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[普贝生用于足月妊娠引产的临床评估]

[Clinical evaluation of propess for induction of term pregnancy].

作者信息

Gai Ming-ying, Zhang Jian-ping, Li Yang, Han Hong-jing, Yang Jian-qiu, Wang Shan-mi, Su Qi-feng, Wu Lian-fang

机构信息

Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, China.

出版信息

Zhonghua Fu Chan Ke Za Zhi. 2003 Apr;38(4):210-2.

PMID:12885366
Abstract

OBJECTIVE

To explore the efficacy and safety of continuously released prostaglandin E(2) (PGE(2)) suppository-propess used for induction of term pregnancy.

METHODS

A multicenter, prospective, case control clinical study was carried out, propess was used in 100 cases as study group, the suppository without PGE(2) was used in 49 cases as control group. The cervical maturity (by Bishop scoring), the time to labor starting, membrane rupture and delivery, the application of oxytocin, ceserean section rate, fetal and neonatal condition were compared between 2 groups after inserting of the suppository. At the same time, side effects caused by propess were investigated.

RESULTS

Bishop score was increased >or= 2 points in 93% cases, >or= 3 points in 87% cases in study group, whereas only 4% cases whose Bishop score increased >or= 2 points in control group. The time to labor starting, membrane rupture, and delivery was shortened obviously in study group than that in control group after inserting suppository. The application of oxytocin was much less in study group, cesarean section rate was reduced in study group (32% vs 61%). There was no significant difference between 2 groups in fetal and neonatal conditions. The overstimulation of uterine contraction and mild gastrointestinal tract reaction occurred in 3 cases and 2 cases respectively in study groups.

CONCLUSION

Propess can be used for induction of term pregnancy effectively and safely.

摘要

目的

探讨持续释放前列腺素E₂(PGE₂)栓剂—普贝生用于足月妊娠引产的有效性和安全性。

方法

进行一项多中心、前瞻性、病例对照临床研究,100例使用普贝生作为研究组,49例使用不含PGE₂的栓剂作为对照组。比较两组在放置栓剂后宫颈成熟度(采用Bishop评分)、开始宫缩时间、胎膜破裂及分娩时间、缩宫素应用情况、剖宫产率、胎儿及新生儿情况。同时,调查普贝生引起的副作用。

结果

研究组93%的病例Bishop评分增加≥2分,87%的病例增加≥3分,而对照组仅有4%的病例Bishop评分增加≥2分。放置栓剂后,研究组开始宫缩、胎膜破裂及分娩时间明显短于对照组。研究组缩宫素应用少得多,研究组剖宫产率降低(32%对61%)。两组胎儿及新生儿情况无显著差异。研究组分别有3例和2例发生子宫收缩过强和轻度胃肠道反应。

结论

普贝生可有效、安全地用于足月妊娠引产。

相似文献

1
[Clinical evaluation of propess for induction of term pregnancy].[普贝生用于足月妊娠引产的临床评估]
Zhonghua Fu Chan Ke Za Zhi. 2003 Apr;38(4):210-2.
2
[Study of the effect of Propess for ripening of the unfavorable cervix for the induction of labor due to medical indications].[普贝生用于因医学指征引产时宫颈条件不佳促成熟效果的研究]
Akush Ginekol (Sofiia). 2003;42(3):5-8.
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[Dinoprostone: slow release vaginal insert (Propess) and intracervical gel (Prepidil) for the induction of labour with unriped cervix].地诺前列酮:用于未成熟宫颈引产的缓释阴道栓剂(普贝生)和宫颈内凝胶(普贝生)
Minerva Ginecol. 2004 Oct;56(5):413-8.
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Zhonghua Fu Chan Ke Za Zhi. 2010 Jul;45(7):492-6.
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Gynecol Obstet Fertil. 2006 Jun;34(6):489-92. doi: 10.1016/j.gyobfe.2006.02.020. Epub 2006 May 19.
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Comparative efficacy and safety of vaginal misoprostol versus dinoprostone vaginal insert in labor induction at term: a randomized trial.足月引产时阴道用米索前列醇与地诺前列酮阴道栓剂的疗效及安全性比较:一项随机试验
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A randomized trial of prostaglandin E2 gel and extra-amniotic saline infusion with high dose oxytocin for cervical ripening.一项关于前列腺素E2凝胶联合羊膜外高剂量缩宫素盐水输注用于宫颈成熟的随机试验。
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[Dose study of methyl carboprost suppository for planned delivery at term].卡前列甲酯栓足月计划分娩的剂量研究
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[Pharmacological induction of labour: benefits and risks].[药物引产:益处与风险]
Minerva Ginecol. 2007 Aug;59(4):347-55.

引用本文的文献

1
Clinical parameters for prediction of successful labor induction after application of intravaginal dinoprostone in nulliparous Chinese women.经阴道应用地诺前列酮后预测中国初产妇引产成功的临床参数。
Med Sci Monit. 2012 Aug;18(8):CR518-522. doi: 10.12659/msm.883273.