Abstract

ObjectiveTo compare costs and efficacy of reflex and recall prenatal DNA screening for trisomy 21, 18 and 13 (affected pregnancies). In both methods women have Combined test markers measured. With recall screening, women with a high Combined test risk are recalled for counselling and offered a DNA blood test or invasive diagnostic testing. With reflex screening, a DNA analysis is automatically performed on plasma collected when blood was collected for measurement of the Combined test markers.MethodsPublished data were used to estimate, for each method, using various unit costs and risk cut-offs, the cost per woman screened, cost per affected pregnancy diagnosed, and for a given number of women screened, numbers of affected pregnancies diagnosed, unaffected pregnancies with positive results, and women with unaffected pregnancies having invasive diagnostic testing.ResultsCost per woman screened is lower with reflex v recall screening: £37 v £38, and £11,043 v £11,178 per affected pregnancy diagnosed (DNA £250, Combined test markers risk cut-off 1 in 150). Reflex screening results in similar numbers of affected pregnancies diagnosed, with 100-fold fewer false-positives and 20-fold fewer women with unaffected pregnancies having invasive diagnostic testing.ConclusionsReflex DNA screening is less expensive, more cost-effective, and safer than recall screening.

Highlights

  • ObjectiveTo compare costs and efficacy of reflex and recall prenatal DNA screening for trisomy 21, 18 and 13 (affected pregnancies)

  • Prenatal screening for trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), and trisomy 13 (Patau syndrome) using plasma DNA analysis detects most affected pregnancies with a much lower positive rate compared with conventional screening methods based on the measurement of ultrasound and serum markers.[1,2]

  • The recall method has a detection rate similar to that of conventional screening. [5,6] In one study [5] about 18% of women with a positive Combined test were sufficiently worried by their Combined test risk to choose an invasive diagnostic test without having a DNA test first

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Summary

Objective

To compare costs and efficacy of reflex and recall prenatal DNA screening for trisomy 21, 18 and 13 (affected pregnancies). In both methods women have Combined test markers measured. Women with a high Combined test risk are recalled for counselling and offered a DNA blood test or invasive diagnostic testing. A DNA analysis is automatically performed on plasma collected when blood was collected for measurement of the Combined test markers

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