TY - JOUR
T1 - Comparison of 10-mg and 5-mg Warfarin Initiation Nomograms Together with Low-Molecular-Weight Heparin for Outpatient Treatment of Acute Venous Thromboembolism
T2 - A Randomized, Double-Blind, Controlled Trial
AU - Kovacs, Michael J.
AU - Rodger, Marc
AU - Anderson, David R.
AU - Morrow, Beverly
AU - Kells, Gertrude
AU - Kovacs, Judy
AU - Boyle, Eleanor
AU - Wells, Philip S.
PY - 2003/5/6
Y1 - 2003/5/6
N2 - Background: The optimal means of achieving therapeutic oral anticoagulation in the outpatient setting has not been determined. Objective: To compare a 10-mg dosing nomogram with a 5-mg nomogram that has been suggested to be sufficient for warfarin initiation. Design: Randomized, controlled clinical trial. Setting: Outpatient venous thromboembolism services of four tertiary care hospitals. Patients: 201 of 210 consecutive patients with objectively confirmed diagnoses of acute venous thromboembolism. Intervention: All patients were treated with subcutaneous low-molecular-weight heparin for a minimum of 5 days until a therapeutic international normalized ratio (INR) was achieved. Patients were randomly assigned to initially receive a 10-mg or 5-mg dose of warfarin. Measurements: The primary end point was time in days to therapeutic INR. Secondary end points were the proportion of patients who had achieved a therapeutic INR by day 5, the total number of INR assessments, the number of INR measurements greater than 5.0, incidence of recurrent venous thromboembolism and major bleeding, and survival. Results: 210 consecutive patients met the inclusion criteria. Of these, 9 were excluded and 201 were randomly assigned to study groups (104 to the 10-mg group and 97 to the 5-mg group). Demographic characteristics of both groups were similar. Patients in the 10-mg group achieved therapeutic INR 1.4 days earlier than patients in the 5-mg group (P < 0.001). Eighty-three percent of patients in the 10-mg group achieved a therapeutic INR by day 5 versus 46% in the 5-mg group (P < 0.001). Fewer INR assessments were performed in the 10-mg group than in the 5-mg group (8.1 vs. 9.1; P = 0.04). There were no significant differences between the two groups in recurrent events, major bleeding, survival, and number of INR measurements greater than 5.0. Conclusion: The 10-mg warfarin initiation nomogram is superior to the 5-mg nomogram because it allows more rapid achievement of a therapeutic INR.
AB - Background: The optimal means of achieving therapeutic oral anticoagulation in the outpatient setting has not been determined. Objective: To compare a 10-mg dosing nomogram with a 5-mg nomogram that has been suggested to be sufficient for warfarin initiation. Design: Randomized, controlled clinical trial. Setting: Outpatient venous thromboembolism services of four tertiary care hospitals. Patients: 201 of 210 consecutive patients with objectively confirmed diagnoses of acute venous thromboembolism. Intervention: All patients were treated with subcutaneous low-molecular-weight heparin for a minimum of 5 days until a therapeutic international normalized ratio (INR) was achieved. Patients were randomly assigned to initially receive a 10-mg or 5-mg dose of warfarin. Measurements: The primary end point was time in days to therapeutic INR. Secondary end points were the proportion of patients who had achieved a therapeutic INR by day 5, the total number of INR assessments, the number of INR measurements greater than 5.0, incidence of recurrent venous thromboembolism and major bleeding, and survival. Results: 210 consecutive patients met the inclusion criteria. Of these, 9 were excluded and 201 were randomly assigned to study groups (104 to the 10-mg group and 97 to the 5-mg group). Demographic characteristics of both groups were similar. Patients in the 10-mg group achieved therapeutic INR 1.4 days earlier than patients in the 5-mg group (P < 0.001). Eighty-three percent of patients in the 10-mg group achieved a therapeutic INR by day 5 versus 46% in the 5-mg group (P < 0.001). Fewer INR assessments were performed in the 10-mg group than in the 5-mg group (8.1 vs. 9.1; P = 0.04). There were no significant differences between the two groups in recurrent events, major bleeding, survival, and number of INR measurements greater than 5.0. Conclusion: The 10-mg warfarin initiation nomogram is superior to the 5-mg nomogram because it allows more rapid achievement of a therapeutic INR.
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U2 - 10.7326/0003-4819-138-9-200305060-00007
DO - 10.7326/0003-4819-138-9-200305060-00007
M3 - Article
C2 - 12729425
AN - SCOPUS:0038750759
SN - 0003-4819
VL - 138
SP - 714-719+I50
JO - Annals of Internal Medicine
JF - Annals of Internal Medicine
IS - 9
ER -