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dc.contributor.authorFukasawa, Toshikien
dc.contributor.authorNakanishi, Etsuroen
dc.contributor.authorShimoda, Hirooen
dc.contributor.authorShinoda, Katsumien
dc.contributor.authorIto, Satoruen
dc.contributor.authorAsada, Shinjien
dc.contributor.authorYoshida, Satomien
dc.contributor.authorTanaka-Mizuno, Sachikoen
dc.contributor.authorMizuno, Kayokoen
dc.contributor.authorTakahashi, Ryosukeen
dc.contributor.authorKawakami, Kojien
dc.date.accessioned2025-06-09T06:35:03Z-
dc.date.available2025-06-09T06:35:03Z-
dc.date.issued2024-07-15-
dc.identifier.urihttp://hdl.handle.net/2433/294603-
dc.description.abstractBackground: 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.isoeng-
dc.publisherElsevier BVen
dc.rights© 2024 The Authors. Published by Elsevier B.V.en
dc.rightsThis is an open access article under the CC BY license.en
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectAdherenceen
dc.subjectGroup-based trajectory modelingen
dc.subjectHeterogeneityen
dc.subjectIstradefyllineen
dc.subjectParkinson's diseaseen
dc.titleAdherence to istradefylline in patients with Parkinson's disease: A group-based trajectory analysisen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleJournal of the Neurological Sciencesen
dc.identifier.volume462-
dc.relation.doi10.1016/j.jns.2024.123092-
dc.textversionpublisher-
dc.identifier.artnum123092-
dc.identifier.pmid38925070-
dcterms.accessRightsopen access-
dc.identifier.pissn0022-510X-
dc.identifier.eissn1878-5883-
出現コレクション:学術雑誌掲載論文等

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