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The application of amniocytes culture for the detection of Down syndrome (DS) is not recommended for neonatal screening due to the potential harms of invasive procedure. Therefore, a novel non-invasive method using cell-free fetal DNA in maternal plasma has been developed. Thus, our aim is to compare the performance of the cytogenetic analysis (CA) with the novel method in identifying fetuses with DS. The data on all 10,940 pregnant women delivering at Siriraj Hospital between November 2011 and December 2014 was retrospectively analyzed. Out of those 10,940 samples, 209 fetuses were confirmed as trisomy 21, of which 179 were confirmed by CA, but 14 were missed by the CA. The sensitivity of CA for detection of DS is 99.9% (95% confidence interval; CI 95.6-99.9), while that of the novel method is 97.7% (CI 95.5-99.1). Since the specificity of the novel method is lower than that of CA (37.8% vs. 100%), the negative predictive value of the novel method is very low (4.6%). In conclusion, this novel screening method is not recommended for the screening of DS, because of its lower specificity and positive predictive value.Marks, Scars

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