Evaluation of a modified thrombelastography assay initiated with recombinant human tissue factor in clinically healthy horses
Article first published online: 22 JUN 2009
©2009 American Society for Veterinary Clinical Pathology
Veterinary Clinical Pathology
Volume 38, Issue 4, pages 462–466, December 2009
How to Cite
Leclere, M., Lavoie, J.-P., Dunn, M. and Bédard, C. (2009), Evaluation of a modified thrombelastography assay initiated with recombinant human tissue factor in clinically healthy horses. Veterinary Clinical Pathology, 38: 462–466. doi: 10.1111/j.1939-165X.2009.00157.x
- Issue published online: 1 DEC 2009
- Article first published online: 22 JUN 2009
- tissue factor
Background: Thrombelastography (TEG) is used to evaluate the viscoelastic properties of blood during clotting and provides a global assessment of hemostasis and clot lysis. TEG analysis initiated with recombinant human tissue factor (TF) has not been evaluated in clinically healthy horses.
Objectives: The purpose of this study was to determine whether TEG results are affected by the time elapsed between sampling and analysis (storage time) of equine blood samples and to establish a preliminary equine reference interval for a modified TEG assay, using recombinant human TF to initiate coagulation.
Methods: Citrated blood samples were obtained from 20 clinically healthy adult horses. Thirteen samples were stored for 30, 60, and 120 minutes at room temperature before TEG analysis. Coagulation was initiated by adding 20 μL of CaCl2 to 330 μL of blood and 10 μL of diluted recombinant TF for a final dilution of 1:3600. Reaction (R) and clotting (K) times, angle (α), and maximum amplitude (MA) were compared between time points. A preliminary reference interval (minimum–maximum values) was determined using data from all 20 horses after 30 minutes of sample storage.
Results: There was a significant effect of storage time on R, K, and α but not MA. Reference intervals were: R, 3.65–6.4 minutes; K, 1.8–5.45 minutes; α, 33.4–66.2°; MA, 41.2–64.1 mm; lysis at 30 minutes post-MA (LY30), <2.75%; and lysis at 60 minutes post-MA (LY60), 1.55–9.5%.
Conclusions: TEG can be performed on equine citrated blood samples using recombinant human TF to activate clot formation. TEG parameters were significantly affected by storage time, suggesting an incomplete inhibition of coagulation in citrated blood.