胸部血管内大動脈修復術におけるステント延長のタイプB大動脈解離に対する長期予後
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Updated: Jan 18, 2026

Novel and Innovative Hybrid Technique for Type A Aortic Dissection
Published on: March 28, 2025
Qingsong Wu1, Kailong Ye2, Siying Luo1
1Department of Cardiovascular Surgery, Fujian Medical University Union Hospital, Fuzhou, Fujian, China; Fujian Medical University, Fuzhou, Fujian, China.
Background:
The long-term efficacy of stent extension in thoracic endovascular aortic repair (TEVAR) for Stanford type B aortic dissection (TBAD) has not been thoroughly evaluated.
Methods:
This retrospective, multicenter study included TBAD patients undergoing TEVAR between 2014 and 2021. On the basis of distal descending aorta coverage, patients were stratified into Stent Extension (SE) and Non-Stent Extension (Non-SE) groups. Stent extension was defined as the intentional distal placement of an additional covered stent to lengthen the repair zone within the descending aorta. After 1:1 propensity score matching (PSM) to balance baseline and perioperative characteristics, long-term outcomes were compared. Multivariate regression analysis identified risk factors.
Results:
Among 511 enrolled patients with the median age was 56 (51, 63) years, 241 received stent extension, and the average follow-up time was 69.4 months. After PSM (131 pairs), the groups were comparable. The SE group showed significantly lower rates of aortic-related mortality(3.8% vs. 10.7%; P=0.032), negative aortic remodeling(13.7% vs. 23.7%; P=0.039), follow-up entry flow(8.4% vs. 18.3%; P=0.018), and reoperation(3.8% vs. 11.5%; P=0.020). Stent extension was a protective factor against entry flow(odds ratio[OR] 0.67, P=0.014) and negative remodeling(OR 0.73, P=0.002). Risk factors included smaller true lumen diameter and patent false lumen for entry flow and patent false lumen with multiple distal tears for negative remodeling. Entry flow independently predicted aortic-related mortality(OR 3.54, P<0.001) and reoperation(OR 5.63, P<0.001).
Conclusion:
Stent extension during TEVAR for TBAD is associated with improved long-term outcomes, reducing complications and reinterventions. Prospective trials are warranted for validation.
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