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Iliofemoral lysis for DVT remains ATTRACTive

机译:DVT的em股溶解仍然具有吸引力

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摘要

Following the publication of a landmark paper on comparative effectiveness of anticoagulation against thrombolysis, the authors of the Acute Venous Thrombosis: Thrombus Removal with Adjunctive Catheter-Directed Thrombolysis (ATTRACT) trial released a subanalysis targeting the iliofemoral vein thrombosis, which excluded the femoropopliteal deep vein thrombosis (DVT) population. Similar to the primary publication, the ATTRACT-iliofemoral results again challenge the utility of pharmacomechanical thrombolysis (PMT) and catheter-directed thrombolysis (CDT) in preventing post-thrombotic syndrome (PTS) ( , ). Their analysis reported no difference in the development of PTS (defined as Villalta score ≥5) between patients with proximal DVT treated with PMT/CDT and anticoagulation alone [relative risk (RR), 0.95; 95% confidence interval (CI), 0.78–1.15; P=0.59] at 24 months after treatment. This result contradicts that of their Norwegian contemporaries of the 2012 Catheter-directed Venous Thrombolysis (CaVenT) trial—a smaller randomized control trial which reported a lower rate of PTS in patients treated with CDT over anticoagulation alone ( ).
机译:在发表有关抗凝抗溶栓的相对有效性的里程碑式论文发表之后,“急性静脉血栓形成:辅助导管导向溶栓的血栓清除术”(ATTRACT)试验的作者发布了针对股静脉血栓形成的亚分析,其中排除了股pop深静脉血栓形成(DVT)人群。与主要出版物相似,ATTRACT ili股的结果再次挑战了药物机械溶栓(PMT)和导管定向溶栓(CDT)在预防血栓形成后综合征(PTS)中的实用性()。他们的分析报告说,接受PMT / CDT治疗的近端DVT患者和单独抗凝治疗的患者,PTS的发展(定义为Villalta评分≥5)没有差异[相对危险度(RR)为0.95;而相对危险度为0.95。 95%置信区间(CI)为0.78-1.15; P = 0.59]在治疗后24个月。该结果与他们在挪威同时代的2012年导管导向静脉溶栓试验(CaVenT)的研究相矛盾,该试验是一项较小的随机对照试验,该研究报道CDT治疗的患者中PTS的发生率比单纯抗凝治疗的要低()。

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