Early and midterm outcomes of thoracic endovascular aortic repair with Lifetech Ankura™ thoracic endograft: A single tertiary center experience

Sabir Hasanzade, Yunus Emre Ergin, Murat Gevrek, Naim Boran Tumer, H. L. Mavioğlu, H. Iscan
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Abstract

Aim: Thoracic aortic pathologies describe a wide spectrum of potentially life-threatening diseases almost always in a comorbid aged patient cohort. Thoracic endovascular aortic repair (TEVAR) is a less invasive treatment choice, offering reduced mortality and morbidity compared to open surgery. We decided to reveal our experience over safety and efficacy data with Lifetech Ankura™ Thoracic endografts with early and midterm outcomes, retrospectivelytiology. Material and Methods: Between January 2018 and January 2023, for a 5-year period, 203 patients who experienced TEVAR procedure with Lifetech Ankura™ Thoracic endograft were retrospectively evaluated. For the patients who required revascularization of the vessel branches originating from the aortic segments, all types of assistive techniques were performed. Intentional coverage of Left subclavian artery was also performed mostly in urgent patients. Results: 251 endografts were implanted in 203 patients. The most frequent aortic pathologies were the thoracic aortic fusiform aneurysm (56.6%) and type B aortic dissection (25.6%), respectively. Early (30-day/in-hospital) mortality occurred in 9 patients in total (4.4%). Technical success rate was 100%, and there was no conversion to open surgery. No other major adverse event, including cerebral, cardiac, or renal complication requiring dialysis, was observed. The average intensive care unit time was 16.9±11 hours (2-160), length of stay was 5.1±3.2 days. CSF drainage was performed in 51 patients inserted before the procedure prophylactically (25.1%). All patients who survived the operation were followed for 18.6±9.3 months. In the follow up period, four patients needed extension for endoleaks and two additive petticoat procedures were performed. One patient who had TEVAR due to a malperfused type B aortic dissection in the acute phase experienced RTAD 2 weeks after the initial procedure. Conclusion: TEVAR with LifeTech Ankura™ Thoracic Stent Graft system provides a safe, effective, and durable treatment with successful early outcomes and technical success. Wide spectrum in length and non-identical radiopaque proximal markers seem to facilitate some advanced endovascular skills. Long-term durability of the endograft should be tested.
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使用Lifetech Ankura™胸腔内移植物修复胸腔血管内主动脉的早期和中期结果:单一三级中心体验
目的:胸主动脉病变描述了广泛的潜在威胁生命的疾病,几乎总是在合并症的老年患者队列。胸椎血管内主动脉修复术(TEVAR)是一种侵入性较小的治疗选择,与开放手术相比,其死亡率和发病率都较低。我们决定通过回顾性研究揭示我们使用Lifetech Ankura™胸腔内移植物的早期和中期结果的安全性和有效性数据。材料和方法:在2018年1月至2023年1月的5年期间,回顾性评估203例使用Lifetech Ankura™胸腔内移植物进行TEVAR手术的患者。对于需要主动脉段血管分支血运重建的患者,进行了所有类型的辅助技术。故意覆盖左锁骨下动脉也主要是在紧急患者中进行的。结果:203例患者共植入251颗内移植物。最常见的主动脉病变为胸主动脉梭状动脉瘤(56.6%)和B型主动脉夹层(25.6%)。早期(30天/住院)死亡共发生9例(4.4%)。技术成功率100%,无中转开腹手术。未观察到其他主要不良事件,包括需要透析的脑、心或肾并发症。平均重症监护时间16.9±11小时(2 ~ 160),住院时间5.1±3.2天。51例患者在手术前预防性插入脑脊液引流(25.1%)。术后随访18.6±9.3个月。在随访期间,有4例患者需要延长内窥镜,并进行了2次添加衬裙手术。1例急性期因B型主动脉夹层灌注不良而发生TEVAR的患者在初始手术后2周发生了RTAD。结论:TEVAR与LifeTech Ankura™胸腔支架移植系统提供了安全、有效和持久的治疗,具有成功的早期结果和技术上的成功。广谱长度和不相同的不透射线近端标记物似乎有助于一些先进的血管内技术。应测试内移植物的长期耐久性。
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