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Economic burden of Parkinson’s disease : a multinational, real-world, cost-of-illness study

datacite.subject.fosCiências Médicas::Ciências da Saúde
datacite.subject.sdg03:Saúde de Qualidade
dc.contributor.authorChaudhuri, K. Ray
dc.contributor.authorAzulay, Jean-Philippe
dc.contributor.authorOdin, Per
dc.contributor.authorLindvall, Susanna
dc.contributor.authorDomingos, Josefa
dc.contributor.authorAlobaidi, Ali
dc.contributor.authorKandukuri, Prasanna L.
dc.contributor.authorChaudhari, Vivek S.
dc.contributor.authorParra, Juan Carlos
dc.contributor.authorYamazaki, Toru
dc.contributor.authorOddsdottir, Julia
dc.contributor.authorWright, Jack
dc.contributor.authorMartinez-Martin, Pablo
dc.date.accessioned2026-03-25T12:38:58Z
dc.date.available2026-03-25T12:38:58Z
dc.date.issued2024-03
dc.description.abstractBackground: Parkinson’s disease is now one of the fastest-growing neurodegenerative disorders in the developed world, with an increasing prevalence and associated socioeconomic costs. Progression of the disease leads to a gradual deterioration in patients’ quality of life, despite optimal treatment, and both medical and societal needs increase, often with the assistance of paid and/or unpaid caregivers. Objective: We aimed to quantify the incremental economic burden of Parkinson’s disease by disease severity in a real-world setting across differing geographic regions. Methods: Demographics, clinical characteristics, health status, patient quality of life, caregiver burden, and healthcare resource utilization data were drawn from the Adelphi Parkinson’s Disease Specific Program™, conducted in the USA, five European countries, and Japan. Results: A total of 563 neurologists provided data for 5299 individuals with Parkinson’s disease; 61% were male, with a mean age of 64 years. Approximately 15% of individuals were deemed to have advanced disease, with significantly more comorbidities, and a poorer quality of life, than those with non-advanced disease. Overall, the mean annual healthcare resource utilization increased significantly with advancing disease, and resulted in a three-fold difference in the USA and Europe. The main drivers behind the high economic burden included hospitalizations, prescription medications, and indirect costs. Conclusions: People with Parkinson’s disease, and their caregivers, incur a higher economic burden as their disease progresses. Future interventions that can control symptoms or slow disease progression could reduce the burden on people with Parkinson’s disease and their caregivers, whilst also substantially impacting societal costs.eng
dc.identifier.citationChaudhuri, K.R., Azulay, JP., Odin, P. et al. Economic Burden of Parkinson’s Disease: A Multinational, Real-World, Cost-of-Illness Study. Drugs - Real World Outcomes 11, 1–11 (2024). https://doi.org/10.1007/s40801-023-00410-1
dc.identifier.doi10.1007/s40801-023-00410-1
dc.identifier.issn2198-9788
dc.identifier.urihttp://hdl.handle.net/10400.26/62430
dc.language.isoeng
dc.peerreviewedyes
dc.publisherSpringer Nature
dc.relation.hasversionhttps://doi.org/10.1007/s40801-023-00410-1
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjecteconomic burden
dc.subjectParkinson’s disease
dc.titleEconomic burden of Parkinson’s disease : a multinational, real-world, cost-of-illness studyeng
dc.typecontribution to journal
dspace.entity.typePublication
oaire.citation.endPage11
oaire.citation.startPage1
oaire.citation.titleDrugs - Real World Outcomes
oaire.citation.volume11
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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