Author:
Josowitz Rebecca,Rogers Lindsay S.
Abstract
Purpose of review
There has been much variability in the definition of double outlet right ventricle (DORV) spanning the last century. Historically, emphasis has been placed on the assignment of the great arteries to the right ventricle as a definition of DORV. In this review, we aim to underscore the importance of conal muscle, rather than rules surrounding assignment of great arteries to ventricles. We will be outlining the variability in patient anatomy that results from variations in conal muscle development in DORV, which may not fit perfectly into predefined constructs. This anatomic variability directly determines physiology and surgical repair options.
Recent findings
There is a growing appreciation of the utility of cross-sectional imaging in complex DORV, and the generation of patient-specific 3D models with virtual reality simulations for surgical planning. These models improve the prediction of candidacy for biventricular repair and allow the mapping of complex baffle pathways preoperatively.
Summary
DORV is not a disease entity in itself, but rather a vast spectrum of disorders associated with maldevelopment of conal muscle and often abnormal expansion of one the great vessels. Patient-specific 3D models will be crucial for improved surgical planning and patient outcomes.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Reference25 articles.
1. Double outlet right ventricle: anatomic types and developmental implications based on a study of 101 autopsied cases;Van Praagh;Coeur,1982
2. Congenital Heart Surgery Nomenclature and Database Project: double outlet right ventricle;Walters;Ann Thorac Surg,2000
3. Normally and abnormally related great arteries: what have we learned?;Praagh;World J Pediatr Congenit Heart Surg,2010
4. Development and morphology of the ventricular outflow tracts;Anderson;World J Pediatr Congenit Heart Surg,2016
5. A concept of double-outlet right ventricle;Lev;J Thorac Cardiovasc Surg,1972