Effectiveness and safety of non-vitamin K antagonist oral anticoagulants and warfarin in atrial fibrillation: a Scandinavian population-based cohort study

被引:9
|
作者
Halvorsen, Sigrun [1 ,2 ]
Johnsen, Soren P. [3 ]
Madsen, Morten [4 ]
Linder, Marie [5 ]
Sulo, Gerhard [6 ]
Ghanima, Waleed [2 ,7 ]
Gislason, Gunnar [8 ]
Hohnloser, Stefan H. [9 ]
Jenkins, Aaron [10 ]
Al-Khalili, Faris [11 ]
Tell, Grethe S. [12 ]
Ehrenstein, Vera [4 ]
机构
[1] Oslo Univ Hosp Ulleval, Dept Cardiol, POB 4956, NO-0424 Oslo, Norway
[2] Univ Oslo, Inst Clin Med, Oslo, Norway
[3] Aalborg Univ, Danish Ctr Clin Hlth Serv Res, Dept Clin Med, Aalborg, Denmark
[4] Aarhus Univ Hosp, Dept Clin Epidemiol, Aarhus, Denmark
[5] Karolinska Inst, Ctr Pharmacoepidemiol, Stockholm, Sweden
[6] Norwegian Inst Publ Hlth, Ctr Dis Burden, Bergen, Norway
[7] Ostfold Hosp Trust, Kalnes, Norway
[8] Copenhagen Univ Hosp Herlev & Gentofte, Dept Cardiol, DK-2900 Hellerup, Denmark
[9] Goethe Univ Frankfurt, Dept Cardiol, Frankfurt, Germany
[10] Pfizer Ltd, Tadworth, England
[11] Sophiahemmets Hosp, Heart Lung & Allergy Clin, Stockholm, Sweden
[12] Univ Bergen, Dept Global Publ Hlth & Primary Care, Bergen, Norway
关键词
Anticoagulants; Atrial fibrillation; Bleeding; Cohort study; Stroke; PATIENT REGISTRY; RIVAROXABAN; VALIDATION; DABIGATRAN; MANAGEMENT; APIXABAN; EFFICACY; QUALITY; WORLD;
D O I
10.1093/ehjqcco/qcab048
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Using Scandinavian population-based registries, we assessed risk of stroke/systemic embolism (SE) and bleeding with non-vitamin K antagonist oral anticoagulants compared with warfarin in anticoagulation-naive patients with atrial fibrillation (AF). Methods and results This historical cohort study included 219 545 AF patients [median age 74 years; 43% women; mean CHA(2)DS(2)-VASc (congestive heart failure, hypertension, age >= 75 years, diabetes mellitus, stroke or transient ischaemic attack, vascular disease, age 65-74 years, sex category) score 3.3] initiating apixaban, dabigatran, rivaroxaban, or warfarin in Denmark, Norway, and Sweden (1 January 2013 to 31 December 2016). The primary endpoints were stroke/SE and major bleeding. The median follow-up times were 9.7 (3.9-21.5) months for stroke/SE and 9.6 (3.8-21.3) months for bleeding. Apixaban and warfarin initiators were older and had higher CHA(2)DS(2)-VASc scores compared with dabigatran and rivaroxaban initiators. After 1:1 propensity score matching, three cohorts were created: apixaban-warfarin (n = 111 162), dabigatran-warfarin (n = 56 856), and rivaroxaban-warfarin (n = 61 198). Adjusted hazard ratios (HRs) were estimated using a Cox regression. For stroke/SE, adjusted HRs against warfarin were 0.96 [95% confidence interval (CI): 0.87-1.06] for apixaban, 0.89 (95% CI: 0.80-1.00) for dabigatran, and 1.03 (95% CI: 0.92-1.14) for rivaroxaban. For major bleeding, the HRs against warfarin were 0.73 (95% CI: 0.67-0.78) for apixaban, 0.89 (95% CI: 0.82-0.97) for dabigatran, and 1.15 (95% CI: 1.07-1.25) for rivaroxaban. The results in the dabigatran cohort did not hold in all dose-defined subgroups. Conclusion In this large Scandinavian study among AF patients initiating oral anticoagulation, those initiating dabigatran, apixaban, and rivaroxaban had similar rates of stroke/SE to patients initiating warfarin. Rates of major bleeding were lower with apixaban and dabigatran and higher with rivaroxaban, each compared with warfarin.
引用
收藏
页码:577 / 587
页数:11
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