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The Annals of Thoracic Surgery, Vol 52, 722-726, Copyright © 1991 by The Society of Thoracic Surgeons
AH Menkis, FN McKenzie, RJ Novick, WJ Kostuk, PW Pflugfelder, M Goldbach and H Rosenberg
The number of heart transplantations performed over the past 3 years has
plateaued. However, the number of pediatric transplantations continues to
slowly increase. Unlike adult heart transplantation, for which
cardiomyopathy remains the most frequent indication, structural congenital
heart disease is the primary indication in children. This report reviews
our experience with orthotopic heart transplantation in the presence of
structural congenital heart disease with and without prior palliative
repair. The diagnoses included transposition of the great arteries, common
atrium, left superior vena cava with and without a bridging innominate
vein, dextrocardia, and univentricular configurations. The palliative
repairs included Blalock-Taussig shunt, bilateral Glenn shunt, Fontan
repair, and Mustard and Rastelli procedure. There were no early deaths. Two
rejection-related late deaths have occurred at 8 months and at 3 years
postoperatively. Extended use of donor tissue and modifications to surgical
technique allowed for successful orthotopic heart transplantation in these
patients who had structural congenital heart disease with and without prior
surgical palliation.
ARTICLES
Expanding applicability of transplantation after multiple prior palliative procedures. The Paediatric Heart Transplant Group
University Hospital, London, Ontario, Canada.
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