The price of performance: a cost and performance analysis of the implementation of cell-free fetal DNA testing for Down syndrome in Ontario, Canada

ABSTRACT Objective To examine the cost and performance implications of introducing cell‐free fetal DNA (cffDNA) testing within modeled scenarios in a publicly funded Canadian provincial Down syndrome (DS) prenatal screening program. Method Two clinical algorithms were created: the first to represent...

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Veröffentlicht in:Prenatal diagnosis 2014-04, Vol.34 (4), p.350-356
Hauptverfasser: Okun, N., Teitelbaum, M., Huang, T., Dewa, C. S., Hoch, J. S.
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container_end_page 356
container_issue 4
container_start_page 350
container_title Prenatal diagnosis
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creator Okun, N.
Teitelbaum, M.
Huang, T.
Dewa, C. S.
Hoch, J. S.
description ABSTRACT Objective To examine the cost and performance implications of introducing cell‐free fetal DNA (cffDNA) testing within modeled scenarios in a publicly funded Canadian provincial Down syndrome (DS) prenatal screening program. Method Two clinical algorithms were created: the first to represent the current screening program and the second to represent one that incorporates cffDNA testing. From these algorithms, eight distinct scenarios were modeled to examine: (1) the current program (no cffDNA), (2) the current program with first trimester screening (FTS) as the nuchal translucency‐based primary screen (no cffDNA), (3) a program substituting current screening with primary cffDNA, (4) contingent cffDNA with current FTS performance, (5) contingent cffDNA at a fixed price to result in overall cost neutrality,(6) contingent cffDNA with an improved detection rate (DR) of FTS, (7) contingent cffDNA with higher uptake of FTS, and (8) contingent cffDNA with optimized FTS (higher uptake and improved DR). Results This modeling study demonstrates that introducing contingent cffDNA testing improves performance by increasing the number of cases of DS detected prenatally, and reducing the number of amniocenteses performed and concomitant iatrogenic pregnancy loss of pregnancies not affected by DS. Costs are modestly increased, although the cost per case of DS detected is decreased with contingent cffDNA testing. Conclusion Contingent models of cffDNA testing can improve overall screening performance while maintaining the provision of an 11‐ to 13‐week scan. Costs are modestly increased, but cost per prenatally detected case of DS is decreased. © 2013 John Wiley & Sons, Ltd. What's already known about this topic? Cell‐free fetal DNA testing has been validated scientifically in the high‐risk population. Other cost analyses have documented potential cost savings via reductions in diagnostic tests required. What does this study add? This study provides a detailed analysis of both cost and performance implications of several potential implementation scenarios of cell‐free fetal DNA testing in a population‐based prenatal screening program.
doi_str_mv 10.1002/pd.4311
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S. ; Hoch, J. S.</creator><creatorcontrib>Okun, N. ; Teitelbaum, M. ; Huang, T. ; Dewa, C. S. ; Hoch, J. S.</creatorcontrib><description>ABSTRACT Objective To examine the cost and performance implications of introducing cell‐free fetal DNA (cffDNA) testing within modeled scenarios in a publicly funded Canadian provincial Down syndrome (DS) prenatal screening program. Method Two clinical algorithms were created: the first to represent the current screening program and the second to represent one that incorporates cffDNA testing. From these algorithms, eight distinct scenarios were modeled to examine: (1) the current program (no cffDNA), (2) the current program with first trimester screening (FTS) as the nuchal translucency‐based primary screen (no cffDNA), (3) a program substituting current screening with primary cffDNA, (4) contingent cffDNA with current FTS performance, (5) contingent cffDNA at a fixed price to result in overall cost neutrality,(6) contingent cffDNA with an improved detection rate (DR) of FTS, (7) contingent cffDNA with higher uptake of FTS, and (8) contingent cffDNA with optimized FTS (higher uptake and improved DR). Results This modeling study demonstrates that introducing contingent cffDNA testing improves performance by increasing the number of cases of DS detected prenatally, and reducing the number of amniocenteses performed and concomitant iatrogenic pregnancy loss of pregnancies not affected by DS. Costs are modestly increased, although the cost per case of DS detected is decreased with contingent cffDNA testing. Conclusion Contingent models of cffDNA testing can improve overall screening performance while maintaining the provision of an 11‐ to 13‐week scan. Costs are modestly increased, but cost per prenatally detected case of DS is decreased. © 2013 John Wiley &amp; Sons, Ltd. What's already known about this topic? Cell‐free fetal DNA testing has been validated scientifically in the high‐risk population. Other cost analyses have documented potential cost savings via reductions in diagnostic tests required. What does this study add? 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S.</creatorcontrib><creatorcontrib>Hoch, J. S.