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

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: Medi...

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Autores principales: Navaratnam, Prakash, Arcona, Steve, Friedman, Howard S., Leoni, Matthew, Shaik, Shajahan, Sasane, Rahul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671728/
https://www.ncbi.nlm.nih.gov/pubmed/34950865
http://dx.doi.org/10.1016/j.prdoa.2021.100125
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author Navaratnam, Prakash
Arcona, Steve
Friedman, Howard S.
Leoni, Matthew
Shaik, Shajahan
Sasane, Rahul
author_facet Navaratnam, Prakash
Arcona, Steve
Friedman, Howard S.
Leoni, Matthew
Shaik, Shajahan
Sasane, Rahul
author_sort Navaratnam, Prakash
collection PubMed
description 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: 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: 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: 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.
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spelling pubmed-86717282021-12-22 Natural history and patterns of treatment change in Parkinson’s disease: A retrospective chart review Navaratnam, Prakash Arcona, Steve Friedman, Howard S. Leoni, Matthew Shaik, Shajahan Sasane, Rahul Clin Park Relat Disord Original Article 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: 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: 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: 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. Elsevier 2021-12-08 /pmc/articles/PMC8671728/ /pubmed/34950865 http://dx.doi.org/10.1016/j.prdoa.2021.100125 Text en © 2021 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Navaratnam, Prakash
Arcona, Steve
Friedman, Howard S.
Leoni, Matthew
Shaik, Shajahan
Sasane, Rahul
Natural history and patterns of treatment change in Parkinson’s disease: A retrospective chart review
title Natural history and patterns of treatment change in Parkinson’s disease: A retrospective chart review
title_full Natural history and patterns of treatment change in Parkinson’s disease: A retrospective chart review
title_fullStr Natural history and patterns of treatment change in Parkinson’s disease: A retrospective chart review
title_full_unstemmed Natural history and patterns of treatment change in Parkinson’s disease: A retrospective chart review
title_short Natural history and patterns of treatment change in Parkinson’s disease: A retrospective chart review
title_sort natural history and patterns of treatment change in parkinson’s disease: a retrospective chart review
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671728/
https://www.ncbi.nlm.nih.gov/pubmed/34950865
http://dx.doi.org/10.1016/j.prdoa.2021.100125
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