Bisdas Theodosios, Stavroulakis Konstantinos, Beropoulis Efthymios, Schwindt Arne, Stachmann Arne, Austermann Martin, Torsello Giovanni
1 Department of Vascular Surgery, St Franziskus Hospital Münster GmbH, Münster, Germany.
J Endovasc Ther. 2017 Aug;24(4):604-610. doi: 10.1177/1526602817710492. Epub 2017 May 26.
To examine the safety and effectiveness of the new large-bore Indigo thrombectomy catheters to treat patients with acute renovisceral occlusion without the need of thrombolytic agents.
Between November 2015 and 2016, 7 consecutive patients (mean age 65±5 years; 5 men) with acute renovisceral artery occlusion were treated with the new large-bore (6-F and 8-F) vacuum-assisted thrombectomy catheters. The occluded vessels were 6 renal arteries and 3 superior mesenteric arteries (SMAs); 5 of the 9 thromboses were in bridging stent-grafts associated with branched endografts. Mean lesion length was 63±36 mm. For the SMA and all bridging stent-grafts, 8-F catheters are routinely used through a brachial access, whereas 6-F aspiration catheters were used in native renal arteries. Technical success was defined as restoration of antegrade blood flow without the need of lysis or alternative thrombectomy/revascularization strategies. Safety endpoints were any in-hospital major adverse events. Pre- and postoperative hemoglobin and hematocrit levels were compared.
Technical success was 100% with no major adverse events or fatal bleeding. The mean amount of aspirated blood was 219±97 mL. The mean hemoglobin and hematocrit values were 13.1±2.1 g/dL and 39%±6% prior to and 11.6±2.2 g/dL (p=0.001) and 34%±6% (p<0.0001) directly after the intervention, respectively.
The first assessment of the new large-bore Indigo thrombectomy catheters showed them to be an effective and safe lysis-free frontline therapy for acute renovisceral artery occlusion in a small cohort of patients. New users should be fully aware of the potential blood loss during aspiration.
探讨新型大口径靛蓝血栓切除术导管在无需溶栓药物的情况下治疗急性肾内脏动脉闭塞患者的安全性和有效性。
2015年11月至2016年期间,连续7例(平均年龄65±5岁;5例男性)急性肾内脏动脉闭塞患者接受了新型大口径(6F和8F)真空辅助血栓切除术导管治疗。闭塞血管为6条肾动脉和3条肠系膜上动脉(SMA);9处血栓中有5处位于与分支型腔内移植物相关的桥接支架移植物中。平均病变长度为63±36mm。对于SMA和所有桥接支架移植物,常规通过肱动脉入路使用8F导管,而在肾动脉主干中使用6F抽吸导管。技术成功定义为无需溶栓或采用其他血栓切除术/血管重建策略即可恢复顺行血流。安全终点为任何院内重大不良事件。比较术前和术后血红蛋白和血细胞比容水平。
技术成功率为100%,无重大不良事件或致命出血。平均吸出血量为219±97mL。干预前平均血红蛋白和血细胞比容值分别为13.1±2.1g/dL和39%±6%,干预后直接分别为11.6±2.2g/dL(p=0.001)和34%±6%(p<0.0001)。
对新型大口径靛蓝血栓切除术导管的首次评估表明,在一小群患者中,它们是治疗急性肾内脏动脉闭塞的一种有效且安全的无需溶栓的一线治疗方法。新使用者应充分意识到抽吸过程中潜在的失血情况。