scholarly journals Right aortic arch with isolation of the left innominate artery in a case of double chamber right ventricle and ventricular septal defect

2014 ◽  
Vol 7 (2) ◽  
pp. 148 ◽  
Author(s):  
Chirantan Mangukia ◽  
Sonali Sethi ◽  
Saket Agarwal ◽  
Smita Mishra ◽  
DeepakKumar Satsangi
Keyword(s):  
Ventricular Septal Defect ◽  
Right Ventricle ◽  
Aortic Arch ◽  
Septal Defect ◽  
Innominate Artery ◽  
Right Aortic Arch ◽  
Double Chamber

One-Stage Repair of Cardiac and Arch Anomalies without Circulatory Arrest

2003 ◽  
Vol 11 (3) ◽  
pp. 250-254 ◽  
Author(s):  
Kona Samba Murthy ◽  
Robert Coelho ◽  
Christopher Roy ◽  
Snehal Kulkarni ◽  
Benjamin Ninan ◽  
...  
Keyword(s):  
Ventricular Septal Defect ◽  
Aortic Arch ◽  
Septal Defect ◽  
Circulatory Arrest ◽  
Coarctation Of The Aorta ◽  
Innominate Artery ◽  
Double Outlet Right Ventricle ◽  
Interrupted Aortic Arch ◽  
Ischemic Time ◽  
Arch Obstruction

Between 1999 and 2002, 23 patients underwent single-stage complete repair of cardiac anomalies and aortic arch obstruction, without circulatory arrest. Median age was 1.2 years. Intracardiac defects included ventricular septal defect in 9, double-outlet right ventricle in 6, d-transposition of the great arteries and ventricular septal defect in 2, subaortic obstruction in 3, and atrial septal defect in 3. Fourteen patients had coarctation of the aorta, 6 had coarctation with hypoplastic aortic arch, and 3 had interrupted aortic arch. Simple techniques were employed such as cannulation of the ascending aorta near the innominate artery and maintaining cerebral and myocardial perfusion. After correction of arch obstruction, intracardiac repair was undertaken. The mean cardiopulmonary bypass time was 169 min, aortic crossclamp time was 51 min, and arch repair took 16 min. There was no operative mortality or neurological deficit. In follow-up of 1–43 months, no patient had residual coarctation. This simplified technique avoids additional procedures, reduces ischemic time, and prevents problems related to circulatory arrest.

Retroesophageal Right Aortic Arch Associated with an Aortic Aneurysm and a Ventricular Septal Defect

2018 ◽  
pp. 47-61
Author(s):  
Marcus Vinícius Silva Ferreira ◽  
Gabrielle Santos Oliveira ◽  
Ana Carolina Gonçalves e Silva ◽  
Fernando Antibas Atik ◽  
Cláudio Ribeiro da Cunha
Keyword(s):  
Aortic Aneurysm ◽  
Ventricular Septal Defect ◽  
Aortic Arch ◽  
Septal Defect ◽  
Right Aortic Arch

Incomplete isolation of the left innominate artery from the right aortic arch: a rare case of double-outlet right ventricle with pulmonary stenosis

2019 ◽  
Vol 29 (5) ◽  
pp. 717-719
Author(s):  
Jun Sato ◽  
Atsuko Kato ◽  
Naoki Ohashi
Keyword(s):  
Right Ventricle ◽  
Aortic Arch ◽  
Rare Case ◽  
Surgical Repair ◽  
Pulmonary Stenosis ◽  
Innominate Artery ◽  
Double Outlet Right Ventricle ◽  
Right Aortic Arch ◽  
Female Infant ◽  
The Right

AbstractIsolation of the left innominate artery from the right aortic arch is a rare anomaly. Herein, we present an even rarer case of incomplete isolation of the proximal left innominate artery with the right aortic arch in a 3-month-old female infant with a double-outlet right ventricle and pulmonary stenosis. Surgical repair at 6 months of age was successful, leading to the restoration of adequate flow in the left arm.

Long-term prognosis after repair of double-chamber right ventricle with ventricular septal defect

1984 ◽  
Vol 54 (10) ◽  
pp. 1292-1295 ◽  
Author(s):  
Daniel Kveselis ◽  
Amnon Rosenthal ◽  
Pauline Ferguson ◽  
Douglas Behrendt ◽  
Herbert Sloan
Keyword(s):  
Ventricular Septal Defect ◽  
Right Ventricle ◽  
Septal Defect ◽  
Long Term Prognosis ◽  
Double Chamber
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