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不明原因复发性流产女性受孕前孕酮治疗:一项随机双盲安慰剂对照试验

Peri-conceptional progesterone treatment in women with unexplained recurrent miscarriage: a randomized double-blind placebo-controlled trial.

作者信息

Ismail Alaa M, Abbas Ahmed M, Ali Mohammed K, Amin Ahmed F

机构信息

a Department of Obstetrics and Gynecology , Women's Health Hospital, Assiut University , Assiut , Egypt.

出版信息

J Matern Fetal Neonatal Med. 2018 Feb;31(3):388-394. doi: 10.1080/14767058.2017.1286315. Epub 2017 Feb 15.

DOI:10.1080/14767058.2017.1286315
PMID:28114846
Abstract

OBJECTIVE

The current study aims to evaluate the effect of peri-conceptional progesterone started early in the luteal phase before confirmation of pregnancy in preventing miscarriage in women with history of unexplained recurrent miscarriage (RM).

MATERIALS AND METHODS

The current study was a randomized double-blind controlled trial (NCT01608347) conducted at Assiut Women's Health Hospital from 2012 through 2015 included patients of unexplained RM. Participants were randomly assigned to receive either 400 mg progesterone pessaries or placebo twice daily, started in the luteal phase and continued after a positive pregnancy test till 28 weeks of gestation. The main study outcome was the miscarriage rate.

RESULTS

Seven hundred women were enrolled (n = 350 in each group). The miscarriage rate was significantly lower in progesterone group (12.4 versus 23.3% in the placebo group, p = 0.001). There was significant improvement in rate of pregnancy continuation beyond 20 weeks as well as the live birth rate in the progesterone group in comparison to placebo group (87.6 versus 76.7% and 91.6 versus 77.4%, respectively, p < 0.05).

CONCLUSIONS

Progesterone is more effective than placebo in reducing the risk of miscarriage if administered in the luteal phase of the cycle, before confirmation of pregnancy in women with history of unexplained RM.

摘要

目的

本研究旨在评估在黄体期早期、妊娠确认前开始使用的围受孕孕酮对有不明原因复发性流产(RM)病史的女性预防流产的效果。

材料与方法

本研究是一项随机双盲对照试验(NCT01608347),于2012年至2015年在阿斯尤特妇女健康医院进行,纳入有不明原因RM的患者。参与者被随机分配,每天两次接受400毫克孕酮阴道栓剂或安慰剂,从黄体期开始,在妊娠试验呈阳性后继续使用至妊娠28周。主要研究结局是流产率。

结果

共纳入700名女性(每组n = 350)。孕酮组的流产率显著低于安慰剂组(12.4%对23.3%,p = 0.001)。与安慰剂组相比,孕酮组妊娠持续超过20周的比率以及活产率有显著改善(分别为87.

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