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Costs of Parkinson’s Disease in a Privately Insured Population
BACKGROUND: This is the first analysis to estimate the costs of commercially insured patients with Parkinson’s disease (PD) in the USA. Prior analyses of PD have not examined costs in patients aged under 65 years, a majority of whom are in the workforce. OBJECTIVE: Our objective was to estimate dire...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757266/ https://www.ncbi.nlm.nih.gov/pubmed/23907717 http://dx.doi.org/10.1007/s40273-013-0075-0 |
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author | Johnson, Scott J. Kaltenboeck, Anna Diener, Melissa Birnbaum, Howard G. Grubb, ElizaBeth Castelli-Haley, Jane Siderowf, Andrew D. |
author_facet | Johnson, Scott J. Kaltenboeck, Anna Diener, Melissa Birnbaum, Howard G. Grubb, ElizaBeth Castelli-Haley, Jane Siderowf, Andrew D. |
author_sort | Johnson, Scott J. |
collection | PubMed |
description | BACKGROUND: This is the first analysis to estimate the costs of commercially insured patients with Parkinson’s disease (PD) in the USA. Prior analyses of PD have not examined costs in patients aged under 65 years, a majority of whom are in the workforce. OBJECTIVE: Our objective was to estimate direct and indirect costs associated with PD in patients under the age of 65 years who are newly diagnosed or have evidence of advanced PD. METHODS: PD patients were selected from a commercially insured claims database (N > 12,000,000; 1999–2009); workloss data were available for a sub-sample of enrollees. Newly diagnosed patients with evidence of similar disorders were excluded. Patients with evidence of advanced PD disease, including ambulatory assistance device users (PDAAD) and institutionalized (PDINST) patients, as well as newly diagnosed PD patients, were analyzed. Each PD cohort was age-, gender- and region-matched to controls without PD. Direct (i.e. insurer payments to providers) and indirect (i.e. workloss) costs were reported in $US, year 2010 values, and were descriptively compared using Wilcoxon rank sum tests. RESULTS: Patients had excess mean direct PD-related costs of $US4,072 (p < 0.001; N = 781) in the year after diagnosis. The PDAAD cohort (N = 214) had excess direct PD-related costs of $US26,467 (p < 0.001) and the PDINST cohort (N = 156) had excess direct PD-related costs of $US37,410 (p < 0.001) in the year after entering these states. Outpatient care was the most expensive cost source for newly diagnosed patients, while inpatient care was the most expensive for PDAAD and PDINST patients. Excess indirect costs were $US3,311 (p < 0.05; N = 173) in the year after initial diagnosis. CONCLUSIONS: Direct costs for newly diagnosed PD patients exceeded costs for controls without PD, and increased with PD progression. Direct costs were approximately 6–7 times higher in patients with advanced PD than in matched controls. Indirect costs represented 45 % of total excess costs for newly diagnosed PD patients. |
format | Online Article Text |
id | pubmed-3757266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-37572662013-09-04 Costs of Parkinson’s Disease in a Privately Insured Population Johnson, Scott J. Kaltenboeck, Anna Diener, Melissa Birnbaum, Howard G. Grubb, ElizaBeth Castelli-Haley, Jane Siderowf, Andrew D. Pharmacoeconomics Original Research Article BACKGROUND: This is the first analysis to estimate the costs of commercially insured patients with Parkinson’s disease (PD) in the USA. Prior analyses of PD have not examined costs in patients aged under 65 years, a majority of whom are in the workforce. OBJECTIVE: Our objective was to estimate direct and indirect costs associated with PD in patients under the age of 65 years who are newly diagnosed or have evidence of advanced PD. METHODS: PD patients were selected from a commercially insured claims database (N > 12,000,000; 1999–2009); workloss data were available for a sub-sample of enrollees. Newly diagnosed patients with evidence of similar disorders were excluded. Patients with evidence of advanced PD disease, including ambulatory assistance device users (PDAAD) and institutionalized (PDINST) patients, as well as newly diagnosed PD patients, were analyzed. Each PD cohort was age-, gender- and region-matched to controls without PD. Direct (i.e. insurer payments to providers) and indirect (i.e. workloss) costs were reported in $US, year 2010 values, and were descriptively compared using Wilcoxon rank sum tests. RESULTS: Patients had excess mean direct PD-related costs of $US4,072 (p < 0.001; N = 781) in the year after diagnosis. The PDAAD cohort (N = 214) had excess direct PD-related costs of $US26,467 (p < 0.001) and the PDINST cohort (N = 156) had excess direct PD-related costs of $US37,410 (p < 0.001) in the year after entering these states. Outpatient care was the most expensive cost source for newly diagnosed patients, while inpatient care was the most expensive for PDAAD and PDINST patients. Excess indirect costs were $US3,311 (p < 0.05; N = 173) in the year after initial diagnosis. CONCLUSIONS: Direct costs for newly diagnosed PD patients exceeded costs for controls without PD, and increased with PD progression. Direct costs were approximately 6–7 times higher in patients with advanced PD than in matched controls. Indirect costs represented 45 % of total excess costs for newly diagnosed PD patients. Springer International Publishing 2013-08-02 2013 /pmc/articles/PMC3757266/ /pubmed/23907717 http://dx.doi.org/10.1007/s40273-013-0075-0 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.5/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Research Article Johnson, Scott J. Kaltenboeck, Anna Diener, Melissa Birnbaum, Howard G. Grubb, ElizaBeth Castelli-Haley, Jane Siderowf, Andrew D. Costs of Parkinson’s Disease in a Privately Insured Population |
title | Costs of Parkinson’s Disease in a Privately Insured Population |
title_full | Costs of Parkinson’s Disease in a Privately Insured Population |
title_fullStr | Costs of Parkinson’s Disease in a Privately Insured Population |
title_full_unstemmed | Costs of Parkinson’s Disease in a Privately Insured Population |
title_short | Costs of Parkinson’s Disease in a Privately Insured Population |
title_sort | costs of parkinson’s disease in a privately insured population |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757266/ https://www.ncbi.nlm.nih.gov/pubmed/23907717 http://dx.doi.org/10.1007/s40273-013-0075-0 |
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