Use of aortic wall patches as leaflet replacement material during aortic valve repair.

Objectives: Aortic valve repair can be limited by inadequate leaflet tissue for proper coaptation. Various kinds of pericardium have been used for cusp augmentation, but most have failed because of tissue degeneration. A more durable leaflet substitute is needed. Methods: In this report, 8 consecutive cases are presented in which autologous ascending aortic tissue was used to augment inadequate native cusps during aortic valve repair. Biologically, aortic wall is a living autologous tissue that could have exceptional durability as a leaflet substitute. Techniques for insertion are described in detail, along with procedural videos. Results: Early surgical outcomes were excellent, with no operative mortalities or complications, and all valves were competent with low valve gradients. Patient follow-up and echocardiograms to a maximum of 8 months' postrepair remain excellent. Conclusions: Because of superior biologic characteristics, aortic wall has the potential to provide a better leaflet substitute during aortic valve repair and to expand patient categories amenable to autologous reconstruction. More experience and follow-up should be generated.

Conversion of the atriopulmonary Fontan connection to a total cavopulmonary connection.

Right atrial-to-pulmonary artery anastomosis (modified Fontan-Kreutzer operation) often results in substantial enlargement of the right atrium over time. Massive right atrial dilatation can cause loss of laminar flow, stasis, compression of the right pulmonary veins posteriorly, and leftward shift of the atrial septum. Some patients may develop arrhythmias related to atrial distension and multiple suture lines. Chronic elevation of the central venous pressure may cause liver dysfunction and/or protein-losing enteropathy in some patients. Some patients with atriopulmonary Fontan connections who develop a decline in functional status may benefit from conversion to a total cavopulmonary connection. Patients with significant ventricular dysfunction can usually only be treated by cardiac transplantation. However, other problems may be successfully managed by revision of the atriopulmonary Fontan connection to a total cavopulmonary anastomosis. Conversion to a total cavopulmonary connection should improve cardiac output by restoring laminar flow, by relieving compression of the right pulmonary veins, and by alleviating the leftward displacement of the atrial septum. Copyright 1998 by W.B. Saunders Company