孕早期胎儿解剖研究和主要异常的鉴定使用10个标准化扫描。

Enrico Colosi, Rosalia Musone, Gilda Filardi, Alma Fabbo
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引用次数: 5

摘要

目的:验证孕早期扫描不仅作为染色体异常的筛查工具,而且作为一种通过10次标准化扫描识别主要解剖异常的方法。方法:对5924例孕早期单胎妊娠患者进行5年的前瞻性研究,对其进行染色体病变筛查。使用了一份由10个预先确定的扫描组成的检查清单。根据当地协议,随访包括在妊娠中期和晚期进行两次以上扫描,并在出生时对新生儿结局进行最终评估。结果:5924例患者中,重大畸形检出率为0.74%,以妊娠早期检出率最高(47.7%)。与神经系统有关的畸形检出率约为50%,腹部、心脏和骨骼的畸形检出率略低(43.5%)。结论:采用10次标准化扫描的妊娠早期超声是一种有效的染色体病变筛查方法,也是识别许多主要胎儿解剖异常的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First trimester fetal anatomy study and identification of major anomalies using 10 standardized scans.

Objective: to validate the use of the first trimester scan not just as a screening tool for chromosomal anomalies, but also as a method to identify the major anatomic anomalies using 10 standardized scans.

Methods: five years of prospective study analyzing the fetal anatomy of 5924 patients with a singleton pregnancy during the first trimester screening for chromosomopathies. A check list of 10 predetermined scans had been used. The follow up consisted of two more scans in the second and third trimester, according to the local protocol, and a final evaluation of neonatal outcome at birth.

Results: in the 5924 examined patients, the percentage of major malformations is 0.74%, most of all discovered in the first trimester (47.7%). The Detection Rate for the malformations related to the nervous system is about 50% and for the malformations of the abdomen, heart and skeleton is slightly lower (43.5%).

Conclusions: first trimester ultrasound using 10 standardized scans is a valid screening method for chromosomopathies and also an effective method to identify many of the major fetal anato - mical anomalies.

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