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不明病因复发性流产女性预防流产的孕激素治疗

Progestogen for preventing miscarriage in women with recurrent miscarriage of unclear etiology.

作者信息

Haas David M, Hathaway Taylor J, Ramsey Patrick S

机构信息

Department of Obstetrics and Gynecology, Indiana University School of Medicine, 1001 West 10th Street, F-5, Indianapolis, Indiana, USA, 46202.

出版信息

Cochrane Database Syst Rev. 2018 Oct 8;10(10):CD003511. doi: 10.1002/14651858.CD003511.pub4.

Abstract

BACKGROUND

Progesterone, a female sex hormone, is known to induce secretory changes in the lining of the uterus essential for successful implantation of a fertilized egg. It has been suggested that a causative factor in many cases of miscarriage may be inadequate secretion of progesterone. Therefore, clinicians use progestogens (drugs that interact with the progesterone receptors), beginning in the first trimester of pregnancy, in an attempt to prevent spontaneous miscarriage. This is an update of a review, last published in 2013.

OBJECTIVES

To assess the efficacy and safety of progestogens as a preventative therapy against recurrent miscarriage.

SEARCH METHODS

For this update, we searched Cochrane Pregnancy and Childbirth's Trials Register, ClinicalTrials.gov, the WHO International Clinical Trials Registry Platform (ICTRP) (6 July 2017) and reference lists from relevant articles, attempting to contact trial authors where necessary, and contacted experts in the field for unpublished works.

SELECTION CRITERIA

Randomized or quasi-randomized controlled trials comparing progestogens with placebo or no treatment given in an effort to prevent miscarriage.

DATA COLLECTION AND ANALYSIS

Two review authors independently assessed trials for inclusion and risk of bias, extracted data and checked them for accuracy. Two reviewers assessed the quality of the evidence using the GRADE approach.

MAIN RESULTS

Thirteen trials (2556 women) met the inclusion criteria. Nine of the included trials compared treatment with placebo and the remaining four trials compared progestogen administration with no treatment. The trials were a mix of multicenter and single-center trials, conducted in Egypt, India, Jordan, UK and USA. In six trials women had had three or more consecutive miscarriages and in seven trials women had suffered two or more consecutive miscarriages. Routes, dosage and duration of progestogen treatment varied across the trials. The majority of trials were at low risk of bias for most domains. Eleven trials (2359 women) contributed data to the analyses.The meta-analysis of all women, suggests that there is probably a reduction in the number of miscarriages for women given progestogen supplementation compared to placebo/controls (average risk ratio (RR) 0.69, 95% confidence interval (CI) 0.51 to 0.92, 11 trials, 2359 women, moderate-quality evidence). A subgroup analysis comparing placebo-controlled versus non-placebo-controlled trials and different routes of administration showed no differences between subgroups for miscarriage. However, there appears to be a subgroup difference for miscarriage between women with three or more prior miscarriages compared to women with two or more miscarriages, with a more pronounced effect in women with three or more prior miscarriages. However, it should be noted that there was high heterogeneity in the subgroup of women with three or more prior miscarriages.None of the trials reported on any secondary maternal outcomes, including severity of morning sickness, thromboembolic events, depression, admission to a special care unit, or subsequent fertility.There was probably a slight benefit for women receiving progestogen seen in the outcome of live birth rate (RR 1.11, 95% CI 1.00 to 1.24, 7 trials, 2086 women, moderate-quality evidence). While the rate of preterm birth is probably reduced for women receiving progestogen, this outcome was mainly driven by one trial and thus should be interpreted with great caution (RR 0.59, 95% CI 0.39 to 0.89, 5 trials, 811 women, moderate-quality evidence). No clear differences were seen for women receiving progestogen for the other secondary outcomes of neonatal death or fetal genital abnormalities. A possible reduction in stillbirth was seen, but again this outcome was driven mainly by one trial and should be interpreted with caution (RR 0.38, 95% CI 0.24 to 0.58, 3 trials, 1199 women). There may be little or no difference in the rate of low birthweight and trials did not report on the secondary child outcomes of teratogenic effects or admission to a special care unit.

