目的:探讨血清学筛查在高龄孕妇产前诊断中的应用价值。方法回顾性分析2012年1月1日-2012年10月31日行胎儿染色体核型分析的高龄孕妇314例,按预产期年龄分为35~39岁组和≥40岁组;按血清学筛查情况分为血清学筛查低危组、血清学筛查高危组和未做血清学筛查组,分析各组胎儿染色体异常率。结果胎儿染色体异常率4.14%(13/314)。≥40岁组胎儿染色体异常率13.21%(7/53),高于35~39岁组2.30%(6/261)( P=0.001)。血清学筛查高危组胎儿染色体异常率7.69%(7/91),高于血清学筛查低危组0(0/64)( P=0.022)。结论对高龄孕妇进行血清学筛查,有助于减少介入性产前诊断率。
Objective To investigate the incidence of chromosome abnormalities in advanced maternalage(AMA) ,and to investigate the value of prenatal screening in AMA . Methods Retrospective analysis of 314 cases of AMA which had invasive prenatal diagnosis .314 cases of AMA were divided into two groups according to expected date of childbirth age :35~39 years old and older than 40 years old . And they were also divided into three groups according to serum screening :low-risk serum screening group ,high-risk serum screening and without serum screeningand ,to analyze the percentage of fetal chro-mosome abnormalities in these groups . Results The percentage of fetal chromosomal abnormalities of 314 AMA was 4 .14% (13/314) . The percentage of fetal chromosomal abnormalities in AMA whose ma-ternal age older than 40 years old was 13 .21% (7/53) ,which was higher than that in AMA whose mater-nal age 35~39 years old 2 .30% (6/261) (P=0 .001) . In high-risk serum screening group ,the percent-age of fetal chromosome abnormalities was 7 .69% (7/91) ,which was higher than that in low-risk serum screening group 0 (0/64) (P=0 .022) . Conclusions Maternal prenatal screening tests could be applied in AMA .