| Literature DB >> 27258224 |
Veli K Topkara1, Robert J Knotts, Douglas L Jennings, A Reshad Garan, Allison P Levin, Alexander Breskin, Francesco Castagna, Barbara Cagliostro, Melana Yuzefpolskaya, Koji Takeda, Hiroo Takayama, Nir Uriel, Donna M Mancini, Andrew Eisenberger, Yoshifumi Naka, Paolo C Colombo, Ulrich P Jorde.
Abstract
Bleeding and thrombotic complications continue to plague continuous-flow left ventricular assist device (CF-LVAD) therapy in patients with end-stage heart failure. Warfarin genotyping information can be incorporated into decision making for initial dosing as recommended by the Food and Drug Administration; however, clinical utility of this data in the CF-LVAD population has not been well studied. Genotypes testing for CYP2C9 and VCORC1 polymorphisms were determined in 90 CF-LVAD patients. Outcomes studied were the association of CYP2C9 (*1, *2, or *3) and VKORC1 (-1639 G>A) gene variants with time-to-target international normalized ratio (INR), total warfarin dose, maintenance warfarin dose. Continuous-flow left ventricular assist device patients carrying a rare variant in the VKORC1 gene had a significantly lower cumulative warfarin dose until target INR achieved (18.9 vs. 35.0 mg, p = 0.002), days spent until INR target achieved (4.9 vs. 7.0 days, p = 0.021), and discharge warfarin dose (3.2 vs. 5.6 mg, p = 0.001) compared with patients with wild-type genotype. Genotype-guided warfarin dosing may lead to safer anticoagulation and potentially improve outcomes in CF-LVAD patients.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27258224 DOI: 10.1097/MAT.0000000000000390
Source DB: PubMed Journal: ASAIO J ISSN: 1058-2916 Impact factor: 2.872