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Fontan's procedure in two stages.

Abstract

Since 1985, 381 patients with various cardiac malformations that share the central common feature of only one effective ventricle have been treated with some modification of Fontan's operation. Since 1989, the Fontan operation has been staged by associating the superior vena cava with the branch pulmonary arteries (hemi-Fontan) initially followed, some months later, by associating the inferior vena cava to the branch pulmonary arteries (completion Fontan). The difference in early mortality for a primary-Fontan operation (16%) compared with a completion-Fontan operation (7%) is substantial (p < 0.05). Since January 1991, mortality associated with the hemi-Fontan operation has been 5.5% (7 deaths in 127 patients). A systematic staged approach to Fontan's operation has been undertaken with a hemi-Fontan operation in patients who are 6 months of age and a completion Fontan operation when those patients are 12 to 18 months of age in an effort to reduce the volume load of the ventricle as early as possible, to minimize intermediate mortality from the palliated state, and to reduce the impact of rapid changes in ventricular geometry and diastolic function that can accompany either the hemi-Fontan or primary Fontan operation, but that are lethal only after a primary Fontan operation.

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BibTeXRIS

W I Norwood, M L Jacobs. 1993. Fontan's procedure in two stages.. https://doi.org/10.1016/s0002-9610(05)81151-1

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Morphologic features of the uniatrial but biventricular atrioventricular connection.

OBJECTIVES: Hearts with an absent atrioventricular connection and a straddling of the solitary atrioventricular valve are rare but significant lesions. They are suitable only for Fontan-like palliation, in which atrioventricular valvar abnormalities play a significant role in determining the outcome. We studied the segmental arrangements in such lesions and clarified the valvar morphology, particularly its surgical implications. METHODS: We made a macroscopic review of all specimens with an absent atrioventricular connection and a straddling atrioventricular valve that were held in the collections of 3 institutes. We included only those specimens with the straddling valve supported exclusively by either the right-sided or left-sided atrioventricular junction and excluded those with a common atrioventricular junction. RESULTS: We found 11 hearts with an absent right atrioventricular connection and a straddling left atrioventricular valve, and 3 with an absent left atrioventricular connection and a straddling right atrioventricular valve. Most had right-hand ventricular topology and discordant ventriculoarterial connections. We found multiple valvar abnormalities, including dysplastic leaflets, short cords, abnormal attachments, and abnormal papillary muscles. The most consistent features were a line of maximal coaptation between the bridging leaflets always perpendicular to the plane of the ventricular septum and a free-floating bridging anterosuperior leaflet. CONCLUSIONS: Straddling of a solitary atrioventricular valve with an absent atrioventricular connection produces a uniatrial but biventricular connection. In this setting, the valve guarding the abnormal solitary atrioventricular junction cannot be classified morphologically as mitral or tricuspid. The markedly variable valvar morphology likely makes these valves prone to insufficiency in the long term.

Heart Defects, Congenital↗