2012•Chinese Journal of Birth Health & HeredityRequires access

Evaluation of clinical findings on 10 063 prognance women for second-trimester antenatal screening in Lanzhou

JI Wei-li

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Abstract

Objective: To investigate the clinic value of screening chromosomal diseases and abnormal pregnancy by maternal serum examination during second trimester of pregnancy.Methods: Auto-DELFLA are used to test the concentrations of AFP and free β-HCG in the serum of mid-pregnant women,then the results were analyzed with 2T Risk calculator and managing software to determine the fetal risk of DS and NTD,considering weight,maternal age,gestational week,etc.Results: of the 10,063 pregnant women undergoing antenatal screening,327(3.25%) were considered as high risk of DS,45(0.45%)cases suggest trisomy-18,277(2.75%) cases are NTD.315 of the high-risk cases underwent amino fluid examination,of which 9 were diagnosed DS,3 were trisomy-18 and 4 were other chromosome abnormities.By B ultrasonic,69 were diagnosed NTD.Conclusions: This study suggests that complementary measures,such as routine antenatal US,maternal serum screening and antenatal diagnosis,have important values in predicting fetal chromosomal diseases and help reduce the birth defect rate.

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Objective: To investigate the clinic value of screening chromosomal diseases and abnormal pregnancy by maternal serum examination during second trimester of pregnancy.Methods: Auto-DELFLA are used to test the concentrations of AFP and free β-HCG in the serum of mid-pregnant women,then the results were analyzed with 2T Risk calculator and managing software to determine the fetal risk of DS and NTD,considering weight,maternal age,gestational week,etc.Results: of the 10,063 pregnant women undergoing antenatal screening,327(3.25%) were considered as high risk of DS,45(0.45%)cases suggest trisomy-18,277(2.75%) cases are NTD.315 of the high-risk cases underwent amino fluid examination,of which 9 were diagnosed DS,3 were trisomy-18 and 4 were other chromosome abnormities.By B ultrasonic,69 were diagnosed NTD.Conclusions: This study suggests that complementary measures,such as routine antenatal US,maternal serum screening and antenatal diagnosis,have important values in predicting fetal chromosomal diseases and help reduce the birth defect rate.

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Available abstract

Objective: To investigate the clinic value of screening chromosomal diseases and abnormal pregnancy by maternal serum examination during second trimester of pregnancy.Methods: Auto-DELFLA are used to test the concentrations of AFP and free β-HCG in the serum of mid-pregnant women,then the results were analyzed with 2T Risk calculator and managing software to determine the fetal risk of DS and NTD,considering weight,maternal age,gestational week,etc.Results: of the 10,063 pregnant women undergoing antenatal screening,327(3.25%) were considered as high risk of DS,45(0.45%)cases suggest trisomy-18,277(2.75%) cases are NTD.315 of the high-risk cases underwent amino fluid examination,of which 9 were diagnosed DS,3 were trisomy-18 and 4 were other chromosome abnormities.By B ultrasonic,69 were diagnosed NTD.Conclusions: This study suggests that complementary measures,such as routine antenatal US,maternal serum screening and antenatal diagnosis,have important values in predicting fetal chromosomal diseases and help reduce the birth defect rate.

Key concepts: Medicine, Trisomy, Obstetrics, Pregnancy, Fetus, Advanced maternal age, Second trimester, Down syndrome

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