Natural history and patterns of treatment change in Parkinson's disease: A retrospective chart review.

Discontinuation Disease progression Dopaminergic agonists Levodopa Monoamine oxidase B Parkinson’s disease Patterns Switch

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:
2022
Historique:
received: 29 09 2021
revised: 08 11 2021
accepted: 02 12 2021
entrez: 24 12 2021
pubmed: 25 12 2021
medline: 25 12 2021
Statut: epublish

Résumé

Parkinson's disease (PD) management seeks to balance the benefits and harms of current medications and evolves as the disease progresses. The natural history of PD and associated patterns of treatment change were analyzed to identify unmet needs in treatment of PD symptoms. Medical charts of patients from clinics across the US diagnosed on or before June 30th, 2014 were retrospectively reviewed. Index date was the first clinic visit, and the post-index period was through study end (June 30th, 2019). Outcomes included the frequency of therapy changes in the post-index period, reasons for therapy change, and adverse events (AE). Patients (n = 203) at index were receiving levodopa-peripheral dopa decarboxylase inhibitor (PDDI) monotherapy (47%), dopaminergic agonist (DA) monotherapy (15%), monoamine oxidase B inhibitor (MAOBI) monotherapy (14%), or combination therapies. The percentage of patients in Hoehn-Yahr disease Stage 1-2 was 52% at index and 20% by the end of the study. Frequencies of motor, non-motor, and neuropsychiatric symptoms increased during the enrollment. Levodopa-PDDI monotherapy and levodopa-PDDI + MAOBI had the lowest rates of therapy changes. Symptom relapse was the most common reason for dose escalation, add-on, and dose reduction, whereas AEs were the most common reason for discontinuation and switching. Dose escalation, add-on, and forward switch were most likely to occur in the first 6 months of treatment. Therapy changes during the study period reflected the challenging and evolving management of PD as the disease progresses. New or add-on symptomatic treatments are needed that are well-tolerated and able to control PD symptoms.

Sections du résumé

BACKGROUND BACKGROUND
Parkinson's disease (PD) management seeks to balance the benefits and harms of current medications and evolves as the disease progresses. The natural history of PD and associated patterns of treatment change were analyzed to identify unmet needs in treatment of PD symptoms.
METHODS METHODS
Medical charts of patients from clinics across the US diagnosed on or before June 30th, 2014 were retrospectively reviewed. Index date was the first clinic visit, and the post-index period was through study end (June 30th, 2019). Outcomes included the frequency of therapy changes in the post-index period, reasons for therapy change, and adverse events (AE).
RESULTS RESULTS
Patients (n = 203) at index were receiving levodopa-peripheral dopa decarboxylase inhibitor (PDDI) monotherapy (47%), dopaminergic agonist (DA) monotherapy (15%), monoamine oxidase B inhibitor (MAOBI) monotherapy (14%), or combination therapies. The percentage of patients in Hoehn-Yahr disease Stage 1-2 was 52% at index and 20% by the end of the study. Frequencies of motor, non-motor, and neuropsychiatric symptoms increased during the enrollment. Levodopa-PDDI monotherapy and levodopa-PDDI + MAOBI had the lowest rates of therapy changes. Symptom relapse was the most common reason for dose escalation, add-on, and dose reduction, whereas AEs were the most common reason for discontinuation and switching. Dose escalation, add-on, and forward switch were most likely to occur in the first 6 months of treatment.
CONCLUSIONS CONCLUSIONS
Therapy changes during the study period reflected the challenging and evolving management of PD as the disease progresses. New or add-on symptomatic treatments are needed that are well-tolerated and able to control PD symptoms.

Identifiants

pubmed: 34950865
doi: 10.1016/j.prdoa.2021.100125
pii: S2590-1125(21)00037-2
pmc: PMC8671728
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100125

Informations de copyright

© 2021 Published by Elsevier Ltd.

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.

Références

Parkinsonism Relat Disord. 2020 Apr;73:31-34
pubmed: 32224439
Am J Manag Care. 2008 Mar;14(2 Suppl):S40-8
pubmed: 18402507
J Parkinsons Dis. 2019;9(4):749-759
pubmed: 31424419
Lancet Neurol. 2020 May;19(5):452-461
pubmed: 32171387
Yale J Biol Med. 2016 Mar 24;89(1):37-47
pubmed: 27505015
Mov Disord. 2011 Oct;26 Suppl 3:S42-80
pubmed: 22021174
Neuroimage. 2019 Apr 15;190:79-93
pubmed: 30465864
J Neurochem. 2016 Oct;139 Suppl 1:318-324
pubmed: 27401947
Expert Opin Drug Saf. 2014 Aug;13(8):1055-69
pubmed: 24962891
Mov Disord. 2018 Aug;33(8):1248-1266
pubmed: 29570866
J Neural Transm (Vienna). 2018 Jun;125(6):953-963
pubmed: 29484495
JAMA. 2014 Apr 23-30;311(16):1670-83
pubmed: 24756517
Neurology. 2018 Dec 11;91(24):e2238-e2243
pubmed: 30404780
N Engl J Med. 2019 Jan 24;380(4):315-324
pubmed: 30673543
Front Aging Neurosci. 2020 Sep 03;12:571185
pubmed: 33101007
Lancet. 2014 Sep 27;384(9949):1196-205
pubmed: 24928805

Auteurs

Prakash Navaratnam (P)

DataMed Solutions, LLC, New York, NY, India.

Steve Arcona (S)

Cerevel Therapeutics, Cambridge, MA, India.

Howard S Friedman (HS)

DataMed Solutions, LLC, New York, NY, India.

Matthew Leoni (M)

Cerevel Therapeutics, Cambridge, MA, India.

Shajahan Shaik (S)

Indegene, Inc, Bangalore, India.

Rahul Sasane (R)

Cerevel Therapeutics, Cambridge, MA, India.

Classifications MeSH