Bailey, LL and Gundry, SR (1990) Hypoplastic left heart syndrome. (Vol.37).
Full text not available from this repository.
HLHS is a complex developmental malformation of the left ventricle, aorta, and associated valves. Survival beyond neonatal life is the exception in untreated infants. The prognosis, however, is no longer hopeless. Newer surgical strategies of staged palliative reconstruction and heart replacement by transplantation appear promising. These options on occasion will become complementary in the management of individual patients. Those children surviving Fontan operations are frequently able to lead NYHA Class I or II lives without drugs, while transplant recipients will require one or more immunoregulative medications indefinitely. Exercise tolerance and work capacity following the Fontan procedure are reported to be 40 to 60 per cent of expected normals. Full functional capacity of successfully palliated children may never be normal. In contrast, exercise capability after heart transplantation is generally better than that following a Fontan operation, with cardiac ejection fractions approaching normal for age. Durability of these new management technologies will make inappropriate the traditional "do nothing" approach to HLHS in all but a few cases.
|Title:||Hypoplastic left heart syndrome.|
|Keywords:||Decision Trees, Heart Defects, Congenital, Heart Transplantation, Humans, Infant, Newborn, Palliative Care, Syndrome|
|UCL classification:||UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Child Health|
Archive Staff Only: edit this record