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Published on: July 7, 2013
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Endovascular Repair in High-Risk Uncomplicated Type B Aortic Dissection: A Systematic Review and Single-Arm
Milton Sérgio Bohatch Júnior1, Beatriz de Melo Silva2, Elisabeth Amanda Gomes Soares3
1Hospital de Base de São José do Rio Preto, São José do Rio Preto, Brazil.
Summary
Thoracic endovascular aortic repair (TEVAR) for high-risk type B aortic dissection shows low early mortality and good long-term survival. Further trials are needed to confirm efficacy and refine patient selection for this high-risk group.
Area of Science:
- Vascular Surgery
- Cardiovascular Research
- Medical Technology Assessment
Background:
- Optimal medical therapy (OMT) alone is associated with poor prognosis in high-risk uncomplicated type B aortic dissection (hrTBAD).
- The role of thoracic endovascular aortic repair (TEVAR) in hrTBAD remains controversial due to potential risks versus benefits in aortic remodeling and complication reduction.
Purpose of the Study:
- To systematically review and meta-analyze early and long-term outcomes of TEVAR in hrTBAD patients.
- To evaluate the safety and efficacy of TEVAR for hrTBAD, addressing uncertainties in current management strategies.
Main Methods:
- Systematic review and single-arm meta-analysis of MEDLINE, Embase, and Cochrane Library up to January 2025.
- Inclusion of 10 retrospective cohort studies (1971 patients) meeting Society for Vascular Surgery criteria for hrTBAD.
- Data synthesis using random-effects models; individual patient data reconstructed from Kaplan-Meier curves.
Main Results:
- Pooled early mortality: 1.22%; stroke: 3.29%; spinal cord ischemia: 1.10%.
- Long-term survival rates: 88.0% at 1 year, 84.0% at 3 years, 77.4% at 5 years; reintervention rate: 6.63%.
- Favorable aortic remodeling observed, with mean thoracic diameter reduction of 4.29 mm and 14.65% false lumen thrombosis.
Conclusions:
- TEVAR in hrTBAD patients demonstrates low early mortality, favorable long-term survival, and encouraging aortic remodeling, particularly in the subacute phase.
- Current evidence stems from non-randomized studies, necessitating further prospective trials for refined patient selection and long-term efficacy confirmation.
- TEVAR should be considered judiciously on a case-by-case basis, integrating risk profiles and multidisciplinary assessment until randomized evidence is available.
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