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Appraisal of current vitamin K dosing algorithms for the reversal of over‐anticoagulation with warfarin: the need for a more tailored dosing regimen
Author(s) -
Sconce Elizabeth A.,
Kamali Farhad
Publication year - 2006
Publication title -
european journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.904
H-Index - 84
eISSN - 1600-0609
pISSN - 0902-4441
DOI - 10.1111/j.0902-4441.2006.t01-1-ejh2957.x
Subject(s) - dosing , warfarin , medicine , vitamin k antagonist , regimen , vkorc1 , asymptomatic , anticoagulant , cyp2c9 , intensive care medicine , algorithm , atrial fibrillation , cytochrome p450 , metabolism , computer science
Warfarin is the most commonly prescribed oral anticoagulant in the UK for the treatment and prevention of thromboembolic disorders. Vitamin K administration is an effective way of reversing excessive anticoagulation. Over‐anticoagulated patients present with a wide range of international normalized ratio (INR) values and may respond differently to a fixed dose of vitamin K. Current dosing algorithms for vitamin K administration in the non‐urgent treatment of over‐anticoagulation do not take this variability in response into account. Consequently, over a third of over‐anticoagulated patients still remain outside their target INR 24 h after treatment. Such patients are therefore prone to either haemorrhage (if the patient is still over‐anticoagulated) or thromboembolism (if the INR reversal is over‐corrected). A number of factors such as patient age, body weight, co‐morbidity, frailty, warfarin daily dose and CYP2C9 and VKORC1 polymorphism could affect response to vitamin K and thus the rate and extent of INR reversal. There is a need for a more individualized approach to the reversal of over‐anticoagulation in asymptomatic or mildly haemorrhagic patients in order to improve the safety of warfarin therapy.
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