Key result
The synthetic Factor Xa inhibitor DX-9065a maintained 100% graft patency compared to 30% with unfractionated heparin in a highly thrombogenic rabbit venous graft model.
Why the study?
Does DX-9065a improve graft patency compared to heparin or argatroban in a rabbit venous graft model?
Does DX-9065a improve graft patency compared to heparin or argatroban in a rabbit venous graft model?
Absolute Event Rate: 100% vs 30%
The synthetic Factor Xa inhibitor DX-9065a demonstrated potent in vivo antithrombotic effects comparable to argatroban and superior to heparin in a highly thrombogenic rabbit venous graft model.
Supports preclinical testing of selective Factor Xa inhibition for grafts; leaves open translation to human bypass surgery.
An in vivo effect of a novel synthetic Xa inhibitor, DX-9065a, was evaluated in a highly thrombogenic venous graft model. A woven Tetron tube graft was interposed in the inferior vena cava of rabbits. All the grafts were completely occluded within 5 hours after a bolus injection of heparin (50 U/kg) given just prior to the grafting. The following agents were continuously given to the respective group of rabbits for 2 h after the bolus injection of heparin; heparin (50 U/kg/h, UFH-group), DX-9065a (0.05 mg/kg/h, DX-group) and argatroban (32 microG/kg/h, MD-group). During a 5-h observation period, the anti-Xa activity in circulating blood between the UFH- and DX-group and the anti-thrombin activity between the UFH- and MD-group were not significantly different. The graft patency in the DX-group (4/4) and MD-group (4/4) was significantly better than that in the UFH-group (3/10). Ultrastructural analysis of the luminal surface of the harvested graft by scanning electron microscopy revealed the reduced formation of fibrin networks entrapping erythrocytes in the DX- and MD-group in comparison with the patent UFH-group. In conclusion, a novel synthetic Xa inhibitor DX-9065a exerts a potent in vivo antithrombotic effect, which was comparable with argatroban, a synthetic thrombin inhibitor.
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Kim et al. (1996) studied Experimental vein graft thrombosis (n=22). DX-9065a vs. Unfractionated heparin (50 U/kg/h) was evaluated on Graft patency at 5 hours. The synthetic Factor Xa inhibitor DX-9065a maintained 100% graft patency compared to 30% with unfractionated heparin in a highly thrombogenic rabbit venous graft model.
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