Department of Vascular and Endovascular Surgery, Heidelberg University Hospital, Germany.
Institute of Medical Biometry and Informatics, University of Heidelberg, Heidelberg, Germany.
Vascular. 2021 Aug;29(4):486-498. doi: 10.1177/1708538120970033. Epub 2020 Nov 2.
To describe the outcome of thoracic endovascular aortic repair (TEVAR) in thoracic aortic aneurysm and penetrating aortic ulcer with respect to instructions for use status.
Between October 2009 and September 2017, a total of 532 patients underwent TEVAR; of which 195 have been treated using the Conformable GORE® TAG® thoracic endoprosthesis (CTAG). Fifty-six patients of this cohort underwent TEVAR for thoracic aortic aneurysm/penetrating aortic ulcer using the CTAG. Depending on the preoperative computed tomography angiography findings, patients were classified as inside or outside the device's instructions for use. All inside instruction for use patients underwent postoperative reclassification regarding the instructions for use status. Study endpoints included TEVAR-related reintervention, exclusion of the pathology (endoleak type I/III), TEVAR-related mortality, and graft-related serious adverse events. The median duration of follow-up was 29.7 months (range: 0-109.4 months).
Of the 56 patients, 17 were primarily classified as outside instruction for use, and in additional 13 patients, TEVAR was performed outside instruction for use, leading to 30 outside instruction for use patients (53.6%). Twenty-six patients (46.4%) were treated inside instruction for use. Reintervention-free survival was lower in outside instruction for use patients ( = 0.016) with a hazard ratio of 9.74 (confidence interval 1.2-80.2; = 0.034) for TEVAR-related reintervention. With respect to endoleak type I/III, relevant difference was detected between inside/outside instruction for use status ( = 0.012). The serious adverse event rate was 30.4%, mainly in outside instruction for use patients ( = 0.004). Logistic regression analysis indicated an association between graft-related serious adverse event/instructions for use status (odds ratio 6.11; confidence interval 1.6-30.06; = 0.012). In-hospital death was seen more frequently in outside instruction for use patients ( = 0.12) as was procedure-related death (log-rank test: = 0.21).
TEVAR for thoracic aortic aneurysm/penetrating aortic ulcer is frequently performed outside instruction for use despite preoperative inside instruction for use eligibility, leading to important consequences for technical/clinical outcome. Instructions for use adherence in TEVAR should be of interest for further large-scale studies.
描述胸主动脉腔内修复术(TEVAR)治疗胸主动脉瘤和穿透性主动脉溃疡的结果,重点关注适应证使用情况。
2009 年 10 月至 2017 年 9 月,共有 532 例患者接受了 TEVAR 治疗;其中 195 例使用顺应性戈尔®TAG®胸主动脉覆膜支架(CTAG)进行治疗。该队列中有 56 例患者使用 CTAG 治疗胸主动脉瘤/穿透性主动脉溃疡。根据术前计算机断层血管造影(CTA)检查结果,将患者分为在适应证范围内和不在适应证范围内。所有在适应证范围内的患者均在术后重新分类,以确定适应证使用情况。研究终点包括 TEVAR 相关再干预、排除病变(Ⅰ/Ⅲ型内漏)、TEVAR 相关死亡率和移植物相关严重不良事件。中位随访时间为 29.7 个月(0-109.4 个月)。
56 例患者中,17 例最初被归类为不在适应证范围内,另外 13 例患者的 TEVAR 治疗不在适应证范围内,因此有 30 例患者(53.6%)不在适应证范围内。26 例(46.4%)患者在适应证范围内接受治疗。不在适应证范围内的患者无再干预生存率较低(=0.016),TEVAR 相关再干预的风险比为 9.74(95%置信区间 1.2-80.2;=0.034)。关于Ⅰ/Ⅲ型内漏,适应证内/外使用状态之间存在显著差异(=0.012)。严重不良事件发生率为 30.4%,主要发生在不在适应证范围内的患者(=0.004)。Logistic 回归分析表明,移植物相关严重不良事件与适应证使用状态之间存在关联(比值比 6.11;95%置信区间 1.6-30.06;=0.012)。不在适应证范围内的患者院内死亡率和手术相关死亡率均较高(log-rank 检验:=0.21)。
尽管术前有适应证内治疗的资格,但 TEVAR 治疗胸主动脉瘤/穿透性主动脉溃疡经常在适应证外进行,这对技术/临床结果产生了重要影响。TEVAR 的适应证使用应成为进一步开展大规模研究的关注点。