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孕11至14周胎儿结构异常的诊断

Diagnosis of Fetal Structural Anomalies at 11 to 14 Weeks.

作者信息

Vayna Ana Maria, Veduta Alina, Duta Simona, Panaitescu Anca Maria, Stoica Sabrina, Buinoiu Natalia, Nedelea Florina, Peltecu Gheorghe

机构信息

Fetal Medicine Department, Filantropia Clinical Hospital, Bucharest, Romania.

Carol Davila University of Medicine, Bucharest, Romania.

出版信息

J Ultrasound Med. 2018 Aug;37(8):2063-2073. doi: 10.1002/jum.14561. Epub 2018 Feb 24.

Abstract

OBJECTIVES

To assess the performance of first-trimester ultrasound (US) in identifying major fetal structural abnormalities in an unselected population.

METHODS

We conducted a retrospective analysis of all pregnancies that underwent the 11- to 14-week scan in the Fetal Medicine Department of Filantropia Hospital in Bucharest, which were prospectively examined within our screening program. The purpose of the first-trimester US was to evaluate the risk for chromosomal abnormalities and to conduct fetal anatomic examination using a detailed protocol.

RESULTS

Our population consisted of 7480 pregnant patients (7576 fetuses). The follow-up was completed for 6045 patients (6114 fetuses). The prevalence of major structural anomalies was 1.89%. In the first trimester, we identified 79% of all major structural anomalies. The highest detection rates were achieved for abdominal wall defects (100%), major central nervous system anomalies (88%), cardiac defects (74%), and skeletal anomalies (71%). The nuchal translucency was increased in 35% of the cases with structural anomalies, and 95% of these were diagnosed in the first trimester. Seventy percent of the patients who presented with structural anomalies and a normal nuchal translucency were diagnosed in the first trimester.

CONCLUSIONS

Our results emphasize the importance of performing a detailed US examination at 11 to 14 weeks' gestation in identification of fetal structural defects.

摘要

目的

评估孕早期超声检查(US)在未选择人群中识别主要胎儿结构异常的性能。

方法

我们对在布加勒斯特慈善医院胎儿医学科接受11至14周扫描的所有妊娠进行了回顾性分析,这些妊娠在我们的筛查项目中进行了前瞻性检查。孕早期超声检查的目的是评估染色体异常风险,并使用详细方案进行胎儿解剖学检查。

结果

我们的研究对象包括7480名孕妇(7576例胎儿)。对6045名患者(6114例胎儿)完成了随访。主要结构异常的患病率为1.89%。在孕早期,我们识别出了所有主要结构异常的79%。腹壁缺陷(100%)、主要中枢神经系统异常(88%)、心脏缺陷(74%)和骨骼异常(71%)的检出率最高。35%的结构异常病例中颈项透明层增厚,其中95%在孕早期被诊断出来。70%有结构异常且颈项透明层正常的患者在孕早期被诊断出来。

结论

我们的结果强调了在妊娠11至14周进行详细超声检查以识别胎儿结构缺陷的重要性。

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