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dc.contributor.authorWalker, Robert
dc.contributor.authorSchulz, Mark
dc.contributor.authorArora, Birendra
dc.contributor.authorChung, Eric
dc.contributor.authorJuneja, Prabhjot
dc.contributor.authorVerhaeghe, Stephane
dc.contributor.authorSpelman, Tim
dc.contributor.authorBroadley, Simon
dc.date.accessioned2021-03-01T05:47:40Z
dc.date.available2021-03-01T05:47:40Z
dc.date.issued2018
dc.identifier.issn0022-3050en_US
dc.identifier.doi10.1136/jnnp-2018-ANZAN.56en_US
dc.identifier.urihttp://hdl.handle.net/10072/402707
dc.description.abstractIntroduction This study aimed to examine and compare patient persistence of fingolimod to all reimbursed disease modifying therapies (DMTs) for relapsing-remitting multiple sclerosis (RRMS) in Australia. Method The Pharmaceutical Benefits Scheme (PBS) 10% sample supplied by the Department of Human Services was used in this study. Eligible patients must have received a script for a reimbursed DMT for RRMS between September 2011 and February 2016. Patient demographics were summarised using mean and standard deviation or frequency percentage. Persistence was defined as a patient that remained on a DMT with a gap in scripts of no longer than 4 months. Individual patients could be included multiple times if they initiated a new DMT during the study period. Persistence was derived using the Kaplan-Meier method and hazard ratios (HR). Persistence to individual treatments was then compared to the average persistence observed across all treatments; p-values were based on the log-rank test. Results 720 unique patients were eligible for the study, contributing 1827 observations that for analysis (2.5 new initiations/patient). Overall the median persistence (MP) to therapy was 29.6 months with 67.7% of patients remaining on therapy for 12 months. The only DMT with significantly better persistence compared to the overall average was fingolimod (HR 0.65 (95%CI 0.57–0.73; p<0.001). Patients had an MP of 60 months on fingolimod with 79.5% of patients persistent at 12 months. Patients were significantly less persistent to interferon Beta-1a, interferon Beta-1b, glatiramer acetate and dimethyl fumarate (hazard ratios above 1.27 (p values all≤0.001) whilst the remaining DMTs, teriflunomide and natalizumab, showed no significant difference from the average persistence. Conclusion In this analysis of PBS sample data, patients were most persistent to fingolimod treatment amongst all DMTs.en_US
dc.languageEnglishen_US
dc.publisherBMJ Publishing Groupen_US
dc.relation.ispartofconferencenameAnnual Scientific Meeting of the Australian-and-New Zealand-Association-of-Neurologists (ANZAN)en_US
dc.relation.ispartofconferencetitleJournal of Neurology Neurosurgery and Psychiatryen_US
dc.relation.ispartofdatefrom2018-05-29
dc.relation.ispartofdateto2018-06-01
dc.relation.ispartoflocationDarwin, Australiaen_US
dc.relation.ispartofpagefromE23en_US
dc.relation.ispartofpagetoE24en_US
dc.relation.ispartofissue6en_US
dc.relation.ispartofvolume89en_US
dc.subject.fieldofresearchMedical and Health Sciencesen_US
dc.subject.fieldofresearchPsychology and Cognitive Sciencesen_US
dc.subject.fieldofresearchcode11en_US
dc.subject.fieldofresearchcode17en_US
dc.subject.keywordsScience & Technologyen_US
dc.subject.keywordsLife Sciences & Biomedicineen_US
dc.subject.keywordsClinical Neurologyen_US
dc.subject.keywordsPsychiatryen_US
dc.subject.keywordsSurgeryen_US
dc.titleReal world evidence (RWE) on long-term persistence of fingolimod in relapsing-remitting multiple sclerosis (RRMS) in australiaen_US
dc.typeConference outputen_US
dc.type.descriptionE3 - Conferences (Extract Paper)en_US
dcterms.bibliographicCitationWalker, R; Schulz, M; Arora, B; Chung, E; Juneja, P; Verhaeghe, S; Spelman, T; Broadley, S, Real world evidence (RWE) on long-term persistence of fingolimod in relapsing-remitting multiple sclerosis (RRMS) in australia, Journal of Neurology Neurosurgery and Psychiatry, 2018, 89 (6), pp. E23-E24en_US
dc.date.updated2021-03-01T05:46:38Z
gro.hasfulltextNo Full Text
gro.griffith.authorBroadley, Simon


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