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The Economic Benefit of Remission for Patients with Rheumatoid Arthritis

INTRODUCTION: In patients with rheumatoid arthritis (RA), attaining remission or low disease activity (LDA), as recommended by the treat-to-target approach, has shown to yield improvement in symptoms and quality of life. However, limited evidence from real-world settings is available to support the...

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Autores principales: Curtis, Jeffrey R., Fox, Kathleen M., Xie, Fenglong, Su, Yujie, Collier, David, Clinton, Cassie, Oko-osi, Hafiz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9510082/
https://www.ncbi.nlm.nih.gov/pubmed/35834162
http://dx.doi.org/10.1007/s40744-022-00473-6
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author Curtis, Jeffrey R.
Fox, Kathleen M.
Xie, Fenglong
Su, Yujie
Collier, David
Clinton, Cassie
Oko-osi, Hafiz
author_facet Curtis, Jeffrey R.
Fox, Kathleen M.
Xie, Fenglong
Su, Yujie
Collier, David
Clinton, Cassie
Oko-osi, Hafiz
author_sort Curtis, Jeffrey R.
collection PubMed
description INTRODUCTION: In patients with rheumatoid arthritis (RA), attaining remission or low disease activity (LDA), as recommended by the treat-to-target approach, has shown to yield improvement in symptoms and quality of life. However, limited evidence from real-world settings is available to support the premise that better disease control is associated with lower healthcare costs. This study fills in evidence gaps regarding the cost of care by RA disease activity (DA) states and by therapy. METHODS: This retrospective cohort study linked medical and prescription claims from Optum Clinformatics Data Mart to electronic health record data from Illumination Health over 1/1/2010–3/31/2020. Mean annual costs for payers and patients were examined, stratifying on DA state and baseline use of conventional synthetic disease-modifying antirheumatic drugs (csDMARDs), biologics, and targeted synthetic (ts)DMARDs. Subgroup analysis examining within-person change in costs pre- and post-initiation of new therapy was also performed. Descriptive statistics, means, and boot-strapped confidence intervals were analyzed by DA state and by RA therapy. Furthermore, multivariate negative binomial regression analysis adjusting for key baseline characteristics was conducted. RESULTS: Of 2339 eligible patients, 19% were in remission, 40% in LDA, 29% in moderate DA (MDA), and 12% in high DA (HDA) at baseline. Mean annual costs during follow-up were substantially less for patients in remission ($40,072) versus those in MDA ($56,536) and HDA ($59,217). For patients in remission, csDMARD use was associated with the lowest mean annual cost ($25,575), tsDMARD was highest ($75,512), and tumor necrosis factor inhibitor (TNFi) ($69,846) and non-TNFi ($57,507) were intermediate. Among new TNFi (n = 137) and non-TNFi initiators (n = 107), 31% and 26% attained LDA/remission, respectively, and the time to achieve remission/LDA was numerically shorter in TNFi vs. non-TNFi initiators. For those on biologics, mean annual within-person medical and inpatient costs were lower after achieving LDA/remission, although pharmacy costs were higher. CONCLUSIONS: Cost of care increased with increasing DA state, with patients in remission having the lowest costs. Optimizing DA has the potential for substantial savings in healthcare costs, although may be partially offset by the high cost of targeted RA therapies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40744-022-00473-6.
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spelling pubmed-95100822022-09-27 The Economic Benefit of Remission for Patients with Rheumatoid Arthritis Curtis, Jeffrey R. Fox, Kathleen M. Xie, Fenglong Su, Yujie Collier, David Clinton, Cassie Oko-osi, Hafiz Rheumatol Ther Original Research INTRODUCTION: In patients with rheumatoid arthritis (RA), attaining remission or low disease activity (LDA), as recommended by the treat-to-target approach, has shown to yield improvement in symptoms and quality of life. However, limited evidence from real-world settings is available to support the premise that better disease control is associated with lower healthcare costs. This study fills in evidence gaps regarding the cost of care by RA disease activity (DA) states and by therapy. METHODS: This retrospective cohort study linked medical and prescription claims from Optum Clinformatics Data Mart to electronic health record data from Illumination Health over 1/1/2010–3/31/2020. Mean annual costs for payers and patients were examined, stratifying on DA state and baseline use of conventional synthetic disease-modifying antirheumatic drugs (csDMARDs), biologics, and targeted synthetic (ts)DMARDs. Subgroup analysis examining within-person change in costs pre- and post-initiation of new therapy was also performed. Descriptive statistics, means, and boot-strapped confidence intervals were analyzed by DA state and by RA therapy. Furthermore, multivariate negative binomial regression analysis adjusting for key baseline characteristics was conducted. RESULTS: Of 2339 eligible patients, 19% were in remission, 40% in LDA, 29% in moderate DA (MDA), and 12% in high DA (HDA) at baseline. Mean annual costs during follow-up were substantially less for patients in remission ($40,072) versus those in MDA ($56,536) and HDA ($59,217). For patients in remission, csDMARD use was associated with the lowest mean annual cost ($25,575), tsDMARD was highest ($75,512), and tumor necrosis factor inhibitor (TNFi) ($69,846) and non-TNFi ($57,507) were intermediate. Among new TNFi (n = 137) and non-TNFi initiators (n = 107), 31% and 26% attained LDA/remission, respectively, and the time to achieve remission/LDA was numerically shorter in TNFi vs. non-TNFi initiators. For those on biologics, mean annual within-person medical and inpatient costs were lower after achieving LDA/remission, although pharmacy costs were higher. CONCLUSIONS: Cost of care increased with increasing DA state, with patients in remission having the lowest costs. Optimizing DA has the potential for substantial savings in healthcare costs, although may be partially offset by the high cost of targeted RA therapies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40744-022-00473-6. Springer Healthcare 2022-07-14 /pmc/articles/PMC9510082/ /pubmed/35834162 http://dx.doi.org/10.1007/s40744-022-00473-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 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 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-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Curtis, Jeffrey R.
Fox, Kathleen M.
Xie, Fenglong
Su, Yujie
Collier, David
Clinton, Cassie
Oko-osi, Hafiz
The Economic Benefit of Remission for Patients with Rheumatoid Arthritis
title The Economic Benefit of Remission for Patients with Rheumatoid Arthritis
title_full The Economic Benefit of Remission for Patients with Rheumatoid Arthritis
title_fullStr The Economic Benefit of Remission for Patients with Rheumatoid Arthritis
title_full_unstemmed The Economic Benefit of Remission for Patients with Rheumatoid Arthritis
title_short The Economic Benefit of Remission for Patients with Rheumatoid Arthritis
title_sort economic benefit of remission for patients with rheumatoid arthritis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9510082/
https://www.ncbi.nlm.nih.gov/pubmed/35834162
http://dx.doi.org/10.1007/s40744-022-00473-6
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