胎儿游离DNA
医学
产前诊断
怀孕
流产
先天性肾上腺增生
产科
置信区间
胎儿
内科学
遗传学
生物
作者
Melissa Hill,S Taffinder,Lyn S. Chitty,Stephen Morris
摘要
Abstract Objectives Fetal sex determination is performed for women who carry X‐linked conditions, for example Duchenne muscular dystrophy (DMD), or those associated with ambiguous genitalia, for example congenital adrenal hyperplasia (CAH). Non‐invasive prenatal diagnosis (NIPD) using cell‐free fetal DNA (cffDNA) in maternal plasma is an alternative to invasive prenatal diagnosis (IPD), which carries a 1% risk of miscarriage. This study aimed to evaluate the incremental cost of NIPD compared with IPD of fetal sex. Methods Diagnostic accuracy, invasive testing rate, and pregnancy outcome following NIPD were ascertained from an audit of all cases referred to two laboratories in 2006 to 2009. Care pathways for DMD and CAH were established and key cost drivers for IPD and NIPD identified using costs derived from published estimates and local laboratory values. Results The differences in mean costs per pregnancy for NIPD versus IPD were small for DMD [mean difference − £87, 95% confidence interval (CI) − £303 to £131] and CAH (−£193, 95% CI − £301 to − £84). Testing costs associated with NIPD were offset by fewer women requiring invasive testing. Conclusions The costs of NIPD and IPD of fetal sex are similar. NIPD can provide benefits for many women by avoiding the risks of invasive testing, without incurring additional costs. Copyright © 2011 John Wiley & Sons, Ltd.
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