Medication adherence/persistence among patients with active multiple sclerosis in Finland

dc.contributor.authorSanni Lahdenperä
dc.contributor.authorMerja Soilu-Hänninen
dc.contributor.authorHanna-Maija Kuusisto
dc.contributor.authorSari Atula
dc.contributor.authorJouni Junnila
dc.contributor.authorAnders Berglund
dc.contributor.organizationfi=kliiniset neurotieteet|en=Clinical Neurosciences|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.74845969893
dc.converis.publication-id49805462
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/49805462
dc.date.accessioned2022-10-28T14:31:36Z
dc.date.available2022-10-28T14:31:36Z
dc.description.abstractObjectives To explore adherence, persistence, and treatment patterns in patients with multiple sclerosis (MS) in Finland treated with disease-modifying therapies (DMTs) for active MS in 2005-2018. <div>Materials and Methods The study cohort was identified using the Drug Prescription Register of Social Insurance Institute, Finland. All patients had at least one prescription of glatiramer acetate (GA), beta-interferons, teriflunomide, or delayed-release dimethyl fumarate (DMF). Adherence was calculated using proportion of days covered (PDC) (cutoff >= 0.8). Time to non-persistence was calculated by the number of days on index DMT treatment before the first treatment gap (>= 90 days) or switch and analyzed with time-to-event methodology. </div><div>Results The cohort included 7474 MS patients (72.2% female; mean age 38.9 years). Treatment switches were steady over 2005-2012, peaked in 2015. PDC means (standard deviations) were GA, 0.87 (0.17); beta-interferons, 0.88 (0.15); DMF, 0.89 (0.14); teriflunomide, 0.93 (0.10). Adherence frequencies were GA, 78.4%; beta-interferons, 81.3%; DMF, 86.9%; teriflunomide, 91.7%. Logistic regression showed that age group, DMT and the starting year, sex, and hospital district independently affected adherence. Patients receiving teriflunomide and DMF, males, and older patients were more likely to persist on treatment. There was no difference in persistence between patients prescribed teriflunomide and DMF, or between GA and beta-interferons. </div><div>Conclusions Oral DMTs had greater adherence and persistence than injectable DMTs.</div>
dc.identifier.eissn1600-0404
dc.identifier.jour-issn0001-6314
dc.identifier.olddbid188785
dc.identifier.oldhandle10024/171879
dc.identifier.urihttps://www.utupub.fi/handle/11111/43845
dc.identifier.urnURN:NBN:fi-fe2021042826928
dc.language.isoen
dc.okm.affiliatedauthorSoilu-Hänninen, Merja
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3112 Neurosciencesen_GB
dc.okm.discipline3112 Neurotieteetfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherWILEY
dc.publisher.countryDenmarken_GB
dc.publisher.countryTanskafi_FI
dc.publisher.country-codeDK
dc.relation.doi10.1111/ane.13301
dc.relation.ispartofjournalActa Neurologica Scandinavica
dc.relation.issue6
dc.relation.volume142
dc.source.identifierhttps://www.utupub.fi/handle/10024/171879
dc.titleMedication adherence/persistence among patients with active multiple sclerosis in Finland
dc.year.issued2020

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