Abstract

The safety and efficacy of a standardized periprocedural anticoagulation regimen with low -rnolecular-weight (LIH) heparin vvas studied n 650 cat-ients who hao eumbolic stroke, chronic atria! fibrillation, or a mechanical neart valve and required interrup ton of warfarin therapy because of an nvasive procedure. Warfarin was stopped 5 or 6 days before the procedure and NIH hepadin (subcutaneous dalteparin sodium' was begun 3 days before the procedure, Patients who had a procedure considered at low risk of bleeding and whose postprocedural hemostas:s was adequate resumed warfarin on the everrng of the procedure and dalteparin was resumed the Fext itay. Dalteparin was delayed if hemostasis was unstab e. Patients wino underwent a procedure at high risk of bleeding resurned warfarin or, the evening of the procedure but dalteparin was not given after the procedure. In 542 patients who underwernt a procedure at low risk for bleeding, 2 thromboermiulic events, 4 mrajor bleeding episodes, and 32 episodes of rncrea...

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