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Oral Anticoagulant Use for Patients with Atrial Fibrillation with Concomitant Anemia and/or Thrombocytopenia

  • Yung-Hsin Yeh
    Affiliations
    Cardiovascular Department, Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan

    College of Medicine, Chang Gung University, Taoyuan, Taiwan
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  • Yi-Hsin Chan
    Affiliations
    Cardiovascular Department, Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan

    College of Medicine, Chang Gung University, Taoyuan, Taiwan

    Microscopy Core Laboratory, Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan
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  • Shao-Wei Chen
    Affiliations
    Division of Thoracic and Cardiovascular Surgery, Department of Surgery, Chang Gung Memorial Hospital, Linkou Medical Center, Chang Gung University, Taoyuan City, Taiwan

    Center for Big Data Analytics and Statistics, Chang Gung Memorial Hospital, Taoyuan, Taiwan
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  • Shang-Hung Chang
    Affiliations
    Cardiovascular Department, Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan

    College of Medicine, Chang Gung University, Taoyuan, Taiwan

    Center for Big Data Analytics and Statistics, Chang Gung Memorial Hospital, Taoyuan, Taiwan
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  • Chun-Li Wang
    Affiliations
    Cardiovascular Department, Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan

    College of Medicine, Chang Gung University, Taoyuan, Taiwan
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  • Chi-Tai Kuo
    Affiliations
    Cardiovascular Department, Chang Gung Memorial Hospital, Linkou, Taoyuan, Taiwan

    College of Medicine, Chang Gung University, Taoyuan, Taiwan
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  • Gregory Y.H. Lip
    Affiliations
    Liverpool Centre for Cardiovascular Science, University of Liverpool & Liverpool Heart and Chest Hospital, Liverpool, UK

    Aalborg Thrombosis Research Unit, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark
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  • Shih-Ann Chen
    Affiliations
    Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan

    Institute of Clinical Medicine, and Cardiovascular Research Center, National Yang Ming Chiao Tung University, Taipei, Taiwan

    Cardiovascular Center, Taichung Veterans General Hospital, Taichung, Taiwan
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  • Tze-Fan Chao
    Correspondence
    Requests for reprints should be addressed to Tze-Fan Chao, MD, Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, No. 201, Sec. 2, Shih-Pai Road, Taipei, Taiwan.
    Affiliations
    Division of Cardiology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan

    Institute of Clinical Medicine, and Cardiovascular Research Center, National Yang Ming Chiao Tung University, Taipei, Taiwan
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      Abstract

      Objective

      Hemoglobin levels and platelet counts have been associated with adverse clinical outcomes in patients with cardiovascular conditions. We aimed to assess the impact of oral anticoagulant use for patients with atrial fibrillation and concomitant anemia or thrombocytopenia.

      Methods

      We used medical data from a multicenter health care system in Taiwan including 37,074 patients with atrial fibrillation. Patients were categorized into 3 groups based on hemoglobin and platelet levels: Group 1 (hemoglobin >10g/dL and platelet>100 K/µL; n = 29,147), Group 2 (hemoglobin<10 g/dL or platelet<100 K/µL; n = 7078), and Group 3 (hemoglobin <10 g/dL and platelet <100 K/µL; n = 849). Patients in each category were further stratified as 3 groups according to their stroke prevention strategies: no oral anticoagulant use (non-OAC), warfarin, or nonvitamin K antagonist oral anticoagulants (NOACs).

      Results

      A higher hemoglobin or platelet level was associated with a higher risk of ischemic stroke/systemic embolism but lower risks of intracranial hemorrhage and major bleeding. The composite risks of ischemic stroke/systemic embolism, intracranial hemorrhage and major bleeding were higher in Group 3 or Group 2, compared with Group 1 (6.79% a year vs 6.41% year vs 4.13% year). Compared to non-OACs, warfarin was not associated with a lower composite risk in the 3 groups. NOACs were associated with a lower composite risk in Group 1 (adjusted hazard ratio:0.68, [95% confidence interval:0.60-0.76]) and Group 2 (adjusted hazard ratio:0.73, [95% confidence interval:0.53-0.99]) but was nonsignificant in Group 3.

      Conclusions

      Patients with atrial fibrillation with anemia or thrombocytopenia were a high-risk population. Compared with no OAC use, NOACs were associated with better clinical outcomes for patients with atrial fibrillation and advanced anemia (hemoglobin <10g/dL) or thrombocytopenia (platelet <100 K/µL) but not for those with both conditions.

      Keywords

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