Comparison of analytical performances between clot waveform analysis and FibWave in edoxaban-treated patients and healthy controls

被引:2
作者
Evrard, Jonathan [1 ]
Siriez, Romain [1 ]
Bouvy, Celine [2 ]
Favresse, Julien [1 ,3 ]
Yildiz, Halil [4 ]
Hainaut, Philippe [4 ]
Mullier, Francois [5 ]
Dogne, Jean-Michel [1 ]
Douxfils, Jonathan [1 ,2 ]
机构
[1] Univ Namur, Namur Res Inst Life Sci NARILIS, Namur Thrombosis & Hemostasis Ctr NTHC, Dept Pharm, B-5000 Namur, Belgium
[2] Qualiblood Sa, Namur, Belgium
[3] Clin St Luc Bouge, Dept Lab Med, Namur, Belgium
[4] Catholic Univ Louvain, Clin Univ St Luc, Dept Internal Med & Infect Dis, Brussels, Belgium
[5] Catholic Univ Louvain, CHU UCL Namur, Namur Thrombosis & Hemostasis Ctr NTHC, Namur Res Inst Life Sci NARILIS,Hematol Lab, Yvoir, Belgium
关键词
activated partial thromboplastin time; anticoagulants; clot waveform analysis; edoxaban; fibrin; fibrinolysis; prothrombin time; DIRECT ORAL ANTICOAGULANTS; PARTIAL THROMBOPLASTIN TIME; COAGULATION ASSAYS; LABORATORY ASSESSMENT; LC-MS/MS; THROMBIN; HEMOSTASIS; DABIGATRAN; ROUTINE; TESTS;
D O I
10.1002/rth2.12804
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction The activated partial thromboplastin time (aPTT) and the prothrombin time (PT) are widely available coagulation parameters which are however poor predictors of the anticoagulant effect of direct oral anticoagulants (DOACs). Some coagulometers use the clot waveform analysis (CWA) to assess the clotting time but mainly based on a unique parameter. The improvement of these methodologies and the evaluation of the other waveform parameters may increase the sensitivity to DOACs. Objectives To assess the performance of an improved clot waveform an method (i.e. FibWave) to detect the impact of edoxaban on the coagulation and the fibrinolytic systems. Methods Seventy-one samples from patients treated with edoxaban collected at minimum concentration (C-TROUGH) and/or maximum concentration (C-MAX), and 45 control samples were included. The aPTT- and PT-based CWA as well as the FibIn, FibEx, and FibLysis methodologies of the FibWave were implemented and performed on an ACL-TOP 700. Results PT and FibEx clotting time were strongly correlated to edoxaban concentration (Pearson r = 0.80 and 0.89, respectively). The FibEx clotting time allowed a better discrimination for samples with 30 and 50 ng/ml of edoxaban compared to PT (cutoffs of 96.5 and 114.2 s for the FibEx versus a unique cutoff of 13.1 s for the PT). The fibrinolytic process was impaired in the presence of edoxaban in a dose-dependent manner. Conclusion FibEx is more sensitive than aPTT- and PT-based CWA for the detection of the clinically relevant anticoagulant level of edoxaban.
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共 48 条
[1]   Concomitant assessment of rivaroxaban concentration and its impact on thrombin generation [J].
Bloemen, Saartje ;
Zwaveling, Suzanne ;
Mullier, Francois ;
Douxfils, Jonathan .
THROMBOSIS RESEARCH, 2019, 184 :8-15
[2]   The anticoagulant effect of dabigatran is reflected in the lag time and time-to-peak, but not in the endogenous thrombin potential or peak, of thrombin generation [J].
Bloemen, Saartje ;
Zwaveling, Suzanne ;
Douxfils, Jonathan ;
Roest, Mark ;
Kremers, Romy ;
Mullier, Francois .
THROMBOSIS RESEARCH, 2018, 171 :160-166
[3]  
Braun PJ, 1997, THROMB HAEMOSTASIS, V78, P1079
[4]   Rivaroxaban and apixaban induce clotting factor Xa fibrinolytic activity [J].
Carter, R. L. R. ;
Talbot, K. ;
Hur, W. S. ;
Meixner, S. C. ;
Van der Gugten, J. G. ;
Holmes, D. T. ;
Cote, H. C. F. ;
Kastrup, C. J. ;
Smith, T. W. ;
Lee, A. Y. Y. ;
Pryzdial, E. L. G. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2018, 16 (11) :2276-2288
[5]   Laboratory testing in patients treated with direct oral anticoagulants: a practical guide for clinicians [J].
Douxfils, J. ;
Ageno, W. ;
Samama, C. -M. ;
Lessire, S. ;
ten Cate, H. ;
Verhamme, P. ;
Dogne, J. -M. ;
Mullier, F. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2018, 16 (02) :209-219
[6]   2021 Update of the International Council for Standardization in Haematology Recommendations for Laboratory Measurement of Direct Oral Anticoagulants [J].
Douxfils, Jonathan ;
Adcock, Dorothy M. ;
Bates, Shannon M. ;
Favaloro, Emmanuel J. ;
Gouin-Thibault, Isabelle ;
Guillermo, Cecilia ;
Kawai, Yohko ;
Lindhoff-Last, Edelgard ;
Kitchen, Steve ;
Gosselin, Robert C. .
THROMBOSIS AND HAEMOSTASIS, 2021, 121 (08) :1008-1020
[7]   Assessment of the analytical performances and sample stability on ST Genesia system using the STG-DrugScreen application [J].
Douxfils, Jonathan ;
Morimont, Laure ;
Bouvy, Celine ;
de Saint-Hubert, Marie ;
Devalet, Berangere ;
Devroye, Celia ;
Dincq, Anne-Sophie ;
Dogne, Jean-Michel ;
Guldenpfennig, Maite ;
Baudar, Justine ;
Larock, Anne-Sophie ;
Lessire, Sarah ;
Mullier, Francois .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2019, 17 (08) :1273-1287
[8]   Laboratory Assessment of Direct Oral Anticoagulants [J].
Douxfils, Jonathan ;
Gosselin, Robert C. .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2017, 43 (03) :277-290
[9]   Edoxaban: Impact on routine and specific coagulation assays A practical laboratory guide [J].
Douxfils, Jonathan ;
Chatelain, Bernard ;
Chatelain, Christian ;
Dogne, Jean-Michel ;
Mullier, Francois .
THROMBOSIS AND HAEMOSTASIS, 2016, 115 (02) :368-381
[10]   Measurement of non-VKA oral anticoagulants versus classic ones: The appropriate use of hemostasis assays [J].
Douxfils J. ;
Tamigniau A. ;
Chatelain B. ;
Goffinet C. ;
Dogné J.-M. ;
Mullier F. .
Thrombosis Journal, 12 (1)