Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6240744 | Journal of Cystic Fibrosis | 2013 | 8 Pages |
BackgroundSwitzerland introduced newborn screening (NBS) for CF in 2011, using an IRT/DNA/IRT protocol. This paper describes the results of the first year and compares two versions of the protocol with different IRT cut-offs, particularly effects on recall rate, sensitivity and specificity.MethodsIRT cut-offs were > 45 ng/ml (99.0th percentile) in period 1 (months 1-4) and > 50 ng/ml (99.2nd percentile) in period 2 (months 5-12). In period 2 we abstained from recalls when none of the 7 most common CF mutations were detected and IRT was < 60 ng/ml.ResultsIn periods 1 and 2, 26,535 and 56,663 tests were performed. Recall rates were 0.94% and 0.48%, respectively (p < 0.001), PPV increased from 23% to 47% (p = 0.024) and sensitivity was 90% and 100%.ConclusionsRaising initial IRT cut-off from the 99.0th to the 99.2nd percentile and abstaining from recalls for children with an IRT < 60 ng/ml and carrying no major CFTR mutation significantly reduced the recall rate without affecting sensitivity.