Dopamine agonist monotherapy utilization in patients with Parkinson’s disease

Objectives: To characterize patients with Parkinson’s disease (PD) who initiated dopamine agonist (DA) monotherapy, describe medication utilization and provider types, and estimate medication adherence and discontinuation rates. Methods: Retrospective study identified patients with PD in the Optum R...

Full description

Bibliographic Details
Main Authors: Monica Frazer, Steve Arcona, Lisa Le, Rahul Sasane
Format: Article
Language:English
Published: Elsevier 2023-01-01
Series:Clinical Parkinsonism & Related Disorders
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2590112522000445
_version_ 1827948425229893632
author Monica Frazer
Steve Arcona
Lisa Le
Rahul Sasane
author_facet Monica Frazer
Steve Arcona
Lisa Le
Rahul Sasane
author_sort Monica Frazer
collection DOAJ
description Objectives: To characterize patients with Parkinson’s disease (PD) who initiated dopamine agonist (DA) monotherapy, describe medication utilization and provider types, and estimate medication adherence and discontinuation rates. Methods: Retrospective study identified patients with PD in the Optum Research Database and included those with ≥1 claim for DA or levodopa between 09/01/2012 and 12/31/2018, ≥2 PD diagnoses, commercial or Medicare Advantage Part D (MAPD) insurance, ≥40 years old, and continuous medical and pharmacy coverage ≥12 months before and after index date. A subset of patients receiving DA monotherapy was selected for this analysis. Variables were analyzed descriptively. Adherence was measured with medication possession ratio (MPR) and proportion of days covered (PDC); defined as ≥0.80. Results: Patients (N = 642) had mean (SD) age of 70.2 (9.9) years, 70.6 % had MAPD coverage, and 61.7 % were male. Neurologists prescribed 64.6 % of DA monotherapy, and 56.9 % of patients had ≥2 PD diagnoses before or on the index date. Index therapy was discontinued by 44.1 % of patients, and 55.9 % persisted for 12 months without change. Mean (SD) time to discontinuation was 102 (79) days. Mean (SD) MPR for patients (n = 562) with ≥2 fills was 0.84 (0.2); 70.3 % were MPR adherent. Mean (SD) PDC for all 642 patients was 0.66 (0.3); 50.5 % were PDC adherent. Conclusion: Adherence and continuation of therapy were suboptimal, which could translate into poor patient outcomes. Future studies could provide insights on the impact of low adherence and persistence with DA monotherapy.
first_indexed 2024-04-09T12:54:02Z
format Article
id doaj.art-a7403977a7264ae58b331915b5389c34
institution Directory Open Access Journal
issn 2590-1125
language English
last_indexed 2024-04-09T12:54:02Z
publishDate 2023-01-01
publisher Elsevier
record_format Article
series Clinical Parkinsonism & Related Disorders
spelling doaj.art-a7403977a7264ae58b331915b5389c342023-05-14T04:29:27ZengElsevierClinical Parkinsonism & Related Disorders2590-11252023-01-018100173Dopamine agonist monotherapy utilization in patients with Parkinson’s diseaseMonica Frazer0Steve Arcona1Lisa Le2Rahul Sasane3QualityMetric, USACerevel Therapeutics, USAOptum HEOR, USA; Corresponding author at: Optum Life Sciences, 11000 Optum Circle, Eden Prairie, MN 55344, USA.Cerevel Therapeutics, USAObjectives: To characterize patients with Parkinson’s disease (PD) who initiated dopamine agonist (DA) monotherapy, describe medication utilization and provider types, and estimate medication adherence and discontinuation rates. Methods: Retrospective study identified patients with PD in the Optum Research Database and included those with ≥1 claim for DA or levodopa between 09/01/2012 and 12/31/2018, ≥2 PD diagnoses, commercial or Medicare Advantage Part D (MAPD) insurance, ≥40 years old, and continuous medical and pharmacy coverage ≥12 months before and after index date. A subset of patients receiving DA monotherapy was selected for this analysis. Variables were analyzed descriptively. Adherence was measured with medication possession ratio (MPR) and proportion of days covered (PDC); defined as ≥0.80. Results: Patients (N = 642) had mean (SD) age of 70.2 (9.9) years, 70.6 % had MAPD coverage, and 61.7 % were male. Neurologists prescribed 64.6 % of DA monotherapy, and 56.9 % of patients had ≥2 PD diagnoses before or on the index date. Index therapy was discontinued by 44.1 % of patients, and 55.9 % persisted for 12 months without change. Mean (SD) time to discontinuation was 102 (79) days. Mean (SD) MPR for patients (n = 562) with ≥2 fills was 0.84 (0.2); 70.3 % were MPR adherent. Mean (SD) PDC for all 642 patients was 0.66 (0.3); 50.5 % were PDC adherent. Conclusion: Adherence and continuation of therapy were suboptimal, which could translate into poor patient outcomes. Future studies could provide insights on the impact of low adherence and persistence with DA monotherapy.http://www.sciencedirect.com/science/article/pii/S2590112522000445Parkinson’s diseaseDopamine agonistDopamine agonist monotherapyAdherenceDiscontinuation ratesMedication utilization
spellingShingle Monica Frazer
Steve Arcona
Lisa Le
Rahul Sasane
Dopamine agonist monotherapy utilization in patients with Parkinson’s disease
Clinical Parkinsonism & Related Disorders
Parkinson’s disease
Dopamine agonist
Dopamine agonist monotherapy
Adherence
Discontinuation rates
Medication utilization
title Dopamine agonist monotherapy utilization in patients with Parkinson’s disease
title_full Dopamine agonist monotherapy utilization in patients with Parkinson’s disease
title_fullStr Dopamine agonist monotherapy utilization in patients with Parkinson’s disease
title_full_unstemmed Dopamine agonist monotherapy utilization in patients with Parkinson’s disease
title_short Dopamine agonist monotherapy utilization in patients with Parkinson’s disease
title_sort dopamine agonist monotherapy utilization in patients with parkinson s disease
topic Parkinson’s disease
Dopamine agonist
Dopamine agonist monotherapy
Adherence
Discontinuation rates
Medication utilization
url http://www.sciencedirect.com/science/article/pii/S2590112522000445
work_keys_str_mv AT monicafrazer dopamineagonistmonotherapyutilizationinpatientswithparkinsonsdisease
AT stevearcona dopamineagonistmonotherapyutilizationinpatientswithparkinsonsdisease
AT lisale dopamineagonistmonotherapyutilizationinpatientswithparkinsonsdisease
AT rahulsasane dopamineagonistmonotherapyutilizationinpatientswithparkinsonsdisease