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The Annals of Thoracic Surgery, Vol 47, 415-420, Copyright © 1989 by The Society of Thoracic Surgeons
E Mazzera, A Corno, S Picardo, R Di Donato, B Marino, D Costa and C Marcelletti
A standard Glenn anastomosis between the superior vena cava and the right
pulmonary artery has been the accepted mode of treatment for patients with
complex cyanotic congenital heart disease. We report our experience in 18
patients with such disease who underwent a bidirectional cavopulmonary
shunt because of increasing cyanosis and growth cessation. All patients
were considered less than "ideal" candidates for a Fontan procedure. We
divided the patients into two groups: group 1 had azygos continuation and
group 2 did not. Fourteen patients required hypothermic cardiopulmonary
bypass. Bidirectional pulmonary blood flow was achieved in all patients.
Only 1 death occurred (group 2). The improvement in oxygen saturation and
overall clinical condition of these patients, together with the low
mortality and morbidity, is encouraging. However, long-term follow-up is
mandatory for a comprehensive evaluation of this surgical approach as
definitive palliation or as a first stage for a Fontan operation.
ARTICLES
Bidirectional cavopulmonary shunts: clinical applications as staged or definitive palliation
Department of Pediatric Cardiac Surgery, Bambino Gesu Hospital, Rome, Italy.
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