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Evaluation of Real-World Healthcare Resource Utilization and Associated Costs in Children with Juvenile Idiopathic Arthritis: A Canadian Retrospective Cohort Study

INTRODUCTION: Juvenile idiopathic arthritis (JIA) is a chronic rheumatic disease, whose multifaceted care path can lead to significant expenditure for the healthcare system. We aim to assess the real-world healthcare resource use (HCRU) and associated cost for children with JIA in a single center in...

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Autores principales: Grazziotin, Luiza R., Currie, Gillian, Twilt, Marinka, Ijzerman, Maarten J., Kip, Michelle M. A., Koffijberg, Hendrik, Benseler, Susanne M., Swart, Joost F., Vastert, Sebastiaan J., Wulffraat, Nico M., Yeung, Rae S. M., Johnson, Nicole, Luca, Nadia J., Miettunen, Paivi M., Schmeling, Heinrike, Marshall, Deborah A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8380593/
https://www.ncbi.nlm.nih.gov/pubmed/34275124
http://dx.doi.org/10.1007/s40744-021-00331-x
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author Grazziotin, Luiza R.
Currie, Gillian
Twilt, Marinka
Ijzerman, Maarten J.
Kip, Michelle M. A.
Koffijberg, Hendrik
Benseler, Susanne M.
Swart, Joost F.
Vastert, Sebastiaan J.
Wulffraat, Nico M.
Yeung, Rae S. M.
Johnson, Nicole
Luca, Nadia J.
Miettunen, Paivi M.
Schmeling, Heinrike
Marshall, Deborah A.
author_facet Grazziotin, Luiza R.
Currie, Gillian
Twilt, Marinka
Ijzerman, Maarten J.
Kip, Michelle M. A.
Koffijberg, Hendrik
Benseler, Susanne M.
Swart, Joost F.
Vastert, Sebastiaan J.
Wulffraat, Nico M.
Yeung, Rae S. M.
Johnson, Nicole
Luca, Nadia J.
Miettunen, Paivi M.
Schmeling, Heinrike
Marshall, Deborah A.
author_sort Grazziotin, Luiza R.
collection PubMed
description INTRODUCTION: Juvenile idiopathic arthritis (JIA) is a chronic rheumatic disease, whose multifaceted care path can lead to significant expenditure for the healthcare system. We aim to assess the real-world healthcare resource use (HCRU) and associated cost for children with JIA in a single center in Canada. METHODS: A single-center consecutive cohort of newly diagnosed patients with JIA attending the pediatric rheumatology clinic from 2011 to 2019 was identified using an administrative data algorithm and electronic medical charts. HCRU was estimated from six administrative health databases that included hospital admissions, emergency, outpatient care, practitioners’ visits, medication, and laboratory and imaging tests. Costs were assigned using appropriate sources. We reported the yearly overall and JIA-associated HCRU and costs 5 years prior to and 6 years after the first visit to the pediatric rheumatologist. The Zhao and Tian estimator was used to calculate cumulative mean costs over a 6-year timeframe. Results were stratified by disease subtype. RESULTS: A total of 389 patients were identified. The yearly total overall mean costs per patient ranged between $804 and $4460 during the 5 years prior to the first visit to the pediatric rheumatologist and $8529 and $10,651 for the 6 years after. Medication cost, driven by use of biologic therapies, and outpatient visits were the greatest contributor to the total cost. The overall cumulative mean cost for 6 years of care was $48,649 per patient, while the JIA-associated cumulative mean cost was $26,820 per patient. During the first year of rheumatology care, systemic onset JIA had the highest cumulative mean overall cost, while oligoarticular JIA had the lowest cumulative mean cost. CONCLUSION: The care pathway for children with JIA can be expensive, and complex—and varies by JIA subtype. Although the yearly total mean cost per patient was constant, the distribution of costs changes over time with the introduction of biologic therapies later in the care pathway. This study provides a better understanding of the JIA costs profile and can help inform future economic studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40744-021-00331-x.
