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J Thorac Cardiovasc Surg ; 147(5): 1568-72, 2014 May.
Article in English | MEDLINE | ID: mdl-23988293

ABSTRACT

OBJECTIVES: Extracardiac conduits are widely used to complete a Fontan circulation in patients with univentricular hearts. Although polytetrafluoroethylene conduits have proven good long-term patency, Dacron (polyethylene terephthalate) prostheses are still infrequently applied, with, as yet, no information on the long-term patency. METHODS: All patients who received an extracardiac Dacron conduit (n = 12) were retrospectively studied. The initial conduit size was 16 mm in all recipients. The mean age at Fontan completion was 3.1 ± 0.7 years. Patients with clinical symptoms and/or significant conduit stenosis (>50% of diameter) underwent reoperation. RESULTS: Of the 12 patients, 8 underwent reoperation (75%) at a mean interval of 6.5 ± 1.8 years after the Fontan operation. All conduits were replaced by an 18-mm polytetrafluoroethylene graft. The explants showed ubiquitous tissue deposits on the inner surface, with a residual internal diameter from 8 to 11 mm. All patients survived the extracardiac conduit replacement. Recovery was uneventful, except that 1 patient experienced long-lasting pleural fluid drainage. The mean hospital stay was 10.6 ± 12.0 days. CONCLUSIONS: The incidence of extracardiac Dacron conduit stenosis in total cavopulmonary connection patients is high. These data indicate that the use of this type of conduit should be avoided. Vigilant follow-up is advised for those patients who have undergone Fontan completion with a Dacron extracardiac conduit.


Subject(s)
Blood Vessel Prosthesis Implantation/adverse effects , Blood Vessel Prosthesis Implantation/instrumentation , Blood Vessel Prosthesis , Fontan Procedure/adverse effects , Graft Occlusion, Vascular/epidemiology , Heart Defects, Congenital/surgery , Polyethylene Terephthalates , Child, Preschool , Constriction, Pathologic , Device Removal , Graft Occlusion, Vascular/diagnosis , Graft Occlusion, Vascular/surgery , Heart Defects, Congenital/physiopathology , Humans , Incidence , Length of Stay , Netherlands/epidemiology , Prosthesis Design , Reoperation , Retrospective Studies , Time Factors , Treatment Outcome
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