Hybrid treatment of interrupted aortic arch in a newborn with contraindications for extracorporeal circulation: case report including 1.5 year follow-up

2013 ◽  
pp. 396-398
Author(s):  
Tomasz Moszura ◽  
Waldemar Bobkowski ◽  
Michał Wojtalik ◽  
Rafał Surmacz ◽  
Bartłomiej Mroziński ◽  
...  
Keyword(s):  
Case Report ◽  
Aortic Arch ◽  
Extracorporeal Circulation ◽  
Interrupted Aortic Arch ◽  
Hybrid Treatment

Isolated interrupted aortic arch in 42-year-old adult-case report

2012 ◽  
Vol 41 (8) ◽  
pp. 521-523 ◽  
Author(s):  
Chen Liping ◽  
Dipesh Pradhan ◽  
Zhang Jing ◽  
Zhou Hongwei ◽  
Rajina Shrestha
Keyword(s):  
Case Report ◽  
Aortic Arch ◽  
Interrupted Aortic Arch ◽  
Adult Case ◽  
Old Adult

Surgical repair of interrupted aortic arch with ventricular septal defect

1998 ◽  
Vol 8 (2) ◽  
pp. 217-220 ◽  
Author(s):  
Lindsey D Allan ◽  
Howard D Apfel ◽  
Yosef Levenbrown ◽  
Jan M Quaegebeur
Keyword(s):  
Ventricular Septal Defect ◽  
Aortic Arch ◽  
Septal Defect ◽  
Ventricular Outflow Tract ◽  
Interrupted Aortic Arch ◽  
Left Ventricular ◽  
Subaortic Stenosis ◽  
Current Debate ◽  
Aortic Orifice

AbstractBackgroundInterrupted aortic arch is often associated with subaortic narrowing and hypoplasia of the aortic orifice. The best surgical strategy for the management of these additional lesions is a matter of current debate.Methods and ResultsBetween 1986 and 1996, 19 patients underwent repair of interrupted aortic arch with closure of ventricular septal defect in a single stage, with no attempt at subaortic resection, irrespective of the dimensions of the left ventricular outflow tract. There was no perioperative hospital mortality, and all patients were alive at 1 year. Follow-up ranges from 0.75 −10 years, with a mean 4.2 ± 3.0 years. Seven patients (37%) have required reintervention for relief of subaortic stenosis, 2 of whom have died.ConclusionsOur results suggest that primary one-stage biventricular repair can be accomplished with low perioperative mortality without addressing the subaortic region. Further long-term follow-up will determine whether this is accomplished at the expense of later morbidity and mortality.

Echocardiography of coarctation of the aorta, aortic arch hypoplasia, and arch interruption: strategies for evaluation of the aortic arch

2016 ◽  
Vol 26 (8) ◽  
pp. 1553-1562 ◽  
Author(s):  
Suma P. Goudar ◽  
Sanket S. Shah ◽  
Girish S. Shirali
Keyword(s):  
Aortic Arch ◽  
Coarctation Of The Aorta ◽  
The United States ◽  
Interrupted Aortic Arch ◽  
Hypoplastic Left Heart ◽  
Live Births ◽  
Additional Information ◽  
Non Invasive ◽  
Aortic Arch Hypoplasia

AimEchocardiography is the modality of choice for the diagnosis and serial follow-up of aortic arch pathology. In this article, we review the types of obstruction of the aortic arch, various classification schemes of coarctation of the aorta and interrupted aortic arch, methodology for optimal echocardiographic imaging of the aortic arch, and key echocardiographic measurements for accurate diagnosis of obstruction and hypoplasia of the aortic arch. Finally, we will discuss the limitations of echocardiography in optimal imaging of the aortic arch and the use of other non-invasive imaging modalities such as CT or MRI to provide additional information in these cases.BackgroundCoarctation of the aorta is the more common lesion of the two, with an estimated incidence of four in every 10,000 live births in the United States of America. Interrupted aortic arch is rarer, with an incidence of 19 per one million live births.1 There is a spectrum of pathology of obstruction of the aortic arch, ranging from coarctation of the aorta with and without hypoplasia of the arch to interrupted aortic arch. Both these lesions are frequently encountered in congenital cardiology practice, and will be discussed in the remainder of this article. Obstruction of the aortic arch in the setting of hypoplastic left heart structures or atresia of the aortic valve is beyond the scope of this review and will not be discussed further.

scholarly journals Co-occurrence of interrupted aortic arch and Apert syndrome: A case report

2020 ◽  
Author(s):  
Serap Nur Ergor ◽  
Mehmet Serdar Kutuk ◽  
Nilgun Duman ◽  
Can Yilmaz Yozgat ◽  
Hafize Otcu Temur ◽  
...  
Keyword(s):  
Case Report ◽  
Aortic Arch ◽  
Interrupted Aortic Arch ◽  
Apert Syndrome

Anesthesia for noncardiac surgery in a neonate with interrupted aortic arch - A case report -

2008 ◽  
Vol 55 (3) ◽  
pp. 358
Author(s):  
Won-Kyoung Kwon ◽  
Duk Kyung Kim ◽  
Tae Gyoon Yoon ◽  
Seong Hyop Kim ◽  
Joo-eun Kang
Keyword(s):  
Case Report ◽  
Aortic Arch ◽  
Interrupted Aortic Arch ◽  
Noncardiac Surgery

Interrupted Aortic Arch or Extreme Coarctation? A Case Report and Review of the Literature

2011 ◽  
Vol 14 (3) ◽  
pp. 188 ◽  
Author(s):  
Onder Teskin ◽  
A. Umit Gullu ◽  
Sahin Senay ◽  
E. Murat Okten ◽  
Cem Alhan
Keyword(s):  
Case Report ◽  
Aortic Arch ◽  
Aortic Coarctation ◽  
Interrupted Aortic Arch ◽  
Review Of The Literature ◽  
Adult Age ◽  
Microscopic Pathology ◽  
Hallmark Feature ◽  
Aortic Interruption

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.

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