Key result
Acute-phase TEVAR for uncomplicated type B aortic dissection demonstrated higher 30-day mortality (0.5%-7.5%) and reintervention rates (0.8%-11.4%) compared with subacute-phase TEVAR.
Why the study?
Patients with uncomplicated type B aortic dissection on medical therapy often require emergent crossover TEVAR with poorer outcomes, raising consideration for preemptive TEVAR stratified by timing.
Does the timing of TEVAR (subacute/chronic vs acute) improve mortality and reintervention rates in patients with uncomplicated type B aortic dissection?
Systematic Review
Does the timing of TEVAR (subacute/chronic vs acute) improve mortality and reintervention rates in patients with uncomplicated type B aortic dissection?
Subacute-phase TEVAR appears to offer optimal outcomes with lower mortality and reintervention rates compared to acute-phase intervention for uncomplicated type B aortic dissection.
Urges closer surveillance or earlier TEVAR in uTBAD on OMT; confirms poorer outcomes with emergent crossover TEVAR.
Background Uncomplicated type B aortic dissection (uTBAD) is primarily managed through optimal medical therapy, whereas complicated cases typically require thoracic endovascular aortic repair (TEVAR). There are published data that suggest that patients managed long-term with optimal medical therapy have an increased likelihood of requiring crossover TEVAR in the emergent acute setting, which are generally associated with poorer outcomes when compared with the nonacute setting. These findings raise consideration for whether TEVAR may be used for patient populations that remain asymptomatic to prevent these delayed acute encounters. This systematic review aims to evaluate mortality, surgical reintervention, and adverse outcomes after TEVAR in patients with uTBAD, stratified by timing of intervention. Methods In accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, we searched MEDLINE and Embase for studies on TEVAR outcome data for uTBAD published between 2014 and 2024. Eligible studies reported 30-day or 1-year incidence of mortality, surgical reintervention, and/or adverse events after TEVAR, with data stratified by intervention timing. Risk of bias was assessed using the Risk Of Bias In Non-randomized Studies of Interventions (ROBINS-I) tool, and evidence quality was evaluated using a modified Grading of Recommendations, Assessment, Development and Evaluation (GRADE) approach. Results Eleven studies from a screen of 2308 were included, comprising retrospective cohort analyses of 70 to 1536 patients. Acute-phase TEVAR demonstrated 30-day mortality rates ranging from 0.5% to 7.5%, compared with 0.0% to 2.7% in the subacute phase and 1.6% to 2.4% in the chronic phase. One-year mortality ranged from 4.7% to 15.7% in acute interventions and up to 8.2% in subacute interventions, with no data for chronic cases. Reintervention rates were higher in acute-phase TEVAR, ranging from 0.8% to 11.4%, compared with 0.7% to 6.8% in the subacute phase. Adverse outcomes, including endoleak, stroke, and retrograde type A aortic dissection, were more frequent in acute-phase interventions. Conclusions Subacute-phase TEVAR appears to offer optimal outcomes in patients with uTBAD, balancing the risks of acute hemodynamic instability and challenges of chronic anatomical changes. Although emerging evidence supports earlier intervention, high-quality contemporary studies are needed to refine patient selection and intervention timing. Furthermore, there are limited consistent end points for long-term outcome data, which is necessary to improve on treatment guidelines.
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Shah et al. (2025) conducted a systematic review in uncomplicated type B aortic dissection (uTBAD). Thoracic endovascular aortic repair (TEVAR) timing (acute phase) vs. Subacute and chronic phase TEVAR was evaluated on 30-day or 1-year incidence of mortality, surgical reintervention, and adverse events. Acute-phase TEVAR for uncomplicated type B aortic dissection demonstrated higher 30-day mortality (0.5%-7.5%) and reintervention rates (0.8%-11.4%) compared with subacute-phase TEVAR.
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