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Patient concern regarding bleeding side effects from oral anticoagulation therapy for atrial fibrillation: An analysis from the multicenter KiCS-AF registry.
Ueda, Ikuko; Kohsaka, Shun; Ikemura, Nobuhiro; Kimura, Takehiro; Katsumata, Yoshinori; Takemura, Ryo; Suzuki, Masahiro; Takatsuki, Seiji; Koide, Daisuke; Fukuda, Keiichi.
Affiliation
  • Ueda I; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.
  • Kohsaka S; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.
  • Ikemura N; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.
  • Kimura T; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.
  • Katsumata Y; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.
  • Takemura R; Clinical and Translational Research Center, Keio University Hospital, Tokyo, Japan.
  • Suzuki M; Department of Cardiology, National Hospital Organization Saitama Hospital, Wako, Japan.
  • Takatsuki S; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.
  • Koide D; Department of Biostatistics & Bioinformatics, Graduate School of Medicine, The University of Tokyo, Japan.
  • Fukuda K; Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.
Article in En | MEDLINE | ID: mdl-37694609
ABSTRACT

AIMS:

The purpose of this study is to utilize PROs to determine the percentage of patients concerned about mild to moderate bleeding side effects of anticoagulants. METHODS AND

RESULTS:

We consecutively enrolled 3,312 newly diagnosed or referred patients for atrial fibrillation (AF) management from 11 sites within the Keio interhospital Cardiovascular Studies-Atrial Fibrillation Registry between September 2012 and May 2018. Of these patients, 2,636 (79.5%) were taking oral anticoagulants at enrollment. Using the Atrial Fibrillation Effect on Quality-of-life questionnaire (AFEQT), the patients who responded "1 not at all bothered" or "2 hardly bothered" on the seven-point scale regarding bleeding side effects were classified as the "no OAC concern" group while those responding "3 a little bothered" to "7 extremely bothered" were classified as the "OAC concern" group. On baseline analysis, 29.3% (n = 772) were "concerned" about bleeding side effects. The proportion of women and patients with AF-related symptoms was higher in the OAC concern vs. no OAC concern group (36.9% vs. 29.8%, p < 0.0004 and 66.2% vs. 56.7%, p < 0.0001, respectively). The CHADS2 scores ≥ 2 were comparable between groups. Of the 430 patients in the 1-year follow-up analysis, the proportion of the continued OAC concern group (1 year from enrollment) was 41.6%.The dabigatran, rivaroxaban, and apixaban usage rates were comparable between the two groups in baseline and 1-year follow-up analysis.

CONCLUSION:

Approximately one-third of all patients with AF on anticoagulant therapy were concerned regarding bleeding from short-and long-term anticoagulant use.
Key words

Full text: 1 Database: MEDLINE Language: En Journal: Eur J Cardiovasc Nurs Journal subject: ANGIOLOGIA / CARDIOLOGIA / ENFERMAGEM Year: 2023 Type: Article Affiliation country: Japan

Full text: 1 Database: MEDLINE Language: En Journal: Eur J Cardiovasc Nurs Journal subject: ANGIOLOGIA / CARDIOLOGIA / ENFERMAGEM Year: 2023 Type: Article Affiliation country: Japan