常规早孕期超声筛查在中枢神经系统异常中的作用:一项使用未经选择的 3 年经验队列的纵向单中心研究。

The role of routine first-trimester ultrasound screening for central nervous system abnormalities: a longitudinal single-center study using an unselected cohort with 3-year experience.

机构信息

Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, P. R. China.

Beijing Maternal and Child Health Care Hospital, Beijing, P. R. China.

出版信息

BMC Pregnancy Childbirth. 2023 May 3;23(1):312. doi: 10.1186/s12884-023-05644-z.

Abstract

BACKGROUND

To evaluate the role of a standardized first-trimester scan in screening different kinds of central nervous system malformations and to report a 3-year experience from a tertiary center using an unselected cohort.

METHODS

This was a retrospective analysis of prospectively collected data from a single center evaluating first-trimester scans with predesigned standardized protocols performed between 1 May 2017 and 1 May 2020, involving 39,526 pregnancies. All pregnant women underwent a series of prenatal ultrasound scans at 11-14, 20-24, 28-34 and 34-38 weeks of gestation. Abnormalities were confirmed by magnetic resonance imaging, postmortem examination or trained ultrasound professionals. Pregnancy outcomes and some postnatal follow-up were obtained from maternity medical records and telephone calls.

RESULTS

A total of 38,586 pregnancies included in the study. The detection rates of CNS anomalies by ultrasound in the first, second, third and late third trimester were 32%, 22%, 25%, and 16%, respectively. And there were 5% of CNS anomalies missed by prenatal ultrasound. In the first-trimester scan, we diagnosed all cases of exencephaly, anencephaly, alobar holoprosencephaly and meningoencephalocele, and some cases of posterior cranial fossa anomalies (20%), open spina bifida (67%), semilobar holoprosencephaly (75%) and severe ventriculomegaly (8%). Vein of Galen aneurysmal malformation, closed spina bifida, lobar holoprosencephaly, intracranial infection, arachnoid cyst, agenesis of the corpus callosum, cysts of the septum pellucidum and isolated absence of the septum pellucidum were never detected during the first trimester. The abortion rates of fetal CNS anomalies detected by first-trimester scan, second-trimester scan, and third- trimester scan were 96%, 84% and 14%, respectively.

CONCLUSIONS

The study showed that almost 1/3 of central nervous system anomalies were detected by the standard first-trimester scan and these cases were associated with a high rate of abortion. Early screening for fetal abnormalities gives parents more time for medical advice and safer abortion if needed. It is therefore recommended that some major CNS anomalies should be screened in the first trimester. The standardized anatomical protocol, consisting of four fetal brain planes, were recommended for routine first trimester ultrasound screening.

摘要

背景

评估标准化早孕期超声检查在筛查不同类型中枢神经系统畸形中的作用,并报告一家三级中心使用未经选择的队列进行的 3 年经验。

方法

这是一项对 2017 年 5 月 1 日至 2020 年 5 月 1 日期间在一家单中心进行的前瞻性收集数据的回顾性分析,涉及 39526 例妊娠。所有孕妇均在 11-14 周、20-24 周、28-34 周和 34-38 周进行一系列产前超声检查。异常通过磁共振成像、尸检或经过培训的超声专业人员进行确认。妊娠结局和一些产后随访从产妇病历和电话中获得。

结果

共纳入 38586 例妊娠。超声在早孕期、中孕期、晚孕期诊断中枢神经系统畸形的检出率分别为 32%、22%、25%和 16%。产前超声漏诊率为 5%。在早孕期超声检查中,我们诊断了所有无脑畸形、无脑回畸形、全前脑无叶型和脑膜脑膨出,以及一些后颅窝异常(20%)、开放性脊柱裂(67%)、半叶脑全前脑畸形(75%)和严重脑室扩大(8%)。静脉窦动脉瘤畸形、闭合性脊柱裂、脑裂畸形、颅内感染、蛛网膜囊肿、胼胝体发育不全、透明隔囊肿和单纯透明隔缺如在早孕期从未被发现过。早孕期超声检查、中孕期超声检查和晚孕期超声检查检测到的胎儿中枢神经系统畸形的流产率分别为 96%、84%和 14%。

结论

该研究表明,近 1/3的中枢神经系统畸形可通过标准早孕期超声检查发现,这些病例流产率较高。早期筛查胎儿异常可使父母有更多的时间获得医学建议,并在需要时进行更安全的流产。因此,建议在早孕期筛查一些主要的中枢神经系统畸形。建议采用包括四个胎儿脑平面的标准化解剖学方案进行常规早孕期超声筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9836/10157940/24bca8566a58/12884_2023_5644_Fig1_HTML.jpg

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