Endovascular Aortic Arch Repair with Mini-Cardiopulmonary Bypass to Prevent Stroke

2016 ◽  
Vol 36 ◽  
pp. 320-324 ◽  
Author(s):  
Masaaki Ryomoto ◽  
Hiroe Tanaka ◽  
Tetsuya Kajiyama ◽  
Masataka Mitsuno ◽  
Mitsuhiro Yamamura ◽  
...  
Author(s):  
Tomohiro Yamamoto ◽  
Takeshi Saito ◽  
Shuichi Shiraishi ◽  
Boulos Asfour ◽  
Victor Hraska ◽  
...  

AbstractWe previously presented a cardiopulmonary bypass (CPB) method with blood delivery via femoral artery cannulation for pediatric aortic arch repair operations using the Radifocus Introducer sheath. However, the flow rate with the Radifocus Introducer sheath is limited by accessory parts with the same structure having a smaller inner diameter among different sizes, rather than the sheath body. Therefore, we further devised a combination of the JELCO IV catheter, an extension tube, and a three-way stopcock with a larger opening to obtain more flow rate keeping the CPB circuit pressure significantly lower than when using the Radifocus Introducer sheath successfully.


2008 ◽  
Vol 56 (S 1) ◽  
Author(s):  
M Czerny ◽  
R Gottardi ◽  
D Zimpfer ◽  
M Dorfmeister ◽  
J Holfeld ◽  
...  

2008 ◽  
Vol 56 (S 1) ◽  
Author(s):  
A Rüffer ◽  
M Kondruweit ◽  
K Ntalakoura ◽  
L Hakami ◽  
M Weyand ◽  
...  

2005 ◽  
Vol 53 (S 01) ◽  
Author(s):  
M Kondruweit ◽  
L Hakami ◽  
R Tandler ◽  
M Weyand ◽  
R Cesnjevar

2013 ◽  
Vol 61 (S 01) ◽  
Author(s):  
A Rüffer ◽  
S Kellermann ◽  
C Janssen ◽  
F Münch ◽  
M Demuth ◽  
...  

2015 ◽  
Vol 63 (S 01) ◽  
Author(s):  
A. Martens ◽  
N. Koigeldiyev ◽  
E. Beckmann ◽  
F. Fleissner ◽  
T. Kaufeld ◽  
...  

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>


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