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dc.contributor.authorBrkic, Alen
dc.contributor.authorDiamantopoulos, Andreas P.
dc.contributor.authorHoff, Mari
dc.contributor.authorHaavardsholm, Espen A.
dc.contributor.authorFevang, Bjørg T. S.
dc.contributor.authorBrekke, Lene K.
dc.contributor.authorLoli, Liz
dc.contributor.authorZettel, Camilla
dc.contributor.authorBakland, Gunnstein
dc.contributor.authorMielnik, Pawel
dc.contributor.authorHaugeberg, Glenn
dc.date.accessioned2023-09-12T05:02:21Z
dc.date.available2023-09-12T05:02:21Z
dc.date.issued2023
dc.identifier.citationBMC Health Services Research. 2023 Sep 07;23(1):968
dc.identifier.urihttp://hdl.handle.net/10852/104975
dc.description.abstractBackground Biologic and targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARDs) are highly effective in treating rheumatoid arthritis (RA), albeit high drug cost has restricted their use in many countries. As a countermeasure, Norway implemented pharmaceutical tendering as a cost-reducing strategy. The aim of this study was to assess the annual proportion of different b/tsDMARDs registered to treat RA patients under the influence of a Norwegian pharmaceutical tendering between 2010 and 2019. Method The data is collected from ten Norwegian outpatient centers. The included patients are categorized as naïve, non-naïve, and current b/tsDMARD users. 13 individual b/tsDMARDs are assessed and compared with the tender rankings from each year. Overview of subcutaneous (sc) with per oral vs. intravenous (iv) and biosimilars vs. non-biosimilar are also described. Result The tender-winning b/tsDMARD was the most or second most used drug in nine out of ten years for naïve users, seven for non-naïve users, and twice for current users. The average sum of the highest and second highest proportion among naïve, non-naïve, and current b/tsDMARD users were 75%, 53%, and 50% during the ten years, respectively. The tender-winning drug was iv in eight out of ten years. However, the average total proportion of sc and per oral b/tsDMARDs was about 70% for naïve b/tsDMARD users, 50% for non-naïve b/tsDMARD users, and 60% for current b/tsDMARD users. The main contributors to sc and per oral b/tsDMARD were etanercept (reference and biosimilar) and certolizumab pegol. The main contributors to iv b/tsDMARD were rituximab reference and infliximab biosimilar. Despite low-ranking offers, rituximab reference (offered as a second-line drug) often achieved a high proportion among non-naïve and current b/tsDMARD users. After the introduction of biosimilars, their average proportion was about 40%, 40%, and 20% for naïve, non-naïve, and current b/tsDMARD users, respectively. Conclusion Based on observed data, a higher tender rank was associated with a higher proportion among naïve and non-naïve b/tsDMARD users. However, in most cases, sc b/tsDMARDs achieved a higher proportion with lower tender ranks than iv b/tsDMARDs with higher tender ranks.
dc.language.isoeng
dc.rightsBioMed Central Ltd., part of Springer Nature
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleExploring the impact of the national tender system on the use of costly drugs treating rheumatoid arthritis patients in ten rheumatology centers in Norway (2010–2019)
dc.typeJournal article
dc.date.updated2023-09-12T05:02:22Z
dc.creator.authorBrkic, Alen
dc.creator.authorDiamantopoulos, Andreas P.
dc.creator.authorHoff, Mari
dc.creator.authorHaavardsholm, Espen A.
dc.creator.authorFevang, Bjørg T. S.
dc.creator.authorBrekke, Lene K.
dc.creator.authorLoli, Liz
dc.creator.authorZettel, Camilla
dc.creator.authorBakland, Gunnstein
dc.creator.authorMielnik, Pawel
dc.creator.authorHaugeberg, Glenn
dc.identifier.cristin2181631
dc.identifier.doihttps://doi.org/10.1186/s12913-023-09975-7
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.type.versionPublishedVersion
cristin.articleid968


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