Ex vivo reversal of effects of rivaroxaban evaluated using thromboelastometry and thrombin generation assay. (13th September 2016)

• Record Type: Journal Article
• Authors: Schenk, B.; Würtinger, P.; Streif, W.; Sturm, W.; Fries, D.; Bachler, M.
• Editors: Hemmings, H. C.
• Is Part Of: British journal of anaesthesia. Volume 117:Number 5(2016:Nov.)
• Page Start: 583
• Page End: 591
• Publication Date: 2016-09-13
• Subjects: blood, anticoagulants -- complications, haemorrhage -- thromboelastography; Anesthesiology -- Periodicals; Anesthesia -- Periodicals; 617.9605
• DOI: 10.1093/bja/aew259
• Languages: English
• ISSNs: 0007-0912

Abstract

Abstract : Background: In major bleeding events, the new direct oral anticoagulants pose a great challenge for physicians. The aim of the study was to test for ex vivo reversal of the direct oral anticoagulant rivaroxaban with various non-specific reversal agents: prothrombin complex concentrate (PCC), activated prothrombin complex concentrate (aPCC), recombinant activated factor VII (rFVIIa), and fibrinogen concentrate (FI). Methods: Blood was obtained from healthy volunteers and from patients treated with rivaroxaban. Blood samples from healthy volunteers were spiked with rivaroxaban to test the correlation between rivaroxaban concentration and coagulation tests. Patient blood samples were spiked with various concentrations of the above-mentioned agents and analysed using thromboelastometry and thrombin generation. Results: When added in vitro, rivaroxaban was significantly ( P <0.05) correlated with ROTEM ® thromboelastometry EXTEM (extrinsic coagulation pathway) clotting time (CT), time to maximal velocity (Max V − t ), and with all measured thrombin generation parameters. In vivo, CT, Max V − t, lag time, and peak thrombin generation ( C max ) were significantly correlated with rivaroxaban concentrations. Regarding reversal of rivaroxaban, all tested agents significantly ( P <0.05) reduced EXTEM CT, but to different extents: rFVIIa by 68%, aPCC by 47%, PCC by 17%, and FI by 9%. Only rFVIIa reversed EXTEM CT to baseline values. Both PCC (+102%) and aPCC (+232%) altered overall thrombin generation (area under the curve) and increased C max (+461% for PCC, +87.5% for aPCC). Conclusions: Thromboelastometry and thrombin generation assays do not favour the same reversal agents for rivaroxaban anticoagulation. Controlled clinical trials are urgently needed to establish doses and clinical efficacy of potential reversal agents. Clinical trial registration: EudracCT trial no. 213-00474-30.