group. Following allocation into groups, induction of labor was carried out using either oral titrated-dose misoprostol solution or fixeddose misoprostol solution.Successful induction of labour was higher in fixed -dose group (Group F) (80%) as compared to 65.53% in titrated-dose group (Group T), the difference was statistically significant (p=0.0439). The need for augmentation was lower in group F (30.67%) than in group T (56%). Statistically, this difference was significant (p = 0.0017). Uterine hyper stimulation and atonic post-partum haemorrhage were noted more in group T but this difference was not significant (p = 0.1461; p = 0.3108). Requirement of newborn resuscitation was observed higher in group T [34 (45.34%)] than group F [16(21.33%)]. Statistically, this difference was significant [p=0.0081]. NICU admissions were more in group T (21.34%) than group F (13.33%), but difference was not significant (p = 0.0574).This study concludes that both fixed- dose and titrated-dose oral misoprostol solution regimens are effective in induction of labour but fixed-dose regimen has an advantage of less mean total dose of misoprostol administered, reduced induction to delivery interval, less uterine hyperstimulation, atonic postpartum hemorrhage and better fetomaternal and neonatal safety profile.
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