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Population Screening for Hereditary Haemochromatosis in Australia: Construction and Validation of a State-Transition Cost-Effectiveness Model

INTRODUCTION: HFE-associated haemochromatosis, the most common monogenic disorder amongst populations of northern European ancestry, is characterised by iron overload. Excess iron is stored in parenchymal tissues, leading to morbidity and mortality. Population screening programmes are likely to impr...

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Autores principales: de Graaff, Barbara, Si, Lei, Neil, Amanda L., Yee, Kwang Chien, Sanderson, Kristy, Gurrin, Lyle C., Palmer, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691808/
https://www.ncbi.nlm.nih.gov/pubmed/29442300
http://dx.doi.org/10.1007/s41669-016-0005-0
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author de Graaff, Barbara
Si, Lei
Neil, Amanda L.
Yee, Kwang Chien
Sanderson, Kristy
Gurrin, Lyle C.
Palmer, Andrew J.
author_facet de Graaff, Barbara
Si, Lei
Neil, Amanda L.
Yee, Kwang Chien
Sanderson, Kristy
Gurrin, Lyle C.
Palmer, Andrew J.
author_sort de Graaff, Barbara
collection PubMed
description INTRODUCTION: HFE-associated haemochromatosis, the most common monogenic disorder amongst populations of northern European ancestry, is characterised by iron overload. Excess iron is stored in parenchymal tissues, leading to morbidity and mortality. Population screening programmes are likely to improve early diagnosis, thereby decreasing associated disease. Our aim was to develop and validate a health economics model of screening using utilities and costs from a haemochromatosis cohort. METHODS: A state-transition model was developed with Markov states based on disease severity. Australian males (aged 30 years) and females (aged 45 years) of northern European ancestry were the target populations. The screening strategy was the status quo approach in Australia; the model was run over a lifetime horizon. Costs were estimated from the government perspective and reported in 2015 Australian dollars ($A); costs and quality-adjusted life-years (QALYs) were discounted at 5% annually. Model validity was assessed using goodness-of-fit analyses. Second-order Monte-Carlo simulation was used to account for uncertainty in multiple parameters. RESULTS: For validity, the model reproduced mortality, life expectancy (LE) and prevalence rates in line with published data. LE for C282Y homozygote males and females were 49.9 and 40.2 years, respectively, slightly lower than population rates. Mean (95% confidence interval) QALYS were 15.7 (7.7–23.7) for males and 14.4 (6.7–22.1) for females. Mean discounted lifetime costs for C282Y homozygotes were $A22,737 (3670–85,793) for males and $A13,840 (1335–67,377) for females. Sensitivity analyses revealed discount rates and prevalence had the greatest impacts on outcomes. CONCLUSION: We have developed a transparent, validated health economics model of C282Y homozygote haemochromatosis. The model will be useful to decision makers to identify cost-effective screening strategies.
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spelling pubmed-56918082017-12-18 Population Screening for Hereditary Haemochromatosis in Australia: Construction and Validation of a State-Transition Cost-Effectiveness Model de Graaff, Barbara Si, Lei Neil, Amanda L. Yee, Kwang Chien Sanderson, Kristy Gurrin, Lyle C. Palmer, Andrew J. Pharmacoecon Open Original Research Article INTRODUCTION: HFE-associated haemochromatosis, the most common monogenic disorder amongst populations of northern European ancestry, is characterised by iron overload. Excess iron is stored in parenchymal tissues, leading to morbidity and mortality. Population screening programmes are likely to improve early diagnosis, thereby decreasing associated disease. Our aim was to develop and validate a health economics model of screening using utilities and costs from a haemochromatosis cohort. METHODS: A state-transition model was developed with Markov states based on disease severity. Australian males (aged 30 years) and females (aged 45 years) of northern European ancestry were the target populations. The screening strategy was the status quo approach in Australia; the model was run over a lifetime horizon. Costs were estimated from the government perspective and reported in 2015 Australian dollars ($A); costs and quality-adjusted life-years (QALYs) were discounted at 5% annually. Model validity was assessed using goodness-of-fit analyses. Second-order Monte-Carlo simulation was used to account for uncertainty in multiple parameters. RESULTS: For validity, the model reproduced mortality, life expectancy (LE) and prevalence rates in line with published data. LE for C282Y homozygote males and females were 49.9 and 40.2 years, respectively, slightly lower than population rates. Mean (95% confidence interval) QALYS were 15.7 (7.7–23.7) for males and 14.4 (6.7–22.1) for females. Mean discounted lifetime costs for C282Y homozygotes were $A22,737 (3670–85,793) for males and $A13,840 (1335–67,377) for females. Sensitivity analyses revealed discount rates and prevalence had the greatest impacts on outcomes. CONCLUSION: We have developed a transparent, validated health economics model of C282Y homozygote haemochromatosis. The model will be useful to decision makers to identify cost-effective screening strategies. Springer International Publishing 2016-11-16 /pmc/articles/PMC5691808/ /pubmed/29442300 http://dx.doi.org/10.1007/s41669-016-0005-0 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Research Article
de Graaff, Barbara
Si, Lei
Neil, Amanda L.
Yee, Kwang Chien
Sanderson, Kristy
Gurrin, Lyle C.
Palmer, Andrew J.
Population Screening for Hereditary Haemochromatosis in Australia: Construction and Validation of a State-Transition Cost-Effectiveness Model
title Population Screening for Hereditary Haemochromatosis in Australia: Construction and Validation of a State-Transition Cost-Effectiveness Model
title_full Population Screening for Hereditary Haemochromatosis in Australia: Construction and Validation of a State-Transition Cost-Effectiveness Model
title_fullStr Population Screening for Hereditary Haemochromatosis in Australia: Construction and Validation of a State-Transition Cost-Effectiveness Model
title_full_unstemmed Population Screening for Hereditary Haemochromatosis in Australia: Construction and Validation of a State-Transition Cost-Effectiveness Model
title_short Population Screening for Hereditary Haemochromatosis in Australia: Construction and Validation of a State-Transition Cost-Effectiveness Model
title_sort population screening for hereditary haemochromatosis in australia: construction and validation of a state-transition cost-effectiveness model
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691808/
https://www.ncbi.nlm.nih.gov/pubmed/29442300
http://dx.doi.org/10.1007/s41669-016-0005-0
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