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The economic burden of idiopathic pulmonary fibrosis in Australia: a cost of illness study
PURPOSE: Idiopathic pulmonary fibrosis (IPF) is a type of interstitial lung disease found mostly in elderly persons, characterized by a high symptom burden and frequent encounters with health services. This study aimed to quantify the economic burden of IPF in Australia with a focus on resource util...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406709/ https://www.ncbi.nlm.nih.gov/pubmed/36289130 http://dx.doi.org/10.1007/s10198-022-01538-7 |
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author | Cox, Ingrid A. de Graaff, Barbara Ahmed, Hasnat Campbell, Julie Otahal, Petr Corte, Tamera J. Moodley, Yuben Goh, Nicole Hopkins, Peter Macansh, Sacha Walters, E. Haydn Palmer, Andrew J. |
author_facet | Cox, Ingrid A. de Graaff, Barbara Ahmed, Hasnat Campbell, Julie Otahal, Petr Corte, Tamera J. Moodley, Yuben Goh, Nicole Hopkins, Peter Macansh, Sacha Walters, E. Haydn Palmer, Andrew J. |
author_sort | Cox, Ingrid A. |
collection | PubMed |
description | PURPOSE: Idiopathic pulmonary fibrosis (IPF) is a type of interstitial lung disease found mostly in elderly persons, characterized by a high symptom burden and frequent encounters with health services. This study aimed to quantify the economic burden of IPF in Australia with a focus on resource utilization and associated direct costs. METHODS: Participants were recruited from the Australian IPF Registry (AIPFR) between August 2018 and December 2019. Data on resource utilization and costs were collected via cost diaries and linked administrative data. Clinical data were collected from the AIPFR. A “bottom up” costing methodology was utilized, and the costing was performed from a partial societal perspective focusing primarily on direct medical and non-medical costs. Costs were standardized to 2021 Australian dollars ($). RESULTS: The average annual total direct costs per person with IPF was $31,655 (95% confidence interval (95% CI): $27,723–$35,757). Extrapolating costs based on prevalence estimates, the total annual costs in Australia are projected to be $299 million (95% CI: $262 million–$338 million). Costs were mainly driven by antifibrotic medication, hospital admissions and medications for comorbidities. Disease severity, comorbidities and antifibrotic medication all had varying impacts on resource utilization and costs. CONCLUSION: This cost-of-illness study provides the first comprehensive assessment of IPF-related direct costs in Australia, identifies the key cost drivers and provides a framework for future health economic analyses. Additionally, it provided insight into the major cost drivers which include antifibrotic medication, hospital admissions and medications related to comorbidities. Our findings emphasize the importance of the appropriate management of comorbidities in the care of people with IPF as this was one of the main reasons for hospitalizations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10198-022-01538-7. |
format | Online Article Text |
id | pubmed-10406709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-104067092023-08-09 The economic burden of idiopathic pulmonary fibrosis in Australia: a cost of illness study Cox, Ingrid A. de Graaff, Barbara Ahmed, Hasnat Campbell, Julie Otahal, Petr Corte, Tamera J. Moodley, Yuben Goh, Nicole Hopkins, Peter Macansh, Sacha Walters, E. Haydn Palmer, Andrew J. Eur J Health Econ Original Paper PURPOSE: Idiopathic pulmonary fibrosis (IPF) is a type of interstitial lung disease found mostly in elderly persons, characterized by a high symptom burden and frequent encounters with health services. This study aimed to quantify the economic burden of IPF in Australia with a focus on resource utilization and associated direct costs. METHODS: Participants were recruited from the Australian IPF Registry (AIPFR) between August 2018 and December 2019. Data on resource utilization and costs were collected via cost diaries and linked administrative data. Clinical data were collected from the AIPFR. A “bottom up” costing methodology was utilized, and the costing was performed from a partial societal perspective focusing primarily on direct medical and non-medical costs. Costs were standardized to 2021 Australian dollars ($). RESULTS: The average annual total direct costs per person with IPF was $31,655 (95% confidence interval (95% CI): $27,723–$35,757). Extrapolating costs based on prevalence estimates, the total annual costs in Australia are projected to be $299 million (95% CI: $262 million–$338 million). Costs were mainly driven by antifibrotic medication, hospital admissions and medications for comorbidities. Disease severity, comorbidities and antifibrotic medication all had varying impacts on resource utilization and costs. CONCLUSION: This cost-of-illness study provides the first comprehensive assessment of IPF-related direct costs in Australia, identifies the key cost drivers and provides a framework for future health economic analyses. Additionally, it provided insight into the major cost drivers which include antifibrotic medication, hospital admissions and medications related to comorbidities. Our findings emphasize the importance of the appropriate management of comorbidities in the care of people with IPF as this was one of the main reasons for hospitalizations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10198-022-01538-7. Springer Berlin Heidelberg 2022-10-27 2023 /pmc/articles/PMC10406709/ /pubmed/36289130 http://dx.doi.org/10.1007/s10198-022-01538-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Paper Cox, Ingrid A. de Graaff, Barbara Ahmed, Hasnat Campbell, Julie Otahal, Petr Corte, Tamera J. Moodley, Yuben Goh, Nicole Hopkins, Peter Macansh, Sacha Walters, E. Haydn Palmer, Andrew J. The economic burden of idiopathic pulmonary fibrosis in Australia: a cost of illness study |
title | The economic burden of idiopathic pulmonary fibrosis in Australia: a cost of illness study |
title_full | The economic burden of idiopathic pulmonary fibrosis in Australia: a cost of illness study |
title_fullStr | The economic burden of idiopathic pulmonary fibrosis in Australia: a cost of illness study |
title_full_unstemmed | The economic burden of idiopathic pulmonary fibrosis in Australia: a cost of illness study |
title_short | The economic burden of idiopathic pulmonary fibrosis in Australia: a cost of illness study |
title_sort | economic burden of idiopathic pulmonary fibrosis in australia: a cost of illness study |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406709/ https://www.ncbi.nlm.nih.gov/pubmed/36289130 http://dx.doi.org/10.1007/s10198-022-01538-7 |
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