Division of Pharmacology and Clinical Evaluation, Medicines for Human Use, Spanish Agency for Medicines and Medical Devices, Parque Empresarial Las Mercedes, Madrid, Spain.
BMJ. 2012 Jun 14;344:e3675. doi: 10.1136/bmj.e3675.
To analyse clinical outcomes with new oral anticoagulants for prophylaxis against venous thromboembolism after total hip or knee replacement.
Systematic review, meta-analysis, and indirect treatment comparisons.
Medline and CENTRAL (up to April 2011), clinical trials registers, conference proceedings, and websites of regulatory agencies.
Randomised controlled trials of rivaroxaban, dabigatran, or apixaban compared with enoxaparin for prophylaxis against venous thromboembolism after total hip or knee replacement. Two investigators independently extracted data. Relative risks of symptomatic venous thromboembolism, clinically relevant bleeding, deaths, and a net clinical endpoint (composite of symptomatic venous thromboembolism, major bleeding, and death) were estimated using a random effect meta-analysis. RevMan and ITC software were used for direct and indirect comparisons, respectively.
16 trials in 38,747 patients were included. Compared with enoxaparin, the risk of symptomatic venous thromboembolism was lower with rivaroxaban (relative risk 0.48, 95% confidence interval 0.31 to 0.75) and similar with dabigatran (0.71, 0.23 to 2.12) and apixaban (0.82, 0.41 to 1.64). Compared with enoxaparin, the relative risk of clinically relevant bleeding was higher with rivaroxaban (1.25, 1.05 to 1.49), similar with dabigatran (1.12, 0.94 to 1.35), and lower with apixaban (0.82, 0.69 to 0.98). The treatments did not differ on the net clinical endpoint in direct or indirect comparisons.
A higher efficacy of new anticoagulants was generally associated with a higher bleeding tendency. The new anticoagulants did not differ significantly for efficacy and safety.
分析新型口服抗凝药物用于预防全髋关节或膝关节置换术后静脉血栓栓塞症的临床结局。
系统评价、荟萃分析和间接治疗比较。
Medline 和CENTRAL(截至 2011 年 4 月)、临床试验注册处、会议记录以及监管机构的网站。
比较利伐沙班、达比加群或阿哌沙班与依诺肝素预防全髋关节或膝关节置换术后静脉血栓栓塞症的随机对照试验。两位研究者独立提取数据。使用随机效应荟萃分析估计症状性静脉血栓栓塞症、临床相关出血、死亡和净临床终点(症状性静脉血栓栓塞症、大出血和死亡的复合终点)的相对风险。RevMan 和 ITC 软件分别用于直接和间接比较。
纳入 38747 例患者的 16 项试验。与依诺肝素相比,利伐沙班降低症状性静脉血栓栓塞症风险(相对风险 0.48,95%置信区间 0.31 至 0.75),与达比加群相似(0.71,0.23 至 2.12),与阿哌沙班相似(0.82,0.41 至 1.64)。与依诺肝素相比,利伐沙班发生临床相关出血的风险较高(相对风险 1.25,1.05 至 1.49),与达比加群相似(1.12,0.94 至 1.35),而阿哌沙班较低(0.82,0.69 至 0.98)。直接或间接比较均未显示在净临床终点方面治疗有显著差异。
新型抗凝药物的更高疗效通常与更高的出血倾向相关。新型抗凝药物在疗效和安全性方面没有显著差异。