Mostrar el registro sencillo del ítem
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
| dc.creator | Ntaios, G. | en |
| dc.creator | Papavasileiou, V. | en |
| dc.creator | Diener, H. C. | en |
| dc.creator | Makaritsis, K. | en |
| dc.creator | Michel, P. | en |
| dc.date.accessioned | 2015-11-23T10:41:28Z | |
| dc.date.available | 2015-11-23T10:41:28Z | |
| dc.date.issued | 2012 | |
| dc.identifier | 10.1161/strokeaha.112.673558 | |
| dc.identifier.issn | 0039-2499 | |
| dc.identifier.uri | http://hdl.handle.net/11615/31438 | |
| dc.description.abstract | 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.) | en |
| dc.source.uri | <Go to ISI>://WOS:000311497600034 | |
| dc.subject | anticoagulants | en |
| dc.subject | apixaban | en |
| dc.subject | atrial fibrillation | en |
| dc.subject | dabigatran | en |
| dc.subject | rivaroxaban | en |
| dc.subject | stroke | en |
| dc.subject | transient ischemic attack | en |
| dc.subject | warfarin | en |
| dc.subject | COST-EFFECTIVENESS | en |
| dc.subject | DABIGATRAN ETEXILATE | en |
| dc.subject | SUBGROUP ANALYSIS | en |
| dc.subject | WARFARIN | en |
| dc.subject | PREVENTION | en |
| dc.subject | THROMBOEMBOLISM | en |
| dc.subject | RIVAROXABAN | en |
| dc.subject | APIXABAN | en |
| dc.subject | EMBOLISM | en |
| dc.subject | AF | en |
| dc.subject | Clinical Neurology | en |
| dc.subject | Peripheral Vascular Disease | en |
| dc.title | 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 | en |
| dc.type | journalArticle | en |
Ficheros en el ítem
| Ficheros | Tamaño | Formato | Ver |
|---|---|---|---|
|
No hay ficheros asociados a este ítem. |
|||