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Use of direct oral anticoagulants in the first year after market entry of edoxaban: A Danish nationwide drug utilization study

    • Aarhus Universitetshospital
    • Aarhus Universitet

    Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

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    Abstract

    Objectives: To describe the early uptake of edoxaban; the fourth direct oral anticoagulant (DOAC) to enter the market. Methods: Using the Danish nationwide health registries, we identified new users of edoxaban (n = 609) from June 6 (day of marketing) through June 2017. For comparison, we also identified new users of dabigatran (n = 2211), rivaroxaban (n = 19 227), and apixaban (n = 14 736). Users were described regarding indication of use, previous anticoagulant experience, comorbidity, and co-medication. Results: The rate of edoxaban initiation increased to 2.0 per 100 000 person months in June 2017, compared with 6.3, 37.5, and 27.0 for dabigatran, rivaroxaban, and apixaban. Atrial fibrillation was the most common registered indication for edoxaban (67%) as well as the other DOACs (41–55%). Overall, users of edoxaban were comparable to users of other DOACs (median age 75 vs 72–76 years and 57% vs 53–59% males), except for a generally lower concomitant use of other drugs. Noticeably, 95% of edoxaban users had previously received anticoagulant treatment compared with 31% to 43% for new users of other DOACs, with 77% switching directly from another anticoagulant treatment to edoxaban (45% directly from VKA and 32% directly from DOACs). Conclusions: While the use of edoxaban is still limited compared with other DOACs, it is increasing. The majority of edoxaban users switch to edoxaban from other anticoagulant treatments. Continued monitoring of the utilization of DOACs, including effectiveness and safety, is considered essential to the safe and rational use of these drugs.

    OriginalsprogEngelsk
    TidsskriftPharmacoepidemiology and Drug Safety
    Vol/bind27
    Udgave nummer2
    Sider (fra-til)174-181
    ISSN1053-8569
    DOI
    StatusUdgivet - 2018

    Finansiering

    Anton Pottegård reports participation in research projects funded by Boehringer‐Ingelheim with funds paid to the institution where he was employed (no personal fees). Erik L. Grove has received speaker honoraria from AstraZeneca, Baxter, Bayer, Boehringer Ingelheim, Bristol‐Myers Squibb, MSD, and Pfizer and has previously participated in advisory board meetings for AstraZeneca, Bayer, Boehringer Ingelheim, and Bristol‐Myers Squibb. Maja Hellfritzsch reports speaker honorarium from Bristol‐Myers Squibb and Pfizer.

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