Background: Excessive anticoagulation due to warfarin use is associated with hemorrhage. Subcutaneously administered vitamin K has not been evaluated for the treatment of warfarin-associated coagulopathy, yet it is widely used. Objective: To show that oral vitamin K is more effective than subcutaneous vitamin K in the treatment of warfarin-associated coagulopathy. Design: Randomized, controlled trial. Setting: Two teaching hospitals. Patients: Patients with an international normalized ratio (INR) between 4.5 and 10.0. Intervention: Warfarin therapy was withheld, and 1 mg of vitamin K was given orally or subcutaneously. Measurements: The primary outcome measure was the INR on the day after administration of vitamin K. Secondary outcome measures were hemorrhage and thrombosis during a 1-month follow-up period. Results: 15 of 26 patients receiving oral vitamin K and 6 of 25 patients receiving subcutaneous vitamin K had therapeutic INRs on the day after study drug administration (P = 0.015; odds ratio, 4.32 [95% Cl, 1.13 to 17.44]). Conclusion: Oral vitamin K lowers INR more rapidly than subcutaneous vitamin K in asymptomatic patients who have supratherapeutic INR values while receiving warfarin.

Oral vitamin K lowers the international normalized ratio more rapidly than subcutaneous vitamin K in the treatment of warfarin-associated coagulopathy: A randomized, controlled trial

AGENO, WALTER
2002-01-01

Abstract

Background: Excessive anticoagulation due to warfarin use is associated with hemorrhage. Subcutaneously administered vitamin K has not been evaluated for the treatment of warfarin-associated coagulopathy, yet it is widely used. Objective: To show that oral vitamin K is more effective than subcutaneous vitamin K in the treatment of warfarin-associated coagulopathy. Design: Randomized, controlled trial. Setting: Two teaching hospitals. Patients: Patients with an international normalized ratio (INR) between 4.5 and 10.0. Intervention: Warfarin therapy was withheld, and 1 mg of vitamin K was given orally or subcutaneously. Measurements: The primary outcome measure was the INR on the day after administration of vitamin K. Secondary outcome measures were hemorrhage and thrombosis during a 1-month follow-up period. Results: 15 of 26 patients receiving oral vitamin K and 6 of 25 patients receiving subcutaneous vitamin K had therapeutic INRs on the day after study drug administration (P = 0.015; odds ratio, 4.32 [95% Cl, 1.13 to 17.44]). Conclusion: Oral vitamin K lowers INR more rapidly than subcutaneous vitamin K in asymptomatic patients who have supratherapeutic INR values while receiving warfarin.
2002
Crowther, Ma; Douketis, Jd; Schnurr, T; Steidl, L; Mera, V; Ultori, C; Venco, A; Ageno, Walter
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11383/1488020
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