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2.1 Estimation of detection rates of aneuploidy using an approach based on nuchal translucency and non-invasive prenatal testing (NIPT)
  1. A Khalil1,
  2. N Mahmoodian1,
  3. A Kulkarni2,
  4. T Homfray2,
  5. A Papageorghiou1,
  6. A Bhide1,
  7. B Thilaganathan1
  1. 1Fetal Medicine Unit, St George’s University of London, London, UK
  2. 2Department of Clinical Genetics, St George’s, University of London, London, UK


Objectives To investigate the detection rates of aneuploidy using nuchal translucency (NT) and non-invasive prenatal testing (NIPT).

Methods A retrospective cohort study including 5306 pregnancies that underwent chorionic villus sampling (CVS) for full karyotyping after fetal NT measurement at 11+0–13+6 weeks of gestation. All abnormal karyotypes were reviewed by a clinical geneticist and grouped according to whether the chromosome anomaly would be detectable by NIPT and whether it might be clinically significant.

Results The fetal karyotype was normal in 4172 (78.6%) and abnormal in 1134 (21.4%), including 1009 likely to result in clinically significant adverse outcome. Universal CVS with full karyotyping would lead to the diagnosis of all clinically significant abnormalities. A policy of NIPT only in all of these cases would have led to the diagnosis of 88.9% of clinically significant abnormalities. A strategy whereby NIPT is the main method of analysis for increased combined screening risk, with invasive testing reserved for those with NT thickness ≥3.0 mm, would require CVS in 20.1%, identify 94.8% of significant abnormalities and avoid miscarriage in 42 (79.2%) pregnancies compared to CVS for all. With a current UK price for NIPT of £400 and the need to confirm abnormal results by CVS, the cost of the three policies would be £2.0 m, £2.5 m and £2.2 m, respectively.

Conclusions A policy of NIPT for increased first trimester aneuploidy risk and CVS with full karyotype only for fetal NT thickness ≥3.0 mm would reduce the risk of procedure-related miscarriage five-fold, yet identify 95% of clinically significant chromosomal abnormalities.

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