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石卫武, 干灵红, 章鸯, 徐丹萍, 陈雪娇, 章卫国, 戴美珍, 周美英. 台州地区孕妇孕中期母血清产前筛查结果分析[J]. 中国公共卫生, 2013, 29(1): 120-121. DOI: 10.11847/zgggws2013-29-01-40
引用本文: 石卫武, 干灵红, 章鸯, 徐丹萍, 陈雪娇, 章卫国, 戴美珍, 周美英. 台州地区孕妇孕中期母血清产前筛查结果分析[J]. 中国公共卫生, 2013, 29(1): 120-121. DOI: 10.11847/zgggws2013-29-01-40
SHI Wei-wu, GAN Ling-hong, ZHANG Yang.et al, . Prenatal serum screening among pregnant women at second-trimester in Taizhou region[J]. Chinese Journal of Public Health, 2013, 29(1): 120-121. DOI: 10.11847/zgggws2013-29-01-40
Citation: SHI Wei-wu, GAN Ling-hong, ZHANG Yang.et al, . Prenatal serum screening among pregnant women at second-trimester in Taizhou region[J]. Chinese Journal of Public Health, 2013, 29(1): 120-121. DOI: 10.11847/zgggws2013-29-01-40

台州地区孕妇孕中期母血清产前筛查结果分析

Prenatal serum screening among pregnant women at second-trimester in Taizhou region

  • 摘要: 目的探讨孕中期母血清产前筛查系统对唐氏综合征(DS)和18-三体综合征及神经管畸形(NTD)检出的临床应用价值。方法应用时间分辨荧光免疫分析技术(DELFIA)对120 309名孕中期(15~21周)孕妇进行血清标记物甲胎蛋白+游离人绒毛膜促性腺激素(AFP+free β-HCG)两联指标检测,筛查结果应用Lifecycle 3.0软件进行出生缺陷风险评估。结果120 309名孕中期孕妇筛查出高风险孕妇5 022例,阳性率为4.17%;4 494例21-三体综合征和18-三体综合征高风险孕妇中有3 573例接受羊水或脐血穿刺产前诊断,占79.51%,发现胎儿核型异常49例,异常检出率为1.37%,其中DS 22例、18-三体综合征6例、其他异常核型21例。结论孕中期母血清标记物两联指标的产前筛查是预测DS 和18-三体综合征、NTD的有效指标。

     

    Abstract: Objective To investigate the clinical value of second trimester maternal serum screening for Down's syndrome(DS),18-trisomy syndrome,and neural tube defects(NTD).Methods The serum markers(alpha-fetoprotein and beta human chroionic gonadotrophin) were detected in 120 309 pregnant women at second trimester(15-21 weeks) with time-resolved fluorescence immunoassay(DELFIA).The detection data were analyzed with Lifecycle 3.0 software.Results There were 5 022 pregnant women identified as at high-risk,with a positive rate of 4.17%.Amniotic fluid or umbilical cord blood puncture was conducted among 79.51% of the women with high risk of DS and 18-trisomy syndrome(3 573/4 494).There were 49(1.37%) cases of abnormal fetal karyotype, 22 cases of DS,6 cases of 18-trisomy syndrome,and 21 cases of other abnormal karyotype.In high-risk pregnant women who were younger or older than 35 years,the abnormal karyotype detection rate was 1.37%.Conclusion Second trimester maternal serum markers(AFP and β-HCG) detection is efficient in prenatal screening for DS,18-trisomy syndrome,and NTD.

     

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