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美国妇产科医师学会委员会意见第296号:孕早期胎儿非整倍体筛查

ACOG Committee Opinion #296: first-trimester screening for fetal aneuploidy.

出版信息

Obstet Gynecol. 2004 Jul;104(1):215-7.

Abstract

First-trimester screening for chromosomal abnormalities offers potential advantages over second-trimester screening. Studies in the 1900s demonstrated an association between chromosomal abnormalities and the ultrasonographic finding of abnormally increased nuchal translucency (an echo-free area at the back of the fetal neck) between 10 and 14 weeks of gestation. First-trimester screening using nuchal translucency, free beta-hCG, and pregnancy-associated plasma protein-A has comparable detection rates and positive screening rates for Down syndrome as second-trimester screening using 4 serum markers (alpha-fetoprotein, beta-hCG, unconjugated estriol, and inhibin-A). Although first-trimester screening for Down syndrome and trisomy 18 is an option, it should be offered only if certain criteria can be met.

摘要

孕早期染色体异常筛查相比孕中期筛查具有潜在优势。20世纪的研究表明,染色体异常与妊娠10至14周时超声检查发现的颈部半透明带异常增厚(胎儿颈部后方的无回声区)之间存在关联。使用颈部半透明带、游离β-人绒毛膜促性腺激素(β-hCG)和妊娠相关血浆蛋白-A进行的孕早期筛查,对于唐氏综合征的检出率和阳性筛查率与使用4种血清标志物(甲胎蛋白、β-hCG、未结合雌三醇和抑制素-A)进行的孕中期筛查相当。虽然孕早期唐氏综合征和18三体筛查是一种选择,但只有在满足特定标准时才应提供该项筛查。

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