Thiagarajah S, Stroud C B, Vavelidis F, Schnorr J A, Schnatterly P T, Ferguson J E
Department of Obstetrics and Gynecology, University of Virginia Health Sciences Center, Charlottesville 22908, USA.
Am J Obstet Gynecol. 1995 Aug;173(2):388-91; discussion 391-2. doi: 10.1016/0002-9378(95)90257-0.
Our purpose was to present the findings of a project to determine the efficacy of including routine fetal karyotyping in the investigation of an elevated maternal serum alpha-fetoprotein concentration.
Targeted ultrasonographic examinations were performed in 658 patients with elevated maternal serum alpha-fetoprotein levels. The scans were normal in 557 women, of whom 427 consented to amniocentesis; 435 fetuses were karyotyped. In the 101 patients with abnormal ultrasonographic examinations 75 had fetal karyotyping.
In the 435 fetuses with normal scans, two had karyotypic anomalies, a 47,XYY and an inherited balanced translocation. Three fetuses with normal karyotypes and high amniotic fluid alpha-fetoprotein levels had congenital nephrosis. In the 101 patients with abnormal scans, 75 fetuses were karyotyped. There were four aneuploidies. Among the 26 patients with abnormal scans who declined amniocentesis one fetus with multiple anomalies was karyotyped after delivery and triploidy was discovered.
These results provide little justification for including fetal karyotyping in the investigation of elevated maternal serum alpha-fetoprotein when the targeted ultrasonographic examination is normal. When it is abnormal, selective rather than routine karyotyping is more appropriate.
我们的目的是展示一个项目的研究结果,该项目旨在确定在孕妇血清甲胎蛋白浓度升高的检查中纳入常规胎儿核型分析的有效性。
对658名孕妇血清甲胎蛋白水平升高的患者进行了针对性超声检查。557名女性的扫描结果正常,其中427人同意进行羊膜穿刺术;对435例胎儿进行了核型分析。在101名超声检查异常的患者中,75例进行了胎儿核型分析。
在扫描结果正常的435例胎儿中,有2例存在核型异常,1例为47,XYY,1例为遗传性平衡易位。3例核型正常但羊水甲胎蛋白水平高的胎儿患有先天性肾病。在101名超声检查异常的患者中,75例胎儿进行了核型分析。有4例非整倍体。在26例拒绝羊膜穿刺术的超声检查异常患者中,1例有多发性畸形的胎儿在出生后进行了核型分析,发现为三倍体。
当针对性超声检查正常时,这些结果几乎没有理由在孕妇血清甲胎蛋白升高的检查中纳入胎儿核型分析。当超声检查异常时,选择性而非常规核型分析更为合适。