Strategies for Implementing Cell-Free DNA Testing

被引:2
作者
Cuckle, Howard [1 ,2 ,3 ]
机构
[1] Hy Labs Ltd, Venadis Diagnost AB, PerkinElmer Inc, Rehovot, Israel
[2] Genome Ltd, Hyderabad, Andhra Pradesh, India
[3] Columbia Univ, Med Ctr, Dept Obstet & Gynecol, 622 West 168th St, New York, NY 10032 USA
关键词
cfDNA; Aneuploidy; Screening; Prenatal; Maternal plasma; MATERNAL PLASMA DNA; NONINVASIVE PRENATAL DETECTION; FETAL ANEUPLOIDY DETECTION; DOWN-SYNDROME; NUCHAL TRANSLUCENCY; CHROMOSOMES; 13; TRISOMIES; 21; BLOOD; PERFORMANCE; PREGNANCIES;
D O I
10.1016/j.cll.2016.01.010
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Maternal plasma cell-free (cf) DNA testing has higher discriminatory power for aneuploidy than any conventional multi-marker screening test. Several strategies have been suggested for introducing it into clinical practice. Secondary cfDNA, restricted only to women with positive conventional screening test, is generally cost saving and minimizes the need for invasive prenatal diagnosis but leads to a small loss in detection. Primary cfDNA, replacing conventional screening or retaining the nuchal translucency scan, is not currently cost-effective for third-party payers. Contingent cfDNA, testing about 20% of women with the highest risks based on a conventional test, is the preferred approach.
引用
收藏
页码:213 / +
页数:15
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