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全膝关节置换术后短期与长期血栓预防:随机比较。

Short versus extended thromboprophylaxis after total knee arthroplasty: a randomized comparison.

机构信息

University Hospital, Caen, France.

出版信息

Thromb Res. 2010 Oct;126(4):e298-304. doi: 10.1016/j.thromres.2010.07.018. Epub 2010 Aug 24.

Abstract

INTRODUCTION

The optimal duration of thromboprophylaxis after total knee arthroplasty remains uncertain.

MATERIAL AND METHODS

We performed a randomized, open trial to determine whether to stop thromboprophylactic therapy at Day 10±2 ('short thromboprophylaxis') was non-inferior to continue thromboprophylactic therapy up to Day 35±5 ('extended thromboprophylaxis') after total knee arthroplasty. At Day 7±2, subjects were screened by ultrasonography for asymptomatic deep-vein thrombosis and randomized. The primary outcome was a composite of proximal deep-vein thrombosis, any symptomatic deep-vein thrombosis, non-fatal symptomatic pulmonary embolism, major bleeding, heparin-induced thrombocytopenia, or all-cause death up to Day 35±5. The secondary outcome was ultrasonographic (extension or new onset) distal deep-vein thrombosis at Day 35±5.

RESULTS

Twenty-one patients (2.4%) were not randomized, because of asymptomatic proximal deep-vein thrombosis on systematic ultrasonography at Day 7±2. Among the 857 randomized patients, mean (SD) duration of anticoagulant treatment was 11.2 (6.7) and 33.9 (3.7) days in the short and extended thromboprophylaxis groups, respectively. The respective rates of the primary outcome were 4.0% (17/420) and 2.4% (10/422), with an absolute difference of 1.7% (90% confidence interval, -0.3 to 3.7). In 285 patients with asymptomatic distal deep-vein thrombosis at Day 7±2, the respective rates of the primary outcome were 7.8% and 2.8% (p=0.067). The rates of the secondary outcome were 14.8% (62/420) and 4.5% (19/422), respectively (p<0.001).

CONCLUSIONS

Short thromboprophylaxis was not non-inferior to extended thromboprophylaxis after total knee arthroplasty. In this setting, the thromboembolic risk persisted longer than seven days, notably in patients with asymptomatic distal deep-vein thrombosis at discharge. ClinicalTrials.gov number: NCT00362492.

摘要

简介

全膝关节置换术后最佳的血栓预防持续时间仍不确定。

材料和方法

我们进行了一项随机、开放性试验,以确定在全膝关节置换术后第 10±2 天(“短时间血栓预防”)停止血栓预防治疗是否不劣于继续治疗至第 35±5 天(“长时间血栓预防”)。在第 7±2 天,通过超声筛查无症状深静脉血栓形成并进行随机分组。主要结局是包括近端深静脉血栓形成、任何有症状的深静脉血栓形成、非致命性有症状的肺栓塞、大出血、肝素诱导的血小板减少症或全因死亡在内的复合终点,随访至第 35±5 天。次要结局是第 35±5 天的超声(扩展或新发)远端深静脉血栓形成。

结果

由于在第 7±2 天系统超声检查发现无症状的近端深静脉血栓形成,21 名患者(2.4%)未被随机分组。在 857 名随机患者中,短时间和长时间血栓预防组的抗凝治疗平均(SD)持续时间分别为 11.2(6.7)和 33.9(3.7)天。主要结局的发生率分别为 4.0%(17/420)和 2.4%(10/422),绝对差异为 1.7%(90%置信区间,-0.3 至 3.7)。在第 7±2 天无症状的 285 名远端深静脉血栓形成患者中,主要结局的发生率分别为 7.8%和 2.8%(p=0.067)。次要结局的发生率分别为 14.8%(62/420)和 4.5%(19/422),差异有统计学意义(p<0.001)。

结论

在全膝关节置换术后,短时间血栓预防并不劣于长时间血栓预防。在这种情况下,血栓栓塞风险持续时间超过 7 天,尤其是在出院时无症状的远端深静脉血栓形成患者中。临床试验注册编号:NCT00362492。

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