HealthDay News – Among older patients undergoing hip or knee replacement, low-intensity compared with standard-intensity warfarin prophylaxis did not meet the noninferiority criterion for the composite outcome of risk for venous thromboembolism or death, according to a study recently published in the Journal of the American Medical Association.
Within 6 different medical centers throughout the United States, Brian F. Gage, MD, of Washington University in St. Louis, and colleagues initiated warfarin therapy in 1650 patients ages 65 years and older who were undergoing elective knee or hip replacement. Using a two-by-two factorial design, study participants were randomly assigned to a target international normalized ratio (INR) of either 1.8 (low-intensity warfarin group, 823 patients) or 2.5 (standard-intensity warfarin group, 827 patients) and to either genotype-guided or clinically guided dosing.
Among the patients, 1597 (98.6%) received at least one dose of warfarin. The researchers found that the rate of the primary composite outcome of deep vein thrombosis or death was 5.1% (41 of 804) in the low-intensity warfarin group (INR target, 1.8) versus 3.8% (30 of 793) in the standard-treatment warfarin group (INR target, 2.5), for a difference of 1.3% (one-sided 95% confidence interval [CI], −∞ to 3.05%; P =.06 for noninferiority). Major bleeding occurred in 0.4% of patients in the low-intensity group and 0.9% of patients in the standard-intensity group (difference of −0.5%; 95% CI, −1.6 to 0.4%). INR values of four or more occurred in 4.5% of patients in the low-intensity group and 12.2% in the standard-intensity group (difference of −7.8%; 95% CI, −10.5 to −5.1%).
“Future research could help address which patients at high risk of bleeding might benefit from low-intensity warfarin,” the authors write.
Several authors disclosed financial ties to orthopedic equipment and pharmaceutical companies, including Stryker and Bristol-Myers Squibb.