Abstract
Congenitally corrected transposition of the great arteries (CCTGA) is a rare congenital heart disease that commonly results in congestive heart failure due to exposure of the anatomic right ventricle to systemic pressures. Additional anatomic abnormalities, such as situs inversus, in which the viscera are mirror images of normal anatomy, or dextrocardia in which the heart apex is located on the patient’s right, once were contraindications to transplant in the treatment of advanced heart failure. However, recent advancements now allow for the management of heart failure through mechanical circulatory support and subsequent transplant. This case presents a 52 year-old man with advanced heart failure secondary to CCTGA and dextrocardia situs inversalis totalis that was managed with a ventricular assist device (VAD) after maximal medical treatment, and subsequently received an orthotopic heart transplant. This case will also review CCTGA in relation to heart failure and the surgical challenges faced in terms of ventricular assist device implantation and orthotopic heart transplant. Citation: Young, B. et al. (2016). Orthotopic heart transplant following implantation of a systemic ventricular assist device in a patient with congenitally corrected transposition of the great arteries and dextrocardia situs inversus totalis” The VAD Journal, 2. doi: http://dx.doi.org/10.13023/VAD.2 016.09 Editor-in-Chief: Maya Guglin, University of Kentucky Received: February 22, 2016 Accepted: May 5, 2016 Published: May 5, 2016 © 2016 The Author(s). This is an open access article published under the terms of the Creative Commons AttributionNonCommercial 4.0 International License (https://creativecommons.org/lice nses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided that the original author(s) and the publication source are credited. Funding: Not applicable Competing interests: Not applicable
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