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希美加群与华法林预防全膝关节置换术后静脉血栓栓塞的比较。

Comparison of ximelagatran with warfarin for the prevention of venous thromboembolism after total knee replacement.

作者信息

Francis Charles W, Berkowitz Scott D, Comp Philip C, Lieberman Jay R, Ginsberg Jeffrey S, Paiement Guy, Peters Gary R, Roth Anne W, McElhattan Jennifer, Colwell Clifford W

机构信息

Department of Medicine, University of Rochester, Rochester, NY, USA.

出版信息

N Engl J Med. 2003 Oct 30;349(18):1703-12. doi: 10.1056/NEJMoa035162.

Abstract

BACKGROUND

In a previous study of the prevention of venous thromboembolism after total knee replacement, the efficacy of ximelagatran, an oral direct thrombin inhibitor that does not require monitoring of coagulation or dose adjustment, was found to be similar to that of warfarin at a dose of 24 mg of ximelagatran twice daily. The purpose of the present study was to determine whether a higher dose of ximelagatran is superior to warfarin.

METHODS

This randomized, double-blind trial compared a regimen of 7 to 12 days of oral ximelagatran, at a dose of 24 or 36 mg twice daily, starting the morning after surgery, with warfarin therapy started the evening of the day of surgery. The composite end point of venous thromboembolism and death from all causes and the incidence of bleeding were the primary outcome measures.

RESULTS

Among the 1851 patients in the efficacy analysis, oral ximelagatran at a dose of 36 mg twice daily was superior to warfarin with respect to the primary composite end point of venous thromboembolism and death from all causes (20.3 percent vs. 27.6 percent; P=0.003). There were no significant differences between these two groups with respect to major bleeding (incidence, 0.8 percent and 0.7 percent, respectively), perioperative indicators of bleeding, wound characteristics, or the composite secondary end point of proximal deep-vein thrombosis, pulmonary embolism, and death (2.7 percent vs. 4.1 percent; P=0.17).

CONCLUSIONS

The efficacy of oral ximelagatran, administered starting the morning after total knee replacement, was superior to that of warfarin for prevention of venous thromboembolism. Rates of hemorrhagic complications with the two drugs were similar.

摘要

背景

在先前一项关于全膝关节置换术后预防静脉血栓栓塞的研究中,发现希美加群(一种无需监测凝血或调整剂量的口服直接凝血酶抑制剂)在每日两次服用24毫克希美加群时的疗效与华法林相似。本研究的目的是确定更高剂量的希美加群是否优于华法林。

方法

这项随机、双盲试验比较了术后次日早晨开始口服希美加群(每日两次,剂量为24毫克或36毫克,疗程7至12天)与手术当天晚上开始的华法林治疗。静脉血栓栓塞和全因死亡的复合终点以及出血发生率是主要结局指标。

结果

在疗效分析的1851例患者中,每日两次服用36毫克剂量的口服希美加群在静脉血栓栓塞和全因死亡的主要复合终点方面优于华法林(分别为20.3%对27.6%;P = 0.003)。两组在大出血(发生率分别为0.8%和0.7%)、围手术期出血指标、伤口特征或近端深静脉血栓形成、肺栓塞和死亡的复合次要终点方面无显著差异(分别为2.7%对4.1%;P = 0.17)。

结论

全膝关节置换术后次日早晨开始服用的口服希美加群在预防静脉血栓栓塞方面的疗效优于华法林。两种药物的出血并发症发生率相似。

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