Extended duration rivaroxaban versus short-term enoxaparin for the prevention of venous thromboembolism after total hip arthroplasty: a double-blind, randomised controlled trial

被引:835
作者
Kakkar, Ajay K. [1 ,2 ]
Brenner, Benjamin [3 ]
Dahl, Ola E. [2 ]
Eriksson, Bengt I. [4 ]
Mouret, Patrick [5 ]
Muntz, Jim [6 ,7 ]
Soglian, Andrea G. [8 ]
Pap, Akos F. [9 ]
Misselwitz, Frank [9 ]
Haas, Sylvia [10 ]
机构
[1] Barts & London Queen Marys Sch Med & Dent, London E1 2AD, England
[2] Thrombosis Res Inst, London SW3 6LR, England
[3] Rambam Med Ctr, Haifa, Israel
[4] Sahlgrens Univ Hosp, Gothenburg, Sweden
[5] Frankfurt Hochst Clin, Frankfurt, Germany
[6] Methodist Hosp, Houston, TX 77030 USA
[7] St Lukes Episcopal Hosp, Houston, TX 77030 USA
[8] Bayer HealthCare, Milan, Italy
[9] Bayer HealthCare, Wuppertal, Germany
[10] Tech Univ Munich, Inst Expt Oncol & Therapy Res, Munich, Germany
关键词
D O I
10.1016/S0140-6736(08)60880-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The risk of venous thromboembolism is high after total hip arthroplasty and could persist after hospital discharge. Our aim was to compare the use of rivaroxaban for extended thromboprophylaxis with short-term thromboprophylaxis with enoxaparin. Methods 2509 patients scheduled to undergo elective total hip arthroplasty were randomly assigned, stratified according to Centre, with a computer-generated randomisation code, to receive,oral rivaroxaban 10 mg once daily for 31-39 days (with placebo injection for 10-14 days; n=1252), or enoxaparin 40 mg once daily subcutaneously for 10-14 days (with placebo tablet for 31-39 days; n=1257). The primary efficacy outcome was the composite of deep-vein thrombosis (symptomatic or asymptornatic detected by mandatory, bilateral venography), non-fatal pulmonary embolism, and all-cause mortality up to day 30-42. Analyses were done in the modified intention-to-treat population, which consisted of all patients who had received at least one dose of study medication, had undergone planned surgery, and had adequate assessment of thromboembolism. This study is registered at ClinicalTrials.gov, number NCT00332020. Findings The modified intention-to-treat population for the analysis of the primary efficacy outcome consisted of 864 patients in the rivaroxaban group and 869 in the enoxaparin group. The primary outcome occurred in 17 (2 . 0%) patients in the rivaroxaban group, compared with 81 (9.3%) in the enoxaparin group (absolute risk reduction 7.3%, 95% CI 5.2-9.4; p<0 . 0001). The incidence of any on-treatment bleeding was much the same in both groups (81 [6.6%] events in 1228 patients in the rivaroxaban safety population vs 68 [5. 5%] of 1229 patients in the enoxaparin safety population; p=0 . 25). Interpretation Extended thromboprophylaxis with rivaroxaban was significantly more effective than short-term enoxaparin plus placebo for the prevention of venous thromboembolism, including symptomatic events, in patients undergoing total hip arthroplasty. Funding Bayer HealthCare AG, Johnson & Johnson Pharmaceutical Research and Development LLC.
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页码:31 / 39
页数:9
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