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Patients’ Preferences for Adjunctive Parkinson’s Disease Treatments: A Discrete-Choice Experiment
BACKGROUND: Several adjunctive medications are available to reduce OFF time between levodopa/carbidopa (LD/CD) doses for people with Parkinson’s disease (PD). OBJECTIVE: To explore how individuals with PD balance benefits and burdens when considering adjunctive medications. METHODS: US adults (30–83...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10505378/ https://www.ncbi.nlm.nih.gov/pubmed/37724313 http://dx.doi.org/10.2147/PPA.S420051 |
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author | Serbin, Michael Marras, Connie Mansfield, Carol Leach, Colton Yonan, Charles Sheehan, Margaret Donnelly, Anne Klepitskaya, Olga |
author_facet | Serbin, Michael Marras, Connie Mansfield, Carol Leach, Colton Yonan, Charles Sheehan, Margaret Donnelly, Anne Klepitskaya, Olga |
author_sort | Serbin, Michael |
collection | PubMed |
description | BACKGROUND: Several adjunctive medications are available to reduce OFF time between levodopa/carbidopa (LD/CD) doses for people with Parkinson’s disease (PD). OBJECTIVE: To explore how individuals with PD balance benefits and burdens when considering adjunctive medications. METHODS: US adults (30–83 years) with self-reported PD, currently treated with LD/CD, who experienced OFF episodes were recruited through the Fox Insight study to complete a discrete-choice experiment survey. Respondents selected among experimentally designed profiles for hypothetical adjunctive PD treatments that varied in efficacy (additional ON time), potential adverse effects (troublesome dyskinesia, risk of diarrhea, risk of change in bodily fluid color), and dosing frequency or the option “No additional medicine”. Data were analyzed with random-parameters logit models. RESULTS: Respondents (N=480) would require ≥60 additional minutes of daily ON time to accept either a 40% risk of change in bodily fluid color or 10 additional minutes with troublesome dyskinesia daily. Respondents would require 40 additional minutes of daily ON time to accept a 10% risk of diarrhea and 22 additional minutes of daily ON time to switch from 1 additional pill each day to 1 pill with each LD/CD dose. On average, respondents preferred adjunctive PD medication over no additional medication. Results predicted that 59.1% of respondents would select a hypothetical treatment profile similar to opicapone, followed by no additional medication (27.5%) and a hypothetical treatment profile similar to entacapone (13.4%). LIMITATIONS: The data collected were based on responses to hypothetical choice profiles in the survey questions. The attributes and levels selected for this study were intended to reflect the characteristics of opicapone and entacapone; attributes associated with other adjunctive therapies were not evaluated. CONCLUSION: Patients with PD expressed interest in adjunctive treatment to increase ON time and would accept reduced ON time to avoid adverse effects. |
format | Online Article Text |
id | pubmed-10505378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-105053782023-09-18 Patients’ Preferences for Adjunctive Parkinson’s Disease Treatments: A Discrete-Choice Experiment Serbin, Michael Marras, Connie Mansfield, Carol Leach, Colton Yonan, Charles Sheehan, Margaret Donnelly, Anne Klepitskaya, Olga Patient Prefer Adherence Original Research BACKGROUND: Several adjunctive medications are available to reduce OFF time between levodopa/carbidopa (LD/CD) doses for people with Parkinson’s disease (PD). OBJECTIVE: To explore how individuals with PD balance benefits and burdens when considering adjunctive medications. METHODS: US adults (30–83 years) with self-reported PD, currently treated with LD/CD, who experienced OFF episodes were recruited through the Fox Insight study to complete a discrete-choice experiment survey. Respondents selected among experimentally designed profiles for hypothetical adjunctive PD treatments that varied in efficacy (additional ON time), potential adverse effects (troublesome dyskinesia, risk of diarrhea, risk of change in bodily fluid color), and dosing frequency or the option “No additional medicine”. Data were analyzed with random-parameters logit models. RESULTS: Respondents (N=480) would require ≥60 additional minutes of daily ON time to accept either a 40% risk of change in bodily fluid color or 10 additional minutes with troublesome dyskinesia daily. Respondents would require 40 additional minutes of daily ON time to accept a 10% risk of diarrhea and 22 additional minutes of daily ON time to switch from 1 additional pill each day to 1 pill with each LD/CD dose. On average, respondents preferred adjunctive PD medication over no additional medication. Results predicted that 59.1% of respondents would select a hypothetical treatment profile similar to opicapone, followed by no additional medication (27.5%) and a hypothetical treatment profile similar to entacapone (13.4%). LIMITATIONS: The data collected were based on responses to hypothetical choice profiles in the survey questions. The attributes and levels selected for this study were intended to reflect the characteristics of opicapone and entacapone; attributes associated with other adjunctive therapies were not evaluated. CONCLUSION: Patients with PD expressed interest in adjunctive treatment to increase ON time and would accept reduced ON time to avoid adverse effects. Dove 2023-09-13 /pmc/articles/PMC10505378/ /pubmed/37724313 http://dx.doi.org/10.2147/PPA.S420051 Text en © 2023 Serbin et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Serbin, Michael Marras, Connie Mansfield, Carol Leach, Colton Yonan, Charles Sheehan, Margaret Donnelly, Anne Klepitskaya, Olga Patients’ Preferences for Adjunctive Parkinson’s Disease Treatments: A Discrete-Choice Experiment |
title | Patients’ Preferences for Adjunctive Parkinson’s Disease Treatments: A Discrete-Choice Experiment |
title_full | Patients’ Preferences for Adjunctive Parkinson’s Disease Treatments: A Discrete-Choice Experiment |
title_fullStr | Patients’ Preferences for Adjunctive Parkinson’s Disease Treatments: A Discrete-Choice Experiment |
title_full_unstemmed | Patients’ Preferences for Adjunctive Parkinson’s Disease Treatments: A Discrete-Choice Experiment |
title_short | Patients’ Preferences for Adjunctive Parkinson’s Disease Treatments: A Discrete-Choice Experiment |
title_sort | patients’ preferences for adjunctive parkinson’s disease treatments: a discrete-choice experiment |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10505378/ https://www.ncbi.nlm.nih.gov/pubmed/37724313 http://dx.doi.org/10.2147/PPA.S420051 |
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