An assessment of Parkinson's disease medication treatment patterns in the Medicaid population.

Dopamine agonist Levodopa Medicaid Medication adherence Parkinson’s disease

Journal

Clinical parkinsonism & related disorders
ISSN: 2590-1125
Titre abrégé: Clin Park Relat Disord
Pays: England
ID NLM: 101761473

Informations de publication

Date de publication:
2021
Historique:
received: 03 06 2021
revised: 17 09 2021
accepted: 20 09 2021
entrez: 25 10 2021
pubmed: 26 10 2021
medline: 26 10 2021
Statut: epublish

Résumé

Most Parkinson's disease (PD) medication adherence studies have focused on patients with commercial or Medicare health insurance coverage. However, less is known regarding medication treatment patterns within the Medicaid population. This retrospective cohort study utilized 2011-2019 administrative healthcare claims from 7 state Medicaid programs. We compared newly diagnosed patients with PD started on either levodopa or a dopamine agonist (DA). Baseline comorbidities were compared. Outcomes were assessed during a 12-month post-index observation period, and included total medication days, proportion of days covered (PDC), adherence status, persistence to initiating PD medication, and time to non-persistence of initiating PD medication. Our study sample of 805 Medicaid patients had an average age of 54.1 years, with 52.0% being female. Levodopa was the predominant PD medication at initiation (75.4%). Roughly half of patients had a baseline depressive disorder and nearly 40% had an anxiety disorder. Levodopa patients had a significantly higher PDC compared to DA patients (0.621 vs. 0.546, p = 0.007). An adjusted logistic regression model showed no significant difference in the number of adherent patients between the two groups (p = 0.058). An adjusted Cox proportional hazards model controlling for demographic and baseline variables showed a 26% lower risk of non-persistence for levodopa patients versus DA patients (HR 0.740, CI 0.597-0.917, p = 0.006). Adherence and persistence rates were suboptimal following initiation of either levodopa or DA medication for patients with PD in Medicaid programs, though rates were better for those initiated on levodopa.

Identifiants

pubmed: 34693271
doi: 10.1016/j.prdoa.2021.100109
pii: S2590-1125(21)00021-9
pmc: PMC8512608
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100109

Informations de copyright

© 2021 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Michael Johnsrud (M)

TxCORE (Texas Center for Health Outcomes Research and Education), The University of Texas at Austin, 2409 University Avenue, Austin, TX 78712, USA.

Kristin Richards (K)

TxCORE (Texas Center for Health Outcomes Research and Education), The University of Texas at Austin, 2409 University Avenue, Austin, TX 78712, USA.

Steve Arcona (S)

Cerevel Therapeutics, 222 Jacobs Street, Suite 200, Cambridge, MA 02141, USA.

Rahul Sasané (R)

Cerevel Therapeutics, 222 Jacobs Street, Suite 200, Cambridge, MA 02141, USA.

Matthew Leoni (M)

Cerevel Therapeutics, 222 Jacobs Street, Suite 200, Cambridge, MA 02141, USA.

Classifications MeSH