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Isolated echogenic intracardiac foci and the role of cell‐free fetal DNA: A cost‐effectiveness analysis

Objectives Cell‐free fetal DNA (cfDNA) has been increasingly incorporated into prenatal aneuploidy screening paradigms given its relatively high sensitivity for Down syndrome (DS). This is often the case when fetal ultrasonographic soft markers are present, such as the relatively common echogenic in...

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Published in:Prenatal diagnosis 2020-12, Vol.40 (12), p.1517-1524
Main Authors: Hacker, Francis M, Hersh, Alyssa R, Shaffer, Brian L, Caughey, Aaron B
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Language:English
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container_title Prenatal diagnosis
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creator Hacker, Francis M
Hersh, Alyssa R
Shaffer, Brian L
Caughey, Aaron B
description Objectives Cell‐free fetal DNA (cfDNA) has been increasingly incorporated into prenatal aneuploidy screening paradigms given its relatively high sensitivity for Down syndrome (DS). This is often the case when fetal ultrasonographic soft markers are present, such as the relatively common echogenic intracardiac focus (EIF). We sought to evaluate the cost‐effectiveness of a screening strategy that included cfDNA screening when an isolated EIF is identified in a low‐risk population with prior aneuploidy screening. Methods A decision‐analytic model was constructed using TreeAge software with probabilities derived from the literature. Our model compared cfDNA screening following isolated EIF detection in women less than 35 years with prior reassuring first trimester screen compared to a strategy of no further aneuploidy screening. Strategies were compared to generate an incremental cost‐effectiveness ratio with a threshold of $100 000/quality‐adjusted life year (QALY) and applied to a theoretical cohort. Results The cfDNA strategy resulted in 21 fewer DS births and 52 additional QALYs, however, increased costs by $51.3 million. This yielded an incremental cost‐effectiveness ratio of $986 503; therefore, it was not a cost‐effective strategy. Conclusion In a low‐risk population with prior reassuring aneuploidy screening, it is not cost effective to offer cfDNA after identification of an isolated EIF.
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This is often the case when fetal ultrasonographic soft markers are present, such as the relatively common echogenic intracardiac focus (EIF). We sought to evaluate the cost‐effectiveness of a screening strategy that included cfDNA screening when an isolated EIF is identified in a low‐risk population with prior aneuploidy screening. Methods A decision‐analytic model was constructed using TreeAge software with probabilities derived from the literature. Our model compared cfDNA screening following isolated EIF detection in women less than 35 years with prior reassuring first trimester screen compared to a strategy of no further aneuploidy screening. Strategies were compared to generate an incremental cost‐effectiveness ratio with a threshold of $100 000/quality‐adjusted life year (QALY) and applied to a theoretical cohort. Results The cfDNA strategy resulted in 21 fewer DS births and 52 additional QALYs, however, increased costs by $51.3 million. This yielded an incremental cost‐effectiveness ratio of $986 503; therefore, it was not a cost‐effective strategy. 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This is often the case when fetal ultrasonographic soft markers are present, such as the relatively common echogenic intracardiac focus (EIF). We sought to evaluate the cost‐effectiveness of a screening strategy that included cfDNA screening when an isolated EIF is identified in a low‐risk population with prior aneuploidy screening. Methods A decision‐analytic model was constructed using TreeAge software with probabilities derived from the literature. Our model compared cfDNA screening following isolated EIF detection in women less than 35 years with prior reassuring first trimester screen compared to a strategy of no further aneuploidy screening. Strategies were compared to generate an incremental cost‐effectiveness ratio with a threshold of $100 000/quality‐adjusted life year (QALY) and applied to a theoretical cohort. Results The cfDNA strategy resulted in 21 fewer DS births and 52 additional QALYs, however, increased costs by $51.3 million. This yielded an incremental cost‐effectiveness ratio of $986 503; therefore, it was not a cost‐effective strategy. 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This is often the case when fetal ultrasonographic soft markers are present, such as the relatively common echogenic intracardiac focus (EIF). We sought to evaluate the cost‐effectiveness of a screening strategy that included cfDNA screening when an isolated EIF is identified in a low‐risk population with prior aneuploidy screening. Methods A decision‐analytic model was constructed using TreeAge software with probabilities derived from the literature. Our model compared cfDNA screening following isolated EIF detection in women less than 35 years with prior reassuring first trimester screen compared to a strategy of no further aneuploidy screening. Strategies were compared to generate an incremental cost‐effectiveness ratio with a threshold of $100 000/quality‐adjusted life year (QALY) and applied to a theoretical cohort. Results The cfDNA strategy resulted in 21 fewer DS births and 52 additional QALYs, however, increased costs by $51.3 million. 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source Wiley-Blackwell Read & Publish Collection
subjects Aneuploidy
Cost analysis
Decision analysis
Deoxyribonucleic acid
DNA
Down's syndrome
Fetuses
Genetic screening
Mathematical models
Prenatal diagnosis
Screening
Strategy
title Isolated echogenic intracardiac foci and the role of cell‐free fetal DNA: A cost‐effectiveness analysis
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