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Healthcare Cost of Multiple Sclerosis and in Relation to Disability Level in Alberta.
McCombe, Jennifer A; Smyth, Penelope; Kate, Mahesh; So, Helen; Vu, Khanh; Luu, Huong; Martins, Karen J B; Aponte-Hao, Sylvia; Nguyen, Phuong Uyen; Richer, Lawrence; Williamson, Tyler; Klarenbach, Scott W.
Afiliação
  • McCombe JA; Faculty of Medicine and Dentistry, Department of Medicine, University of Alberta, Edmonton, AB, Canada.
  • Smyth P; Faculty of Medicine and Dentistry, Department of Medicine, University of Alberta, Edmonton, AB, Canada.
  • Kate M; Faculty of Medicine and Dentistry, Department of Medicine, University of Alberta, Edmonton, AB, Canada.
  • So H; Faculty of Medicine and Dentistry, Real World Evidence Unit, University of Alberta, Edmonton, AB, Canada.
  • Vu K; Faculty of Medicine and Dentistry, Real World Evidence Unit, University of Alberta, Edmonton, AB, Canada.
  • Luu H; Faculty of Medicine and Dentistry, Real World Evidence Unit, University of Alberta, Edmonton, AB, Canada.
  • Martins KJB; Faculty of Medicine and Dentistry, Real World Evidence Unit, University of Alberta, Edmonton, AB, Canada.
  • Aponte-Hao S; Data and Research Services, Alberta SPOR SUPPORT Unit Data Platform, Calgary, AB, Canada.
  • Nguyen PU; The Centre for Health Informatics, University of Calgary, Calgary, AB, Canada.
  • Richer L; The Centre for Health Informatics, University of Calgary, Calgary, AB, Canada.
  • Williamson T; College of Health Sciences, University of Alberta, Edmonton, AB, Canada.
  • Klarenbach SW; Faculty of Medicine and Dentistry, Department of Pediatrics, University of Alberta, Edmonton, AB, Canada.
Can J Neurol Sci ; : 1-12, 2024 Oct 02.
Article em En | MEDLINE | ID: mdl-39356041
ABSTRACT

BACKGROUND:

We aimed to (1) report updated estimates of direct healthcare costs for people living with MS (pwMS), (2) contrast costs to a control population and (3) explore differences between disability levels among pwMS.

METHODS:

Administrative data were used to identify adult pwMS (MS cohort) and without (control cohort) in Alberta, Canada; disability level (based on the Expanded Disability Status Scale) among pwMS was estimated. One- and two-part generalized linear models with gamma distribution were used to estimate the incremental direct healthcare cost (2021 $CDN) of MS during a 1-year observation period.

RESULTS:

Adjusting for confounders, the total healthcare cost ratio was higher in the MS cohort (n = 13,089) versus control (n = 150,080) (5.24 [95% CI 5.08, 5.41]) with a predicted incremental cost of $15,016 (95% CI $14,497, $15,535) per person-year. Among the MS cohort, total predicted direct healthcare costs were higher with greater disability, $14,430 (95% CI $13,980, $14,880) to $58,697 ($51,514, $65,879) per person-year in mild and severe disability, respectively. The primary health resource cost component shifted from disease-modifying therapies in mild disability to supportive care in moderate and severe disability.

CONCLUSION:

Adult pwMS had greater direct healthcare costs than those without. Extrapolating to the population level (where 14,485 adult pwMS were identified in the study), it is estimated that $218 million per year in healthcare costs may be attributable to MS in Alberta. The significantly larger economic impact associated with greater disability underscores the importance of preventing or delaying disease progression and functional impairment in MS.
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Can J Neurol Sci Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Can J Neurol Sci Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá