Thrombophilia: disorders predisposing to venous thromboembolism

Citation
Gf. Pineo et Rd. Hull, Thrombophilia: disorders predisposing to venous thromboembolism, BAIL CLIN H, 11(3), 1998, pp. 525-540
Citations number
95
Categorie Soggetti
Hematology
Journal title
BAILLIERES CLINICAL HAEMATOLOGY
ISSN journal
09503536 → ACNP
Volume
11
Issue
3
Year of publication
1998
Pages
525 - 540
Database
ISI
SICI code
0950-3536(199809)11:3<525:TDPTVT>2.0.ZU;2-2
Abstract
Venous thromboembolism continues to present a challenge to clinicians. Over the years, a number of risk factors which predispose to venous thromboembo liism have been identified, and these risk factors are taken into account i n the formulation of recommendations for the prevention and treatment of th ese disorders. In more recent years; there have, been major advances in our understanding of congenital or acquired defects that predispose to thrombo sis leading to these so-called acquired or inherited forms of thrombophilia . The list of acquired forms of thrombophilia now includes anti-thrombin, p rotein C, protein S, activated protein C resistance, the prothrombin 20210A mutant, homocysteinemia and a number of rare defects which either enhance coagulation or interfere with fibrinolysis. In spite of these advances, the re are numerous families with thrombophilia in whom none of the known defec ts can be demonstrated. The challenge for the future is to discover some of these as yet unknown factors and to determine the most appropriate methods for the prevention and treatment of venous thromboembolism in susceptible individuals with thrombophilia.