AUTHORS' CONCLUSIONS: For women with unexplained recurrent miscarriages, supplementation with progestogen therapy probably reduces the rate of miscarriage in subsequent pregnancies.

摘要

背景

孕酮是一种女性性激素,已知其能诱导子宫内膜发生分泌期变化,这对受精卵成功着床至关重要。有人认为,许多流产病例的一个致病因素可能是孕酮分泌不足。因此,临床医生从妊娠早期开始使用孕激素(即与孕酮受体相互作用的药物),试图预防自然流产。这是一篇综述的更新版,上一版于2013年发表。

目的

评估孕激素作为预防复发性流产的治疗方法的有效性和安全性。

检索方法

为了进行此次更新,我们检索了Cochrane妊娠与分娩试验注册库、ClinicalTrials.gov、世界卫生组织国际临床试验注册平台(ICTRP)(2017年7月6日)以及相关文章的参考文献列表,必要时试图联系试验作者,并联系该领域的专家以获取未发表的研究。

入选标准

比较孕激素与安慰剂或不进行治疗以预防流产的随机或半随机对照试验。

数据收集与分析

两位综述作者独立评估试验是否纳入以及偏倚风险,提取数据并检查其准确性。两位评审员使用GRADE方法评估证据质量。

主要结果

13项试验(2556名女性)符合纳入标准。纳入的试验中有9项将治疗与安慰剂进行了比较,其余4项试验将孕激素给药与不治疗进行了比较。这些试验包括多中心和单中心试验,在埃及、印度、约旦、英国和美国开展。在6项试验中,女性有过三次或更多次连续流产,在7项试验中,女性有过两次或更多次连续流产。孕激素治疗的途径、剂量和持续时间在各项试验中有所不同。大多数试验在大多数领域的偏倚风险较低。11项试验(2359名女性)为分析提供了数据。对所有女性进行的荟萃分析表明,与安慰剂/对照组相比,补充孕激素的女性流产数量可能减少(平均风险比(RR)0.69,95%置信区间(CI)0.51至0.92,11项试验,2359名女性,中等质量证据)。一项比较安慰剂对照试验与非安慰剂对照试验以及不同给药途径的亚组分析显示,各亚组在流产方面无差异。然而,与有两次或更多次流产的女性相比,有三次或更多次既往流产的女性在流产方面似乎存在亚组差异,在有三次或更多次既往流产的女性中效果更明显。然而,应注意的是,有三次或更多次既往流产的女性亚组存在高度异质性。没有一项试验报告任何次要的孕产妇结局,包括孕吐严重程度、血栓栓塞事件、抑郁症、入住特殊护理病房或后续生育能力。在活产率结局方面,接受孕激素治疗的女性可能略有获益(RR 1.11,95%CI 1.00至1.24,7项试验,2086名女性,中等质量证据)。虽然接受孕激素治疗的女性早产率可能降低,但这一结局主要由一项试验驱动,因此应极为谨慎地解读(RR 0.59,95%CI 0.39至0.89,5项试验,811名女性,中等质量证据)。对于接受孕激素治疗的女性,在新生儿死亡或胎儿生殖器异常等其他次要结局方面未观察到明显差异。观察到死产率可能降低,但同样这一结局主要由一项试验驱动,应谨慎解读(RR 0.38,95%CI 0.24至0.58,3项试验,1199名女性)。低出生体重率可能几乎没有差异,且试验未报告致畸作用或入住特殊护理病房等次要儿童结局。

作者结论

对于原因不明的复发性流产女性,补充孕激素治疗可能会降低后续妊娠的流产率。

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Human chorionic gonadotrophin (hCG) for preventing miscarriage.用于预防流产的人绒毛膜促性腺激素(hCG)。
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