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Prospective study of prenatal screening for Downs syndrome with free beta human chorionic gonadotrophin.

机译:用游离β人绒毛膜促性腺激素对唐氏综合征进行产前筛查的前瞻性研究。

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摘要

OBJECTIVE--To assess the value and impact of a screening programme for Down's syndrome that uses the two maternal serum markers: alpha fetoprotein and free beta human chorionic gonadotrophin. DESIGN--All women booked into clinics were screened. Further tests were offered to women with a risk of one in 300 or greater of having an affected baby. Follow up of outcome of all pregnancies. SETTING--Biochemical screening laboratory serving two health districts. SUBJECTS--8179 women of all ages with singleton pregnancies screened between 15 and 22 weeks' gestation from 1 April 1991 to 31 March 1992. MAIN OUTCOME MEASURES--Detection rate of Down's syndrome, false positive rate, uptake of screening, uptake of amniocentesis in women identified as at increased risk, prevalence of Down's syndrome at birth. RESULTS--Overall 89% (8317/9345) of women underwent screening. The rate of detection of Down's syndrome was 69% (11/16; 95% confidence interval 41 to 89%) with a 5.2% false positive rate (426/179; 4.7 to 5.7%). In women under 30 the detection rate was 50% (four out of eight; 32 to 86%) Uptake of amniocentesis was 89% (389/437), resulting in a reduction of prevalence of Down's syndrome at birth from 1.1 per 1000 in previous years (66/59,696) to 0.4 per 1000 during the screening year (4/9345). Additionally, several other abnormalities were identified. CONCLUSION--The benefit of a high detection rate with this approach and the additional anomalies identified should encourage others to introduce screening programmes for Down's syndrome that use free beta human chorionic gonadotrophin and alpha fetoprotein.
机译:目的-评估唐氏综合症筛查程序的价值和影响,该筛查程序使用两种母体血清标志物:甲胎蛋白和游离β人绒毛膜促性腺激素。设计-对所有进入诊所的女性进行筛查。对于患患病婴儿的风险大于或等于300的妇女,提供了进一步的测试。跟进所有怀孕的结果。地点-为两个卫生区服务的生化筛查实验室。主题--8179,从1991年4月1日至1992年3月31日,在15至22周的妊娠中对所有年龄的单胎妊娠妇女进行了筛查。主要观察指标-唐氏综合症的检测率,假阳性率,筛查的摄取,羊膜穿刺的摄取。在被确定为患病风险增加的妇女中,唐氏综合症在出生时的患病率较高。结果-共有89%(8317/9345)妇女接受了筛查。唐氏综合症的检出率为69%(11/16; 95%置信区间41至89%),假阳性率为5.2%(426/179; 4.7至5.7%)。在30岁以下的女性中,检出率为50%(八分之四; 32%至86%),羊膜穿刺术的摄取率为89%(389/437),从而使唐氏综合症的患病率从以前的每1000例降低到1.1例。年(66 / 59,696)至筛选年(4/9345)中的每1000个0.4。此外,还发现了其他几种异常情况。结论-这种方法具有较高检测率的优势以及发现的其他异常现象应鼓励其他人引入唐氏综合症的筛查程序,该程序使用游离的β人绒毛膜促性腺激素和甲胎蛋白。

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