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达比加群酯和利伐沙班预防静脉血栓栓塞症——系统评价和调整后的间接比较。

Dabigatran and rivaroxaban for prevention of venous thromboembolism--systematic review and adjusted indirect comparison.

机构信息

School of Medicine, Health Policy and Practice, University of East Anglia, Norwich, UK.

出版信息

J Clin Pharm Ther. 2011 Feb;36(1):111-24. doi: 10.1111/j.1365-2710.2010.01162.x.

Abstract

WHAT IS KNOWN AND OBJECTIVE

Dabigatran and rivaroxaban are new oral anticoagulants for thromboprophylaxis after elective orthopaedic surgery. We aimed to systematically compare their relative benefits and harms through meta-analysis, and adjusted indirect comparison.

METHODS

We searched PubMed, EMBASE, trial registries and regulatory documents through May 2009 for randomized controlled trials (RCTs) of dabigatran (150 and 220 mg daily) and rivaroxaban (10 mg daily) compared with enoxaparin (40-60 mg daily) in elective orthopaedic surgery. We used random effects meta-analysis to calculate pooled relative risks (RRs) and 95% confidence intervals (95% CI) for the outcomes of total venous thromboembolism, VTE (deep venous thrombosis, non-fatal pulmonary embolism and all-cause mortality), and haemorrhagic adverse events (major and clinically relevant non-major bleeds). Adjusted indirect comparison was used for the pooled RRs of dabigatran and rivaroxaban with enoxaparin as the common control.

RESULTS

Rivaroxaban was superior to enoxaparin for the prevention of venous thromoboembolism (RR 0.56, 95% CI 0.43-0.73, P<0.0001), with a trend for increased haemorrhage (RR 1.26, 95% CI 0.94-1.69, P=0.13). Dabigatran was not superior to enoxaparin for prevention of VTE (RR 1.12, 95% 0.97-1.29, P=0.12), and did not reduce haemorrhage risk (RR 1.10, 95% 0.90-1.35, P=0.32). Adjusted indirect comparison showed that rivaroxaban was superior to dabigatran in preventing VTE, RR 0.50 (95% CI 0.37-0.68), but with a slight trend towards increased haemorrhage RR 1.14 (95% CI 0.80-1.64).

WHAT IS NEW AND CONCLUSION

Rivaroxaban may be more effective than dabigatran for prevention of VTE after elective orthopaedic surgery but might also slightly increase the risk of haemorrhage.

摘要

已知和目的

达比加群和利伐沙班是用于择期骨科手术后血栓预防的新型口服抗凝剂。我们旨在通过荟萃分析和调整间接比较来系统比较它们的相对益处和危害。

方法

我们检索了PubMed、EMBASE、试验注册处和监管文件,以查找达比加群(每日 150 毫克和 220 毫克)和利伐沙班(每日 10 毫克)与依诺肝素(每日 40-60 毫克)在择期骨科手术中的随机对照试验(RCT),直至 2009 年 5 月。我们使用随机效应荟萃分析计算了总静脉血栓栓塞、VTE(深静脉血栓形成、非致命性肺栓塞和全因死亡率)和出血不良事件(主要和临床相关非主要出血)的汇总相对风险(RR)和 95%置信区间(95%CI)。调整间接比较用于达比加群和利伐沙班与依诺肝素作为共同对照的汇总 RR。

结果

利伐沙班在预防静脉血栓栓塞方面优于依诺肝素(RR 0.56,95%CI 0.43-0.73,P<0.0001),且出血风险有增加趋势(RR 1.26,95%CI 0.94-1.69,P=0.13)。达比加群在预防 VTE 方面并不优于依诺肝素(RR 1.12,95%CI 0.97-1.29,P=0.12),且并未降低出血风险(RR 1.10,95%CI 0.90-1.35,P=0.32)。调整间接比较显示,利伐沙班在预防 VTE 方面优于达比加群,RR 0.50(95%CI 0.37-0.68),但出血风险略有增加,RR 1.14(95%CI 0.80-1.64)。

新发现和结论

利伐沙班在择期骨科手术后预防 VTE 方面可能比达比加群更有效,但也可能略微增加出血风险。

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