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The economic burden of pulmonary arterial hypertension (PAH) in the US on payers and patients

BACKGROUND: Pulmonary arterial hypertension (PAH) is a rare condition that can ultimately lead to right heart failure and death. In this study we estimated the health care costs and resource utilization associated with PAH in a large US managed care health plan. METHODS: Subjects with claims-based e...

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Autores principales: Sikirica, Mirko, Iorga, Serban R, Bancroft, Tim, Potash, Jesse
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301626/
https://www.ncbi.nlm.nih.gov/pubmed/25539602
http://dx.doi.org/10.1186/s12913-014-0676-0
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author Sikirica, Mirko
Iorga, Serban R
Bancroft, Tim
Potash, Jesse
author_facet Sikirica, Mirko
Iorga, Serban R
Bancroft, Tim
Potash, Jesse
author_sort Sikirica, Mirko
collection PubMed
description BACKGROUND: Pulmonary arterial hypertension (PAH) is a rare condition that can ultimately lead to right heart failure and death. In this study we estimated the health care costs and resource utilization associated with PAH in a large US managed care health plan. METHODS: Subjects with claims-based evidence of PAH from 1/1/2004 to 6/30/2010 (identification period) were selected. To be included in the final PAH study sample, subjects were required to have ≥2 claims with a primary PH diagnosis; ≥2 claims with a PAH related-diagnosis (connective tissue diseases, congenital heart diseases, portal hypertension); and ≥1 claim with evidence of a PAH-indicated medication. The earliest date of a claim with evidence of PAH-indicated medication during the identification period was set as the index date. Health care costs and resource utilization were compared between an annualized baseline period and a 12 month follow-up period. RESULTS: 504 PAH subjects were selected for the final study cohort. Estimated average total health care costs were approximately 16% lower in the follow-up period compared to the baseline period (follow-up costs = $98,243 [SD = 110,615] vs. baseline costs = $116,681 [SD = 368,094], p < 0.001), but substantively high in each period relative to costs reported for other chronic diseases. Pharmacy costs were significantly higher in the follow-up period vs. the baseline period, ($38,514 [SD = 34,817] vs. $6,440 [SD = 12,186], p < 0.001) but medical costs were significantly lower in the follow-up vs. baseline ($59,729 [SD = 106,683] vs. $110,241 [SD = 368,725], p < 0.001). These costs were mirrored in health-care resource utilization estimates. The average counts of ambulatory visits and inpatient stays were lower in the follow-up vs. the baseline (both p < 0.001). Results varied in exploratory analyses when less restrictive subject identification algorithms were used. CONCLUSIONS: Subjects with evidence of PAH had substantively high health care costs. Medical costs appeared to decrease following PAH medication use, but with a concomitant increase in pharmacy costs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12913-014-0676-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-43016262015-01-22 The economic burden of pulmonary arterial hypertension (PAH) in the US on payers and patients Sikirica, Mirko Iorga, Serban R Bancroft, Tim Potash, Jesse BMC Health Serv Res Research Article BACKGROUND: Pulmonary arterial hypertension (PAH) is a rare condition that can ultimately lead to right heart failure and death. In this study we estimated the health care costs and resource utilization associated with PAH in a large US managed care health plan. METHODS: Subjects with claims-based evidence of PAH from 1/1/2004 to 6/30/2010 (identification period) were selected. To be included in the final PAH study sample, subjects were required to have ≥2 claims with a primary PH diagnosis; ≥2 claims with a PAH related-diagnosis (connective tissue diseases, congenital heart diseases, portal hypertension); and ≥1 claim with evidence of a PAH-indicated medication. The earliest date of a claim with evidence of PAH-indicated medication during the identification period was set as the index date. Health care costs and resource utilization were compared between an annualized baseline period and a 12 month follow-up period. RESULTS: 504 PAH subjects were selected for the final study cohort. Estimated average total health care costs were approximately 16% lower in the follow-up period compared to the baseline period (follow-up costs = $98,243 [SD = 110,615] vs. baseline costs = $116,681 [SD = 368,094], p < 0.001), but substantively high in each period relative to costs reported for other chronic diseases. Pharmacy costs were significantly higher in the follow-up period vs. the baseline period, ($38,514 [SD = 34,817] vs. $6,440 [SD = 12,186], p < 0.001) but medical costs were significantly lower in the follow-up vs. baseline ($59,729 [SD = 106,683] vs. $110,241 [SD = 368,725], p < 0.001). These costs were mirrored in health-care resource utilization estimates. The average counts of ambulatory visits and inpatient stays were lower in the follow-up vs. the baseline (both p < 0.001). Results varied in exploratory analyses when less restrictive subject identification algorithms were used. CONCLUSIONS: Subjects with evidence of PAH had substantively high health care costs. Medical costs appeared to decrease following PAH medication use, but with a concomitant increase in pharmacy costs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12913-014-0676-0) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-24 /pmc/articles/PMC4301626/ /pubmed/25539602 http://dx.doi.org/10.1186/s12913-014-0676-0 Text en © Sikirica et al.; licensee BioMed Central. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Sikirica, Mirko
Iorga, Serban R
Bancroft, Tim
Potash, Jesse
The economic burden of pulmonary arterial hypertension (PAH) in the US on payers and patients
title The economic burden of pulmonary arterial hypertension (PAH) in the US on payers and patients
title_full The economic burden of pulmonary arterial hypertension (PAH) in the US on payers and patients
title_fullStr The economic burden of pulmonary arterial hypertension (PAH) in the US on payers and patients
title_full_unstemmed The economic burden of pulmonary arterial hypertension (PAH) in the US on payers and patients
title_short The economic burden of pulmonary arterial hypertension (PAH) in the US on payers and patients
title_sort economic burden of pulmonary arterial hypertension (pah) in the us on payers and patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301626/
https://www.ncbi.nlm.nih.gov/pubmed/25539602
http://dx.doi.org/10.1186/s12913-014-0676-0
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