Congenital Heart Surgery Nomenclature and Database Project: patent ductus arteriosus, coarctation of the aorta, interrupted aortic arch

2000 ◽  
Vol 69 (3) ◽  
pp. 298-307 ◽  
Author(s):  
Carl L Backer ◽  
Constantine Mavroudis
2013 ◽  
Vol 25 (1) ◽  
pp. 87-94 ◽  
Author(s):  
Ali A. Al Akhfash ◽  
Abdulrahman A. Almesned ◽  
Badr F. Al Harbi ◽  
Abdullah Al Ghamdi ◽  
Maan Hasson ◽  
...  

AbstractBackground: Coarctation of the aorta is a very common congenital heart malformation. It is frequently associated with other abnormalities. Echocardiography is the diagnostic modality for congenital heart disease. The carotid-subclavian artery index and the isthmus/descending aorta index were proposed for establishing the diagnosis of coarctation of the aorta. Objectives: The objectives were to evaluate such indexes and to look for other echocardiographic predictors of coarctation of the aorta. Method Echocardiography was reviewed for infants with coarctation of the aorta, as well as a control group, using the Echo PAC Dimension. Standard measurements were obtained from different sites of the aortic arch. Results: A total of 31 infants 3 months or less with coarctation of the aorta and 50 infants with no coarctation of the aorta were reviewed. Abnormal aortic valve was present in 65% of those with coarctation of the aorta. The diameters of the proximal and the distal transverse aortic arch were smaller in the coarctation of the aorta group. The distance between the aortic arch branches was longer in the coarctation of the aorta group. Apart from the ratio between distance 2 and the ascending aorta, other ratios/indexes were smaller in the coarctation of the aorta group than in the control group. Conclusion: The presence of abnormal aortic valve, a carotid subclavian index <1.1, I/AAo ratio <0.53, and DTA/AAo ratio <0.6 suggest the presence of coarctation of the aorta. Neonates with large patent ductus arteriosus and any of these findings need close observation until the patent ductus arteriosus closes. If the arch is difficult to assess by two-dimensional echocardiography, the patient may need further imaging to rule out coarctation of the aorta.


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

PEDIATRICS ◽  
1980 ◽  
Vol 65 (5) ◽  
pp. 1054-1054
Author(s):  
Thom Mayer

It was with great interest that I read Moss' excellent summary of data concerning congenital heart disease.1 Of particular interest were the well-taken references concerning Gross' "atrial well" and Lillehei's use of crosscirculation. In that vein, however, there is one inaccuracy in the article. In speaking of repair of patent ductus arteriosus, Moss states that it represents "the oldest of all heart operations." Although the 1939 report by Gross2 did signal the onset of surgical therapy of congenital heart disease, the first successful heart operation was performed by Ludwig Rehn of Frankfurt, Germany in 1896,3 only seven years after Theodor Billroth had declared that, "A surgeon who would attempt such an operation should lose the respect of his colleagues."


2019 ◽  
Vol 52 ◽  
pp. 50-54
Author(s):  
Jeremy R. Burt ◽  
Vincent Grekoski ◽  
Fiona Tissavirasingham ◽  
Ryan Parente ◽  
Jorge Garcia

2021 ◽  
pp. 1-2
Author(s):  
Stephen T. Dalby ◽  
Joshua A. Daily ◽  
Lawrence E. Greiten

Abstract We report a case of a newborn infant with coarctation of the aorta and hypoplastic transverse aortic arch who was found to have a circumaortic double left innominate vein on echocardiography. This exceedingly rare finding was important for surgical planning and was confirmed during congenital heart surgery.


2010 ◽  
Vol 58 (5) ◽  
pp. 477
Author(s):  
Hyun-Jeong Kwak ◽  
Hong Soon Kim ◽  
Jong Seok Lee ◽  
Jeongmin Kim ◽  
Joo-Young Chung ◽  
...  

Author(s):  
Jonan Chun Yin Lee ◽  
Jeanie Betsy Chiang ◽  
Boris Chun Kei Chow

Interrupted aortic arch (IAA) is an extremely rare congenital cyanotic heart disease characterized by complete disruption between the ascending and descending aorta. A patent ductus arteriosus (PDA) or other collateral pathways provide blood flow to the distal descending aorta. Mortality is extremely high at early infancy, particularly after the closure of ductus arteriosus. Survival and presentation in adulthood are extremely rare. Here we illustrate a rare case of type B interrupted aortic arch in an adult who presented with secondary polycythaemia. The blood supply to descending aorta and beyond is almost solely by a patent ductus arteriosus. The case demonstrates the value of multimodality imaging including CT and MRI for diagnosis and treatment planning in these patients.


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