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Prescribing trends of atrial fibrillation patients who switched from warfarin to a direct oral anticoagulant

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Abstract

Direct oral anticoagulant (DOAC) agents offer several lifestyle and therapeutic advantages for patients relative to warfarin in the treatment of atrial fibrillation (AF). These alternative agents are increasingly used in the treatment of AF, however the adoption practices, patient profiles, and reasons for switching to a DOAC from warfarin have not been well studied. Through the Michigan Anticoagulation Quality Improvement Initiative, abstracted data from 3873 AF patients, enrolled between 2010 and 2015, were collected on demographics and comorbid conditions, stroke and bleeding risk scores, and reasons for anticoagulant switching. Over the study period, patients who switched from warfarin to a DOAC had similar baseline characteristics, risk scores, and insurance status but differed in baseline CrCl. The most common reasons for switching were patient related ease of use concerns (37.5%) as opposed to clinical reasons (16.5% of patients). Only 13% of patients that switched to a DOAC switched back to warfarin by the end of the study period.

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Acknowledgements

The Michigan Anticoagulation and Quality Improvement Initiative is funded by the Blue Cross Blue Shield of Michigan/Blue Care Network, which did not contribute to data collection, interpretation, or manuscript writing. Dr. Barnes is supported by the National Heart, Lung and Blood Institute (2-T32-HL007853-16).

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Correspondence to Zachary D. Hale.

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ZH, XK, BH, XG, JK, GK—none; EKR—consultant: Janssen, ACP, board member: AC Forum; SA—consulting fees/honoraria: Kona, Trice Orthopedics, Micardia; ownership/partnership/principal: Biostar Ventures, Ablative Solutions, research/research grants: Boston Scientific Watchman, Abbott Absorb trial; SK—consultant: BI, Janssen Dalichi Sankyo, Bristol Myer Squibb, Pfizer, speaker’s bureau: Janssen, Boehringer-Ingelheim, Bristol Myer Squibb, Pfizer, CSL Behring; JF—consultant Merck, Bristol Myer Squibb, Pfizer, Sanofi-Aventis, Janssen Pharmaceuticals; research grants: Fibromuscular Disease Society of America, Blue Cross/Blue Shield of Michigan; GB—consulting for Portola and Aralez, research grants from Blue Cross/Blue Shield of Michigan and BMS/Pfizer.

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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

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Hale, Z.D., Kong, X., Haymart, B. et al. Prescribing trends of atrial fibrillation patients who switched from warfarin to a direct oral anticoagulant. J Thromb Thrombolysis 43, 283–288 (2017). https://doi.org/10.1007/s11239-016-1452-2

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