FACTOR VIIa USED TO STOP BLEEDINGS IN DIFFERENT CONDITIONS ASSOCIATED WITH DIC

July 1, 2001

E. Moisescu *, L Ardelean *, V. Bumbea *, L. Simian **, A. Muresan *, H. Bumbea ***
* Department of Intensive Care, Emergency Hospital, Bucharest
** N. Gh. Lupu Hospital, Bucharest
*** Department of Hematology, Colțea Hospital, Bucharest

Abstract

Recombinant Factor Vlla (NovoSeven®) occurred as a treatment option for patients with hemophilia who developed inhibitors against clot1ing factors Vlll and/or IX. It ensures effective haemostasis at the site of injury, independent of the presence of FVlll and/or FIX, by forming complexes with exposed tissue factor (I’F). Tissue Factor is a membrane­ bound glycoprotein expressed on cells in the sub­ endothelium. It has a high affinity for FVlla with whom it forms complexes with important proteolytic activity. The TF: FVIIa complex activates FX to FXa leading of the generation of small amounts of thrombin (Ila)· This limited amount of thrombin subsequently activates the co­ factors factor V (FV) and FVIII, as well as platelets accumulated at the site of injury. The activated platel_ets expose Phosphatidyl serine on their membrane and proVIde the template for further thrombin generation.


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EFFECT OF RECOMBINANT FACTOR VIIA ASSESSED BY THROMBOCYTE IMMUNO-PHENOTYPING ON THE EXPRESSION OF PLATELET’S FIBRINOGEN RECEPTORS IN BLEEDING DISORDERS – preliminary results

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