Persistent truncus arteriosus is a rare congenital malformation accounting for less than 2% of all the congenital heart defects seen in the first year of life.
IIn the great majority of infants born with this malformation, there is a large left-to-right shunt, with large pulmonary blood flow,2 though normal or low pulmonary flow can be present,3 resulting from pulmonary obstruction. Deformities of the truncal valve are often present, resulting in different degrees of truncal incompetence.4 5 The natural history of patients with persistent truncus arteriosus is poor. Almost all present during the first months of life with intractable congestive cardiac failure.2 3 More than 60% die before the age of 6 months6 7 and more than 80% before 1 year.8 9 In the survivors, pulmonary vascular disease increases progressively after the age of 2 years and one-third are inoperable by the age of 4 years.In the surgical management of infants with persistent truncus arteriosus and intractable congestive cardiac failure, the choice lies between a two-stage procedure involving banding of either the main pulmonary trunk or the individual pulmonary arteries, *