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吉林地区21234例孕中期三联筛查病例及随访分析

Retrospective analysis of 21234 cases pregnancies of second-trimester triple-marker screening in Jilin area
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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
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  • 1张斌,张月萍,张彬,李笑天.高龄孕妇唐氏综合征血清学筛查的价值[J].中国产前诊断杂志(电子版),2010,2(4):9-11. 被引量:7
  • 2王斌,陈英耀,石琦,张洁,李军,钱序,朱怡蓓.我国唐氏综合征的疾病经济负担研究[J].中国卫生经济,2006,25(3):24-26. 被引量:90
  • 3庞振凌,刘红霞,王晓然.171例唐氏综合征患者的细胞遗传学分析[J].中国优生与遗传杂志,2006,14(4):53-54. 被引量:20
  • 4王雪方,施云凤.杭州地区8516例孕中期妇女产前筛查回顾性分析[J].中国优生与遗传杂志,2006,14(7):51-52. 被引量:20
  • 5世界出生缺陷预防机构联盟宣言[J].中华医学遗传学杂志,1995,12(1):53-53.
  • 6Wald N J, Watt HC, Hackshaw AK, et al. First and second trimester antenatal Screening for Down' s syndrome: the results of the Serum, Urine and Ultrasound Screening Study (SURUSS) [ J ]. Health Techol Assess, 2003, 7:1 - 77.
  • 7Boaz W, Charles HR. An update on antenatal screening for Down' s syndrome and specific implications for assisted reproduction pregnan- cies[J]. Human Reproduction Update, 2006, 12(5):513 -518.
  • 8Walg N J, Watt HC, Hackshaw AK, et al. First and second trimester antenatal screening for Down, s syndrome : the results of the serum, unine and Ultrasound Screening Study (SURUSS) [ J]. Health Techol Assess ,2003,7: 12771.
  • 9刘权章.临床遗传学彩色图谱[M]北京:人民卫生出版社,2006200.
  • 10李璞.医学遗传学[M]重庆:重庆大学出版社,2006171.

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