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随机试验筛查低危孕妇早产-早产筛查研究。

Randomized trial of screening for preterm birth in low-risk women - the preterm birth screening study.

机构信息

Department of Neuroscience, Reproductive Sciences and Dentistry, School of Medicine, University of Naples Federico II, Naples, Italy (Drs Saccone, Maruotti, and Sarno; Ms Gragnano; Drs Bartolini, Borrelli, Locci, and Guida).

Department of Neuroscience, Reproductive Sciences and Dentistry, School of Medicine, University of Naples Federico II, Naples, Italy (Drs Saccone, Maruotti, and Sarno; Ms Gragnano; Drs Bartolini, Borrelli, Locci, and Guida).

出版信息

Am J Obstet Gynecol MFM. 2024 May;6(5S):101267. doi: 10.1016/j.ajogmf.2023.101267. Epub 2024 Feb 19.

Abstract

BACKGROUND

Preterm birth is a major cause of perinatal morbidity and mortality. It is unclear whether the introduction of a universal transvaginal ultrasound cervical length screening program in women at low risk for preterm delivery is associated with a reduction in the frequency of preterm birth.

OBJECTIVE

To test the hypothesis that the introduction of a midtrimester universal transvaginal ultrasound cervical length screening program in asymptomatic singleton pregnancies without prior preterm delivery would reduce the rate of preterm birth at <37 weeks of gestation.

STUDY DESIGN

This study was a multicenter nonblinded randomized trial of screening of asymptomatic singleton pregnancies without prior spontaneous preterm birth, who were randomized to either cervical length screening program (ie, intervention group) or no screening (ie, control group). Participants were randomized at the time of their routine anatomy scan between 18 0/7 and 23 6/7 weeks of gestation. Women randomized in the screening group received cervical length measurement. Those who were found to have cervical length ≤25 mm were offered 200 mg vaginal progesterone daily along with cervical pessary. The primary outcome was preterm birth at <37 weeks. The risk of primary outcome was quantified by the relative risk with 95% confidence interval, and was based on the intention-to-screen principle.

RESULTS

A total of 1334 asymptomatic women with singleton pregnancies and without prior preterm birth, were included in the trial. Out of the 675 women randomized in the transvaginal ultrasound cervical length screening group, 13 (1.9%) were found to have transvaginal ultrasound cervical length ≤25 mm during the screening. Preterm birth at <37 weeks of gestation occurred in 48 women in the transvaginal ultrasound cervical length screening group (7.5%), and 54 women in the control group (8.7%) (relative risk, 0.86; 95% confidence interval, 0.59-1.25). Women randomized in the transvaginal ultrasound cervical length screening group had no significant differences in the incidence of preterm birth at less than 34, 32, 30, 28, and 24 weeks of gestation.

CONCLUSION

The introduction of a universal transvaginal ultrasound cervical length screening program at 18 0/6 to 23 6/7 weeks of gestation in singleton pregnancies without prior spontaneous preterm birth, with treatment for those with cervical length ≤25 mm, did not result in significant lower incidence of preterm delivery than the incidence without the screening program.

摘要

背景

早产是围产期发病率和死亡率的主要原因。目前尚不清楚在没有早产史的低危孕妇中引入普遍的经阴道超声宫颈长度筛查方案是否与早产发生率的降低有关。

目的

检验以下假设,即在没有先前自发性早产史的无症状单胎妊娠中引入中期普遍的经阴道超声宫颈长度筛查方案是否会降低<37 孕周的早产率。

研究设计

这是一项多中心非盲随机试验,对无先前自发性早产史的无症状单胎妊娠进行筛查,将其随机分为宫颈长度筛查方案(即干预组)或不筛查(即对照组)。参与者在 18 0/7 至 23 6/7 孕周时在常规解剖扫描时进行随机分组。随机分组在筛查组的女性接受宫颈长度测量。如果发现宫颈长度≤25mm,则提供 200mg 阴道孕酮每日一次,并使用宫颈扩张器。主要结局是<37 孕周的早产。主要结局的风险通过 95%置信区间的相对风险来量化,并基于意向筛查原则。

结果

共有 1334 名无症状的单胎妊娠且无先前早产史的孕妇参加了该试验。在 675 名接受经阴道超声宫颈长度筛查的女性中,有 13 名(1.9%)在筛查期间发现经阴道超声宫颈长度≤25mm。<37 孕周的早产发生在经阴道超声宫颈长度筛查组的 48 名女性中(7.5%),对照组的 54 名女性中(8.7%)(相对风险,0.86;95%置信区间,0.59-1.25)。随机分组在经阴道超声宫颈长度筛查组的女性在<34、32、30、28 和 24 孕周的早产发生率没有显著差异。

结论

在没有自发性早产史的单胎妊娠中,在 18 0/6 至 23 6/7 孕周时引入普遍的经阴道超声宫颈长度筛查方案,并对宫颈长度≤25mm 的患者进行治疗,与不进行筛查方案相比,并未显著降低早产发生率。

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