Naslov
Extended Thromboprophylaxis with Betrixaban in Acutely Ill Medical Patients

Autori
Cohen, Alexander T. ; Harrington, Robert A. ; Goldhaber, Samuel Z. ; Hull, Russell D. ; Wiens, Brian L. ; Gold, Alex ; Hernandez, Adrian F. ; Gibson, C. Michael

Izvornik
New England Journal of Medicine (0028-4793) 375 (2016), 6; 534-544

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Betrixaban ; Thromboprophylaxis ; Acutely Ill Medical Patients

Sažetak
BACKGROUND:Patients with acute medical illnesses are at prolonged risk for venous thrombosis. However, the appropriate duration of thromboprophylaxis remains unknown. METHODS:Patients who were hospitalized for acute medical illnesses were randomly assigned to receive subcutaneous enoxaparin (at a dose of 40 mg once daily) for 10±4 days plus oral betrixaban placebo for 35 to 42 days or subcutaneous enoxaparin placebo for 10±4 days plus oral betrixaban (at a dose of 80 mg once daily) for 35 to 42 days. We performed sequential analyses in three prespecified, progressively inclusive cohorts: patients with an elevated d-dimer level (cohort 1), patients with an elevated d-dimer level or an age of at least 75 years (cohort 2), and all the enrolled patients (overall population cohort). The statistical analysis plan specified that if the between-group difference in any analysis in this sequence was not significant, the other analyses would be considered exploratory. The primary efficacy outcome was a composite of asymptomatic proximal deep-vein thrombosis and symptomatic venous thromboembolism. The principal safety outcome was major bleeding. RESULTS:A total of 7513 patients underwent randomization. In cohort 1, the primary efficacy outcome occurred in 6.9% of patients receiving betrixaban and 8.5% receiving enoxaparin (relative risk in the betrixaban group, 0.81 ; 95% confidence interval [CI], 0.65 to 1.00 ; P=0.054). The rates were 5.6% and 7.1%, respectively (relative risk, 0.80 ; 95% CI, 0.66 to 0.98 ; P=0.03) in cohort 2 and 5.3% and 7.0% (relative risk, 0.76 ; 95% CI, 0.63 to 0.92 ; P=0.006) in the overall population. (The last two analyses were considered to be exploratory owing to the result in cohort 1.) In the overall population, major bleeding occurred in 0.7% of the betrixaban group and 0.6% of the enoxaparin group (relative risk, 1.19 ; 95% CI, 0.67 to 2.12 ; P=0.55). CONCLUSIONS:Among acutely ill medical patients with an elevated d-dimer level, there was no significant difference between extended-duration betrixaban and a standard regimen of enoxaparin in the prespecified primary efficacy outcome. However, prespecified exploratory analyses provided evidence suggesting a benefit for betrixaban in the two larger cohorts.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti

POVEZANOST RADA