Left Subclavian Artery Revascularization With In Situ Laser Fenestration During Thoracic Endovascular Aortic Repair for Acute Complicated or High-Risk Type B Aortic Dissection: Results of the LLTEVAR Trial

左锁骨下动脉血运重建联合原位激光开窗术治疗急性复杂性或高危B型主动脉夹层:LLTEVAR试验结果

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Abstract

BACKGROUND: Coverage of the left subclavian artery (LSA) during thoracic endovascular aortic repair (TEVAR) for type B aortic dissection (TBAD) increases the risk of major adverse events (MAEs). In situ laser-assisted fenestration allows for LSA revascularization in both elective and urgent settings, yet its safety and efficacy lack robust multicenter data. METHODS: LLTEVAR (LSA Revascularization With Laser-Assisted Fenestration During TEVAR) was a prospective, single-arm, multicenter study that enrolled patients with acute complicated or high-risk acute TBAD. The primary safety end point was freedom from composite MAEs (mortality, stroke, myocardial infarction, paraplegia, type Ia endoleak, and retrograde aortic dissection/intramural hematoma) within 30 days after the procedure. Univariate and multivariable analyses identified risk factors for composite MAEs. RESULTS: A total of 100 patients (mean age, 60.5±12.6 years) were enrolled at 5 vascular centers between July 2018 and September 2021. The technical success rate of LSA fenestration was 98.0% (98/100). The 30-day primary safety end point was 86.0%. Complicated TBAD (OR, 4.04; 95% CI, 1.05-15.59; P=0.04) and type II/III aortic arch (OR, 4.61; 95% CI, 1.18-17.95; P=0.03) were significantly associated with a higher risk of composite MAEs within 30 days. CONCLUSION: In situ laser-assisted fenestration for LSA revascularization during TEVAR demonstrates favorable procedural success and acceptable short-term outcomes in patients with acute TBAD. However, periprocedural MAEs remain a critical consideration, particularly in those with complicated TBAD with type II/III aortic arch anatomy. Further studies with comparative groups and long-term follow-up are warranted to validate these outcomes. REGISTRATION: URL: https://clinicaltrials.gov; Unique Identifier: NCT03845829.

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