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Reintervention after thoracic endovascular aortic repair of complicated aortic dissection
Elsa M Faure1, Ludovic Canaud1, Camille Agostini2
1Department of Thoracic and Vascular Surgery, University Hospital, Montpellier, France; U1046, Institut National de la Santé et de la Recherche Médicale, Université Montpellier 1, Montpellier, France.
Insights
Thoracic endovascular aortic repair (TEVAR) is feasible for complicated aortic dissection (C-AD), but reintervention rates are high. Factors like excessive oversizing and anticoagulant therapy increase reintervention risk, while false lumen thrombosis is protective.
Area of Science:
- Vascular Surgery
- Endovascular Repair
- Aortic Dissection
Background:
- Complicated aortic dissection (C-AD) presents significant management challenges.
- Thoracic endovascular aortic repair (TEVAR) has emerged as a less invasive option for C-AD.
- Predicting the need for reintervention after TEVAR in C-AD is crucial for optimizing patient outcomes.
Purpose of the Study:
- To identify predictive factors for reintervention following TEVAR in patients with C-AD.
- To evaluate the long-term efficacy and safety of TEVAR for C-AD.
- To inform clinical decision-making and improve patient selection for TEVAR in C-AD.
Main Methods:
- Retrospective institutional review of consecutive patients undergoing TEVAR for C-AD between 2000 and 2011.
- Analysis of patient demographics, primary indications for TEVAR, technical success rates, and 30-day mortality.
- Multivariate and univariate analyses to identify significant factors associated with secondary procedures.
Main Results:
- Forty-one patients underwent TEVAR for C-AD involving the descending thoracic aorta.
- Technical success was 100%, with a 30-day mortality of 5%.
- Reintervention was required in 32% of patients for various endoleaks, device migration, or aortic expansion. Significant predictors for reintervention included oversizing ≥20%, bare-spring stent in the proximal landing zone, and anticoagulant therapy. Large aortic dilatation was a risk factor, while complete false lumen thrombosis was protective.
Conclusions:
- TEVAR is a feasible treatment for C-AD, but a substantial rate of reintervention necessitates careful patient selection and monitoring.
- Excessive oversizing, proximal bare-spring stent grafts, large aortic dilatation, and anticoagulant therapy are associated with increased reintervention risk.
- Complete false lumen thrombosis at the stent graft level appears to be a protective factor against reintervention.
Objective:
This study assessed predictive factors for reintervention after thoracic endovascular aortic repair (TEVAR) for complicated aortic dissection (C-AD).
Methods:
An institutional review of consecutive TEVAR for C-AD was performed.
Results:
Between 2000 and 2011, 41 patients underwent TEVAR for a C-AD involving the descending thoracic aorta. Primary indications included aneurysm >55 mm in 24, rapid aneurysmal enlargement or impending rupture in 6, saccular aneurysm >20 mm in 1, malperfusion in 1, intractable chest pain in 3, and rupture in 6. Technical success was achieved in 100%. The 30-day mortality rate was 5% (n = 2). Fourteen secondary procedures were performed in 13 patients (32%) for indications of device migration in 2, proximal type I endoleak in 5, distal type I endoleak in 2, type II endoleak in 1, aneurysmal evolution of the descending thoracic aorta in 2, aneurysmal expansion of the dissected abdominal aorta in 1, and retrograde dissection in 1. Multivariate analysis demonstrated that oversizing ≥20% (odds ratio [OR], 16; P = .011), bare-spring stent in the proximal landing zone of the stent graft (OR, 12; P = .032), and anticoagulant therapy (OR, 78; P = .03) were significant factors for reintervention. On univariate analysis, large aneurysm was a risk factor for reintervention (P = .002), whereas complete false lumen thrombosis at the stent graft level was protective (P < .05).
Conclusions:
This study confirms the feasibility of TEVAR for C-AD, although the rate of reintervention is high. Excessive oversizing, a bare-spring stent graft in the proximal landing zone, large aortic dilatation, and anticoagulant therapy were factors associated with reintervention. Complete false lumen thrombosis at the stent graft level was protective.
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