Biologic TNF inhibiting agents for treatment of inflammatory rheumatic diseases: Dosing patterns and related costs in Switzerland from a payers perspective

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dc.identifier.uri http://dx.doi.org/10.15488/563
dc.identifier.uri http://www.repo.uni-hannover.de/handle/123456789/587
dc.contributor.author Zeidler, Jan
dc.contributor.author Mittendorf, Thomas
dc.contributor.author Müller, Rüdiger
dc.contributor.author Kempis, Johannes von
dc.date.accessioned 2016-10-28T09:54:27Z
dc.date.available 2016-10-28T09:54:27Z
dc.date.issued 2012
dc.identifier.citation Zeidler, Jan; Mittendorf, T.; Müller, R.; von Kempis, J.: Biologic TNF inhibiting agents for treatment of inflammatory rheumatic diseases: Dosing patterns and related costs in Switzerland from a payers perspective . In: Health Economics Review 2 (2012), Nr. 1, S. 1-8. DOI: http://dx.doi.org/10.1186/2191-1991-2-20
dc.description.abstract Background: To obtain detailed real-life data on costs and dosing patterns in the utilisation of the TNF inhibitors adalimumab, etanercept, and infliximab in patients treated in Switzerland. Methods: Administrative claims processed by a major Swiss health insurer between 2005 and 2008 were analysed. Patients with inflammatory rheumatic diseases (IRDs) with at least one prescription for adalimumab, etanercept, or infliximab were identified. All-cause and disease-specific costs, as well as daily costs of treatment, were calculated. Dosing patterns and discontinuation rates were analysed. Results: A total of 555 IRD patients were identified. All-cause costs during the 12 months after the index event were 20,555CHF in the etanercept group, 24,152CHF in the adalimumab group, and 27,614CHF in the infliximab group. The most important cost driver was mean TNF inhibitor drug cost, which was 15,613CHF in the etanercept group, 19,166CHF in the adalimumab group, and 21,313CHF in the infliximab group. Discontinuation rates during the first year after the index event were 46.8% in etanercept, 41.3% in adalimumab, and 51.2% in the infliximab group. Rates of dosage increase were 13.3% in the etanercept group, 13.0% in the adalimumab group, and 14.1% in the infliximab group. When time on treatment was considered, daily costs of treatment were similar for etanercept and adalimumab, but were higher for infliximab. Conclusions: Marked differences in costs between subcutaneous and intravenous therapies were observed. Among the three groups of patients defined by TNF inhibitor treatment, costs for the infliximab group were highest during the year after the index event. eng
dc.description.sponsorship Helsana Versicherungen AG
dc.language.iso eng
dc.publisher Heidelberg : Springer Verlag
dc.relation.ispartofseries Health Economics Review 2 (2012), Nr. 1
dc.rights CC BY 2.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by/2.0/
dc.subject Claims data eng
dc.subject Cost analysis eng
dc.subject Dosing patterns eng
dc.subject Inflammatory rheumatic diseases eng
dc.subject Switzerland eng
dc.subject Tumornecrosis factor inhibitor I eng
dc.subject adalimumab eng
dc.subject etanercept eng
dc.subject infliximab eng
dc.subject adult eng
dc.subject ankylosing spondylitis eng
dc.subject article eng
dc.subject billing and claims eng
dc.subject controlled study eng
dc.subject drug cost eng
dc.subject drug dose comparison eng
dc.subject drug dose increase eng
dc.subject drug dose regimen eng
dc.subject drug utilization eng
dc.subject drug withdrawal eng
dc.subject female eng
dc.subject human eng
dc.subject major clinical study eng
dc.subject male eng
dc.subject priority journal eng
dc.subject psoriatic arthritis eng
dc.subject rheumatoid arthritis eng
dc.subject Switzerland eng
dc.subject.ddc 330 | Wirtschaft ger
dc.subject.ddc 610 | Medizin, Gesundheit ger
dc.title Biologic TNF inhibiting agents for treatment of inflammatory rheumatic diseases: Dosing patterns and related costs in Switzerland from a payers perspective eng
dc.type Article
dc.type Text
dc.relation.issn 2191-1991
dc.relation.doi http://dx.doi.org/10.1186/2191-1991-2-20
dc.bibliographicCitation.issue 1
dc.bibliographicCitation.volume 2
dc.bibliographicCitation.firstPage 1
dc.bibliographicCitation.lastPage 8
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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