A decade of non-invasive prenatal screening in Australia: National impact on prenatal screening and diagnostic testing

被引:2
|
作者
Hui, Lisa [1 ,2 ,3 ,4 ,6 ]
Halliday, Jane [1 ,5 ]
机构
[1] Murdoch Childrens Res Inst, Reprod Epidemiol Grp, Melbourne, Vic, Australia
[2] Univ Melbourne, Dept Obstet & Gynaecol, Melbourne, Vic, Australia
[3] Mercy Hosp Women, Dept Perinatal Med, Melbourne, Vic, Australia
[4] Northern Hlth, Dept Obstet & Gynaecol, Melbourne, Vic, Australia
[5] Univ Melbourne, Dept Paediat, Melbourne, Vic, Australia
[6] Mercy Hosp Women, 163 Studley Rd, Melbourne, Vic 3084, Australia
基金
英国医学研究理事会;
关键词
aneuploidy; Down syndrome; obstetrics; pregnancy; prenatal diagnosis; prenatal screening; serum screening; ANEUPLOIDY; ASSOCIATION;
D O I
10.1111/ajo.13638
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Prenatal screening for aneuploidy has undergone immense changes over the past two decades. In 2013 cell-free DNA-based non-invasive prenatal testing (NIPT) became a new self-funded option primarily for Down syndrome screening, but also other aneuploidies and genetic conditions. The numbers of Medicare item claims for prenatal diagnostic procedures have halved since the introduction of NIPT, while billings for serum screening fell by 40% over the same period, on a background of steady births. Australia is now observing historically low rates of prenatal diagnostic testing. These data provide an informative snapshot of historic changes in prenatal screening and diagnosis, as our sector prepares for the impending impacts of other advances in genomics on maternity care. They also highlight the need to address equity and quality issues that arise when consumers must bear the full costs of improved genomic tests in the absence of Medicare funding.
引用
收藏
页码:264 / 267
页数:4
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