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Medication adherence/persistence among patients with active multiple sclerosis in Finland
OBJECTIVES: 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. MATERIALS AND METHODS: The study cohort was identified using the Drug Prescription Register of Social...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689851/ https://www.ncbi.nlm.nih.gov/pubmed/32559310 http://dx.doi.org/10.1111/ane.13301 |
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author | Lahdenperä, Sanni Soilu‐Hänninen, Merja Kuusisto, Hanna‐Maija Atula, Sari Junnila, Jouni Berglund, Anders |
author_facet | Lahdenperä, Sanni Soilu‐Hänninen, Merja Kuusisto, Hanna‐Maija Atula, Sari Junnila, Jouni Berglund, Anders |
author_sort | Lahdenperä, Sanni |
collection | PubMed |
description | OBJECTIVES: 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. 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. 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. CONCLUSIONS: Oral DMTs had greater adherence and persistence than injectable DMTs. |
format | Online Article Text |
id | pubmed-7689851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76898512020-12-05 Medication adherence/persistence among patients with active multiple sclerosis in Finland Lahdenperä, Sanni Soilu‐Hänninen, Merja Kuusisto, Hanna‐Maija Atula, Sari Junnila, Jouni Berglund, Anders Acta Neurol Scand Original Articles OBJECTIVES: 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. 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. 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. CONCLUSIONS: Oral DMTs had greater adherence and persistence than injectable DMTs. John Wiley and Sons Inc. 2020-07-31 2020-12 /pmc/articles/PMC7689851/ /pubmed/32559310 http://dx.doi.org/10.1111/ane.13301 Text en © 2020 The Authors. Acta Neurologica Scandinavica published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Lahdenperä, Sanni Soilu‐Hänninen, Merja Kuusisto, Hanna‐Maija Atula, Sari Junnila, Jouni Berglund, Anders Medication adherence/persistence among patients with active multiple sclerosis in Finland |
title | Medication adherence/persistence among patients with active multiple sclerosis in Finland |
title_full | Medication adherence/persistence among patients with active multiple sclerosis in Finland |
title_fullStr | Medication adherence/persistence among patients with active multiple sclerosis in Finland |
title_full_unstemmed | Medication adherence/persistence among patients with active multiple sclerosis in Finland |
title_short | Medication adherence/persistence among patients with active multiple sclerosis in Finland |
title_sort | medication adherence/persistence among patients with active multiple sclerosis in finland |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689851/ https://www.ncbi.nlm.nih.gov/pubmed/32559310 http://dx.doi.org/10.1111/ane.13301 |
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