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早孕期颈项透明层增厚胎儿的不良妊娠结局:前瞻性队列研究。

Adverse pregnancy outcome in fetuses with early increased nuchal translucency: prospective cohort study.

机构信息

Department of Obstetrics and Gynecology, Amsterdam UMC location University of Amsterdam, Amsterdam, The Netherlands.

Amsterdam Reproduction and Development, Amsterdam, The Netherlands.

出版信息

Ultrasound Obstet Gynecol. 2024 Aug;64(2):164-172. doi: 10.1002/uog.27623.

Abstract

OBJECTIVES

An increased nuchal translucency (NT) thickness of ≥ 3.5 mm is a well-established marker for congenital anomalies and adverse pregnancy outcome between 11 and 14 weeks' gestation, but little is known about its performance as a screening tool before 11 weeks. We aimed to investigate, in a prospective setting, whether fetuses with increased NT before 11 weeks are at risk for adverse pregnancy outcome.

METHODS

This was a prospective cohort study including pregnant women with a viable fetus with NT ≥ 2.5 mm and a crown-rump length (CRL) < 45 mm. All included women were referred to our fetal medicine unit (FMU) and scheduled for a follow-up scan where the NT was remeasured after 1 week when the CRL was > 45 mm. Two groups were evaluated: cases with a normalized NT (< 3.5 mm) and cases with persistently increased NT (≥ 3.5 mm). The cases were monitored until 4 weeks after delivery. The main outcome was a composite adverse outcome of aneuploidy, other genetic disorders, structural anomalies and pregnancy loss. We performed subgroup analyses of NT thickness at inclusion and normalized or persistently increased NT at follow-up.

RESULTS

The study included 109 cases, of which 39 (35.8%) had an adverse pregnancy outcome. Of these, 64.1% (25/39) were aneuploid, corresponding to 22.9% (25/109) of the total study population. In the subgroups of NT thickness at inclusion of 2.5-3.4 mm, 3.5-4.4 mm and ≥ 4.5 mm, an adverse outcome was reported in 22.0% (9/41), 40.0% (18/45) and 52.2% (12/23), respectively. In fetuses with a normalized NT and without ultrasound abnormalities at the follow-up scan, the incidence of adverse outcome was 8.5% (5/59), of which 5.1% (3/59) cases were aneuploid.

CONCLUSIONS

Fetuses with an early increased NT thickness are at considerable risk of an adverse pregnancy outcome, even if the NT normalizes after 11 weeks. Not all congenital anomalies can be diagnosed with routine first-trimester screening, such as non-invasive prenatal testing and/or a first-trimester anomaly scan. Therefore, expectant parents should always be referred to a FMU for detailed ultrasonography. Invasive prenatal testing should be offered if an increased NT of ≥ 2.5 mm is observed before 11 weeks' gestation. © 2024 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.

摘要

目的

颈项透明层(NT)厚度增加≥3.5mm是 11-14 孕周胎儿先天性异常和不良妊娠结局的明确标志物,但目前尚不清楚其在 11 孕周前作为筛查工具的表现。本研究旨在前瞻性研究中探讨 11 孕周前 NT 增加的胎儿是否存在不良妊娠结局的风险。

方法

这是一项前瞻性队列研究,纳入了 NT≥2.5mm 且头臀长(CRL)<45mm 的有存活胎儿的孕妇。所有纳入的孕妇均被转诊至胎儿医学科(FMU),并安排进行后续扫描,当 CRL>45mm 时,1 周后再次测量 NT。评估了两组:NT 正常(<3.5mm)的病例和 NT 持续增加(≥3.5mm)的病例。对这些病例进行了监测,直到分娩后 4 周。主要结局是染色体异常、其他遗传疾病、结构异常和妊娠丢失的复合不良结局。我们对纳入时的 NT 厚度和后续的 NT 正常或持续增加进行了亚组分析。

结果

该研究纳入了 109 例病例,其中 39 例(35.8%)存在不良妊娠结局。其中,64.1%(25/39)为染色体异常,相当于总研究人群的 22.9%(25/109)。在纳入时 NT 厚度为 2.5-3.4mm、3.5-4.4mm 和≥4.5mm 的亚组中,分别报告了 22.0%(9/41)、40.0%(18/45)和 52.2%(12/23)的不良结局。在 NT 正常且在后续扫描中无超声异常的胎儿中,不良结局的发生率为 8.5%(5/59),其中 5.1%(3/59)为染色体异常。

结论

即使在 11 孕周后 NT 正常化,早期 NT 厚度增加的胎儿仍存在相当大的不良妊娠结局风险。并非所有先天性异常都可以通过常规的早孕期筛查来诊断,如非侵入性产前检测和/或早孕期异常扫描。因此,应始终将期待父母转介至 FMU 进行详细的超声检查。如果在 11 孕周前观察到 NT 增加≥2.5mm,则应提供有创性产前检测。© 2024 作者。《超声医学杂志》由 John Wiley & Sons Ltd 出版,代表国际超声协会在妇产科领域出版。

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