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Impact of oral anticoagulation in patients with atrial fibrillation at very low thromboembolic risk.
Verbrugge, Frederik Hendrik; Martin, Anne-Céline; Siegal, Deborah; Pieper, Karen; Illingworth, Laura; Camm, A John; Fox, Keith A A.
Afiliação
  • Verbrugge FH; Department of Cardiovascular Medicine, University Hospitals Leuven, Leuven, Belgium frederik.verbrugge@zol.be.
  • Martin AC; Medico-surgical Valve Unit, Georges Pompidou European Hospital, AP-HP, Paris, France.
  • Siegal D; Paris University, Innovative Therapies in Haemostasis, INSERM, Paris, France.
  • Pieper K; Department of Medicine, Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
  • Illingworth L; Thrombosis Research Institute, London, UK.
  • Camm AJ; Thrombosis Research Institute, London, UK.
  • Fox KAA; Institute of Clinical and Molecular Sciences, Department of Cardiology, St. George's University of London, London, UK.
Heart ; 106(11): 845-851, 2020 06.
Article em En | MEDLINE | ID: mdl-31806700
ABSTRACT

OBJECTIVE:

To investigate reasons for and impact of oral anticoagulation (OAC) in patients with atrial fibrillation (AF) at very low thromboembolic risk.

METHODS:

Individuals with CHA2DS2-VASc score 0 (men) or 1 (women) from the Global Anticoagulant Registry in the FIELD-Atrial Fibrillation (GARFIELD-AF) were studied. Baseline characteristics according to OAC use were evaluated by logistic regression analysis. Non-haemorrhagic stroke or systemic embolism, major bleeding, cardiovascular and all-cause mortality were compared.

RESULTS:

From 2224 low CHA2DS2-VASc patients in GARFIELD-AF, 44% received OAC. In an adjusted model, increasing age up to 65 years (OR (95% CI)=1.31 (1.19 to 1.44)) and persistent AF (OR (95% CI)=3.25 (2.44 to 4.34)) or permanent AF (OR (95% CI)=2.29 (1.59 to 3.30)) versus paroxysmal/unclassified AF were associated with OAC use. Concomitant antiplatelet therapy (OR (95% CI)=0.21 (0.17 to 0.27)) was inversely associated. Crude incidence rates per 100 person-years over 2 years in patients on OAC versus not on OAC were 0.32 (95% CI 0.14 to 0.71) vs 0.30 (95% CI 0.14 to 0.63) for non-haemorrhagic stroke or systemic embolism, 0.21 (95% CI 0.08 to 0.57) vs 0.17 (95% CI 0.06 to 0.46) for major bleeding, 0.26 (95% CI 0.11 to 0.64) vs 0.26 (95% CI 0.12 to 0.57) for cardiovascular mortality and 0.74 (95% CI 0.44 to 1.25) vs 0.99 (95% CI 0.66 to 1.49) for all-cause mortality.

CONCLUSIONS:

In contrast to guideline recommendations, almost half of real-world patients with AF at a very low thromboembolic risk according to the CHA2DS2-VASc score receive OAC. Persistent or permanent AF and increasing age up to 65 years are associated with OAC use, while concomitant antiplatelet therapy shows an inverse association. Regardless whether patients received OAC therapy, few thromboembolic and bleeding events occur, highlighting the low risk of this population.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Tromboembolia / Sistema de Registros / Medição de Risco / Anticoagulantes Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Tromboembolia / Sistema de Registros / Medição de Risco / Anticoagulantes Idioma: En Ano de publicação: 2020 Tipo de documento: Article