Comparison of different strategies in prenatal screening for Down's syndrome: Cost effectiveness analysis of computer simulation

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Abstract

Objectives: To assess and compare the cost effectiveness of three different strategies for prenatal screening for Down's syndrome (integrated test, sequential screening, and contingent screenings) and to determine the most useful cut-off values for risk. Design: Computer simulations to study integrated, sequential, and contingent screening strategies with various cut-offs leading to 19 potential screening algorithms. Data sources: The computer simulation was populated with data from the Serum Urine and Ultrasound Screening Study (SURUSS), real unit costs for healthcare interventions, and a population of 110 948 pregnancies from the province of Québec for the year 2001. Main outcome measures: Cost effectiveness ratios, incremental cost effectiveness ratios, and screening options' outcomes. Results: The contingent screening strategy dominated all other screening options: it had the best cost effectiveness ratio ($C26 833 per case of Down's syndrome) with fewer procedure related euploid miscarriages and unnecessary terminations (respectively, 6 and 16 per 100 000 pregnancies). It also outperformed serum screening at the second trimester. In terms of the incremental cost effectiveness ratio, contingent screening was still dominant: compared with screening based on maternal age alone, the savings were $C30 963 per additional birth with Down's syndrome averted. Contingent screening was the only screening strategy that offered early reassurance to the majority of women (77.81%) in first trimester and minimised costs by limiting retesting during the second trimester (21.05%). For the contingent and sequential screening strategies, the choice of cut-off value for risk in the first trimester test significantly affected the cost effectiveness ratios (respectively, from $C26 833 to $C37 260 and from $C35 215 to $C45 314 per case of Down's syndrome), the number of procedure related euploid miscarriages (from 6 to 46 and from 6 to 45 per 100 000 pregnancies), and the number of unnecessary terminations (from 16 to 26 and from 16 to 25 per 100 000 pregnancies). Conclusions: Contingent screening, with a first trimester cut-off value for high risk of 1 in 9, is the preferred option for prenatal screening of women for pregnancies affected by Down's syndrome.

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Gekas, J., Gagné, G., Bujold, E., Douillard, D., Forest, J. C., Reinharz, D., & Rousseau, F. (2009). Comparison of different strategies in prenatal screening for Down’s syndrome: Cost effectiveness analysis of computer simulation. BMJ (Online), 338(7692), 453–456. https://doi.org/10.1136/bmj.b138

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