摘要
目的 回顾性分析2010-2013年吉林地区孕中期三联筛查临床应用情况及其影响因素。方法 孕中期(15-20+6周)采血,利用时间分辨荧光免疫分析法测定血清AFP、Freeβ-HCG和u E3。结合年龄、体重、孕周等因素,通过Life Cycle风险评估软件估算风险值,筛选高风险孕妇,并对其妊娠结局进行随访。结果 21 234例孕妇中,高风险1266例,筛查阳性率5.96%。不同年龄、体重、孕周分布,筛查阳性率不尽相同。随访15 486例孕妇,发现240例不良妊娠结局。结论 孕中期三联筛查结果受年龄、体重、孕周因素影响。结合产前诊断和随访观察,可有效降低吉林地区缺陷胎儿出生率。
Objective: Analyze retrospectively clinical applications of 21 234 cases pregnancies of second-trimester triple-marker screening in Jilin area during 2010-2013. Methods: Serum samples were collected during second trimester (15-20+Sweeks) and triple markers (AFP, Free β-HCG and uE3) were determined by time-resolved fluoroimmunoassay method. In combination with maternal age, weight and gestational weeks et al, we evaluated the risk with assessment software to select high-risk pregnancies. Results: There are 1266 cases high-risk pregnancies in 21 234 cases pregnancies and the positive rate of screening is 5.96%. The positive rates of screening are different in various groups of maternal age, weight, gestational weeks. There are 240 cases adverse obstetrical outcomes through follow-up visit of 15 486 pregnancies. Conclusion: Second-trimester triple-marker screening (AFP+Free I3-HCG+uE3) is an effective approach to predict abnormal fetuses, which is affected by age, weight, gestational weeks. In combination with follow-up visits and prenatal diagnosis, the screening can reduce birth defects in Jilin area.
出处
《中国优生与遗传杂志》
2015年第6期68-69,123,共3页
Chinese Journal of Birth Health & Heredity
基金
吉林省发改委产业技术研究与开发项目(2011007-12)
关键词
出生缺陷
唐氏综合征
产前筛查
随访
Birth Defects
Downs s syndrome
Prenatal Screening
Follow-Up Studies