Grignaffini A, Soncini E, Anfuso S, Ronzoni E
Dipartimento di Scienze Ginecologiche, Ostetriche e di Neonatologia, Università degli Studi di Parma, Parma.
Minerva Ginecol. 2004 Oct;56(5):413-8.
The purpose of the present study is to compare the effectiveness and safety of a slow release vaginal PGE2 insert (Propess) with intracervical PGE2 gel (Prepidil gel) in the induction of cervical ripening and labour.
For the induction of labour we selected 103 single pregnancies at term presenting a Bishop score of less than 5. Fifty-one were induced with Propess, and 52 with intracervical Prepidil.
The 2 groups were homogeneous as regards indications to induction and obstetric characteristics. The success of induction (achievement of uncomplicated vaginal delivery) was comparable in the 2 groups: Propess 67%, Prepidil 65%. The times needed to induce labour were on average longer with Propess (16 h 59 min) than with Prepidil (12 h 54 min), (p<0.05); nevertheless the time needed to achieve delivery by the vaginal route within 24 hours was comparable (49% vs 48%). The number of patients requiring more than one application of prostaglandin was less in the Propess group (5.9%) than in the Prepidil group (55.8%) (p<0.001). The times relative to dilation and expulsion did not differ significantly. Resort to cesarean section for fetal indication (cardiotocographic changes) was greater in inductions with Prepidil (8 cases) compared to Propess (2 cases), p<0.05.
The systems proved equally effective, nevertheless Propess seems to be safer thanks to the lower incidence of cardiotocographic changes such as to indicate urgent cesarean section. Propess would seem to be more acceptable on the part of patients thanks to the smaller number of applications necessary.
本研究旨在比较缓释阴道用前列地尔栓(普贝生)与宫颈内用前列地尔凝胶(普米克凝胶)在促宫颈成熟及引产方面的有效性和安全性。
对于引产,我们选择了103例足月单胎妊娠且 Bishop 评分小于5分的孕妇。51例使用普贝生引产,52例使用宫颈内普米克引产。
两组在引产指征和产科特征方面具有同质性。两组引产成功率(实现无并发症阴道分娩)相当:普贝生组为67%,普米克组为65%。普贝生引产所需时间平均(16小时59分钟)比普米克(12小时54分钟)长(p<0.05);然而,24小时内经阴道分娩所需时间相当(49%对48%)。普贝生组需要多次应用前列腺素的患者数量(5.9%)少于普米克组(55.8%)(p<0.001)。与扩张和娩出相关的时间无显著差异。因胎儿指征(胎心监护变化)而行剖宫产的比例,普米克引产组(8例)高于普贝生组(2例),p<0.05。
两种方法同样有效,但普贝生似乎更安全,因为胎心监护变化发生率较低,无需紧急剖宫产。由于所需应用次数较少,普贝生似乎更易被患者接受。