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[孕母血清唐氏综合征和神经管缺陷筛查]

[Maternal serum screening for Down syndrome and neural tube defects].

作者信息

van Rijn M, Christiaens G C, van der Schouw Y T, Hagenaars A M, de Pater J M, Visser G H

机构信息

Academisch Ziekenhuis, afd. Obstetrie en Gynaecologie, Utrecht.

出版信息

Ned Tijdschr Geneeskd. 1998 Feb 21;142(8):409-15.

PMID:9562776
Abstract

OBJECTIVE

Evaluation of maternal serum screening for Down's syndrome (DS) and neural tube defects (NTDs).

DESIGN

Longitudinal study.

SETTING

Department of Obstetrics and Gynaecology, University Hospital Utrecht, the Netherlands.

METHOD

6362 pregnant women underwent serum screening for DS and (or) NTD between the 15th and 21st weeks of pregnancy between March 1991 and March 1996. Screening was performed using alpha-foetoprotein, unconjugated oestriol, human chorionic gonadotrophin and maternal age. The result of each individual test was a calculated risk for delivering a child with DS and (or) NTD.

RESULTS

Nine out of 12 singleton pregnancies of a foetus with DS were detected. To this purpose, 573 women who, according to the serum screening had an increased risk of a child with the abnormality, were offered amniocentesis, which was performed in 471 of them. Two twin pregnancies with a total of 3 DS affected foetuses were also detected; one twin pregnancy of a DS foetus was screen-negative. The one case of spina bifida was screen-positive. The proportion of women eligible for invasive prenatal diagnosis because of maternal age increased from 9% to 25% in the course of the study. Of 1118 women aged > or = 36 years 913 (82%) declined invasive investigation compared with 40% in the general population.

CONCLUSION

The results of the maternal serum screening program in Utrecht were comparable with other studies. Maternal serum screening is accepted as an alternative by women above 36 years, and allows to decrease the need for amniocentesis without a significant loss in detection rate.

摘要

目的

评估孕母血清筛查唐氏综合征(DS)和神经管缺陷(NTDs)。

设计

纵向研究。

地点

荷兰乌得勒支大学医院妇产科。

方法

1991年3月至1996年3月期间,6362名孕妇在妊娠第15至21周接受了DS和(或)NTD的血清筛查。筛查采用甲胎蛋白、非结合雌三醇、人绒毛膜促性腺激素和孕妇年龄。每项个体检测结果是分娩患有DS和(或)NTD患儿的计算风险。

结果

12例单胎DS胎儿妊娠中检测出9例。为此,向573名根据血清筛查患异常患儿风险增加的妇女提供了羊膜穿刺术,其中471人接受了该检查。还检测出2例双胎妊娠,共有3个受DS影响的胎儿;1例DS胎儿的双胎妊娠筛查为阴性。1例脊柱裂筛查为阳性。在研究过程中,因孕妇年龄而符合侵入性产前诊断条件的妇女比例从9%增加到25%。在1118名年龄≥36岁的妇女中,913名(82%)拒绝侵入性检查,而普通人群中这一比例为40%。

结论

乌得勒支孕母血清筛查项目的结果与其他研究相当。36岁以上的妇女接受孕母血清筛查作为一种替代方法,并且可以减少羊膜穿刺术的需求,而不会显著降低检出率。

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