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Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen

PURPOSE: Carrier screening identifies couples at high risk for conceiving offspring affected with serious heritable conditions. Minimal guidelines recommend offering testing for cystic fibrosis and spinal muscular atrophy, but expanded carrier screening (ECS) assesses hundreds of conditions simultan...

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Autores principales: Beauchamp, Kyle A., Johansen Taber, Katherine A., Muzzey, Dale
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752320/
https://www.ncbi.nlm.nih.gov/pubmed/30760891
http://dx.doi.org/10.1038/s41436-019-0455-8
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author Beauchamp, Kyle A.
Johansen Taber, Katherine A.
Muzzey, Dale
author_facet Beauchamp, Kyle A.
Johansen Taber, Katherine A.
Muzzey, Dale
author_sort Beauchamp, Kyle A.
collection PubMed
description PURPOSE: Carrier screening identifies couples at high risk for conceiving offspring affected with serious heritable conditions. Minimal guidelines recommend offering testing for cystic fibrosis and spinal muscular atrophy, but expanded carrier screening (ECS) assesses hundreds of conditions simultaneously. Although medical societies consider ECS an acceptable practice, the health economics of ECS remain incompletely characterized. METHODS: Preconception screening was modeled using a decision tree comparing minimal screening and a 176-condition ECS panel. Carrier rates from >60,000 patients, primarily with private insurance, informed disease incidence estimates, while cost and life-years-lost data were aggregated from the literature and a cost-of-care database. Model robustness was evaluated using one-way and probabilistic sensitivity analyses. RESULTS: For every 100,000 pregnancies, 290 are predicted to be affected by ECS-panel conditions, which, on average, increase mortality by 26 undiscounted life-years and individually incur $1,100,000 in lifetime costs. Relative to minimal screening, preconception ECS reduces the affected birth rate and is estimated to be cost-effective (i.e.,<$50,000 incremental cost per life-year), findings robust to perturbation. CONCLUSION: Based on screened patients predominantly with private coverage, preconception ECS is predicted to reduce the burden of Mendelian disease in a cost-effective manner compared with minimal screening. The data and framework herein may facilitate similar assessments in other cohorts.
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spelling pubmed-67523202019-09-23 Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen Beauchamp, Kyle A. Johansen Taber, Katherine A. Muzzey, Dale Genet Med Article PURPOSE: Carrier screening identifies couples at high risk for conceiving offspring affected with serious heritable conditions. Minimal guidelines recommend offering testing for cystic fibrosis and spinal muscular atrophy, but expanded carrier screening (ECS) assesses hundreds of conditions simultaneously. Although medical societies consider ECS an acceptable practice, the health economics of ECS remain incompletely characterized. METHODS: Preconception screening was modeled using a decision tree comparing minimal screening and a 176-condition ECS panel. Carrier rates from >60,000 patients, primarily with private insurance, informed disease incidence estimates, while cost and life-years-lost data were aggregated from the literature and a cost-of-care database. Model robustness was evaluated using one-way and probabilistic sensitivity analyses. RESULTS: For every 100,000 pregnancies, 290 are predicted to be affected by ECS-panel conditions, which, on average, increase mortality by 26 undiscounted life-years and individually incur $1,100,000 in lifetime costs. Relative to minimal screening, preconception ECS reduces the affected birth rate and is estimated to be cost-effective (i.e.,<$50,000 incremental cost per life-year), findings robust to perturbation. CONCLUSION: Based on screened patients predominantly with private coverage, preconception ECS is predicted to reduce the burden of Mendelian disease in a cost-effective manner compared with minimal screening. The data and framework herein may facilitate similar assessments in other cohorts. Nature Publishing Group US 2019-02-14 2019 /pmc/articles/PMC6752320/ /pubmed/30760891 http://dx.doi.org/10.1038/s41436-019-0455-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. If you remix, transform, or build upon this article or a part thereof, you must distribute your contributions under the same license as the original. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/.
spellingShingle Article
Beauchamp, Kyle A.
Johansen Taber, Katherine A.
Muzzey, Dale
Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen
title Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen
title_full Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen
title_fullStr Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen
title_full_unstemmed Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen
title_short Clinical impact and cost-effectiveness of a 176-condition expanded carrier screen
title_sort clinical impact and cost-effectiveness of a 176-condition expanded carrier screen
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752320/
https://www.ncbi.nlm.nih.gov/pubmed/30760891
http://dx.doi.org/10.1038/s41436-019-0455-8
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