Socioeconomic burden of cystic fibrosis in Canada.


Journal

BMJ open respiratory research
ISSN: 2052-4439
Titre abrégé: BMJ Open Respir Res
Pays: England
ID NLM: 101638061

Informations de publication

Date de publication:
09 Aug 2024
Historique:
received: 11 01 2024
accepted: 11 07 2024
medline: 10 8 2024
pubmed: 10 8 2024
entrez: 9 8 2024
Statut: epublish

Résumé

Cost of illness studies are important tools to summarise the burden of disease for individuals, the healthcare system and society. The lack of standardised methods for reporting costs for cystic fibrosis (CF) makes it difficult to quantify the total socioeconomic burden. In this study, we aimed to comprehensively report the socioeconomic burden of CF in Canada. The total cost of CF in Canada was calculated by triangulating information from three sources (Canadian CF Registry, customised Burden of Disease survey and publicly available information). A prevalence-based, bottom-up, human capital approach was applied, and costs were categorised into four perspectives (ie, healthcare system, individual/caregiver, variable (ie, medicines) and society) and three domains (ie, direct, indirect and intangible). All costs were converted into 2021 Canadian dollars (CAD) and adjusted for inflation. The cost of cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapies was excluded. The total socioeconomic burden of CF in Canada in 2021 across the four perspectives was $C414 million. Direct costs accounted for two-thirds of the total costs, with medications comprising half of all direct costs. Out-of-pocket costs to individuals and caregivers represented 18.7% of all direct costs. Indirect costs representing absenteeism accounted for one-third of the total cost. This comprehensive cost of illness study for CF represents a community-oriented approach describing the socioeconomic burden of living with CF and serves as a benchmark for future studies.

Sections du résumé

BACKGROUND BACKGROUND
Cost of illness studies are important tools to summarise the burden of disease for individuals, the healthcare system and society. The lack of standardised methods for reporting costs for cystic fibrosis (CF) makes it difficult to quantify the total socioeconomic burden. In this study, we aimed to comprehensively report the socioeconomic burden of CF in Canada.
METHODS METHODS
The total cost of CF in Canada was calculated by triangulating information from three sources (Canadian CF Registry, customised Burden of Disease survey and publicly available information). A prevalence-based, bottom-up, human capital approach was applied, and costs were categorised into four perspectives (ie, healthcare system, individual/caregiver, variable (ie, medicines) and society) and three domains (ie, direct, indirect and intangible). All costs were converted into 2021 Canadian dollars (CAD) and adjusted for inflation. The cost of cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapies was excluded.
RESULTS RESULTS
The total socioeconomic burden of CF in Canada in 2021 across the four perspectives was $C414 million. Direct costs accounted for two-thirds of the total costs, with medications comprising half of all direct costs. Out-of-pocket costs to individuals and caregivers represented 18.7% of all direct costs. Indirect costs representing absenteeism accounted for one-third of the total cost.
CONCLUSION CONCLUSIONS
This comprehensive cost of illness study for CF represents a community-oriented approach describing the socioeconomic burden of living with CF and serves as a benchmark for future studies.

Identifiants

pubmed: 39122474
pii: 11/1/e002309
doi: 10.1136/bmjresp-2024-002309
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: AS, BSQ, SS and WDW received payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events: Vertex Pharmaceuticals, Educational events (BSQ and AS), Vyaire Medical (SS), Canadian Agency for Drugs and Technologies in Health (WDW) and Formulary Management Expert Committee (WDW). SS received consulting fees from Chiesi Farmaceutricals and Ndd technologies. PDWE, KS, ZMC, EM, JW and SYC are employees of Cystic Fibrosis Canada.

Auteurs

Olivier D Laflamme (OD)

Department of Community Health, and Epidemiology, Dalhousie University, Halifax, Nova Scotia, Canada.

Noah Johnson (N)

Department of Community Health, and Epidemiology, Dalhousie University, Halifax, Nova Scotia, Canada.

Kim Steele (K)

Cystic Fibrosis Canada, Toronto, Ontario, Canada.

Luis Chavez (L)

Department of Community Health, and Epidemiology, Dalhousie University, Halifax, Nova Scotia, Canada.

Stephanie Y Cheng (SY)

Cystic Fibrosis Canada, Toronto, Ontario, Canada.

Harvey R Rabin (HR)

Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

Zain M Cheema (ZM)

Cystic Fibrosis Canada, Toronto, Ontario, Canada.
Department of Medicine, Hamilton, Hamilton, Ontario, Canada.

Eunice Mamic (E)

Cystic Fibrosis Canada, Toronto, Ontario, Canada.

Lilian C Gomez (LC)

Department of Community Health, and Epidemiology, Dalhousie University, Halifax, Nova Scotia, Canada.

Jeanette Leong (J)

Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

Bradley S Quon (BS)

Division of Respiratory Medicine, Department of Medicine, The University of British Columbia, Vancouver, British Columbia, Canada.

Mohsen Sadatsafavi (M)

Respiratory Evaluation Sciences Program, Faculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, British Columbia, Canada.

Anne L Stephenson (AL)

Division of Respirology, St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.

W Dominika Wranik (WD)

Department of Community Health, and Epidemiology, Dalhousie University, Halifax, Nova Scotia, Canada.
Department of Public and International Affairs, Dalhousie University, Halifax, Nova Scotia, Canada.

Paul D W Eckford (PDW)

Cystic Fibrosis Canada, Toronto, Ontario, Canada.

John Wallenburg (J)

Cystic Fibrosis Canada, Toronto, Ontario, Canada.

Cole Bowerman (C)

Department of Community Health, and Epidemiology, Dalhousie University, Halifax, Nova Scotia, Canada.
Department of Medicine, Hamilton, Hamilton, Ontario, Canada.

Sanja Stanojevic (S)

Department of Community Health, and Epidemiology, Dalhousie University, Halifax, Nova Scotia, Canada sanja.stanojevic@dal.ca.

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