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j.jns.2024.123092.pdf | 2.46 MB | Adobe PDF | 見る/開く |
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DCフィールド | 値 | 言語 |
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dc.contributor.author | Fukasawa, Toshiki | en |
dc.contributor.author | Nakanishi, Etsuro | en |
dc.contributor.author | Shimoda, Hiroo | en |
dc.contributor.author | Shinoda, Katsumi | en |
dc.contributor.author | Ito, Satoru | en |
dc.contributor.author | Asada, Shinji | en |
dc.contributor.author | Yoshida, Satomi | en |
dc.contributor.author | Tanaka-Mizuno, Sachiko | en |
dc.contributor.author | Mizuno, Kayoko | en |
dc.contributor.author | Takahashi, Ryosuke | en |
dc.contributor.author | Kawakami, Koji | en |
dc.date.accessioned | 2025-06-09T06:35:03Z | - |
dc.date.available | 2025-06-09T06:35:03Z | - |
dc.date.issued | 2024-07-15 | - |
dc.identifier.uri | http://hdl.handle.net/2433/294603 | - |
dc.description.abstract | Background: Understanding the different patterns of adherence to istradefylline treatment is essential to identifying Parkinson's disease (PD) patients who might benefit from targeted interventions Objectives: This descriptive study aimed to identify longitudinal istradefylline adherence patterns and to characterize factors associated with them. Methods: We identified PD patients aged 21-99 years who initiated istradefylline treatment in a Japanese hospital administrative database. Group-based trajectory modeling was used to model the monthly proportion of days covered over time to identify distinct 360-day adherence patterns. Factors associated with each adherence pattern were assessed using univariable multinomial logistic regression models. Results: Of 2088 eligible PD patients, 4 distinct adherence groups were identified: consistently high adherence (56.8%); rapidly declining adherence (25.8%); gradually declining adherence (8.5%); and gradually declining and then recovering adherence (9.0%). Compared to the consistently high adherence group, the other groups had the following characteristics associated with a likelihood of lower adherence: the rapidly declining adherence group received fewer dopamine agonists (63.8% vs. 69.4%), monoamine oxidase B (MAO-B) inhibitors (26.8% vs. 31.6%), and catechol-O-methyl transferase inhibitors (31.6% vs. 37.0%) and had a higher prevalence of anxiety/mood disorders (29.9% vs. 24.6%); the gradually declining adherence group received fewer MAO-B inhibitors (22.5% vs. 31.6%) and amantadine (8.4% vs. 16.1%) and had a higher prevalence of mild cognitive impairment/dementia (27.0% vs. 18.8%); and the declining and then recovering adherence group had a higher prevalence of anxiety/mood disorders (34.2% vs. 24.6%). Conclusions: Clinicians should be aware of the heterogeneous patterns of adherence to istradefylline. | en |
dc.language.iso | eng | - |
dc.publisher | Elsevier BV | en |
dc.rights | © 2024 The Authors. Published by Elsevier B.V. | en |
dc.rights | This is an open access article under the CC BY license. | en |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | - |
dc.subject | Adherence | en |
dc.subject | Group-based trajectory modeling | en |
dc.subject | Heterogeneity | en |
dc.subject | Istradefylline | en |
dc.subject | Parkinson's disease | en |
dc.title | Adherence to istradefylline in patients with Parkinson's disease: A group-based trajectory analysis | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | Journal of the Neurological Sciences | en |
dc.identifier.volume | 462 | - |
dc.relation.doi | 10.1016/j.jns.2024.123092 | - |
dc.textversion | publisher | - |
dc.identifier.artnum | 123092 | - |
dc.identifier.pmid | 38925070 | - |
dcterms.accessRights | open access | - |
dc.identifier.pissn | 0022-510X | - |
dc.identifier.eissn | 1878-5883 | - |
出現コレクション: | 学術雑誌掲載論文等 |

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