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dc.contributor.authorNorborg, Hilde
dc.contributor.authorRiise, Trond
dc.contributor.authorMyhr, Kjell-Morten
dc.contributor.authorTorkildsen, Nina Agnethe Grytten
dc.contributor.authorWergeland, Stig
dc.date.accessioned2021-08-13T06:37:05Z
dc.date.available2021-08-13T06:37:05Z
dc.date.created2021-06-17T14:04:46Z
dc.date.issued2021
dc.identifier.issn2055-2173
dc.identifier.urihttps://hdl.handle.net/11250/2767667
dc.description.abstractBackground For patients with MS, medication switches increase the risk of disease reactivation. Objective Compare discontinuation rates due to treatment failure or side effects between teriflunomide and dimethyl fumarate, and investigate clinical variables affecting discontinuation rates. Methods All patients who received teriflunomide or dimethyl fumarate at Haukeland University Hospital from 2013 until 2018 were identified. Clinical and demographic variables were extracted from the Norwegian MS Registry. Cause-specific Cox regression models estimated the rate of discontinuation due to treatment failure or side effects. Results We included 354 patients treated with either dimethyl fumarate (n = 185) or teriflunomide (n = 169). We found 38% lower risk of discontinuation because of treatment failure for patients using dimethyl fumarate compared to teriflunomide (p < 0.05). In a treatment-naive subgroup (n = 183), we found a 38% reduced risk of discontinuation for any reason among patients using dimethyl fumarate (p < 0.05). There was no significant difference between treatment groups in discontinuation rate due to side effects, although more patients reported side effects when treated with dimethyl fumarate. Conclusion Our findings suggests that dimethyl fumarate has a lower risk of discontinuation because of treatment failure among both treatment-experienced and treatment-naive patients.en_US
dc.language.isoengen_US
dc.publisherSAGE Publicationsen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleReal-world discontinuation rate of teriflunomide and dimethyl fumarate in multiple sclerosisen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright The Author(s), 2021en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1177/20552173211022027
dc.identifier.cristin1916433
dc.source.journalMultiple Sclerosis Journal, Experimental, Translational and Clinicalen_US
dc.identifier.citationMultiple Sclerosis Journal, Experimental, Translational and Clinical. 2021, 7 (2).en_US
dc.source.volume7en_US
dc.source.issue2en_US


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Navngivelse 4.0 Internasjonal
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