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spelling pubmed-83805932021-09-08 Evaluation of Real-World Healthcare Resource Utilization and Associated Costs in Children with Juvenile Idiopathic Arthritis: A Canadian Retrospective Cohort Study Grazziotin, Luiza R. Currie, Gillian Twilt, Marinka Ijzerman, Maarten J. Kip, Michelle M. A. Koffijberg, Hendrik Benseler, Susanne M. Swart, Joost F. Vastert, Sebastiaan J. Wulffraat, Nico M. Yeung, Rae S. M. Johnson, Nicole Luca, Nadia J. Miettunen, Paivi M. Schmeling, Heinrike Marshall, Deborah A. Rheumatol Ther Original Research INTRODUCTION: Juvenile idiopathic arthritis (JIA) is a chronic rheumatic disease, whose multifaceted care path can lead to significant expenditure for the healthcare system. We aim to assess the real-world healthcare resource use (HCRU) and associated cost for children with JIA in a single center in Canada. METHODS: A single-center consecutive cohort of newly diagnosed patients with JIA attending the pediatric rheumatology clinic from 2011 to 2019 was identified using an administrative data algorithm and electronic medical charts. HCRU was estimated from six administrative health databases that included hospital admissions, emergency, outpatient care, practitioners’ visits, medication, and laboratory and imaging tests. Costs were assigned using appropriate sources. We reported the yearly overall and JIA-associated HCRU and costs 5 years prior to and 6 years after the first visit to the pediatric rheumatologist. The Zhao and Tian estimator was used to calculate cumulative mean costs over a 6-year timeframe. Results were stratified by disease subtype. RESULTS: A total of 389 patients were identified. The yearly total overall mean costs per patient ranged between $804 and $4460 during the 5 years prior to the first visit to the pediatric rheumatologist and $8529 and $10,651 for the 6 years after. Medication cost, driven by use of biologic therapies, and outpatient visits were the greatest contributor to the total cost. The overall cumulative mean cost for 6 years of care was $48,649 per patient, while the JIA-associated cumulative mean cost was $26,820 per patient. During the first year of rheumatology care, systemic onset JIA had the highest cumulative mean overall cost, while oligoarticular JIA had the lowest cumulative mean cost. CONCLUSION: The care pathway for children with JIA can be expensive, and complex—and varies by JIA subtype. Although the yearly total mean cost per patient was constant, the distribution of costs changes over time with the introduction of biologic therapies later in the care pathway. This study provides a better understanding of the JIA costs profile and can help inform future economic studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40744-021-00331-x. Springer Healthcare 2021-07-18 /pmc/articles/PMC8380593/ /pubmed/34275124 http://dx.doi.org/10.1007/s40744-021-00331-x Text en © The Author(s) 2021 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
Grazziotin, Luiza R.
Currie, Gillian
Twilt, Marinka
Ijzerman, Maarten J.
Kip, Michelle M. A.
Koffijberg, Hendrik
Benseler, Susanne M.
Swart, Joost F.
Vastert, Sebastiaan J.
Wulffraat, Nico M.
Yeung, Rae S. M.
Johnson, Nicole
Luca, Nadia J.
Miettunen, Paivi M.
Schmeling, Heinrike
Marshall, Deborah A.
Evaluation of Real-World Healthcare Resource Utilization and Associated Costs in Children with Juvenile Idiopathic Arthritis: A Canadian Retrospective Cohort Study
title Evaluation of Real-World Healthcare Resource Utilization and Associated Costs in Children with Juvenile Idiopathic Arthritis: A Canadian Retrospective Cohort Study
title_full Evaluation of Real-World Healthcare Resource Utilization and Associated Costs in Children with Juvenile Idiopathic Arthritis: A Canadian Retrospective Cohort Study
title_fullStr Evaluation of Real-World Healthcare Resource Utilization and Associated Costs in Children with Juvenile Idiopathic Arthritis: A Canadian Retrospective Cohort Study
title_full_unstemmed Evaluation of Real-World Healthcare Resource Utilization and Associated Costs in Children with Juvenile Idiopathic Arthritis: A Canadian Retrospective Cohort Study
title_short Evaluation of Real-World Healthcare Resource Utilization and Associated Costs in Children with Juvenile Idiopathic Arthritis: A Canadian Retrospective Cohort Study
title_sort evaluation of real-world healthcare resource utilization and associated costs in children with juvenile idiopathic arthritis: a canadian retrospective cohort study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8380593/
https://www.ncbi.nlm.nih.gov/pubmed/34275124
http://dx.doi.org/10.1007/s40744-021-00331-x
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