de Kort Jasper F, Mandigers Tim J, Bissacco Daniele, Domanin Maurizio, Piffaretti Gabriele, Twine Christopher P, Wanhainen Anders, van Herwaarden Joost A, Trimarchi Santi, de Vincentiis Carlo
Cardio Thoracic Vascular Department, Section of Vascular Surgery, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan, Italy; Department of Vascular Surgery, University Medical Centre Utrecht, Utrecht, the Netherlands.
Cardio Thoracic Vascular Department, Section of Vascular Surgery, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milan, Italy; Department of Vascular Surgery, University Medical Centre Utrecht, Utrecht, the Netherlands.
Eur J Vasc Endovasc Surg. 2025 Apr;69(4):531-544. doi: 10.1016/j.ejvs.2024.10.049. Epub 2024 Nov 8.
High risk, inoperable patients with ascending aortic disease are increasingly managed with thoracic endovascular aortic repair (TEVAR). The aim of this study was to assess the available literature on TEVAR confined to the ascending aorta (a-TEVAR), describing study and patient characteristics, procedural and stent graft details, and outcomes.
This was a systematic review and meta-analysis. MEDLINE, Web of Science, and Scopus were systematically searched for eligible studies reporting on outcomes after a-TEVAR (PROSPERO ID: CRD42023440826). Eligible studies reported outcomes after a-TEVAR without adjunctive supra-aortic vessel treatment.
The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement was followed. The ROBINS-I and Joanna Briggs Institute Critical Appraisal Checklist were used as quality assessment tools. A Grading of Recommendations Assessment, Development, and Evaluation (GRADE) evidence certainty analysis was performed for the main outcomes. The main outcome was death. A proportional meta-analysis was performed with a mean and 95% confidence interval (CI) for the main outcomes. All articles were included up to 1 January 2024.
Ninety four studies were included (19 cohort studies, 75 case reports or series), reporting on 259 patients (57.8% male). The mean age was 69.1 (95% CI 65.0 - 73.1) years and mean follow up 19.6 (95% CI 14.5 - 24.6) months. The most common comorbidity was prior cardiac or thoracic surgery (n = 191). The most frequent indications for a-TEVAR (52.1% urgent a-TEVAR) were type A aortic dissection (43.6%) and pseudoaneurysm (38.6%). The most commonly deployed stent grafts were Gore (44.5%), Cook (23.5%), and Medtronic (17.0%). The in hospital mortality rate was 7.3% (95% CI 4.7 - 11.2%), 30 day mortality rate 7.7% (95% CI 5.1 - 11.6%), and overall mortality rate 17.0% (95% CI 12.9 - 22.0%) during follow up. GRADE showed very low evidence certainty for all outcomes. Eighty eight complications were reported and there was a re-operation rate of 13.1% (95% CI 9.5 - 17.8%). In hospital and 30 day mortality rates for type A dissection were 12.4% (95% CI 7.5 - 19.7%) (n = 14) and 13.3% (95% CI 8.2 - 20.8%) (n = 15), respectively, and for pseudoaneurysm 4.0% (95% CI 1.6 - 9.8%) (n = 4) and 4.0% (95% CI 1.6 - 9.8) (n = 4), respectively.
Despite heterogeneous literature and very low GRADE evidence certainty, a-TEVAR seems technically feasible in high risk patients. In addition, there is need for a consensus on when and how to use a-TEVAR and a need for a specific endograft for use in the ascending aorta.
对于升主动脉疾病的高危、无法手术的患者,越来越多地采用胸主动脉腔内修复术(TEVAR)进行治疗。本研究的目的是评估仅限于升主动脉的TEVAR(a-TEVAR)的现有文献,描述研究和患者特征、手术及支架移植物细节以及结局。
这是一项系统评价和荟萃分析。对MEDLINE、科学网和Scopus进行了系统检索,以查找报告a-TEVAR术后结局的符合条件的研究(PROSPERO注册号:CRD42023440826)。符合条件的研究报告了未进行辅助主动脉弓上血管治疗的a-TEVAR术后结局。
遵循系统评价和荟萃分析的首选报告项目(PRISMA)声明。使用ROBINS-I和乔安娜·布里格斯研究所批判性评价清单作为质量评估工具。对主要结局进行了推荐分级评估、制定和评价(GRADE)证据确定性分析。主要结局是死亡。对主要结局进行了比例荟萃分析,给出了均值和95%置信区间(CI)。纳入了截至2024年1月1日的所有文章。
纳入了94项研究(19项队列研究,75项病例报告或系列研究),报告了259例患者(男性占57.8%)。平均年龄为69.1(95%CI 65.0 - 73.1)岁,平均随访时间为19.6(95%CI 14.5 - 24.6)个月。最常见的合并症是既往心脏或胸外科手术(n = 191)。a-TEVAR最常见的适应证(52.1%为急诊a-TEVAR)是A型主动脉夹层(43.6%)和假性动脉瘤(38.6%)。最常用的支架移植物是戈尔(44.5%)、库克(23.5%)和美敦力(17.0%)。住院死亡率为7.3%(95%CI 4.7 - 11.2%),30天死亡率为7.7%(95%CI 5.1 - 11.6%),随访期间总死亡率为17.0%(95%CI 12.9 - 22.0%)。GRADE显示所有结局的证据确定性都非常低。报告了88例并发症,再次手术率为13.1%(95%CI 9.5 - 17.8%)。A型夹层的住院死亡率和30天死亡率分别为12.4%(95%CI 7.5 - 19.7%)(n = 14)和13.3%(95%CI 8.2 - 20.8%)(n = 15),假性动脉瘤的分别为4.0%(95%CI 1.6 - 9.8%)(n = 4)和4.0%(95%CI 1.6 - 9.8)(n = 4)。
尽管文献存在异质性且GRADE证据确定性非常低,但a-TEVAR在高危患者中似乎在技术上是可行的。此外,需要就何时以及如何使用a-TEVAR达成共识,并且需要一种专门用于升主动脉的血管内移植物。