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J Thorac Cardiovasc Surg 2003;125:423-425
© 2003 The American Association for Thoracic Surgery
Brief Communications |
From the Pediatric Cardiac Surgery Department, Children's Hospital La Fe,a Valencia, and Children's Hospital Sant Joan de Deu,b Barcelona, Spain.
Received for publication July 12, 2002. Accepted for publication July 18, 2002. Address for reprints: José M. Caffarena, MD, PhD, Pediatric Cardiac Surgery Department, Hospital Infantil La Fe, C/ Avda de Campanar s/n, 46009 Valencia, Spain (E-mail: josecaffarena{at}telefonica.net).
Tunnel-type subaortic stenosis with aortic valve involvement combined with mitral stenosis and annular hypoplasia, frequently seen with Shone anomaly or related conditions, may have a severe presentation in infancy, with aortic valvulotomy and mitral valve replacement being necessary at an early age.
1 These patients subsequently may have severe gradients across the mitral prosthesis because of body growth, along with frequent complex aortic obstructions that are aggravated by the protrusion of the mitral prosthesis into the left ventricular outflow tract.
Faced with the seeming inevitability of performing a double mitral-aortic valve replacement, we developed an alternative technique that enlarges the mitral annulus, allowing the accommodation of a prosthesis of a greater size and at the same time resolving the complex aortic obstruction. The objective is to minimize the use of prosthetic material and to use autologous tissue in these growing children.
Method
We use deep hypothermic cardiopulmonary bypass. After aortic crossclamping, blood cardioplegic solution is administered through the aortic root. The retrograde route is used for dose maintenance. The aorta is sectioned along the commissural plane, and the aortic valve is resected, with extraction of coronary arteries and a generous circumference of aortic wall. The free wall of the right atrium is opened and extended over the base of the right atrial appendage toward the interatrial septum and roof of the left atrium.
The interatrial septum is cut longitudinally, and the mitral valve, whether native or prosthetic, is removed. On the remnant of the aortic annulus an incision is made on the noncoronaryleft coronary commissure, connecting it with the incision on the roof of the left atrium. The pulmonary autograft is obtained with a double muscular flap, anterior from the free wall and posterior from the septum of the right ventricular infundibulum up to the level permitted by the conal septum (Figure 1). The intercoronary commissure is then opened toward the interventricular septal muscle up to the subaortic obstruction level. The autograft can now be implanted to the base of the enlarged aortic root. The autograft is sutured to the aortic root with the posterior flap for the ventriculoseptoplasty and the anterior muscle flap to enlarge the mitral annulus, with the suture continued along the borders of the incised roof of the left atrium (Figure 2). The new mitral prosthesis is sutured to the muscle of the autograft and to the rest of the mitral annulus. The coronary arteries are then reimplanted in the autograft, and it is subsequently anastomosed to the distal aorta. The procedure is concluded with a cryopreserved pulmonary homograft to reestablish ventriculopulmonary continuity.
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Currently the extended replacement of the aortic root with a pulmonary autograft, the Ross-Konno procedure, is the technique of choice in complex aortic obstructions.
2 However, there have been few solutions described for simultaneous annular enlargement and mitral valve replacement in these patients. The mitral prosthesis in supra-annular position
3 and the Konno aortoventriculoplasy with mitral valve replacement,
4 the techniques most frequently used, are both associated with elevated mortality. Jonas and associates
5 in 1998 described a new technique of mitral annular and left ventricular outflow tract enlargement that but preserved the aortic valve.
The technique that we describe here is original and has a clear indication for patients with complex subaortic obstruction who also require mitral-aortic double-valve replacement. The use of this technique has allowed us to implant prostheses 4 to 5 mm larger than the mean size of the native mitral annulus, avoiding protrusion of the prosthesis into the left ventricular outflow tract, which is naturally reconstructed with the extended pulmonary autograft.
The two major complications in relation to the technique described are bleeding and complete block of cardiac conduction. Bleeding may be reduced by strengthening the suture proximal to the autograft with separate stitches supporting polytetrafluoroethylene patches and by reinforcing the posterior muscle of the autograft with a limited band of autologous pericardium. The unclamping of the aorta before placement of the pulmonary homograft allows us to locate and control any hemorrhage with greater ease.
The high incidence of complete block in these patients is related to the ventriculoseptoplasty and the proximal suture of the autograft. To avoid this complication, we must orient the ventriculoseptoplasty from the intercoronary commissure distally to the left, confining it to the severity of the subaortic obstruction.
The initial results in these 2 cases encourage us to propose this technique as an alternative of choice for mitral-aortic double-valve replacement in this difficult group of patients.
References
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