Contingent screening for Down syndrome is an efficient alternative to non-disclosure sequential screening

Prenat Diagn. 2004 Oct;24(10):762-6. doi: 10.1002/pd.974.

Abstract

Objective: To present a first and second trimester Down syndrome screening strategy, whereby second-trimester marker determination is contingent on the first-trimester results. Unlike non-disclosure sequential screening ('the Integrated test'), which requires all women to have markers in both trimesters, this allows a large proportion of the women to complete screening in the first trimester.

Methods: Two first-trimester risk cut-offs defined three types of results: positive and referred for early diagnosis; negative with screening complete; and intermediate, needing second-trimester markers. Multivariate Gaussian modelling with Monte Carlo simulation was used to estimate the false-positive rate for a fixed 85% detection rate. The false-positive rate was evaluated for various early detection rates and early test completion rates. Model parameters were taken from the SURUSS trial.

Results: Completion of screening in the first trimester for 75% of women resulted in a 30% early detection rate and a 55% second trimester detected rate (net 85%) with a false-positive rate only 0.1% above that achievable by the Integrated test. The screen-positive rate was 0.1% in the first trimester and 4.7% for those continuing to be tested in the second trimester. If the early detection rate were to be increased to 45% or the early completion rate were to be increased to 80%, there would be a further 0.1% increase in the false-positive rate.

Conclusion: Contingent screening can achieve results comparable with the Integrated test but with earlier completion of screening for most women. Both strategies need to be evaluated in large-scale prospective studies particularly in relation to psychological impact and practicability.

MeSH terms

  • Biomarkers / analysis
  • Down Syndrome / diagnosis*
  • Down Syndrome / embryology
  • False Positive Reactions
  • Female
  • Fetal Diseases / diagnosis*
  • Fetal Diseases / embryology
  • Humans
  • Mass Screening / methods*
  • Models, Biological
  • Monte Carlo Method
  • Normal Distribution
  • Predictive Value of Tests
  • Pregnancy
  • Pregnancy Trimester, First
  • Pregnancy Trimester, Second
  • Prenatal Diagnosis / methods*
  • Prospective Studies
  • Risk Factors

Substances

  • Biomarkers