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Incidence of direct oral anticoagulant use in patients with nonvalvular atrial fibrillation and characteristics of users in 6 European countries (2008–2015): A cross‐national drug utilization study

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dc.contributor Háskóli Íslands
dc.contributor University of Iceland
dc.contributor.author Ibáñez, Luisa
dc.contributor.author Sabaté, Mònica
dc.contributor.author Vidal, Xavier
dc.contributor.author Ballarin, Elena
dc.contributor.author Rottenkolber, Marietta
dc.contributor.author Schmiedl, Sven
dc.contributor.author Heeke, Andreas
dc.contributor.author Huerta, Consuelo
dc.contributor.author Martin Merino, Elisa
dc.contributor.author Montero, Dolores
dc.contributor.author Leon‐Muñoz, Luz María
dc.contributor.author Gasse, Christiane
dc.contributor.author Moore, Nicholas
dc.contributor.author Droz, Cécile
dc.contributor.author Lassalle, Régis
dc.contributor.author Aakjær, Mia
dc.contributor.author Andersen, Morten
dc.contributor.author De Bruin, Marie Louise
dc.contributor.author Groenwold, Rolf
dc.contributor.author Ham, Hendrika A.
dc.contributor.author Souverein, Patrick
dc.contributor.author Klungel, Olaf
dc.contributor.author Gardarsdottir, Helga
dc.date.accessioned 2020-03-11T15:47:07Z
dc.date.available 2020-03-11T15:47:07Z
dc.date.issued 2019-09-04
dc.identifier.citation Ibáñez, L, Sabaté, M, Vidal, X, et al. Incidence of direct oral anticoagulant use in patients with nonvalvular atrial fibrillation and characteristics of users in 6 European countries (2008–2015): A cross‐national drug utilization study. Br J Clin Pharmacol. 2019; 85: 2524– 2539. https://doi.org/10.1111/bcp.14071
dc.identifier.issn 0306-5251
dc.identifier.issn 1365-2125 (eISSN)
dc.identifier.uri https://hdl.handle.net/20.500.11815/1586
dc.description Publisher's version (útgefin grein).
dc.description.abstract Aims: To estimate the incidence of direct oral anticoagulant drug (DOAC) use in patients with nonvalvular atrial fibrillation and to describe user and treatment characteristics in 8 European healthcare databases representing 6 European countries. Methods: Longitudinal drug utilization study from January 2008 to December 2015. A common protocol approach was applied. Annual period incidences and direct standardisation by age and sex were performed. Dose adjustment related to change in age and by renal function as well as concomitant use of potentially interacting drugs were assessed. Results: A total of 186 405 new DOAC users (age ≥18 years) were identified. Standardized incidences varied from 1.93–2.60 and 0.11–8.71 users/10 000 (2011–2015) for dabigatran and rivaroxaban, respectively, and from 0.01–8.12 users/10 000 (2012–2015) for apixaban. In 2015, the DOAC incidence ranged from 9 to 28/10 000 inhabitants in SIDIAP (Spain) and DNR (Denmark) respectively. There were differences in population coverage among the databases. Only 1 database includes the total reference population (DNR) while others are considered a population representative sample (CPRD, BIFAP, SIDIAP, EGB, Mondriaan). They also varied in the type of drug data source (administrative, clinical). Dose adjustment ranged from 4.6% in BIFAP (Spain) to 15.6% in EGB (France). Concomitant use of interacting drugs varied between 16.4% (SIDIAP) and 70.5% (EGB). Cardiovascular comorbidities ranged from 25.4% in Mondriaan (The Netherlands) to 82.9% in AOK Nordwest (Germany). Conclusion: Overall, apixaban and rivaroxaban increased its use during the study period while dabigatran decreased. There was variability in patient characteristics such as comorbidities, potentially interacting drugs and dose adjustment. (EMA/2015/27/PH).
dc.description.sponsorship The research leading to these results was conducted as part of the activities of the PE‐PV Consortium (Pharmacoepidemiology and Pharmacovigilance Consortium), which is a public academic partnership coordinated by the University of Utrecht. The project has received support from the European Medicines Agency under the Framework service contract (nr EMA/2015/27/PH) with regard to the reopening of competition no3. K. Janhsen (Witten/Herdecke University, Alfred‐Herrhausen‐ Straße 50, 58448 Witten, Germany (UW/H)) and B. Grave (AOK NORDWEST, Kopenhagener Straße 1, 44269 Dortmund, Germany). R. Gerlach and M. Tauscher (National Association of Statutory Health Insurance Physicians of Bavaria, Elsenheimerstr. 39, D‐80687 Munich, Germany). The authors of the BIFAP database would like to acknowledge the excellent collaboration of the primary care general practitioners and pediatricians, and also the support of the regional governments to the database. This study is based in part on data from the BIFAP fully financed by the Spanish Agency on Medicines and Medical Devices (AEMPS). The views and opinions expressed in this article are those of the authors and do not necessarily reflect the official policy or position of the EMA (European Medicines Agency) or one of its committees or working parties, or AEMPS (Agencia Española de Medicamentos y Productos Sanitarios).
dc.format.extent 2524-2539
dc.language.iso en
dc.publisher Wiley
dc.relation.ispartofseries British Journal of Clinical Pharmacology;85(11)
dc.rights info:eu-repo/semantics/openAccess
dc.subject Anticoagulants
dc.subject Arrhythmia
dc.subject Cardiovascular
dc.subject Drug utilization
dc.subject Pharmacoepidemiology
dc.subject Hjartsláttartruflanir
dc.subject Blóðrásarsjúkdómar
dc.subject Lyfjanotkun
dc.title Incidence of direct oral anticoagulant use in patients with nonvalvular atrial fibrillation and characteristics of users in 6 European countries (2008–2015): A cross‐national drug utilization study
dc.type info:eu-repo/semantics/article
dcterms.license This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
dc.description.version Peer Reviewed
dc.identifier.journal British Journal of Clinical Pharmacology
dc.identifier.doi 10.1111/bcp.14071
dc.contributor.department Faculty of Pharmaceutical Sciences (UI)
dc.contributor.department Lyfjafræðideild (HÍ)
dc.contributor.school Heilbrigðisvísindasvið (HÍ)
dc.contributor.school School of Health Sciences (UI)


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