Yin Chun-yan, Zhou Jing-zhen, Wang Bao-ping, Lü Xiao-yan
Department of Obstetrics, Second People's Hospital of Guangdong Province, Guangzhou 510317, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2006 Feb;26(2):182-4, 188.
To evaluate the effect and risk of misoprostol for stimulating cervical maturity in women with post-term pregnancy negative for insulin-like growth factor binding protein-1 (IGFBP-1) in cervical secretion with modified Bishop score less than 3.
Seventy-one women with post-term pregnancy randomized into misoprostol group (n=37) and control group (n=34) received misoprostol placement at the posterior vaginal fornix and routine intravenous oxytocin infusion, respectively, to stimulate cervical maturity. Failure to respond to the treatment within the initial 24 h necessitated a repeated administration for no more than 3 times in all. Modified Bishop score was recorded and fetal heart monitored once every 24 h, and IGFBP-1 in the cervical secretion was detected at 24 and 48 h after drug administration.
The misoprostol group showed better effect of cervical maturity stimulation than the control group (P<0.001), and the positivity rates of IGFBP-1 24 and 48 h after drug administration were significantly higher than that of the control group (P<0.01 and 0.001). The number of cases with indication for cesarean section was significant higher in the control group (P<0.001). There were no significant differences in postpartum hemorrhage, excessive uterine contraction, incidence of fecal contamination of the amniotic fluid or Apgar score of the newborn between the two groups (P>0.05).
Misoprostol is safe and effective for stimulating cervical maturity in women with post-term pregnancy who have modified Bishop score lower than 3 and are negative for IGPBF-1 in cervical secretion. Oxytocin is not advised for use in such gravida for stimulating cervical maturity. IGFBP-1 in cervical secretion may serve as an important index for evaluating the cervical maturity.
评估米索前列醇对孕周过期、宫颈分泌物中胰岛素样生长因子结合蛋白-1(IGFBP-1)阴性且改良Bishop评分小于3的女性促宫颈成熟的效果及风险。
71例孕周过期的女性被随机分为米索前列醇组(n=37)和对照组(n=34),分别接受阴道后穹窿放置米索前列醇和常规静脉滴注缩宫素以促宫颈成熟。若在最初24小时内治疗无反应,则最多重复给药3次。记录改良Bishop评分,每24小时监测1次胎心,并在给药后24小时和48小时检测宫颈分泌物中的IGFBP-1。
米索前列醇组促宫颈成熟的效果优于对照组(P<0.001),给药后24小时和48小时IGFBP-1的阳性率显著高于对照组(P<0.01和0.001)。对照组剖宫产指征的病例数显著更高(P<0.001)。两组间产后出血、子宫收缩过强、羊水粪染发生率或新生儿Apgar评分无显著差异(P>0.05)。
米索前列醇对孕周过期、改良Bishop评分低于3且宫颈分泌物中IGPBF-1阴性的女性促宫颈成熟安全有效。不建议此类孕妇使用缩宫素促宫颈成熟。宫颈分泌物中的IGFBP-1可作为评估宫颈成熟的重要指标。