scholarly journals Aortic coarctation progresses to become interrupted aortic arch

2017 ◽  
Vol 18 (9) ◽  
pp. 1072-1072 ◽  
Author(s):  
Ting Ting Low ◽  
Lynette Li San Teo ◽  
Shoban Krishna Kumar ◽  
Edgar Lik Wui Tay ◽  
James Wei Lun Yip
2011 ◽  
Vol 14 (3) ◽  
pp. 188 ◽  
Author(s):  
Onder Teskin ◽  
A. Umit Gullu ◽  
Sahin Senay ◽  
E. Murat Okten ◽  
Cem Alhan

The hallmark feature of aortic interruption that is useful in differentiating it from aortic coarctation is the "complete absence" of continuity between both parts of the interrupted segment. In this study, we reviewed the 28 patients diagnosed with isolated interrupted aortic arch (IAA) who reached adult age (> 20 years), aimed to review the validity of the Celoria-Patton classification in the literature, and reported the first microscopic pathology of the IAA in an adult.


Perfusion ◽  
2009 ◽  
Vol 24 (3) ◽  
pp. 185-189 ◽  
Author(s):  
Hui Zhang ◽  
Pei Cheng ◽  
Jia Hou ◽  
Lei Li ◽  
Hu Liu ◽  
...  

One-stage repair of aortic arch obstruction and associated cardiac anomalies is a surgical challenge in infants.The purpose of the present study is to review the current outcome using regional cerebral perfusion (RCP) during a procedure correcting interrupted aortic arch (IAA) and also isolated aortic coarctation (CoA) and CoA combined with hypoplastic aortic arch (CoA-HyAA) in our center. Between January 2007 and July 2008, 24 infant patients with interrupted aortic arch (IAA) (n=3), isolated aortic coarctation (iCoA) (n=9) and aortic coarctation with hypoplastic aortic arch (CoA-HyAA) (n=12) underwent one-stage surgical correction in our hospital. End-to-end anastomosis was employed in 12 infants (IAA n=3 and iCoA n=9); for the other 12 patients with CoA-HyAA, an end-to-end extended anastomosis was used in 8 cases, end-to-side anastomosis in 2 cases, and composite heterologous pericardial patch in 2 cases. RCP with 40 mL/kg/min through the innominate artery during aortic arch reconstruction was employed for all pediatric patients. One single-dose histidine-ketoglutarate-tryptophan (HTK) solution was used for myocardial protection during CPB. Cardiopulmonary bypass time and aortic cross-clamp time were 165.6±32.4min and 81.7±30.0min, respectively. The mean regional cerebral perfusion time was 31.0±10.6min; lowest nasopharyngeal temperature was 19.1±1.1°C. Operative mortality rate in both groups was 8.3%. Mean follow-up was 10.5±4.8 months. There was no late mortality or postoperative neurologic, renal or hepatic complications. All patients are asymptomatic and are developing normally. One-stage total arch repair using the RCP technique is an excellent method that may minimize neurologic and renal complications. Our surgical strategy for arch anomaly has a low rate of residual and recurrent coarctation when performed in these infants.


2010 ◽  
pp. 945-966 ◽  
Author(s):  
J. Andreas Hoschtitzky ◽  
Robert H. Anderson ◽  
Martin J. Elliott

1976 ◽  
Vol 71 (1) ◽  
pp. 35-48 ◽  
Author(s):  
Noel H. Fishman ◽  
Merrill H. Bronstein ◽  
William Berman ◽  
Benson B. Roe ◽  
L. Henry Edmunds ◽  
...  

1995 ◽  
Vol 5 (1) ◽  
pp. 15-20
Author(s):  
Osamu Matsuki ◽  
Toshikatsu Yagihara ◽  
Fumio Yamamoto ◽  
Kyoichi Nishigaki ◽  
Hideki Uemura ◽  
...  

AbstractA one-stage repair was performed for correction of the intracardiac malformations associated with coarctation of aorta in five pateints or interrupted aortic arch in eight patients. The ages ranged from four to 294 (median 35) days. The anomalies within the heart were a ventricular septal defect with or without subaortic stenosis (n=7), an aortopulmonary window (n=2), common arterial trunk (n=2), aortic valvar stenosis (n=1) and the TaussigBing anomaly (n=1). Surgery was performed through a median sternotomy employing cardiopulmonary bypass with moderate to deep hypothermia. In terms of the aortic reconstruction, an extended direct anastomosis was performed in 10 patients, while a vascular graft was interposed in three. So long as the aortic cannula did not interfere with the proximal anastomotic site on the aorta, circulatory arrest was avoided. As for surgery within the heart, the ventricular septal defects were closed via the right atrium with myotomy and myectomy if a morphological substrate for subaortic stenosis was confirmed (n=4). There were two hospital deaths (15.4%) due to low cardiac output. In patients who underwent myotomy and myectomy for subaortic stenosis, the postoperative pressure gradient across the aortic valve was negligible. We conclude that surgical results of one-stage repair for the intracardiac malformations associated with interrupted aortic arch or aortic coarctation are reasonable. We suggest that the early relief of obstruction within the left ventricular outflow tract may have played some role in the favorable outcome.


Surgery Today ◽  
1998 ◽  
Vol 28 (9) ◽  
pp. 889-894 ◽  
Author(s):  
Ryo Aeba ◽  
Toshiyuki Katogi ◽  
Toshihiko Ueda ◽  
Shigeyuki Takeuchi ◽  
Shiaki Kawada

Sign in / Sign up

Export Citation Format

Share Document