首页> 外文期刊>The Lancet >The efficacy and safety of enoxaparin versus unfractionated heparin for the prevention of venous thromboembolism after acute ischaemic stroke (PREVAIL Study): an open-label randomised comparison.
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The efficacy and safety of enoxaparin versus unfractionated heparin for the prevention of venous thromboembolism after acute ischaemic stroke (PREVAIL Study): an open-label randomised comparison.

机译:依诺肝素与普通肝素预防急性缺血性卒中后静脉血栓栓塞的有效性和安全性(PREVAIL研究):开放标签的随机比较。

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BACKGROUND: Venous thromboembolism prophylaxis with low molecular weight heparin or unfractionated heparin is recommended in acute ischaemic stroke, but which regimen provides optimum treatment is uncertain. We aimed to compare the efficacy and safety of enoxaparin with that of unfractionated heparin for patients with stroke. METHODS: 1762 patients with acute ischaemic stroke who were unable to walk unassisted were randomly assigned within 48 h of symptoms to receive either enoxaparin 40 mg subcutaneously once daily or unfractionated heparin 5000 U subcutaneously every 12 h for 10 days (range 6-14). Patients were stratified by National Institutes of Health Stroke Scale (NIHSS) score (severe stroke > or =14, less severe stroke <14). The primary efficacy endpoint was the composite of symptomatic or asymptomatic deep vein thrombosis, symptomatic pulmonary embolism, or fatal pulmonary embolism. Primary safety endpoints were symptomatic intracranial haemorrhage, major extracranial haemorrhage, and all-causemortality. This study is registered with ClinicalTrials.gov, number NCT00077805. FINDINGS: In the efficacy population (ie, one or more dose received, presence of deep vein thrombosis or pulmonary embolism, or assessment for venous thromboembolism), enoxaparin (n=666) and unfractionated heparin (669) were given for 10.5 days (SD 3.2). Enoxaparin reduced the risk of venous thromboembolism by 43% compared with unfractionated heparin (68 [10%] vs 121 [18%]; relative risk 0.57, 95% CI 0.44-0.76, p=0.0001; difference -7.9%, -11.6 to -4.2); this reduction was consistent for patients with an NIHSS score of 14 or more (26 [16%] vs 52 [30%]; p=0.0036) or less than 14 (42 [8%] vs 69 [14%]; p=0.0044). The occurrence of any bleeding was similar with enoxaparin (69 [8%]) or unfractionated heparin (71 [8%]; p=0.83). The frequency of the composite of symptomatic intracranial and major extracranial haemorrhage was small and closely similar between groups (enoxaparin 11 [1%] vs unfractionated heparin 6 [1%]; p=0.23). We noted no difference for symptomatic intracranial haemorrhage between groups (4 [1%] vs 6 [1%], respectively; p=0.55); the rate of major extracranial bleeding was higher with enoxaparin than with unfractionated heparin (7 [1%] vs 0; p=0.015). INTERPRETATION: Our results suggest that for patients with acute ischaemic stroke, enoxaparin is preferable to unfractionated heparin for venous thromboembolism prophylaxis in view of its better clinical benefits to risk ratio and convenience of once daily administration.
机译:背景:在急性缺血性卒中中,建议用低分子量肝素或普通肝素预防静脉血栓栓塞,但尚不确定哪种方案可提供最佳治疗。我们旨在比较依诺肝素和普通肝素对中风患者的疗效和安全性。方法:将1762例无法自主行走的急性缺血性卒中患者随机分配,在症状的48小时内每天皮下注射依诺肝素40 mg一次,或每12 h皮下注射普通肝素5000 U连续10天(范围6-14)。通过国立卫生研究院卒中量表(NIHSS)评分对患者进行分层(重度中风>或= 14,轻度中风<14)。主要疗效终点是有症状或无症状的深静脉血栓形成,有症状的肺栓塞或致命的肺栓塞。主要安全终点为有症状的颅内出血,大颅外出血和全因死亡。该研究已在ClinicalTrials.gov上注册,编号为NCT00077805。结果:在疗效人群中(即接受一剂或多剂,存在深静脉血栓形成或肺栓塞或评估静脉血栓栓塞),给予依诺肝素(n = 666)和普通肝素(669)10.5天(SD) 3.2)。与普通肝素相比,依诺肝素将静脉血栓栓塞的风险降低了43%(68 [10%]对121 [18%];相对风险0.57,95%CI 0.44-0.76,p = 0.0001;相差-7.9%,-11.6至-4.2);对于NIHSS得分为14或更高(26 [16%] vs 52 [30%]; p = 0.0036)或小于14(42 [8%] vs 69 [14%]; p = 0.0044)。依诺肝素(69 [8%])或普通肝素(71 [8%]; p = 0.83)的出血情况相似。有症状的颅内出血和大颅外出血的复合发生频率很小,两组之间非常相似(依诺肝素11 [1%]与普通肝素6 [1%]; p = 0.23)。我们注意到两组之间有症状的颅内出血没有差异(分别为4 [1%]和6 [1%]; p = 0.55);依诺肝素的严重颅外出血发生率高于普通肝素(7 [1%] vs 0; p = 0.015)。解释:我们的结果表明,对于急性缺血性卒中患者,依诺肝素在预防静脉血栓栓塞方面优于普通肝素,因为它具有更高的临床风险比和每天一次给药的便利性。

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