Department of Vascular Surgery, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.
Department of Vascular Surgery, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.
J Vasc Surg. 2021 Sep;74(3):871-879. doi: 10.1016/j.jvs.2021.01.067. Epub 2021 Feb 26.
Complex aortic endografts have evolved to include inner branches to overcome specific challenges with existing technologies. We have reported the early outcomes of endovascular aortic aneurysm repair (EVAR) using a Jotec inner branched endograft (iBEVAR).
All patients who had undergone complex EVARs using extra-design engineering iBEVAR (Jotec GmbH, Hechingen, Germany) from 2018 to 2020 at a single center were reviewed. The patient demographics, cardiovascular risk factors, anatomic features of the aneurysms, and target vessels were recorded. The reasons for using inner branches instead of fenestrated and standard branched endografts and the procedural details, outcomes, and reintervention during follow-up were examined.
A total of 110 patients were treated with branched and fenestrated endografts during the study period, of whom 18 patients had had a patient-specific custom-made iBEVAR endograft with downward inner branches. The technical success rate was 100%. A total of 68 target vessels were cannulated, and bridging stent-grafts were placed successfully in all. The reasons for choosing the iBEVAR design included unfavorable target vessel trajectory for fenestrated repair (n = 15), excessive infrarenal aortic angulation and/or adverse iliac access vessels for fenestrated repair (n = 11), the presence of a narrow aortic lumen (n = 14), and/or to reduce aortic coverage compared with that with standard outer branched repair (n = 14). We also used iBEVAR to treat type Ia endoleaks after failed EVAR with a short main body (n = 5). The median contrast volume used was 120 mL (range, 48-200 mL), with a median fluoroscopy screening time of 66 minutes (range, 35-136 minutes) and a median dose-area product of 17,832 dGy∙cm (range, 8260-55,070 dGycm). No 30-day mortality and no major complications occurred. One early intervention was required for a suspected type Ib endoleak from an iliac limb and one late intervention for in-stent stenosis in a renal bridging stent-graft. One patient had died of non-aortic-related causes at 3 months. All other patients continued with follow-up with their aneurysms excluded, patent target vessels, and no type I or III endoleak identified at a median follow-up of 12 months (range, 1-26 months).
The use of Jotec extra-design engineering endografts incorporating downward inner branches resulted in satisfactory early outcomes with a low reintervention rate. The technology has the potential to be a useful addition to our armamentarium for treating complex aortic endografts; however, long-term outcomes data are needed.
复杂的主动脉内支架已发展到包括内置分支,以克服现有技术的特定挑战。我们报告了使用 Jotec 内置分支(iBEVAR)进行血管内主动脉瘤修复(EVAR)的早期结果。
回顾了 2018 年至 2020 年在单一中心使用额外设计工程 iBEVAR(Jotec GmbH,德国海兴根)进行复杂 EVAR 的所有患者。记录患者的人口统计学、心血管危险因素、动脉瘤的解剖特征和靶血管。检查使用内置分支而不是开窗和标准分支内支架的原因以及程序细节、结果和随访期间的再介入情况。
研究期间,共有 110 名患者接受了分支和开窗内支架治疗,其中 18 名患者接受了定制的 iBEVAR 内支架治疗,内置有向下的分支。技术成功率为 100%。共对 68 个靶血管进行了穿刺,所有靶血管均成功植入了桥接支架。选择 iBEVAR 设计的原因包括:开窗修复靶血管轨迹不佳(n=15)、肾下主动脉过度倾斜和/或髂内血管不良适合开窗修复(n=11)、主动脉管腔狭窄(n=14)和/或与标准外分支修复相比减少主动脉覆盖范围(n=14)。我们还使用 iBEVAR 治疗了 5 例 EVAR 失败后因短主体而导致的 I 型内漏。中位造影剂用量为 120mL(范围,48-200mL),中位透视筛查时间为 66 分钟(范围,35-136 分钟),中位剂量面积乘积为 17832dGy·cm(范围,8260-55070 dGy·cm)。无 30 天死亡率和重大并发症发生。1 例早期干预需要治疗髂内分支疑似 I 型内漏,1 例晚期干预治疗肾桥接支架内狭窄。1 例患者在 3 个月时因非主动脉相关原因死亡。所有其他患者继续接受随访,其动脉瘤被排除,靶血管通畅,中位随访 12 个月(范围,1-26 个月)时未发现 I 型或 III 型内漏。
使用 Jotec 额外设计工程内支架内置分支可获得满意的早期结果,再介入率较低。该技术有可能成为我们治疗复杂主动脉内支架的有用工具;然而,需要长期的结果数据。