首页> 外文期刊>Journal of endovascular therapy: an official journal of the International Society of Endovascular Specialists >Bioabsorbable stent implantation vs. common femoral artery endarterectomy: Early results of a randomized trial
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Bioabsorbable stent implantation vs. common femoral artery endarterectomy: Early results of a randomized trial

机译:生物可吸收支架植入与股总动脉内膜切除术:一项随机试验的早期结果

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Purpose: To compare clinical and hemodynamic outcome in patients undergoing treatment of common femoral artery (CFA) atherosclerotic lesions by bioabsorbable stent implantation (BASI group) or by common femoral artery endarterectomy (CFE group). Methods: A randomized, controlled, single-center, open-label trial was initiated to compare outcomes of BASI or CFE in patients with chronic atherosclerotic occlusive lesions in the CFA. From May 2011 to April 2013, 116 consecutive patients were recruited; after excluding 36 patients, 80 patients (52 men; mean age 72.2±9.6 years) were enrolled 1:1 and are the subject of this intention-to-treat interim analysis (40 patients in each group). The primary endpoint was surgical site infections; secondary outcome measures were technical success, hemodynamic improvement, clinical improvement, patency, limb salvage, and survival. Results: There was no statistically significant difference between both groups regarding demographic data, cardiovascular risk factors, or CFA occlusions. The CFE patients presented with 7 surgical site infections (all minor) vs. none in the BASI group (p=0.002) and a longer mean postoperative hospital stay of 7 vs. 2 days for BASI patients (p<0.001). Technical success rates were 97.5% and 100% for the BASI and CFE groups, respectively. Postoperative ankle-brachial index means were comparable (p=0.38). The 30-day primary patency rates were 92.5% and 100% for the BASI and CFE groups, respectively (p=0.038). There were 6 reconstruction failures in CFE patients vs. none in the BASI group (p=0.02); 5 failures involved initial CFA occlusions. At 1 year, the primary and secondary patency rates were 80% vs. 100% (p=0.007) and 84% vs. 100% (p=0.01) for BASI and CFE patients, respectively. Limb salvage was equivalent, and survival rates were 88% and 90% for BASI vs. CFE patients (p=0.51) at 1 year. Conclusion: This interim analysis suggests that BASI is not an option for CFA occlusion and is only a limited option for CFA stenosis. Clinical and hemodynamic results are comparable for BASI and CFE. An increased rate of redo procedures in the BASI patients outweighs lower surgical site infection rates compared to CFE. Short-term patency rates are significantly worse in patients undergoing CFA stenting with BASI.
机译:目的:比较通过生物可吸收支架植入术(BASI组)或股总动脉内膜切除术(CFE组)对股总动脉(CFA)动脉粥样硬化病变进行治疗的患者的临床和血液动力学结果。方法:开始一项随机,对照,单中心,开放标签的试验,以比较CFA中慢性动脉粥样硬化闭塞性病变患者的BASI或CFE结果。从2011年5月到2013年4月,连续招募了116名患者;在排除36例患者后,以1:1比例纳入了80例患者(52名男性;平均年龄72.2±9.6岁),并接受了此意向性治疗中期分析(每组40例)。主要终点是手术部位感染。次要结果指标是技术成功,血液动力学改善,临床改善,通畅,肢体抢救和生存。结果:两组在人口统计学数据,心血管危险因素或CFA闭塞方面无统计学差异。 CFE患者出现7种手术部位感染(全部为轻度感染),而BASI组则为无(p = 0.002),而BASI患者的平均术后住院时间则更长,为7天与2天(p <0.001)。 BASI和CFE组的技术成功率分别为97.5%和100%。术后踝肱指数均值具有可比性(p = 0.38)。 BASI和CFE组的30天初次通畅率分别为92.5%和100%(p = 0.038)。 CFE患者中有6例重建失败,而BASI组中无6例重建失败(p = 0.02);最初的CFA阻塞涉及5个失败。在1年时,BASI和CFE患者的初次和第二次通畅率分别为80%对100%(p = 0.007)和84%对100%(p = 0.01)。肢体抢救是相当的,在一年中,BASI与CFE患者的存活率分别为88%和90%(p = 0.51)。结论:该中期分析表明,BASI并非CFA闭塞的选择,而只是CFA狭窄的一种有限选择。临床和血液动力学结果与BASI和CFE相当。与CFE相比,BASI患者重做程序的增加率高于较低的手术部位感染率。在接受BASI的CFA支架置入术的患者中,短期通畅率明显较差。

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