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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 |
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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. |
doi_str_mv | 10.1002/pd.5803 |
format | article |
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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.</description><identifier>ISSN: 0197-3851</identifier><identifier>EISSN: 1097-0223</identifier><identifier>DOI: 10.1002/pd.5803</identifier><identifier>PMID: 32716062</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Aneuploidy ; Cost analysis ; Decision analysis ; Deoxyribonucleic acid ; DNA ; Down's syndrome ; Fetuses ; Genetic screening ; Mathematical models ; Prenatal diagnosis ; Screening ; Strategy</subject><ispartof>Prenatal diagnosis, 2020-12, Vol.40 (12), p.1517-1524</ispartof><rights>2020 John Wiley & Sons Ltd</rights><rights>2020 John Wiley & Sons Ltd.</rights><rights>2020 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2603-52bada0090abb5b1981299b11baee2c9309ea39e457cbaa80796b3fed1d02be43</citedby><cites>FETCH-LOGICAL-c2603-52bada0090abb5b1981299b11baee2c9309ea39e457cbaa80796b3fed1d02be43</cites><orcidid>0000-0003-2461-195X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32716062$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hacker, Francis M</creatorcontrib><creatorcontrib>Hersh, Alyssa R</creatorcontrib><creatorcontrib>Shaffer, Brian L</creatorcontrib><creatorcontrib>Caughey, Aaron B</creatorcontrib><title>Isolated echogenic intracardiac foci and the role of cell‐free fetal DNA: A cost‐effectiveness analysis</title><title>Prenatal diagnosis</title><addtitle>Prenat Diagn</addtitle><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.</description><subject>Aneuploidy</subject><subject>Cost analysis</subject><subject>Decision analysis</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Down's syndrome</subject><subject>Fetuses</subject><subject>Genetic screening</subject><subject>Mathematical models</subject><subject>Prenatal diagnosis</subject><subject>Screening</subject><subject>Strategy</subject><issn>0197-3851</issn><issn>1097-0223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp10M1qVDEUB_AgSjv9wDeQgAsFmfYkmfsRd0NbtVDaLnR9OUlObOqdmzG5o8zOR_AZ-yTNOG0XBVcncH75c_gz9lrAkQCQx0t3VLWgXrCJAN1MQUr1kk1AlLdqK7HL9nK-LbCVutlhu0o2ooZaTtiP8xx7HMlxsjfxOw3B8jCMCS0mF9ByH23gODg-3hBPsScePbfU93d__vpExD2N2PPTy_lHPuc25rEsyHuyY_hFA-VcfmO_ziEfsFce-0yHD3Offft09vXky_Ti6vP5yfxiamUNalpJgw4BNKAxlRG6FVJrI4RBImm1Ak2oNM2qxhrEFhpdG-XJCQfS0Ezts_fb3GWKP1eUx24R8uZkHCiucidnsqmkEk1d6Ntn9DauUrl3o2qlQQmhi3q3VTbFnBP5bpnCAtO6E9Bt-u-Wrtv0X-Sbh7yVWZB7co-FF_BhC36Hntb_y-muT__F3QMf-47c</recordid><startdate>202012</startdate><enddate>202012</enddate><creator>Hacker, Francis M</creator><creator>Hersh, Alyssa R</creator><creator>Shaffer, Brian L</creator><creator>Caughey, Aaron B</creator><general>John Wiley & Sons, Ltd</general><general>Wiley Subscription Services, Inc</general><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><orcidid>https://orcid.org/0000-0003-2461-195X</orcidid></search><sort><creationdate>202012</creationdate><title>Isolated echogenic intracardiac foci and the role of cell‐free fetal DNA: A cost‐effectiveness analysis</title><author>Hacker, Francis M ; Hersh, Alyssa R ; Shaffer, Brian L ; Caughey, Aaron B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2603-52bada0090abb5b1981299b11baee2c9309ea39e457cbaa80796b3fed1d02be43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aneuploidy</topic><topic>Cost analysis</topic><topic>Decision analysis</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Down's syndrome</topic><topic>Fetuses</topic><topic>Genetic screening</topic><topic>Mathematical models</topic><topic>Prenatal diagnosis</topic><topic>Screening</topic><topic>Strategy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hacker, Francis M</creatorcontrib><creatorcontrib>Hersh, Alyssa R</creatorcontrib><creatorcontrib>Shaffer, Brian L</creatorcontrib><creatorcontrib>Caughey, Aaron B</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Prenatal diagnosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hacker, Francis M</au><au>Hersh, Alyssa R</au><au>Shaffer, Brian L</au><au>Caughey, Aaron B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolated echogenic intracardiac foci and the role of cell‐free fetal DNA: A cost‐effectiveness analysis</atitle><jtitle>Prenatal diagnosis</jtitle><addtitle>Prenat Diagn</addtitle><date>2020-12</date><risdate>2020</risdate><volume>40</volume><issue>12</issue><spage>1517</spage><epage>1524</epage><pages>1517-1524</pages><issn>0197-3851</issn><eissn>1097-0223</eissn><abstract>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.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>32716062</pmid><doi>10.1002/pd.5803</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-2461-195X</orcidid></addata></record> |
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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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