Bleeding and ischaemic events after first bleed in anticoagulated atrial fibrillation patients: risk and timing

Author:

Meyre Pascal B12ORCID,Blum Steffen12ORCID,Hennings Elisa12,Aeschbacher Stefanie12ORCID,Reichlin Tobias3ORCID,Rodondi Nicolas45ORCID,Beer Jürg H6,Stauber Annina7,Müller Andreas7ORCID,Sinnecker Tim89,Moutzouri Elisavet45,Paladini Rebecca E12,Moschovitis Giorgio10ORCID,Conte Giulio11,Auricchio Angelo11,Ramadani Alexandra12,Schwenkglenks Matthias1213ORCID,Bonati Leo H8,Kühne Michael12ORCID,Osswald Stefan12ORCID,Conen David14

Affiliation:

1. Division of Cardiology, Department of Medicine, University Hospital Basel , Petersgraben 4, 4031 Basel, Basel-Stadt , Switzerland

2. Division of Cardiology, Cardiovascular Research Institute Basel, University Hospital Basel , Spitalstrasse 2, 4056 Basel, Basel-Stadt , Switzerland

3. Department of Cardiology, Inselspital, Bern University Hospital, University of Bern , 3010 Bern , Switzerland

4. Institute of Primary Health Care (BIHAM), University of Bern , Mittelstrasse 43, 3012 Bern , Switzerland

5. Department of General Internal Medicine, Inselspital, Bern University Hospital, University of Bern , Freiburgstrasse 16p, 3010 Bern , Switzerland

6. Department of Medicine, Cantonal Hospital of Baden and Molecular Cardiology, University Hospital of Zurich , Im Ergel 1, 5404 Baden, Aargau , Switzerland

7. Department of Cardiology, Triemli Hospital Zurich , Birmensdorferstrasse 497, 8063 Zurich , Switzerland

8. Department of Neurology and Stroke Center, University Hospital Basel, University of Basel , Petersgraben 4, 4031 Basel, Basel-Stadt , Switzerland

9. Medical Image Analysis Center (MIAC AG) and Department of Biomedical Engineering, University of Basel , Marktgasse 8, 4051 Basel, Basel-Stadt , Switzerland

10. Division of Cardiology, Ospedale Regionale di Lugano , Via Tesserete 46, 6900 Lugano , Switzerland

11. Istituto Cardiocentro Ticino, Ente Ospedaliero Cantonale , Via Tesserete 48, 6900 Lugano , Switzerland

12. Epidemiology, Biostatistics, and Prevention Institute, University of Zurich , Hirschengraben 84, 8001 Zurich , Switzerland

13. Institute of Pharmaceutical Medicine (ECPM), University of Basel , Klingelbergstrasse 61, 4056 Basel , Switzerland

14. Population Health Research Institute, McMaster University , 237 Barton St E, Hamilton, ON L8L 2X2 , Canada

Abstract

Abstract Aims To determine the risk of subsequent adverse clinical outcomes in anticoagulated patients with atrial fibrillation (AF) who experienced a new bleeding event. Methods and results Anticoagulated AF patients were followed in two prospective cohort studies. Information on incident bleeding was systematically collected during yearly follow-up visits and events were adjudicated as major bleeding or clinically relevant non-major bleeding (CRNMB) according to the International Society on Thrombosis and Haemostasis guidelines. The primary outcome was a composite of stroke, myocardial infarction (MI), or all-cause death. Time-updated multivariable Cox proportional-hazards models were used to compare outcomes in patients with and without incident bleeding. Median follow-up was 4.08 years [interquartile range (IQR): 2.93–5.98]. Of the 3277 patients included (mean age 72 years, 28.5% women), 646 (19.7%) developed a new bleeding, 297 (9.1%) a major bleeding and 418 (12.8%) a CRNMB. The incidence of the primary outcome was 7.08 and 4.04 per 100 patient-years in patients with and without any bleeding [adjusted hazard ratio (aHR): 1.36, 95% confidence interval (CI): 1.16–1.61; P < 0.001; median time between a new bleeding and a primary outcome 306 days (IQR: 23–832)]. Recurrent bleeding occurred in 126 patients [incidence, 8.65 per 100 patient-years (95% CI: 7.26–10.30)]. In patients with and without a major bleeding, the incidence of the primary outcome was 11.00 and 4.06 per 100 patient-years [aHR: 2.04, 95% CI: 1.69–2.46; P < 0.001; median time to a primary outcome 142 days (IQR: 9–518)], and 59 had recurrent bleeding [11.61 per 100 patient-years (95% CI: 8.99–14.98)]. The incidence of the primary outcome was 5.29 and 4.55 in patients with and without CRNMB [aHR: 0.94, 95% CI: 0.76–1.15; P = 0.53; median time to a composite outcome 505 days (IQR: 153–1079)], and 87 had recurrent bleeding [8.43 per 100 patient-years (95% CI: 6.83–10.40)]. Patients who had their oral anticoagulation (OAC) discontinued after their first bleeding episode had a higher incidence of the primary composite than those who continued OAC (63/89 vs. 159/557 patients; aHR: 4.46, 95% CI: 3.16–6.31; P < 0.001). Conclusion In anticoagulated AF patients, major bleeding but not CRNMB was associated with a high risk of adverse outcomes, part of which may be explained by OAC discontinuation. Most events occurred late after the bleeding episode, emphasizing the importance of long-term follow-up in these patients.

Funder

Swiss National Science Foundation

Swiss Heart Foundation

Foundation for Cardiovascular Research Basel

University of Basel

Boehringer Ingelheim

Sanofi-Aventis

Merck Sharp & Dome

Bayer

Daiichi-Sankyo

Pfizer

Bristol-Myers Squibb

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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