</creatorcontrib><title>The price of performance: a cost and performance analysis of the implementation of cell-free fetal DNA testing for Down syndrome in Ontario, Canada</title><title>Prenatal diagnosis</title><addtitle>Prenat Diagn</addtitle><description>ABSTRACT Objective To examine the cost and performance implications of introducing cell‐free fetal DNA (cffDNA) testing within modeled scenarios in a publicly funded Canadian provincial Down syndrome (DS) prenatal screening program. Method Two clinical algorithms were created: the first to represent the current screening program and the second to represent one that incorporates cffDNA testing. From these algorithms, eight distinct scenarios were modeled to examine: (1) the current program (no cffDNA), (2) the current program with first trimester screening (FTS) as the nuchal translucency‐based primary screen (no cffDNA), (3) a program substituting current screening with primary cffDNA, (4) contingent cffDNA with current FTS performance, (5) contingent cffDNA at a fixed price to result in overall cost neutrality,(6) contingent cffDNA with an improved detection rate (DR) of FTS, (7) contingent cffDNA with higher uptake of FTS, and (8) contingent cffDNA with optimized FTS (higher uptake and improved DR). Results This modeling study demonstrates that introducing contingent cffDNA testing improves performance by increasing the number of cases of DS detected prenatally, and reducing the number of amniocenteses performed and concomitant iatrogenic pregnancy loss of pregnancies not affected by DS. Costs are modestly increased, although the cost per case of DS detected is decreased with contingent cffDNA testing. Conclusion Contingent models of cffDNA testing can improve overall screening performance while maintaining the provision of an 11‐ to 13‐week scan. Costs are modestly increased, but cost per prenatally detected case of DS is decreased. © 2013 John Wiley &amp; Sons, Ltd. What's already known about this topic? Cell‐free fetal DNA testing has been validated scientifically in the high‐risk population. Other cost analyses have documented potential cost savings via reductions in diagnostic tests required. What does this study add? 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S.</creator><creator>Hoch, J. S.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201404</creationdate><title>The price of performance: a cost and performance analysis of the implementation of cell-free fetal DNA testing for Down syndrome in Ontario, Canada</title><author>Okun, N. ; Teitelbaum, M. ; Huang, T. ; Dewa, C. S. ; Hoch, J. 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S.</au><au>Hoch, J. S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The price of performance: a cost and performance analysis of the implementation of cell-free fetal DNA testing for Down syndrome in Ontario, Canada</atitle><jtitle>Prenatal diagnosis</jtitle><addtitle>Prenat Diagn</addtitle><date>2014-04</date><risdate>2014</risdate><volume>34</volume><issue>4</issue><spage>350</spage><epage>356</epage><pages>350-356</pages><issn>0197-3851</issn><eissn>1097-0223</eissn><abstract>ABSTRACT Objective To examine the cost and performance implications of introducing cell‐free fetal DNA (cffDNA) testing within modeled scenarios in a publicly funded Canadian provincial Down syndrome (DS) prenatal screening program. Method Two clinical algorithms were created: the first to represent the current screening program and the second to represent one that incorporates cffDNA testing. From these algorithms, eight distinct scenarios were modeled to examine: (1) the current program (no cffDNA), (2) the current program with first trimester screening (FTS) as the nuchal translucency‐based primary screen (no cffDNA), (3) a program substituting current screening with primary cffDNA, (4) contingent cffDNA with current FTS performance, (5) contingent cffDNA at a fixed price to result in overall cost neutrality,(6) contingent cffDNA with an improved detection rate (DR) of FTS, (7) contingent cffDNA with higher uptake of FTS, and (8) contingent cffDNA with optimized FTS (higher uptake and improved DR). Results This modeling study demonstrates that introducing contingent cffDNA testing improves performance by increasing the number of cases of DS detected prenatally, and reducing the number of amniocenteses performed and concomitant iatrogenic pregnancy loss of pregnancies not affected by DS. Costs are modestly increased, although the cost per case of DS detected is decreased with contingent cffDNA testing. Conclusion Contingent models of cffDNA testing can improve overall screening performance while maintaining the provision of an 11‐ to 13‐week scan. Costs are modestly increased, but cost per prenatally detected case of DS is decreased. © 2013 John Wiley &amp; Sons, Ltd. What's already known about this topic? Cell‐free fetal DNA testing has been validated scientifically in the high‐risk population. Other cost analyses have documented potential cost savings via reductions in diagnostic tests required. What does this study add? This study provides a detailed analysis of both cost and performance implications of several potential implementation scenarios of cell‐free fetal DNA testing in a population‐based prenatal screening program.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24395030</pmid><doi>10.1002/pd.4311</doi><tpages>7</tpages></addata></record>
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subjects Adult
Amniocentesis - economics
Amniocentesis - methods
Amniocentesis - statistics & numerical data
Chorionic Gonadotropin, beta Subunit, Human - analysis
Cost-Benefit Analysis
Costs and Cost Analysis
DNA - analysis
DNA - blood
Down Syndrome - diagnosis
Female
Fetus - chemistry
Humans
Maternal Age
Nuchal Translucency Measurement - economics
Nuchal Translucency Measurement - statistics & numerical data
Ontario
Pregnancy
Pregnancy-Associated Plasma Protein-A - analysis
Prenatal Diagnosis - economics
Prenatal Diagnosis - methods
Prenatal Diagnosis - statistics & numerical data
Sequence Analysis, DNA - economics
Sequence Analysis, DNA - methods
Sequence Analysis, DNA - statistics & numerical data
title The price of performance: a cost and performance analysis of the implementation of cell-free fetal DNA testing for Down syndrome in Ontario, Canada
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