Gender and contemporary risk of adverse events in atrial fibrillation

Author:

Champsi Asgher123ORCID,Mobley Alastair R123ORCID,Subramanian Anuradhaa4ORCID,Nirantharakumar Krishnarajah234ORCID,Wang Xiaoxia13ORCID,Shukla David24ORCID,Bunting Karina V13ORCID,Molgaard Inge5,Dwight Jeremy5,Casado Arroyo Ruben6ORCID,Crijns Harry J G M78ORCID,Guasti Luigina9ORCID,Lettino Maddalena10ORCID,Lumbers R Thomas1112ORCID,Maesen Bart78ORCID,Rienstra Michiel13ORCID,Svennberg Emma14ORCID,Țica Otilia115ORCID,Traykov Vassil16ORCID,Tzeis Stylianos17ORCID,van Gelder Isabelle13ORCID,Kotecha Dipak123ORCID

Affiliation:

1. Institute of Cardiovascular Sciences, University of Birmingham , Medical School, Vincent Drive, Birmingham B15 2TT , UK

2. West Midlands NHS Secure Data Environment, University Hospitals Birmingham NHS Foundation Trust , Mindelsohn Way, Birmingham B15 2TH , UK

3. NIHR Birmingham Biomedical Research Centre, Institute of Translational Medicine, Queen Elizabeth Hospital , Heritage Building, Mindelsohn Way, Birmingham B15 2TH , UK

4. Institute of Applied Health Research, University of Birmingham , University Road West, Birmingham B15 2TT , UK

5. Patient & Public Representatives, European Society of Cardiology, Sophia Antipolis, France

6. Department of Cardiology, H.U.B.-Hôpital Erasme, Université Libre de Bruxelles , Brussels 1070 , Belgium

7. Department of Cardiology, Maastricht University Medical Center , Maastricht , The Netherlands

8. Cardiovascular Research Institute (CARIM), Maastricht University , Maastricht , The Netherlands

9. Department of Medicine and Surgery, University of Insubria , Varese , Italy

10. Cardiothoracic and Vascular Department, Fondazione IRCCS San Gerardo dei Tintori , Monza , Italy

11. Institute of Health Informatics, University College London , London , UK

12. NIHR University College London Hospitals Biomedical Research Centre , London , UK

13. Department of Cardiology, University of Groningen, University Medical Centre Groningen , Groningen , The Netherlands

14. Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital , Stockholm , Sweden

15. Cardiology Department, Emergency County Clinical Hospital of Oradea , Oradea , Romania

16. Clinic of Cardiology, Acibadem City Clinic Tokuda University Hospital , Sofia , Bulgaria

17. Cardiology Department, Mitera Hospital , Athens , Greece

Abstract

Abstract Background and Aims The role of gender in decision-making for oral anticoagulation in patients with atrial fibrillation (AF) remains controversial. Methods The population cohort study used electronic healthcare records of 16 587 749 patients from UK primary care (2005–2020). Primary (composite of all-cause mortality, ischaemic stroke, or arterial thromboembolism) and secondary outcomes were analysed using Cox hazard ratios (HR), adjusted for age, socioeconomic status, and comorbidities. Results 78 852 patients were included with AF, aged 40–75 years, no prior stroke, and no prescription of oral anticoagulants. 28 590 (36.3%) were women, and 50 262 (63.7%) men. Median age was 65.7 years (interquartile range 58.5–70.9), with women being older and having other differences in comorbidities. During a total follow-up of 431 086 patient-years, women had a lower adjusted primary outcome rate with HR 0.89 vs. men (95% confidence interval [CI] 0.87–0.92; P < .001) and HR 0.87 after censoring for oral anticoagulation (95% CI 0.83–0.91; P < .001). This was driven by lower mortality in women (HR 0.86, 95% CI 0.83–0.89; P < .001). No difference was identified between women and men for the secondary outcomes of ischaemic stroke or arterial thromboembolism (adjusted HR 1.00, 95% CI 0.94–1.07; P = .87), any stroke or any thromboembolism (adjusted HR 1.02, 95% CI 0.96–1.07; P = .58), and incident vascular dementia (adjusted HR 1.13, 95% CI 0.97–1.32; P = .11). Clinical risk scores were only modest predictors of outcomes, with CHA2DS2-VA (ignoring gender) superior to CHA2DS2-VASc for primary outcomes in this population (receiver operating characteristic curve area 0.651 vs. 0.639; P < .001) and no interaction with gender (P = .45). Conclusions Removal of gender from clinical risk scoring could simplify the approach to which patients with AF should be offered oral anticoagulation.

Funder

National Institute for Health and Care Research

NIHR Birmingham Biomedical Research Centre

MRC Health Data Research UK

British Heart Foundation Accelerator Award

Publisher

Oxford University Press (OUP)

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