Stroke and bleeding risk in atrial fibrillation with CHA2DS2-VASC risk score of one: the Norwegian AFNOR study

Author:

Anjum Mariam12ORCID,Ariansen Inger2ORCID,Hjellvik Vidar2,Selmer Randi2,Kjerpeseth Lars J2,Skovlund Eva3,Myrstad Marius14,Ellekjær Hanne56,Christophersen Ingrid E17,Tveit Arnljot18ORCID,Berge Trygve14ORCID

Affiliation:

1. Department of Medical Research, Bærum Hospital, Vestre Viken Hospital Trust , Gjettum , Norway

2. Department of Chronic Diseases, Norwegian Institute of Public Health , Oslo , Norway

3. Department of Public Health and Nursing, Norwegian University of Science and Technology , Trondheim , Norway

4. Department of Internal Medicine, Bærum Hospital, Vestre Viken Hospital Trust , Gjettum , Norway

5. Stroke Unit, Department of Internal Medicine, St.Olavs Hospital , Norway

6. Department of Neuromedicine and Movement Science, Faculty of Medicine and Health Science, Norwegian University of Science and Technology , Norway

7. Department of Medical Genetics, Oslo University Hospital , Oslo , Norway

8. Department of Cardiology, Institute of Clinical Medicine, University of Oslo , Oslo , Norway

Abstract

Abstract Background and Aims The benefit of oral anticoagulant (OAC) therapy in atrial fibrillation (AF) and intermediate stroke risk is debated. In a nationwide Norwegian cohort with a non-sex CHA2DS2-VASc risk score of one, this study aimed to investigate (i) stroke and bleeding risk in AF patients with and without OAC treatment, and (ii) the risk of stroke in non-anticoagulated individuals with and without AF. Methods A total of 1 118 762 individuals including 34 460 AF patients were followed during 2011–18 until ischaemic stroke, intracranial haemorrhage, increased CHA2DS2-VASc score, or study end. One-year incidence rates (IRs) were calculated as events per 100 person-years (%/py). Cox regression models provided adjusted hazard ratios (aHRs [95% confidence intervals]). Results Among AF patients, the ischaemic stroke IR was 0.51%/py in OAC users and 1.05%/py in non-users (aHR 0.47 [0.37–0.59]). Intracranial haemorrhage IR was 0.28%/py in OAC users and 0.19%/py in non-users (aHR 1.23 [0.88–1.72]). Oral anticoagulant use was associated with an increased risk of major bleeding (aHR 1.37 [1.16–1.63]) but lower risk of the combined outcome of ischaemic stroke, major bleeding, and mortality (aHR 0.57 [0.51–0.63]). Non-anticoagulated individuals with AF had higher risk of ischaemic stroke compared to non-AF individuals with the same risk profile (aHR 2.47 [2.17–2.81]). Conclusions In AF patients at intermediate risk of stroke, OAC use was associated with overall favourable clinical outcomes. Non-anticoagulated AF patients had higher risk of ischaemic stroke compared to the general population without AF with the same risk profile.

Funder

Norwegian South-East Regional Health Authority

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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