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Ann Thorac Surg 1998;66:1269-1272
© 1998 The Society of Thoracic Surgeons


Original articles: cardiovascular

Residual aortic valve regurgitation after aortic root remodeling without a direct annuloplasty

Carlo Bassano, MD, PhDa, Ruggero De Paulis, MDa, Alfonso Penta de Peppo, MDa, Antonio Tondo, MDa, Laura Fratticci, MDa, Giovanni M. De Matteis, MDa, Alessandro Ricci, MDa, Luigi Sommariva, MDa, Luigi Chiariello, MDa

a Department of Cardiac Surgery, Tor Vergata University, European Hospital, Rome, Italy

Accepted for publication April 28, 1998.

Address reprint requests to Dr Bassano, Cardiochirurgia, Università Tor Vergata, European Hospital, Via Portuense 700, 00149 Roma, Italy

Background. Aortic insufficiency secondary to degenerative aneurysms of the ascending aorta can be surgically treated with replacement of the valve or with remodeling of the aortic root.

Methods. In 15 patients who underwent aortic root remodeling from January 1994 to December 1996, we evaluated the postoperative aortic regurgitation and correlated it with several anatomic and functional variables. Operative success was defined as a residual aortic regurgitation less than or equal to 1 on a scale of 0 to 4.

Results. Root dimensions and aortic incompetence decreased significantly after the operation (p < 0.0001). The difference between preoperative and postoperative root diameters (p = 0.0006) and the presence of Marfan’s syndrome (p < 0.0001) were independently predictive of persisting significant aortic insufficiency. Operative success was obtained in patients with a difference between preoperative and postoperative root diameters smaller than 30 mm.

Conclusions. Aortic root remodeling is effective in reducing aortic regurgitation. Severe aortic root dilatation may result in excessive geometric alteration, leading to suboptimal results. The choice of a larger graft contributes to avoiding excessive geometric constraint of a profoundly diseased aortic root. Indication to undergo root remodeling should be evaluated cautiously in patients with Marfan’s syndrome.




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