Spencer K, Carpenter P
Department of Clinical Biochemistry, Oldchurch Hospital, Romford, Essex.
BMJ. 1993 Sep 25;307(6907):764-9. doi: 10.1136/bmj.307.6907.764.
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.
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.
Biochemical screening laboratory serving two health districts.
8179 women of all ages with singleton pregnancies screened between 15 and 22 weeks' gestation from 1 April 1991 to 31 March 1992.
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.
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.
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.
评估一项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)进行唐氏综合征筛查计划的价值和影响。
对所有预约到诊所的妇女进行筛查。对怀有患病婴儿风险为三百分之一或更高的妇女提供进一步检测。对所有妊娠结局进行随访。
为两个健康区服务的生化筛查实验室。
1991年4月1日至1992年3月31日期间,8179名年龄各异的单胎妊娠妇女在妊娠15至22周时接受了筛查。
唐氏综合征的检出率、假阳性率、筛查接受率、被确定为高危的妇女接受羊膜穿刺术的比例、出生时唐氏综合征的患病率。
总体而言,89%(8317/9345)的妇女接受了筛查。唐氏综合征的检出率为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%)。30岁以下妇女的检出率为50%(8例中的4例;32%至86%)。羊膜穿刺术的接受率为89%(389/437),导致出生时唐氏综合征的患病率从前几年的每1000人中有1.1例(66/59,696)降至筛查年度的每1000人中有0.4例(4/9345)。此外,还发现了其他几种异常情况。
这种方法具有高检出率以及发现其他异常情况的益处,应促使其他机构推行使用游离β人绒毛膜促性腺激素和甲胎蛋白的唐氏综合征筛查计划。