Aleksander Siniarski, Jakub Michal Zimodro, Aleksandra Gąsecka, Michał Łomiak, Marta Frydrych, Jadwiga Nessler, Grzegorz Gajos
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引用次数: 0
Abstract
Transcatheter aortic valve implantation (TAVI) is an established treatment method in patients with severe aortic stenosis at high surgical risk. TAVI might reduce thrombin generation and fibrin clot resistance to lysis. We aimed to evaluate the predictive value of thrombin generation and clot lysis time on TAVI outcomes. We screened 135 patients referred for TAVI. Thrombin generation (lag time, time to peak, peak thrombin concentration, and endogenous thrombin potential) and clot lysis time were assessed before TAVI and at hospital discharge. Major adverse cardiac and cerebrovascular events (MACCE) including all-cause death, cardiovascular death, myocardial infarction, stroke, transient ischemic attack, heart failure decompensation, and clinical valve thrombosis were assessed during 1-year follow-up. Among 70 patients who underwent TAVI, 14 (20%) experienced MACCE during the median follow-up of 361 days. Before TAVI, thrombin generation and clot lysis time were similar in patients with vs. without MACCE. Post-TAVI peak thrombin concentration was significantly lower in patients with MACCE (157.5 vs. 240.38 nM, p = 0.016), discriminated between those with and without MACCE (AUC: 0.773, p = 0.016), and was predictive for MACCE in both univariable (OR: 10.733, 95% CI: 1.197-96.283, p = 0.034) and multivariable (OR: 11.551, 95% CI: 1.104-120.828, p = 0.041) regression analyses. Pre-TAVI lag time was a predictor of MACCE in univariable regression analysis (OR: 5.304, 95% CI: 1.074-26.182, p = 0.041). Post-TAVI peak thrombin concentration and pre-TAVI lag time might potentially serve as novel predictors of MACCE in patients undergoing TAVI.
期刊介绍:
The Journal of Thrombosis and Thrombolysis is a long-awaited resource for contemporary cardiologists, hematologists, vascular medicine specialists and clinician-scientists actively involved in treatment decisions and clinical investigation of thrombotic disorders involving the cardiovascular and cerebrovascular systems. The principal focus of the Journal centers on the pathobiology of thrombosis and vascular disorders and the use of anticoagulants, platelet antagonists, cell-based therapies and interventions in scientific investigation, clinical-translational research and patient care.
The Journal will publish original work which emphasizes the interface between fundamental scientific principles and clinical investigation, stimulating an interdisciplinary and scholarly dialogue in thrombosis and vascular science. Published works will also define platforms for translational research, drug development, clinical trials and patient-directed applications. The Journal of Thrombosis and Thrombolysis'' integrated format will expand the reader''s knowledge base and provide important insights for both the investigation and direct clinical application of the most rapidly growing fields in medicine-thrombosis and vascular science.