Key result
Warfarin exposure in patients with non-valvar atrial fibrillation was associated with significantly longer adjusted mean survival compared to no warfarin (MD 14.4 months; P<0.001).
Why the study?
Does warfarin improve survival and reduce ischaemic and thromboembolic events in patients with non-valvar atrial fibrillation?
Cohort (n=6,108)
Does warfarin improve survival and reduce ischaemic and thromboembolic events in patients with non-valvar atrial fibrillation?
Mean Difference: 14.4
Absolute Event Rate: 52% vs 38.2%
p-value: p=<0.001
In a general population cohort, warfarin treatment for non-valvular atrial fibrillation was associated with significantly improved survival and reduced ischemic events, despite an increased risk of bleeding.
Warfarin survival association in observational data should not change practice; leaves open causal benefit in non-valvular AF.
OBJECTIVE: To compare survival and adverse outcome of patients with non-valvar atrial fibrillation (NVAF) treated with or without warfarin. DESIGN: Record linkage method to identify patients with a previous hospital diagnosis of atrial fibrillation and to link these patients to international normalised ratio (INR) test results and mortality data. SETTING: Cardiff and the Vale of Glamorgan, Wales. MAIN OUTCOME MEASURES: Mortality, specifically from ischaemic and thromboembolic events. RESULTS: 6108 patients were identified with NVAF, of whom 36.4% received warfarin. Mean survival in the warfarin and non-warfarin groups was 52.0 months and 38.2 months, respectively (p < 0.001), and 14.4 months (p < 0.001) after adjustment for confounding factors. Warfarin treated patients in the upper quartile of INR control had significantly longer survival (57.5 months) than did those in the lowest quartile of control (38.1 months, p < 0.001). The risk of stroke in the warfarin group when treated was lower than that in the non-warfarin group (relative rate (RR) 0.74, p < 0.001). The risk of death from ischaemic stroke was lower in the warfarin group (RR 0.43, p < 0.001). The risk of all ischaemic and embolic events in the warfarin group was lower when they were taking warfarin (RR 0.74, p < 0.001). The risk of bleeding in the warfarin group when treated was greater (RR 1.78, p = 0.001). CONCLUSIONS: Patients with NVAF within the recommended target INR range of 2.0-3.0 survive longer and have reduced morbidity. Probably too few people are anticoagulated with warfarin in NVAF.
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Craig J. Currie (2005) conducted a cohort in Non-valvar atrial fibrillation (n=6,108). Warfarin vs. No warfarin was evaluated on Survival (months) (MD 14.4, p=<0.001). Warfarin exposure in patients with non-valvar atrial fibrillation was associated with significantly longer adjusted mean survival compared to no warfarin (MD 14.4 months; P<0.001).
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