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Updated: May 10, 2026

Biaxial Mechanical Characterizations of Atrioventricular Heart Valves
Published on: April 9, 2019
Anatomy of discordant atrioventricular connections
James L Wilkinson1, Robert H Anderson
1Royal Children's Hospital, Melbourne, Australia.
Insights
Discordant atrioventricular connections involve abnormal heart chamber connections, often leading to congenitally corrected transposition. Accurate anatomical description is crucial for understanding these complex congenital heart defects.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Congenital Heart Disease
Background:
- Discordant atrioventricular connections describe abnormal relationships between atrial and ventricular chambers.
- These anomalies frequently present with abnormal great artery connections, resulting in conditions like congenitally corrected transposition.
Purpose of the Study:
- To detail the complex anatomy of discordant atrioventricular connections.
- To emphasize the importance of a segmental approach in describing these congenital heart malformations.
Main Methods:
- Descriptive anatomical analysis of discordant atrioventricular connections.
- Utilizing a step-by-step segmental approach for documentation.
Main Results:
- Commonly associated defects include ventricular septal defects and outflow tract obstruction.
- Abnormalities of the tricuspid valve and conduction system are frequently observed.
- Complex topological variations, such as criss-cross atrioventricular connections, can occur.
Conclusions:
- Discordant atrioventricular connections represent a spectrum of complex congenital heart defects.
- A systematic segmental approach is essential for accurate diagnosis and communication.
Abstract:
The term discordant atrioventricular connections refers to the situation in which the ventricles are connected inappropriately to the atrial chambers. In most instances, the connections of the great arteries are also abnormal, with the aorta and the pulmonary trunk arising from morphologically inappropriate ventricles. This combination results in the presence of so-called congenitally corrected transposition. Double-outlet right ventricle is occasionally present, while concordant ventriculoarterial connections may be seen rarely. Most such hearts have a range of additional abnormalities, including ventricular septal defects; outflow tract obstruction, usually of the morphologically left ventricle; anomalies of the morphologically tricuspid valve; and a highly abnormal location of the specialized atrioventricular conduction axis. Some examples exhibit bizarre abnormalities of ventricular relationships and topology, including criss-cross atrioventricular connections and superoinferior ventricular relations. In describing the anatomy of these malformations, it is important to use a step-by-step segmental approach to the documentation of the connections and associated defects in each case and to avoid potentially confusing shorthand terms.
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