Granero J, Díaz de Rada P, Lozano L M, Martínez J, Herrera A
Departamento de Cirugía Ortopédica y Traumatología, Hospital Germans Trias i Pujol, Badalona, Barcelona, España.
Departamento de Cirugía Ortopédica y Traumatología, Clínica Universitaria de Navarra, Pamplona, España.
Rev Esp Cir Ortop Traumatol. 2016 Jan-Feb;60(1):44-52. doi: 10.1016/j.recot.2015.05.009. Epub 2015 Jul 17.
To analyse the effectiveness and safety of rivaroxaban vs. standard treatment (ST) in the prevention of venous thromboembolism after hip or knee replacement in daily clinical practice in Spain.
A sub-analysis of the Spanish data in the XAMOS international observational study that included patients>18 years who received 10mg o.d. rivaroxaban or ST.
FOLLOW-UP: up to 3 months after surgery.
incidence of symptomatic/asymptomatic thromboembolic events, bleeding, mortality, and other adverse events;
use of health resources and satisfaction after hospital discharge.
Of the total 801 patients included, 410 received rivaroxaban and 391 ST (64.7% heparin, 24.0% fondaparinux, 11% dabigatran). The incidence of symptomatic thromboembolic events and major bleeding was similar in both groups (0.2% vs. 0.8% wit ST and 0.7% vs. 1.3% with ST [EMA criteria]/0.0% vs. 0.3% with ST [RECORD criteria]). The adverse events incidence associated with the drug was significantly higher rivaroxaban (overall: 4.4% vs. 0.8% with ST, P=.001; serious: 1.5% vs. 0.0% with ST, P=.03). The rivaroxaban used less health resources after discharge, and the majority considered the tolerability as «very good« and the treatment as «very comfortable».
Rivaroxaban is at least as effective as ST in the prevention of venous thromboembolism prevention in daily clinical practice, with a similar incidence of haemorrhages. It provides greater satisfaction/comfort, and less health resources after discharge. These results should be interpreted taking into account the limitations inherent in observational studies.
分析在西班牙日常临床实践中,利伐沙班与标准治疗(ST)在预防髋或膝关节置换术后静脉血栓栓塞方面的有效性和安全性。
对XAMOS国际观察性研究中的西班牙数据进行亚分析,该研究纳入了年龄大于18岁、接受每日10mg利伐沙班或标准治疗的患者。
至术后3个月。
有症状/无症状血栓栓塞事件、出血、死亡率及其他不良事件的发生率;
出院后卫生资源的使用情况及满意度。
在纳入的801例患者中,410例接受利伐沙班治疗,391例接受标准治疗(64.7%使用肝素,24.0%使用磺达肝癸钠,11%使用达比加群)。两组有症状血栓栓塞事件和大出血的发生率相似(利伐沙班组为0.2%,标准治疗组为0.8%;根据欧洲药品管理局(EMA)标准,利伐沙班组为0.7%,标准治疗组为1.3%;根据RECORD标准,利伐沙班组为0.0%,标准治疗组为0.3%)。与药物相关不良事件的发生率利伐沙班显著更高(总体:4.4%对比标准治疗组的0.8%,P = 0.001;严重不良事件:1.5%对比标准治疗组的0.0%,P = 0.03)。利伐沙班出院后使用的卫生资源更少,且大多数患者认为耐受性“非常好”,治疗“非常舒适”。
在日常临床实践中,利伐沙班在预防静脉血栓栓塞方面至少与标准治疗同样有效,出血发生率相似。它能提供更高的满意度/舒适度,且出院后使用的卫生资源更少。应结合观察性研究固有的局限性来解读这些结果。