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  Vol. 293 No. 23, June 15, 2005 TABLE OF CONTENTS
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Safety of Ximelagatran—Reply

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

In Reply: While Dr Brinker and colleagues from the Food and Drug Administration acknowledge the significant limitations of the vitamin K antagonists, the consequence of concern is that a substantial number of patients at serious risk of thrombembolism are left untreated. The resulting impact on mortality and lifelong disabilities may be less visible than a direct drug adverse effect.

Brinker et al state that the 2 long-term atrial fibrillation studies "showed conflicting results." This seems misleading, considering that for the major end points of stroke and systemic embolism, the efficacy of ximelagatran was remarkably consistent, being 2.3% and 2.6%, compared with 3.3% and 1.9%, respectively, for warfarin,1-2 the latter figure giving warfarin a nonsignificantly superior efficacy in one of the studies. Moreover, this result can probably be attributed to the control of warfarin in this study being exceptionally optimal and unlikely to be duplicated in clinical practice. For the second . . . [Full Text of this Article]

Victor Gurewich, MD
vgurewic@bidmc.harvard.edu
Beth Israel-Deaconess Medical Center
Harvard Medical School
Boston, Mass



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