Amon E, Fossick K, Sibai B
Department of Obstetrics and Gynecology, St. Louis University School of Medicine, Missouri 63117, USA.
J Matern Fetal Med. 1999 Jan-Feb;8(1):8-11. doi: 10.1002/(SICI)1520-6661(199901/02)8:1<8::AID-MFM2>3.0.CO;2-0.
The purpose of this study was to evaluate the effects of exogenous administration of PGE2 upon the components of the biophysical profile.
The study group included 17 nulliparas at > or = 38 weeks gestation, with a Bishop score of < or = 4, requiring induction of labor. A controlled release vaginal pessary containing 10 mg of PGE2, designed to release hormones at approximately 0.8 mg per hour in vitro, was used for 12 hours of cervical ripening. The BPP was performed by the same sonographer at three intervals: prior to pessary insertion, at 6 hours, and 12 hours.
None of these patients had membrane rupture or went into spontaneous labor during the ripening process. All patients subsequently required amniotomy and oxytocin. The proportion of patients scoring 2 points for fetal breathing movements decreased from 59% at baseline to 0% at 12 hours, P < 0.0005, and the proportion of patients with fetal body movements decreased from 100% at baseline to 25% at 12 hours, P < 0.0005. However, the other components of the biophysical profile were not affected. The mean maternal plasma PGE2 metabolite concentrations were 235 pg/ml, 475 pg/ml, and 466 pg/ml at 0, 6 and 12 hours, respectively, P < 0.005.
In term patients, vaginal administration of the PGE2 pessary was associated with improved Bishop score over 12 hours and significant increases in maternal plasma PGEM levels at 6 hours and 12 hours. These changes were inversely related to fetal breathing and body movements.
本研究旨在评估外源性给予前列腺素E2(PGE2)对生物物理评分各组成部分的影响。
研究组包括17名孕龄≥38周的初产妇,Bishop评分≤4分,需要引产。使用一种含10mg PGE2的控释阴道栓剂,其在体外约每小时释放0.8mg激素,用于宫颈成熟12小时。由同一位超声检查医师在三个时间点进行生物物理评分:放置栓剂前、6小时和12小时。
在成熟过程中,这些患者均未发生胎膜破裂或自然临产。所有患者随后均需要行人工破膜及使用缩宫素。胎儿呼吸运动评分为2分的患者比例从基线时的59%降至12小时时的0%,P<0.0005;胎儿躯体运动的患者比例从基线时的100%降至12小时时的25%,P<0.0005。然而,生物物理评分的其他组成部分未受影响。母体血浆PGE2代谢物浓度在0小时、6小时和12小时时分别为235pg/ml、475pg/ml和466pg/ml,P<0.005。
对于足月患者,阴道给予PGE2栓剂在12小时内可改善Bishop评分,且在6小时和12小时时母体血浆前列腺素E代谢物(PGEM)水平显著升高。这些变化与胎儿呼吸和躯体运动呈负相关。