Suppr超能文献

孕中期使用甲胎蛋白、人绒毛膜促性腺激素和游离雌三醇进行母体血清筛查:一项区域计划的经验。

Second-trimester maternal serum screening using alpha-fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: experience of a regional programme.

作者信息

Goodburn S F, Yates J R, Raggatt P R, Carr C, Ferguson-Smith M E, Kershaw A J, Milton P J, Ferguson-Smith M A

机构信息

Department of Clinical Genetics, Addenbrooke's Hospital, Cambridge, U.K.

出版信息

Prenat Diagn. 1994 May;14(5):391-402. doi: 10.1002/pd.1970140509.

Abstract

Over a 2-year period from January 1991 to December 1992, second-trimester maternal serum screening for Down's syndrome using alpha-fetoprotein (alpha FP), human chorionic gonadotrophin (hCG), and unconjugated oestriol (uE3) was made available to five health districts in East Anglia, with a total population of 1.2 million. Amniocentesis was offered when the risk of Down's syndrome at term was 1:200 or greater. 25,359 singleton pregnancies were screened, representing an uptake of 77 per cent. The recall rate for the 24 per cent of women who had not had a dating scan prior to the test was 9.4 per cent compared with 3.9 per cent for those who had been scanned (P < 0.0005). Seventy-five per cent (36/48) of Down's syndrome pregnancies were detected for a false-positive rate of 4.0 per cent. Twenty-five out of 36 of detected Down's syndrome pregnancies were dated by scan prior to sampling, and in the 11 remaining cases, the dates were confirmed by scan after a high-risk result was obtained. The exclusion of uE3 from the screening protocol would have reduced the detection rate to 52 per cent (25/48) for the same false-positive rate. Eighty-five per cent of women identified at high risk accepted the offer of an amniocentesis. Other fetal abnormalities detected were trisomy 18 (3), trisomy 13 (2), 45,X (6), 69,XXX (5), other chromosome abnormalities (9), open neural tube defects (26), hydrocephalus (7), abdominal wall defects (4), and steroid sulphatase deficiency (6).

摘要

在1991年1月至1992年12月的两年期间,东盎格利亚的五个卫生区为120万总人口提供了孕中期唐氏综合征母体血清筛查,检测指标包括甲胎蛋白(αFP)、人绒毛膜促性腺激素(hCG)和未结合雌三醇(uE3)。当足月时唐氏综合征风险为1:200或更高时,会建议进行羊膜穿刺术。对25359例单胎妊娠进行了筛查,接受率为77%。检测前未进行孕周扫描的24%的女性召回率为9.4%,而进行过扫描的女性召回率为3.9%(P<0.0005)。75%(36/48)的唐氏综合征妊娠被检测出,假阳性率为4.0%。36例被检测出的唐氏综合征妊娠中有25例在采样前通过扫描确定了孕周,其余11例在获得高危结果后通过扫描确认了孕周。在相同假阳性率的情况下,从筛查方案中排除uE3会使检测率降至52%(25/48)。85%被确定为高危的女性接受了羊膜穿刺术的建议。检测出的其他胎儿异常包括18三体(3例)、13三体(2例)、45,X(6例)、69,XXX(5例)、其他染色体异常(9例)、开放性神经管缺陷(26例)、脑积水(7例)、腹壁缺陷(4例)和类固醇硫酸酯酶缺乏症(6例)。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验