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首页> 外文期刊>Journal of orthopaedic trauma >A Double-Blind, Randomized Controlled Trial of the Prevention of Clinically Important Venous Thromboembolism After Isolated Lower Leg Fractures
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A Double-Blind, Randomized Controlled Trial of the Prevention of Clinically Important Venous Thromboembolism After Isolated Lower Leg Fractures

机译:双盲,随机对照试验预防孤立的小腿骨折后临床上重要的静脉血栓栓塞

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Background:Among patients with isolated below-knee fractures, previous studies have detected asymptomatic deep vein thrombosis in 10%-40% using contrast venography. However, the clinical relevance of these thrombi is unknown; there is considerable uncertainty about the risk: benefit of routine thromboprophylaxis and clinical practice guidelines differ in their recommendations.Methods:In this multicenter, double-blind trial, 265 patients with isolated lower leg fractures requiring surgery were randomized to subcutaneous dalteparin 5000 units or matching placebo once daily for 2 weeks with bilateral Doppler ultrasound (DUS) of the proximal leg veins on postoperative day 142 and 3-month follow-up. The primary effectiveness outcome was clinically important venous thromboembolism (CIVTE), defined as the composite of symptomatic venous thromboembolism within 3 months after surgery and asymptomatic proximal deep vein thrombosis on DUS. The primary safety outcome was major bleeding.Results:Two hundred fifty-eight patients (97%) were included in the primary outcome analysis for effectiveness (130: dalteparin; 128: placebo). Incidence of CIVTE in the dalteparin and placebo groups was 1.5% and 2.3%, respectively (absolute risk reduction, 0.8%; 95% confidence interval, -2.0 to 3.0). There were no fatal pulmonary emboli or major bleeding.Conclusions:The overall incidence of CIVTE after surgically repaired, isolated tibia, fibula, and ankle fractures was low (1.9%; 95% confidence interval, 0.7-4.7), with no observed differences between dalteparin and placebo either for CIVTE or safety. Recruitment was stopped at the first interim analysis. This study also demonstrates the substantial discrepancy in venous thromboembolism rates between trials that use venographic outcomes compared with more clinically relevant outcomes.Level of Evidence:Therapeutic Level I. See Instructions for Authors for a complete description of levels of evidence.
机译:背景:在一些孤立的膝下骨折患者中,以前的研究已经使用造影剂静脉造影在无症状的深静脉血栓形成中发现了10%-40%。但是,这些血栓的临床相关性尚不清楚。方法:在这项多中心,双盲试验中,将265例需要手术的孤立小腿骨折患者随机分为皮下注射达肝素5000单位或相匹配的方法术后第142天和3个月的随访中,每天一次安慰剂,连续2周,接受双侧多普勒超声(DUS)对近端腿部静脉进行检查。主要有效性结果是临床上重要的静脉血栓栓塞症(CIVTE),定义为术后3个月内有症状的静脉血栓栓塞和无症状的DUS近端深静脉血栓形成的复合物。主要安全结果为大出血。结果:258例患者(97%)被纳入主要疗效分析(130:达肝素; 128:安慰剂)。达肝素和安慰剂组的CIVTE发生率分别为1.5%和2.3%(绝对危险度降低为0.8%; 95%的置信区间为-2.0至3.0)。没有致命的肺栓塞或大出血。结论:手术修复,孤立的胫骨,腓骨和踝部骨折后,CIVTE的总发生率较低(1.9%; 95%置信区间为0.7-4.7),两者之间无明显差异达肝素和安慰剂可提高CIVTE或安全性。在第一次中期分析中停止了招聘。这项研究还表明,使用静脉造影结果的试验与临床上相关结果相比,静脉血栓栓塞发生率存在显着差异。证据水平:治疗水平I。有关证据水平的完整说明,请参见《作者说明》。

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