首页> 美国卫生研究院文献>TH Open: Companion Journal to Thrombosis and Haemostasis >Modified IMPROVE VTE Risk Score and Elevated D-Dimer Identify a High Venous Thromboembolism Risk in Acutely Ill Medical Population for Extended Thromboprophylaxis
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Modified IMPROVE VTE Risk Score and Elevated D-Dimer Identify a High Venous Thromboembolism Risk in Acutely Ill Medical Population for Extended Thromboprophylaxis

机译:改良的IMPROVE VTE风险评分和D-二聚体升高可确定在急性疾病医疗人群中长期静脉血栓栓塞的高静脉血栓栓塞风险

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摘要

An individualized approach to identify acutely ill medical patients at increased risk of venous thromboembolism (VTE) and a low risk of bleeding to optimize the benefit and risk of extended thromboprophylaxis (ET) is needed. The International Medical Prevention Registry on Venous Thromboembolism (IMPROVE) VTE risk score has undergone extensive external validation in medically ill patients for in-hospital use and a modified model was used in the MARINER trial of ET also incorporating an elevated D-dimer. The MAGELLAN study demonstrated efficacy with rivaroxaban but had excess bleeding. This retrospective analysis investigated whether the modified IMPROVE VTE model with an elevated D-dimer could identify a high VTE risk subgroup of patients for ET from a subpopulation of the MAGELLAN study, which was previously identified as having a lower risk of bleeding. We incorporated the modified IMPROVE VTE score using a cutoff score of 4 or more or 2 and 3 with an elevated D-dimer (>2 times the upper limit of normal) to the MAGELLAN subpopulation. In total, 56% of the patients met the high-risk criteria. In the placebo group, the total VTE event rate at Day 35 was 7.94% in the high-risk group and 2.83% for patients in the lower-risk group. A reduction in VTE was observed with rivaroxaban in the high-risk group (relative risk [RR]: 0.68, 95% confidence interval [CI]: 0.51–0.91,  = 0.008) and in the lower-risk group (RR: 0.69, 95% CI: 0.40 -1.20,  = 0.187). The modified IMPROVE VTE score with an elevated D-dimer identified a nearly threefold higher VTE risk subpopulation of patients where a significant benefit exists for ET using rivaroxaban.
机译:需要一种个体化的方法来识别急性静脉内血栓栓塞症(VTE)风险增加且出血风险低的急性病患者,以优化获益和延长血栓预防(ET)的风险。国际医学预防静脉血栓栓塞登记处(IMPROVE)VTE风险评分已在住院病人中接受了广泛的外部验证,用于医院内,并且在ET的MARINER试验中使用了改良的模型,该模型还纳入了升高的D-二聚体。 MAGELLAN研究证明利伐沙班具有疗效,但出血过多。这项回顾性分析调查了改良的IMP-VE VTE模型(D-二聚体水平升高)是否可以从MAGELLAN研究的一个亚人群中识别出ET患者的高VTE危险亚组,该亚人群先前已被确定具有较低的出血风险。我们纳入了改良的IMPROVE VTE评分,使用4或更高的截止评分或2和3,D-二聚体水平升高(>正常上限的2倍)至MAGELLAN亚群。总共有56%的患者符合高危标准。在安慰剂组中,高危组在第35天的总VTE事件发生率为7.94%,低危组为2.83%。在高风险组中,利伐沙班观察到VTE降低(相对风险[RR]:0.68,95%置信区间[CI]:0.51-0.91, = 0.008)和较低风险组(RR:0.69,95%CI:0.40 -1.20, = 0.187)。改良的IMPROVE VTE评分与D-二聚体水平升高,确定了使用利伐沙班治疗ET有显着益处的患者,其VTE风险亚群高出近三倍。

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