Reoperations for Aneurysmal Disease of the Ascending Aorta, Aortic Arch, and Descending Aorta: Their Causes and Operative Results

1994 ◽  
Vol 2 (2) ◽  
pp. 95-100 ◽  
Author(s):  
Shigeaki Aoyagi ◽  
Hidetoshi Akashi ◽  
Keiichiro Tayama ◽  
Yuji Hanamoto ◽  
Kazunari Yamana ◽  
...  

Between 1984 and 1993, 20 patients underwent reoperation for the thoracic aorta or ascending aorta and aortic valve. There were 14 male and 6 female patients who ranged in age from 28 to 70 years with a mean of 53.2 years. The mean interval between initial operation and the 2nd operation was 70.4 months. Of the 20 patients, 6 had stigmata of Marfan's syndrome. The primary aortic pathology requiring initial operation was annuloaortic ectasia in 10 patients, aortic valvular disease in 5, aortic dissection in 3, and mega aorta syndrome, aortic aneurysm in multiple segments, or aortic arch aneurysm in 1 each. Cause of reoperation was pseudoaneurysm formation at suture lines in the ascending aorta in 6 patients, new or progressive dilatation in the remaining aortic segment in 5, new or persistent aortic dissection in 4, graft infection in 2, and recurrent aortic arch aneurysm in 1. The remaining 2 patients received a planned two-stage operation for multiple aneurysms or mega aorta syndrome. Six patients died early after reoperation, yielding a hospital mortality rate of 30%; however, 3 of the 6 deaths were related to a compromised preoperative clinical condition and 1 to perioperative contamination. Two operative deaths (10%) were related to operative techniques. Results suggest application of separate grafts for coronary artery reattachment, as in the Cabrol or Piehler techniques, or the aortic button technique for aortic root replacement, may help eliminate pseudoaneurysm formation, which is one of the major complications after operations on the ascending aorta. It is also suggested that early diagnosis and prompt operative treatment for recurrent or residual aneurysmal diseases of the aorta may be essential for successful definitive treatment.

2020 ◽  
Vol 22 (Supplement_N) ◽  
pp. N142-N145
Author(s):  
Alice Benedetti ◽  
Alvise Del Monte ◽  
Maurizio Rubino ◽  
Daniela Mancuso

Abstract A 36-year-old woman at 31 weeks’ gestation presented with exertional dyspnoea and palpitations. She had a history of bicuspid aortic valve treated with surgical aortic valvotomy for severe stenosis, followed by ascending aorta replacement for type A acute aortic dissection and Bentall operation with a mechanical valve for severe aortic regurgitation. Eight years after the last surgery, magnetic resonance angiography showed aortic arch aneurysm (49 mm) with a small intimal flap. Thereafter, the patient was lost to follow-up until the current admission. She was hemodynamically stable on presentation and physical examination was unremarkable apart from a mechanical second heart sound. The electrocardiogram showed sinus rhythm with left bundle branch block (Panel A). Transthoracic echocardiography revealed severe left ventricular dilation (EDV 90 ml/m2) with mild dysfunction (EF 50%), normal prosthetic aortic valve function, and aortic arch dilation (50 mm) (Panel B and C). After a multidisciplinary evaluation, elective cesarean section was performed at 34 weeks’ gestation. A post-delivery aortic computed tomography angiography revealed aortic arch aneurysm (52 mm) with intimal flap and two pseudoaneurysms of the anterior aortic wall causing sternal erosion (Panel D, E, F and G). Subsequently, the patient underwent ascending aorta and aortic arch replacement by Frozen Elephant Trunk technique with a 24 x130 mm prosthesis between the aortic root and the descending aorta. The postoperative course was uneventful, and the patient was discharged to a cardiac rehabilitation centre.


2020 ◽  
Vol 3 ◽  
pp. 54-56
Author(s):  
Shinichi Ishida ◽  
Wataru Koike ◽  
Takashi Fujita ◽  
Kei Yagami

2003 ◽  
Vol 51 (10) ◽  
pp. 545-547 ◽  
Author(s):  
Katsuhiko Matsuyama ◽  
Masahiko Matsumoto ◽  
Takaaki Sugita ◽  
Junichiro Nishizawa ◽  
Yujiro Kawanishi ◽  
...  

Surgery Today ◽  
1999 ◽  
Vol 29 (8) ◽  
pp. 817-820
Author(s):  
Miki Asano ◽  
Akira Mishima ◽  
Shigeru Sasaki ◽  
Takayuki Saito ◽  
Shigeki Yamamoto ◽  
...  

Surgery Today ◽  
1999 ◽  
Vol 29 (8) ◽  
pp. 817-820
Author(s):  
Miki Asano ◽  
Akira Mishima ◽  
Shigeru Sasaki ◽  
Takayuki Saito ◽  
Shigeki Yamamoto ◽  
...  

Author(s):  
Yoshihiro Suematsu ◽  
Satoshi Nishi ◽  
Daisuke Arima ◽  
Akihiro Yoshimoto

We report a successful treatment of type A acute aortic syndrome (AAS)-associated aortic arch aneurysm in a 71-year-old man with major comorbidities. The ascending aorta was wrapped with artificial graft, and supra-aortic debranching was constructed. Then, Zone 0 thoracic endovascular aneurysm repair (TEVAR) with plug occlusion of the left subclavian artery was successfully performed. The patient was discharged in good physical condition without any complications. To our knowledge, this is the first reported case in the literature of successful Zone 0 TEVAR after ascending aorta wrapping and supra-aortic debranching with type A AAS associated with aortic arch aneurysm.


Aorta ◽  
2020 ◽  
Vol 08 (05) ◽  
pp. 144-147
Author(s):  
Davide Margonato ◽  
Valerio Stefano Tolva ◽  
Giuseppe Vaccari ◽  
Paolo Bianchi ◽  
Renato Casana ◽  
...  

AbstractCoexistence of obstructive hypertrophic cardiomyopathy and severe aortic pathology is extremely rare; nonetheless, the association between these two diseases is fascinating. Here we present a unique case report of a patient with obstructive hypertrophic cardiomyopathy and aortic arch aneurysm treated by a single surgical procedure.


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