Comparing thrombin generation in patients with hemophilia A and patients on vitamin K antagonists

被引:15
|
作者
de Koning, M. L. Y. [1 ]
Fischer, K. [1 ]
de laat, B. [2 ]
Huisman, A. [3 ]
Ninivaggi, M. [2 ]
Schutgens, R. E. G. [1 ]
机构
[1] Univ Med Ctr Utrecht, Van Creveldkliniek, Heidelberglaan 100,POB 85060, NL-3508 AB Utrecht, Netherlands
[2] Synapse, Maastricht, Netherlands
[3] Univ Med Ctr Utrecht, Dept Clin Chem & Hematol, Utrecht, Netherlands
关键词
atrial fibrillation; coumarins; factor VIII; hemophilia A; thrombin; INTERNATIONAL-NORMALIZED-RATIO; CORN TRYPSIN-INHIBITOR; CALIBRATED AUTOMATED THROMBOGRAPHY; FACTOR-VIII DEFICIENCY; ATRIAL-FIBRILLATION; CARDIOVASCULAR-DISEASE; CLINICAL SEVERITY; LIFE EXPECTANCY; PLASMA; ASSAY;
D O I
10.1111/jth.13674
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: It is unknown whether patients with hemophilia A with atrial fibrillation require treatment with vitamin K antagonists (VKAs) to the same extent as the normal population. Objective: To compare hemostatic potential in hemophilia patients and patients on VKAs using thrombin generation (TG). Methods: In this cross-sectional study, TG, initiated with 1pM tissue factor, was measured in 133 patients with severe (FVIII < 1%, n = 15) and non-severe (FVIII 1-50%, n = 118) hemophilia A, 97 patients on a VKA with an international normalized ratio (INR) >= 1.5 and healthy controls. Endogenous thrombin potential (ETP) (nM*min) was compared according to FVIII level (< 1%, 1-19% and 20-50%) with healthy controls and patients with sub-therapeutic INR (1.5-1.9) and therapeutic INR (>= 2.0). Medians and interquartile ranges (IQRs) were calculated. Results: Compared with healthy controls (898 [IQR 803-1004]), both hemophilia patients and patients on VKAs had lower median ETPs at 304 (196-449) and 176 (100-250), respectively. ETP was quite similar in severe hemophilia patients (185 [116-307]) and patients with a therapeutic INR (156 [90-225]). Compared with patients with therapeutic INR, ETP in patients with FVIII 1-19% and patients with FVIII 20-50% was higher at 296 (203430) and 397 (219-632), respectively. All patients with therapeutic INR had an ETP < 400. Considering this threshold, 93% of severe hemophilia patients, 70% of patients with FVIII 1-19% and 52% of patients with FVIII 20-50% had an ETP < 400. Conclusion: In severe hemophilia patients, TG was comparable to that in patients with a therapeutic INR. In one-third of non-severe hemophilia patients, TG was higher. These results suggest that anticoagulation therapy should be considered in a substantial proportion of non-severe hemophilia patients.
引用
收藏
页码:868 / 875
页数:8
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