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Updated: May 15, 2026

Anatomical Reconstructions of the Human Cardiac Venous System using Contrast-computed Tomography of Perfusion-fixed Specimens
Published on: April 18, 2013
Rationalising the nomenclature of common arterial trunk
Marshall L Jacobs1, Robert H Anderson
1Department of Pediatric and Congenital Heart Surgery, Cleveland Clinic, Cleveland, Ohio 19073, USA. marshall.jacobs@comcast.net
Insights
Congenital heart malformations with a common arterial trunk are reclassified using a simplified system based on pulmonary or aortic dominance. This new approach aligns with current cardiac development knowledge and predicts surgical outcomes.
Area of Science:
- Cardiology
- Developmental Biology
- Medical Diagnostics
Background:
- Traditional classification systems for congenital cardiac malformations, specifically hearts with a common arterial trunk, suffer from inconsistencies.
- Existing nomenclature presents paradoxes and incompatibilities with current understanding of cardiac development and morphology.
Observation:
- Hearts with a common arterial trunk represent a complex group of congenital cardiac malformations.
- Previous classification methods presented significant challenges due to inherent contradictions.
- A need exists for a more coherent and biologically relevant classification system.
Findings:
- A simplified categorization based on pulmonary or aortic dominance is proposed for hearts with a common arterial trunk.
- This new system reconciles disparate existing categorizations.
- The proposed classification aligns with recent findings in cardiac development and morphology.
Implications:
- This simplified classification provides a more consistent framework for understanding and diagnosing these complex heart conditions.
- It emphasizes the key morphologic determinant influencing surgical outcomes.
- The approach facilitates better communication among clinicians and researchers, improving patient care and advancing the field of congenital heart disease research.
Abstract:
Hearts having a common arterial trunk belong to a family of congenital cardiac malformations for which traditional systems of classification and nomenclature are plagued by internal paradoxes, incompatibility between systems due to the lack of potential for identification of synonyms, or irreconcilable inconsistencies with our current knowledge of cardiac development and morphology. A simplified categorisation that classifies these hearts on the basis of pulmonary or aortic dominance reconciles the existing disparate categorisations, is in keeping with recent findings concerning cardiac development, and emphasises the principal morphologic determinant of surgical outcome.
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