Costs of Illness for Huntington's Disease: A Systematic Review.
Journal
PharmacoEconomics - open
ISSN: 2509-4254
Titre abrégé: Pharmacoecon Open
Pays: Switzerland
ID NLM: 101700780
Informations de publication
Date de publication:
15 Oct 2024
15 Oct 2024
Historique:
accepted:
23
09
2024
medline:
15
10
2024
pubmed:
15
10
2024
entrez:
14
10
2024
Statut:
aheadofprint
Résumé
Huntington's disease (HD) is associated with significant financial burden for patients and payers. The objective was to identify and quantify costs of HD by stage of disease progression. A systematic search of Medline, Embase, Scopus, and Cochrane Library was used to identify types of costs that are frequently reported for individuals diagnosed with HD and to quantify those costs across early, middle, and late stages of HD. Full-text, original research articles were included if they reported costs specific to HD burden. To standardize stage-level costs, Shoulson Fahn and Barthel Index scores were combined to estimate the cost for early, middle-, and late-stage HD. A total of 692 abstracts were identifie,d and following abstract screening, a total of 80 full-text articles were reviewed for inclusion. Only five studies were included for extraction and synthesis including three from the USA, one from the United Kingdom (UK), and one from Peru. Annual inpatient, outpatient, drug costs, and caregiving costs all increased substantially as disease progressed. Outpatient costs were approximately 2.5 times greater than inpatient costs for early and middle stages of HD. Among all the costs associated with HD, annual caregiver cost emerges as the most significant costs in the economic burden of HD, ranging from a minimum of $6041 for early stage to a maximum of $133,200 for late-stage HD. Significant variation was observed across studies, especially comparing costs observed in Peru with the USA and UK. Outpatient costs exceed inpatient costs, especially in early and middle stages, underscoring the importance of outpatient care. All costs seem to rise rapidly, in a nonlinear fashion, as patients advance to later stages. While only two studies reported caregiver burden, these costs were significanly higher in the most severe stage, where patients were completely dependent on a caregiver. This review highlights the complexity of cost assessment in HD and underscores the need for consistent methods and further research to guide effective policy actions.
Sections du résumé
BACKGROUND
BACKGROUND
Huntington's disease (HD) is associated with significant financial burden for patients and payers. The objective was to identify and quantify costs of HD by stage of disease progression.
METHODS
METHODS
A systematic search of Medline, Embase, Scopus, and Cochrane Library was used to identify types of costs that are frequently reported for individuals diagnosed with HD and to quantify those costs across early, middle, and late stages of HD. Full-text, original research articles were included if they reported costs specific to HD burden. To standardize stage-level costs, Shoulson Fahn and Barthel Index scores were combined to estimate the cost for early, middle-, and late-stage HD.
RESULTS
RESULTS
A total of 692 abstracts were identifie,d and following abstract screening, a total of 80 full-text articles were reviewed for inclusion. Only five studies were included for extraction and synthesis including three from the USA, one from the United Kingdom (UK), and one from Peru. Annual inpatient, outpatient, drug costs, and caregiving costs all increased substantially as disease progressed. Outpatient costs were approximately 2.5 times greater than inpatient costs for early and middle stages of HD. Among all the costs associated with HD, annual caregiver cost emerges as the most significant costs in the economic burden of HD, ranging from a minimum of $6041 for early stage to a maximum of $133,200 for late-stage HD. Significant variation was observed across studies, especially comparing costs observed in Peru with the USA and UK.
CONCLUSION
CONCLUSIONS
Outpatient costs exceed inpatient costs, especially in early and middle stages, underscoring the importance of outpatient care. All costs seem to rise rapidly, in a nonlinear fashion, as patients advance to later stages. While only two studies reported caregiver burden, these costs were significanly higher in the most severe stage, where patients were completely dependent on a caregiver. This review highlights the complexity of cost assessment in HD and underscores the need for consistent methods and further research to guide effective policy actions.
Identifiants
pubmed: 39402413
doi: 10.1007/s41669-024-00531-5
pii: 10.1007/s41669-024-00531-5
doi:
Types de publication
Journal Article
Systematic Review
Langues
eng
Informations de copyright
© 2024. The Author(s).
Références
Bruzelius E, Scarpa J, Zhao Y, Basu S, Faghmous JH, Baum A. Huntington’s disease in the United States: variation by demographic and socioeconomic factors. Mov Disord. 2019;34(6):858–65. https://doi.org/10.1002/mds.27653 .
doi: 10.1002/mds.27653
pubmed: 30868663
pmcid: 6579693
George Yohrling LS, Raimundo K, Crowell V, Lovecky D, Vetter L. Prevalence of Huntington’s disease in the US. Neurotherapeutics. 2019;16(4):1387. [Online]. http://ovidsp.ovid.com/ovidweb.cgi?T=JS&PAGE=reference&D=emedx&NEWS=N&AN=631892123 .
