Bristol-Myers
Squibb Company BMY and Pfizer
Inc. PFE today announced results of a post-hoc subanalysis
from the Phase III ARISTOTLE trial. Patients with nonvalvular atrial
fibrillation (NVAF) who are anticoagulated to reduce the risk of stroke
often undergo procedures for which temporary discontinuation of the
anticoagulant prior to and following the procedure is sometimes
warranted. This subanalysis describes the overall rates of key
post-procedural outcomes, such as stroke or systemic embolism and major
bleeding, among Eliquis and warfarin patients who underwent a
procedure during the ARISTOTLE trial, and examined any differences in
post-procedural events according to whether or not study drug was
interrupted. This subanalysis was presented today at the ESC
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