Progression of distal aorta after endovascular fenestration/ stenting in acute type A aortic dissection with malperfusion syndrome

被引:5
作者
Ahmad, Rana-Armaghan [1 ]
Orelaru, Felix [2 ]
Graham, Nathan [1 ]
Titsworth, Marc [1 ]
Monaghan, Katelyn [1 ]
Wu, Xiaoting [1 ]
Kim, Karen M. [1 ]
Fukuhara, Shinichi [1 ]
Patel, Himanshu [1 ]
Deeb, G. Michael [1 ]
Yang, Bo [1 ]
机构
[1] Michigan Med, Dept Cardiac Surg, Ann Arbor, MI USA
[2] St Joseph Mercy, Dept Gen Surg, Ann Arbor, MI USA
关键词
acute type A aortic dissection; endovascular fenestration and stenting; malperfusion; malperfusion syndrome; FALSE LUMEN; REPAIR;
D O I
10.1016/j.xjon.2023.02.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: The study objective was to evaluate the progression of dissected distal aorta in patients with acute type A aortic dissection with malperfusion syndrome treated with endovascular fenestration/stenting and delayed open aortic repair. Methods: From 1996 to 2021, 927 patients presented with acute type A aortic dissection. Of these, 534 had DeBakey I dissection with no malperfusion syndrome and underwent emergency open aortic repair (no malperfusion syndrome group), whereas 97 patients with malperfusion syndrome underwent fenestration/stenting and delayed open aortic repair (malperfusion syndrome group). Sixty-three patients with malperfusion syndrome treated with fenestration/stenting were excluded due to no open aortic repair, including death from organ failure (n = 31), death from aortic rupture (n = 16), and discharged alive (n = 16). Results: Compared with the no malperfusion syndrome group, the malperfusion syndrome group had more patients with acute renal failure (60% vs 4.3%, P < .001). Both groups had similar aortic root and arch procedures. Postoperatively, the malperfusion syndrome group had similar operative mortality (5.2% vs 7.9%, P = .35) and permanent dialysis (4.7% vs 2.9%, P = .50), but more new-onset dialysis (22% vs 7.7%, P < .001) and prolonged ventilation (72% vs 49%, P < .001). The growth rate of the aortic arch (0.38 vs 0.35 mm/year, P = .81) was similar between the malperfusion syndrome and no malperfusion syndrome groups. The descending thoracic aorta growth rate (1.03 vs 0.68 mm/year, P = .001) and abdominal aorta growth rate (0.76 vs 0.59 mm/year, P = .02) were significantly higher in the malperfusion syndrome group. The cumulative incidence of reoperation over 10 years (18% vs 18%, P = .81) and 15-year survival outcome (50% vs 48%, P = .43) were similar between the malperfusion syndrome and no malperfusion syndrome groups. Conclusions: Endovascular fenestration/stenting followed by delayed open aortic repair was a valid approach for patients with malperfusion syndrome.
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页码:11 / 13
页数:3
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