Revised technique of cardiopulmonary bypass in one-stage repair of interrupted aortic arch complex

1993 ◽  
Vol 55 (5) ◽  
pp. 1166-1171 ◽  
Author(s):  
Hisataka Yasui ◽  
Hideaki Kado ◽  
Kunihiro Yonenaga ◽  
Shihori Kawasaki ◽  
Yuichi Shiokawa ◽  
...  
2014 ◽  
Vol 17 (2) ◽  
pp. 80
Author(s):  
Ahmet Ozkara ◽  
Mehmet Ezelsoy ◽  
Levent Onat ◽  
Ilhan Sanisoglu

<p><b>Introduction:</b> Interrupted aortic arch is a rare congenital malformation characterized by a complete loss of luminal continuity between the ascending and descending aorta. It is often diagnosed during the neonatal period.</p><p><b>Case presentation:</b> We presented a 51-year-old male patient with interrupted aortic arch type B who was treated successfully with posterolateral thoracotomy without using cardiopulmonary bypass.</p><p><b>Conclusion:</b> The prognosis for interrupted aortic arch depends on the associated congenital anomalies, but the outcome is usually very poor unless there is surgical treatment. Survival into adulthood depends on the development of collateral circulation.</p>


1993 ◽  
Vol 56 (3) ◽  
pp. 554-556 ◽  
Author(s):  
Gaetano Gargiulo ◽  
Lucio Zannini ◽  
Sonia-Bernadette Albanese ◽  
Guido Frascaroli ◽  
Maria-Cristina Santordli ◽  
...  

1989 ◽  
Vol 98 (2) ◽  
pp. 285-288 ◽  
Author(s):  
S. Aranki ◽  
F. Musumeci ◽  
A. Khaghani ◽  
R. Radley-Smith ◽  
M. Yacoub

1998 ◽  
Vol 65 (3) ◽  
pp. 829-831 ◽  
Author(s):  
Hiroaki Hata ◽  
Motomi Shiono ◽  
Yukiyasu Sezai ◽  
Naokata Sumitomo ◽  
Masahiro Otsuka ◽  
...  

1977 ◽  
Vol 74 (6) ◽  
pp. 913-917 ◽  
Author(s):  
Kenji Ito ◽  
Naoaki Kohguchi ◽  
Yasunori Ohkawa ◽  
Tadayoshi Akasaka ◽  
Hiroshi Ohara ◽  
...  

2012 ◽  
Vol 60 (9) ◽  
pp. 575-577
Author(s):  
Masatoshi Shimada ◽  
Takaya Hoashi ◽  
Koji Kagisaki ◽  
Tatsuya Oda ◽  
Isao Shiraishi ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-3
Author(s):  
Richard Neal ◽  
Katharina Mattishent ◽  
Fiona Reynolds

We report a case of a 32-week-gestation male who presented initially with symptoms suggestive of an interrupted aortic arch. The absence of a VSD prompted further investigations, including a CT angiogram, which revealed that he had an extensive thrombus in his aorta. He underwent a successful aortic thrombectomy with arch repair on cardiopulmonary bypass support. In view of the extensive thrombus, the patient was referred to the haematology team. There was no family history of prothrombotic tendencies.


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