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足月引产中口服米索前列醇片与阴道用前列腺素E2栓的比较。

A comparison of oral misoprostol tablets and vaginal prostaglandin E2 pessary in induction of labour at term.

作者信息

Hassan Anjum Ara

机构信息

Department of Obstetrics and Gynaecology, Hamdard University Hospital, Karachi.

出版信息

J Coll Physicians Surg Pak. 2005 May;15(5):284-7.

Abstract

OBJECTIVE

To compare the cost-effectiveness, mode of delivery, fetal and maternal outcome of oral Misoprostol and vaginal prostaglandin E2 pessary in induction of labour at term.

DESIGN

Randomized clinical trial.

PLACE AND DURATION OF STUDY

Hamdard University Hospital, Imam Clinic and General Hospital from February 2002 to January 2003.

PATIENTS AND METHODS

The trial was conducted over two groups of patient for labour induction such that Group A received 50 microg oral Misoprostol 4 hourly to a maximum of four doses. Group B received prostaglandin E2 vaginal pessary at 6 hourly intervals upto two doses. Labour induction, number of doses, need of augmentation, induction to delivery time interval, mode of delivery and neonatal outcome were the main outcomes. Test of proportions was used to compare the significance between both managements.

RESULTS

Out of a total of 214 women, 106 received oral Misoprostol and 108 received PGE2 vaginal pessary. Ninety-three percent women in misoprostol group were successfully induced compared with 91% in PGE2 group. A significant response of labour induction with the minimal dose (58%, p = 0.001) and earlier induction to vaginal delivery (74%, p = 0.01) was observed in Misoprostol group. Rate of operative delivery was also less (16%, p = 0.16) compared with PGE2 group (25%).

CONCLUSION

Oral Misoprostol administration was more efficient and cost-effective than PGE2 vaginal pessary for induction of labour due to earlier response with minimal dose and less number of operative deliveries.

摘要

目的

比较口服米索前列醇与阴道用前列腺素E2栓在足月引产时的成本效益、分娩方式、胎儿及母亲结局。

设计

随机临床试验。

研究地点及时间

2002年2月至2003年1月在哈姆达德大学医院、伊玛目诊所和综合医院。

患者及方法

该试验在两组引产患者中进行,A组每4小时口服50微克米索前列醇,最多4剂。B组每6小时阴道放置一次前列腺素E2栓,最多2剂。引产、用药剂量、加强宫缩的需求、引产至分娩的时间间隔、分娩方式及新生儿结局为主要观察指标。采用比例检验比较两种治疗方法的差异。

结果

214名女性中,106名接受口服米索前列醇,108名接受阴道用前列腺素E2栓。米索前列醇组93%的女性成功引产,前列腺素E2组为91%。米索前列醇组在最小剂量时引产反应显著(58%,p = 0.001),且引产至阴道分娩时间更早(74%,p = 0.01)。与前列腺素E2组(25%)相比,米索前列醇组的手术分娩率也较低(16%,p = 0.16)。

结论

口服米索前列醇在引产方面比阴道用前列腺素E2栓更有效且成本效益更高,因其起效早、剂量小且手术分娩次数少。

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