Thromb Haemost 2005; 93(03): 475-480
DOI: 10.1160/TH04-10-0706
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Evaluation of thrombin generating capacity in plasma from patients with haemophilia A and B

Yesim Dargaud
1   Laboratoire d’Hémostase Hopital Edouard Herriot, Lyon, France
,
Suzette Béguin
2   Synapse Bv, Cardiovascular Research Institute Maastricht, University of Maastricht, The Netherlands
,
Anne Lienhart
1   Laboratoire d’Hémostase Hopital Edouard Herriot, Lyon, France
,
Raed Al Dieri
2   Synapse Bv, Cardiovascular Research Institute Maastricht, University of Maastricht, The Netherlands
,
Christine Trzeciak
1   Laboratoire d’Hémostase Hopital Edouard Herriot, Lyon, France
,
Jean Claude Bordet
1   Laboratoire d’Hémostase Hopital Edouard Herriot, Lyon, France
,
Coenraad H. Hemker
2   Synapse Bv, Cardiovascular Research Institute Maastricht, University of Maastricht, The Netherlands
,
Claude Negrier
1   Laboratoire d’Hémostase Hopital Edouard Herriot, Lyon, France
› Author Affiliations
Further Information

Publication History

Received 31 October 2004

Accepted after resubmission 29 February 2004

Publication Date:
14 December 2017 (online)

Summary

In haemophilia patients, a relationship is usually observed between the clinical expression of the disease and plasmatic factor VIII/factor IX (FVIII/FIX) activity. However, it is known from clinical experience, that some haemophilia patients, despite similar FVIII/FIX plasma levels, could exhibit different bleeding phenotype. After determining preanalytical test conditions, we evaluated the thrombin generation capacity from haemophilia plasma samples in various conditions and the potential usefulness of thrombin generation test (TGT) in haemophilia patients. In a series of 46 haemophilia patients (34 haemophilia A and 12 haemophilia B patients), we found a significant correlation between plasmatic FVIII/FIX levels and endogenous thrombin potential (ETP), peak and time to peak obtained by thrombin generation measurement. In addition, a correlation was found between severe clinical bleeding phenotype and ETP. Our results suggest that TGT could be a promising tool to evaluate haemostasis capacity in patients with haemophilia. Our ex vivo results, obtained 24 hours after FVIII concentrate administration, showed that in patients presenting similar plasmatic FVIIII levels, thrombin generation capacity may be significantly different. These results suggest that in patients with haemophilia, TGT could be useful for individually tailoring prophylactic regimens as well as for adapting clotting factors infusions in surgical situations, in addition to FVIII/FIX plasma clotting activities.

 
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