ASH Clinical News December 2014 | Page 42

Written in Blood Pre-Procedure Anticoagulation Interruption May Not Be Necessary Patients with atrial fibrillation (AF) on anticoagulation therapies who require a surgical procedure may require an interruption in the therapy – depending on their risk of post-procedural bleeding and the likelihood of periprocedural thrombotic events. According to an analysis of data from the ARISTOTLE trial, though, many patients were able to undergo surgical procedures safely without interrupting or bridging therapy. “These findings corroborate the implications of many other studies,” lead author David Garcia, MD, of the division of hematology, University of Washington, Seattle, told ASH Clinical News. “In 2014, for patients with atrial fibrillation, pre-procedure parenteral bridging therapy looks increasingly unnecessary.” The ARISTOTLE trial compared apixaban (an oral direct factor Xa inhibitor) with warfarin for the prevention of stroke or systemic embolism in AF patients. Apixaban, in contrast to warfarin and other vitamin K antagonists, has a rapid onset and offset of anticoagulant activity – making it an attractive option for patients who require short-term protection from thrombosis before a surgical procedure. According to Dr. Garcia, physicians have more experience with managing patients taking warfarin who require surgical procedures than the newer target-specific oral anticoagulants. In this analysis, investigators explored the management of anticoagulants and surgical outcomes 30 days post-procedure among 5,924 patients from the ARISTOTLE study who underwent a total of 40 ASH Clinical News 10,674 procedures. Overall, 5,439 patients had a procedure that met study eligibility criteria. The most common were dental extraction/ oral surgery (14.6%), colonoscopy (9.9%), and ophthalmic surgery (8.0%). Local investigators chose to interrupt anticoagulant treatment pre-proc VGW&R