Divino V, et al. The direct medical costs of Huntington’s disease by stage. A retrospective commercial and Medicaid claims data analysis. J Med Econ. 2013;16(8):1043–50. https://doi.org/10.3111/13696998.2013.818545 .
doi: 10.3111/13696998.2013.818545
pubmed: 23789925
Huntington’s Disease Society of America. Overview of Huntington’s disease. Hdsa.org. 2019. [Online]. https://hdsa.org/what-is-hd/overview-of-huntingtons-disease/ .
Ahmed M, Mridha D. Unraveling huntington’s disease: a report on genetic testing, clinical presentation, and disease progression. Cureus. 2023. https://doi.org/10.7759/cureus.43377 .
doi: 10.7759/cureus.43377
pubmed: 38299137
pmcid: 10828751
European Huntington’s Disease Network. About Huntington’s disease. ehdn.org. [Online]. https://ehdn.org/about-hd/ .
Ferguson MW, Kennedy CJ, Palpagama TH, Waldvogel HJ, Faull RLM, Kwakowsky A. Current and possible future therapeutic options for Huntington’s disease. J Cent Nerv Syst Dis. 2022;14:11795735221092516. https://doi.org/10.1177/11795735221092517 .
doi: 10.1177/11795735221092517
Moher D, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med. 2009. https://doi.org/10.1371/journal.pmed.1000097 .
doi: 10.1371/journal.pmed.1000097
pubmed: 19753108
pmcid: 2735783
Husereau D, et al. Consolidated health economic evaluation reporting standards (CHEERS)-explanation and elaboration: a report of the ISPOR health economic evaluation publication guidelines good reporting practices task force. Value Health. 2013;16(2):231–50. https://doi.org/10.1016/j.jval.2013.02.002 .
doi: 10.1016/j.jval.2013.02.002
pubmed: 23538175
Covidence systematic review software [Internet]. Melbourne: Veritas Health Innovation. www.covidence.org .
OANDA Corporation. Currency Converter [Internet]. 2019 [cited 2019 Jun 30]. https://www1.oanda.com/currency/converter/ .
Basu A. Estimating costs and valuations of non-health benefits in cost-effectiveness analysis. In: Neumann PJ, Sanders GD, Russell LB, Siegel JE, Ganiats TG, editors. Cost-effectiveness heal. med. Second. New York: Oxford University Press; 2017. p. 20.
Jones C, et al. The societal cost of Huntington’s disease: are we underestimating the burden? Eur J Neurol. 2016;23(10):1588–90. https://doi.org/10.1111/ene.13107 .
doi: 10.1111/ene.13107
pubmed: 27461550
Silva-Paredes G, Urbanos-Garrido RM, Inca-Martinez M, Rabinowitz D, Cornejo-Olivas MR. Economic burden of Huntington’s disease in Peru. BMC Health Serv Res. 2019;19(1):1–10. https://doi.org/10.1186/s12913-019-4806-6 .
doi: 10.1186/s12913-019-4806-6
Wild EJ, Tabrizi SJ. Premanifest and early Huntington’s disease. Huntington’s Dis. 2014. https://doi.org/10.1093/med/9780199929146.003.0005 .
doi: 10.1093/med/9780199929146.003.0005
Patel AM, Chang E, Paydar C, Reddy SR. Healthcare utilization and direct medical costs of Huntington’s disease among Medicaid beneficiaries in the United States. J Med Econ. 2023;26(1):811–20. https://doi.org/10.1080/13696998.2023.2222561 .
doi: 10.1080/13696998.2023.2222561
pubmed: 37285853
Exuzides A, et al. Healthcare utilization and cost burden of Huntington’s disease among Medicare beneficiaries in the United States. J Med Econ. 2021;24(1):1327–36. https://doi.org/10.1080/13696998.2021.2002579 .
doi: 10.1080/13696998.2021.2002579
pubmed: 34730477
Sanders GD, et al. Recommendations for conduct, methodological practices, and reporting of cost-effectiveness analyses: second panel on cost-effectiveness in health and medicine. JAMA. 2016;316(10):1093–103. https://doi.org/10.1001/jama.2016.12195 .
doi: 10.1001/jama.2016.12195
pubmed: 27623463