Literature DB >> 26259499

National decline in invasive prenatal diagnostic procedures in association with uptake of combined first trimester and cell-free DNA aneuploidy screening.

Stephen J Robson1, Lisa Hui2,3,4.   

Abstract

In late 2012, a new screening test for fetal aneuploidy based on circulating cell-free DNA (cfDNA) became available to Australian women. The introduction of this technology in the United States has led to a reduction in invasive diagnostic procedures. Analysis of the number of amniocentesis and chorionic villus sampling (CVS) procedures performed in Australia from 1994 to 2014 shows that the introduction of cfDNA testing has been associated with the most rapid decline in invasive procedures in the last 20 years. This change has important implications for training in, and maintenance of, the procedural skills of amniocentesis and CVS.
© 2015 The Royal Australian and New Zealand College of Obstetricians and Gynaecologists.

Entities:  

Keywords:  amniocentesis; cell-free DNA; chorionic villus sampling; noninvasive prenatal testing; population; prenatal testing

Mesh:

Substances:

Year:  2015        PMID: 26259499     DOI: 10.1111/ajo.12380

Source DB:  PubMed          Journal:  Aust N Z J Obstet Gynaecol        ISSN: 0004-8666            Impact factor:   2.100


  8 in total

Review 1.  Screening for fetal chromosomal and subchromosomal disorders.

Authors:  Sarah Harris; Dallas Reed; Neeta L Vora
Journal:  Semin Fetal Neonatal Med       Date:  2017-11-08       Impact factor: 3.926

2.  Comparison of indications and results of prenatal invasive diagnostic tests before and after the implementation of the use of cell-free fetal DNA: a tertiary referral center experience.

Authors:  Firat Okmen; Huseyin Ekici; Ismet Hortu; Metehan Imamoglu; Duygu Arican; Haluk Akın; Sermet Sagol
Journal:  J Assist Reprod Genet       Date:  2020-05-21       Impact factor: 3.412

3.  Trends in the use of prenatal testing services for fetal aneuploidy in Ontario: a descriptive study.

Authors:  Tianhua Huang; Shelley Dougan; Mark Walker; Christine M Armour; Nan Okun
Journal:  CMAJ Open       Date:  2018-10-05

4.  In-house genetic counseling increases the detection of abnormal karyotypes-a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland.

Authors:  Julia Bijok; Anna Kucińska-Chahwan; Diana Massalska; Alicja Ilnicka; Grzegorz Panek; Tomasz Roszkowski
Journal:  J Assist Reprod Genet       Date:  2020-05-19       Impact factor: 3.412

5.  Implementation of cell-free DNA-based non-invasive prenatal testing in a National Health Service Regional Genetics Laboratory.

Authors:  Fiona S Togneri; Mark D Kilby; Elizabeth Young; Samantha Court; Denise Williams; Michael J Griffiths; Stephanie K Allen
Journal:  Genet Res (Camb)       Date:  2019-12-09       Impact factor: 1.588

6.  'Small cost to pay for peace of mind': Women's experiences with non-invasive prenatal testing.

Authors:  Hilary Bowman-Smart; Julian Savulescu; Cara Mand; Christopher Gyngell; Mark D Pertile; Sharon Lewis; Martin B Delatycki
Journal:  Aust N Z J Obstet Gynaecol       Date:  2019-02-06       Impact factor: 2.100

7.  Population-based impact of noninvasive prenatal screening on screening and diagnostic testing for fetal aneuploidy.

Authors:  Lisa Hui; Briohny Hutchinson; Alice Poulton; Jane Halliday
Journal:  Genet Med       Date:  2017-05-18       Impact factor: 8.822

Review 8.  Has noninvasive prenatal testing impacted termination of pregnancy and live birth rates of infants with Down syndrome?

Authors:  Melissa Hill; Angela Barrett; Mahesh Choolani; Celine Lewis; Jane Fisher; Lyn S Chitty
Journal:  Prenat Diagn       Date:  2017-12       Impact factor: 3.050

  8 in total

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