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.contributorHáskóli Íslandsen_US
dc.contributorUniversity of Icelanden_US
dc.contributor.authorIbáñez, Luisa
dc.contributor.authorSabaté, Mònica
dc.contributor.authorVidal, Xavier
dc.contributor.authorBallarin, Elena
dc.contributor.authorRottenkolber, Marietta
dc.contributor.authorSchmiedl, Sven
dc.contributor.authorHeeke, Andreas
dc.contributor.authorHuerta, Consuelo
dc.contributor.authorMartin Merino, Elisa
dc.contributor.authorMontero, Dolores
dc.contributor.authorLeon‐Muñoz, Luz María
dc.contributor.authorGasse, Christiane
dc.contributor.authorMoore, Nicholas
dc.contributor.authorDroz, Cécile
dc.contributor.authorLassalle, Régis
dc.contributor.authorAakjær, Mia
dc.contributor.authorAndersen, Morten
dc.contributor.authorDe Bruin, Marie Louise
dc.contributor.authorGroenwold, Rolf
dc.contributor.authorHam, Hendrika A.
dc.contributor.authorSouverein, Patrick
dc.contributor.authorKlungel, Olaf
dc.contributor.authorGardarsdottir, Helga
dc.contributor.departmentFaculty of Pharmaceutical Sciences (UI)en_US
dc.contributor.departmentLyfjafræðideild (HÍ)en_US
dc.contributor.schoolHeilbrigðisvísindasvið (HÍ)en_US
dc.contributor.schoolSchool of Health Sciences (UI)en_US
dc.date.accessioned2020-03-11T15:47:07Z
dc.date.available2020-03-11T15:47:07Z
dc.date.issued2019-09-04
dc.descriptionPublisher's version (útgefin grein).en_US
dc.description.abstractAims: 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).en_US
dc.description.sponsorshipThe 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).en_US
dc.description.versionPeer Revieweden_US
dc.format.extent2524-2539en_US
dc.identifier.citationIbáñez, 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.14071en_US
dc.identifier.doi10.1111/bcp.14071
dc.identifier.issn0306-5251
dc.identifier.issn1365-2125 (eISSN)
dc.identifier.journalBritish Journal of Clinical Pharmacologyen_US
dc.identifier.urihttps://hdl.handle.net/20.500.11815/1586
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofseriesBritish Journal of Clinical Pharmacology;85(11)
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAnticoagulantsen_US
dc.subjectArrhythmiaen_US
dc.subjectCardiovascularen_US
dc.subjectDrug utilizationen_US
dc.subjectPharmacoepidemiologyen_US
dc.subjectHjartsláttartruflaniren_US
dc.subjectBlóðrásarsjúkdómaren_US
dc.subjectLyfjanotkunen_US
dc.titleIncidence 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 studyen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dcterms.licenseThis 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.en_US

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