Nonvitamin-K-Antagonist Oral Anticoagulants in Patients With Atrial Fibrillation and Previous Stroke or Transient Ischemic Attack A Systematic Review and Meta-Analysis of Randomized Controlled Trials

被引:129
作者
Ntaios, George [1 ]
Papavasileiou, Vasileios [2 ,3 ]
Diener, Hans-Christoph [4 ,5 ]
Makaritsis, Konstantinos
Michel, Patrik [2 ,3 ]
机构
[1] Univ Thessaly, Dept Med, Biopolis, Larisa 41110, Greece
[2] Univ Lausanne, Lausanne, Switzerland
[3] CHU Vaudois, Neurol Serv, Lausanne, Switzerland
[4] Univ Hosp Essen, Dept Neurol, Essen, Germany
[5] Univ Hosp Essen, Stroke Ctr, Essen, Germany
基金
美国国家卫生研究院;
关键词
anticoagulants; apixaban; atrial fibrillation; dabigatran; rivaroxaban; stroke; transient ischemic attack; warfarin; COST-EFFECTIVENESS; DABIGATRAN ETEXILATE; SUBGROUP ANALYSIS; WARFARIN; PREVENTION; THROMBOEMBOLISM; APIXABAN; EMBOLISM; AF;
D O I
10.1161/STROKEAHA.112.673558
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-To assess whether the combined analysis of all phase III trials of nonvitamin-K-antagonist (non-VKA) oral anticoagulants in patients with atrial fibrillation and previous stroke or transient ischemic attack shows a significant difference in efficacy or safety compared with warfarin. Methods-We searched PubMed until May 31, 2012, for randomized clinical trials using the following search items: atrial fibrillation, anticoagulation, warfarin, and previous stroke or transient ischemic attack. Studies had to be phase III trials in atrial fibrillation patients comparing warfarin with a non-VKA currently on the market or with the intention to be brought to the market in North America or Europe. Analysis was performed on intention-to-treat basis. A fixed-effects model was used as more appropriate than a random-effects model when combining a small number of studies. Results-Among 47 potentially eligible articles, 3 were included in the meta-analysis. In 14 527 patients, non-VKAs were associated with a significant reduction of stroke/systemic embolism (odds ratios, 0.85 [95% CI, 074-0.99]; relative risk reduction, 14%; absolute risk reduction, 0.7%; number needed to treat, 134 over 1.8-2.0 years) compared with warfarin. Non-VKAs were also associated with a significant reduction of major bleeding compared with warfarin (odds ratios, 0.86 [ 95% CI, 075-0.99]; relative risk reduction, 13%; absolute risk reduction, 0.8%; number needed to treat, 125), mainly driven by the significant reduction of hemorrhagic stroke (odds ratios, 0.44 [95% CI, 032-0.62]; relative risk reduction, 57.9%; absolute risk reduction, 0.7%; number needed to treat, 139). Conclusions-In the context of the significant limitations of combining the results of disparate trials of different agents, non-VKAs seem to be associated with a significant reduction in rates of stroke or systemic embolism, hemorrhagic stroke, and major bleeding when compared with warfarin in patients with previous stroke or transient ischemic attack. (Stroke. 2012; 43: 3298-3304.)
引用
收藏
页码:3298 / 3304
页数:7
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