TY - JOUR
T1 - The direct thrombin inhibitors
T2 - Their role and use for rational anticoagulation
AU - Frenkel, Eugene P.
AU - Shen, Yu Min
AU - Haley, Barbara B.
N1 - Funding Information:
This research was funded in part by the Nasher Cancer Research Fund.
PY - 2005
Y1 - 2005
N2 - It is clear that major clinical advantages are achieved when direct thrombin inhibitors are used in venous thromboembolism. These advantages include the inhibition of fibrin-bound thrombin and the inhibition of activation of platelet factor 4. These agents provide more reliable anticoagulant response patterns because they are not significantly bound to plasma proteins and few, if any, drug-drug interactions are seen. The studies to date confirm that not all direct thrombin inhibitors are the same. The new reversible, short-acting catalytic site-specific drugs provide an excellent safety profile and high degree of efficacy for the prophylaxis and treatment of venous thromboembolism and pulmonary embolic states. The availability of the oral prodrug ximelagatran allows reproducible, effective, and safe direct thrombin inhibition without the requirement for coagulation laboratory monitoring; it appears destined to be the oral anticoagulant of the future.
AB - It is clear that major clinical advantages are achieved when direct thrombin inhibitors are used in venous thromboembolism. These advantages include the inhibition of fibrin-bound thrombin and the inhibition of activation of platelet factor 4. These agents provide more reliable anticoagulant response patterns because they are not significantly bound to plasma proteins and few, if any, drug-drug interactions are seen. The studies to date confirm that not all direct thrombin inhibitors are the same. The new reversible, short-acting catalytic site-specific drugs provide an excellent safety profile and high degree of efficacy for the prophylaxis and treatment of venous thromboembolism and pulmonary embolic states. The availability of the oral prodrug ximelagatran allows reproducible, effective, and safe direct thrombin inhibition without the requirement for coagulation laboratory monitoring; it appears destined to be the oral anticoagulant of the future.
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U2 - 10.1016/j.hoc.2004.09.002
DO - 10.1016/j.hoc.2004.09.002
M3 - Review article
C2 - 15639111
AN - SCOPUS:15544379843
SN - 0889-8588
VL - 19
SP - 119
EP - 145
JO - Hematology/Oncology Clinics of North America
JF - Hematology/Oncology Clinics of North America
IS - 1
ER -