首页> 外文期刊>Journal of endovascular therapy: an official journal of the International Society of Endovascular Specialists >Anatomical Applicability of Endovascular Aneurysm Sealing Techniques in a Consecutive Cohort of Fenestrated Endovascular Aneurysm Repairs
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Anatomical Applicability of Endovascular Aneurysm Sealing Techniques in a Consecutive Cohort of Fenestrated Endovascular Aneurysm Repairs

机译:血管内动脉瘤密封技术的解剖学适用性在连续血管内动脉瘤修理中的连续群组中

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Purpose: To determine how many endovascular aneurysm sealing (EVAS) procedures with/without off-label use of chimneys (ChEVAS) could have been performed in a cohort of patients who had undergone fenestrated endovascular aneurysm repair (FEVAR). Methods: Sixty patients (median age 76.3 years; 54 men) who underwent FEVAR in our institution between 2013 and 2015 were selected for the study. The median aneurysm diameter was 62.0 mm (interquartile range 59.3, 69.0). Preoperative computed tomography angiograms (CTA) were anonymized and sent to 2 physicians with experience of more than 40 ChEVAS interventions. These ChEVAS planners were blinded to the study purpose and asked to agree upon an EVAS/ChEVAS plan. The primary outcome was the percentage of the FEVAR patients in whom an EVAS/ChEVAS was technically possible. The secondary outcomes were a comparison of seal zones, number of target vessels, and device cost. Results: An EVAS-based intervention would have been technically possible in 56 (93.3%) of the FEVAR patients. The median proximal aortic seal zone was significantly more distal in the EVAS/ChEVAS procedures vs the FEVAR cases (zone 8 vs zone 7, p < 0.001) and fewer target vessels were involved (median 2 vs 3, p < 0.001). The cost of the EVAS/ChEVAS device was 66% of the FEVAR device. Planners would not currently advocate an EVAS-based intervention in 43 (76.8%) of these 56 patients due to concerns regarding the risk of migration associated with the lumen thrombus ratios observed. Conclusion: EVAS is technically feasible in the majority of patients undergoing FEVAR in our institution but currently advocated in only 23.2%. The seal zone was more distal, fewer target vessels were involved, and the device cost was lower in the planned EVAS/ChEVAS interventions.
机译:目的:确定有多少内血管内动脉瘤密封(EVA)手术(EVA)的手术(EVA)程序可以在经历肠道血管内动脉瘤修复(FEVAR)的患者中进行烟囱(CHEVAS)。方法:六十名患者(中位年龄76.3岁; 54名男子)在2013年至2015年间接受了FEVAR的FEVAR,为这项研究选择了FEVAR。中间动脉瘤直径为62.0毫米(第59.3,69.0级)。术前计算断层扫描血管造影(CTA)被匿名,并送到2个医生,体验超过40个雪兰乳酪干预。这些Chevas规划者对学习目的蒙蔽,并要求在EVAS / CHEVAS计划上同意。主要结果是EVAS / CHEVAS在技术上可能的FEVAR患者的百分比。二次结果是密封区,目标血管数量和装置成本的比较。结果:在56(93.3%)的FEVAR患者中,基于EVAS的干预措施将在技术上是可能的。在EVAS / CHEVAS程序中,近端主动脉密封区的中位数远端vs vs涉及FEVAR案例(区域8 ZS区7,P <0.001)和更少的靶血管(中位数2 Vs 3,P <0.001)。 EVAS / Chevas设备的成本为FEVAR设备的66%。由于关于与观察到的腔血栓比率相关的迁移风险的担忧,规划者目前倡导基于EVAS的干预措施的43(76.8%)。结论:EVAS在我们机构中的FEVAR的大多数患者中是技术上可行的,但目前仅在23.2%中提倡。密封区更远距离,涉及较少的目标血管,计划的EVAS / Chevas干预中的装置成本较低。

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