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The Journal of Thoracic and Cardiovascular Surgery, Vol 105, 398-404, Copyright © 1993 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
RM Di Donato, A Amodeo, DD di Carlo, L Galletti, G Rinelli, L Pasquini and C Marcelletti
Ventricular hypertrophy is a recognized risk factor for the Fontan
operation in cases of complex cardiac anomalies with unrestricted pulmonary
blood flow and subaortic obstruction. Between 1986 and 1991 we have treated
23 such patients with a new type of palliation combining a main pulmonary
artery-ascending aorta anastomosis with a bidirectional cavopulmonary
anastomosis. Their ages averaged 57 +/- 36 months (7 to 155 months). Nine
patients had (S,L,L) single ventricule with transposition and the other 14
had more complex cardiac anomalies unsuitable for biventricular repair.
Subaortic obstruction was defined by a hemodynamic criterion (n = 6) or by
a morphologic criterion (n = 17). There were five hospital deaths (21.7%):
All three patients older than 7 years of age died (p = not significant).
Follow-up averaged 28 +/- 21 months (range 1 to 58 months). Among the 18
hospital survivors, the proportions surviving 1 and 5 years after the
operation were 78% and 63%, respectively. Control cardiac catheterization
in 11 patients showed no or trivial subaortic gradient, a mean
cavopulmonary pressure of 10 +/- 3 mm Hg, and a mean arterial oxygen
saturation of 83%. Nine patients underwent secondary Fontan repair in our
institution 21 +/- 4 months after palliation, without deaths. Another
patient died elsewhere, 3.7 years after palliation, as a result of
hemorrhage at sternal reentry during attempted Fontan operation (overall
mortality at repair, 10%). The other eight patients are awaiting Fontan
operation. This staged approach reduces both pressure and volume
ventricular load and provides adequate oxygenation before the Fontan
operation. In our experience, it resulted in reduced mortality at
definitive repair.
ARTICLES
Staged Fontan operation for complex cardiac anomalies with subaortic obstruction
Department of Pediatric Cardiac Surgery, Bambino Gesu Hospital, Rome, Italy.
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