Panda Subrat, Jha Vandana, Singh Santa
Department of Obstetrics and Gynecology, Neigrihms, India.
J Family Reprod Health. 2013 Dec;7(4):177-9.
To compare efficacy, safety and tolerance of combination of mifepristone and misoprostol versus misoprostol-only in induction of late intrauterine fetal death (IUFD).
This prospective study included a consecutive series of 52 women gravid up to fourth with IUFD after 28 weeks of gestation between January 2008 and June 2011. Women were divided into two groups. First group of women received a single oral dose of 200mg mifepristone, and after 24 hours, 100ug of intravaginal misoprostol was administered, followed by intravaginal 100µg misoprostol at four hourly intervals if required. Second group of women received 100 µg misoprostol at four hourly interval per vaginally (maximum 600µg in 24 hours). Oxytocin was given for augmentation if needed.
The induction-to-delivery time was shorter with the combination regimen (p < 0.001) group. The total dose of misoprostol needed was lower in the group pre-treated with mifepristone (p < 0.001). Oxytocin was required only in misoprostol group. The two groups did not differ as regards complications experienced during labor and delivery significantly.
Both regimens, misoprostol-only and the combination of mifepristone and misoprostol are safe in induction of labor after intrauterine fetal death (IUFD). Pre-treatment with mifepristone is more effective in terms of reducing of induction delivery interval, requirement of lesser dose of misoprostol and no need of augmentation with oxytocin.
比较米非司酮与米索前列醇联合用药和单纯使用米索前列醇引产治疗晚期胎儿宫内死亡(IUFD)的疗效、安全性及耐受性。
本前瞻性研究纳入了2008年1月至2011年6月期间连续收治的52例妊娠28周后发生胎儿宫内死亡的孕妇,孕周最大至孕晚期。将这些孕妇分为两组。第一组孕妇口服单次剂量200mg米非司酮,24小时后阴道给予100μg米索前列醇,必要时每4小时重复阴道给予100μg米索前列醇。第二组孕妇每4小时经阴道给予100μg米索前列醇(24小时最大剂量600μg)。必要时给予缩宫素加强宫缩。
联合用药组引产至分娩的时间较短(p<0.001)。米非司酮预处理组所需米索前列醇的总剂量较低(p<0.001)。仅米索前列醇组需要使用缩宫素。两组在分娩过程中经历的并发症方面无显著差异。
单纯使用米索前列醇以及米非司酮与米索前列醇联合用药这两种方案用于胎儿宫内死亡(IUFD)后的引产都是安全的。米非司酮预处理在缩短引产至分娩间隔、减少米索前列醇剂量需求以及无需使用缩宫素加强宫缩方面更有效。