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Ann Thorac Surg 1998;66:1571-1574
© 1998 The Society of Thoracic Surgeons

Surgical management of isolated congenital tricuspid regurgitation

Toshiyuki Katogi, MDa, Ryo Aeba, MDa, Tsutomu Ito, MDa, Tetsuya Goto, MDa, Yasunori Cho, MDa, Toshihiko Ueda, MDa, Shiaki Kawada, MDa

a Division of Cardiovascular Surgery, Keio University, Tokyo, Japan

Accepted for publication May 18, 1998.

Address reprint requests to Dr Katogi, Division of Cardiovascular Surgery, Keio University, 35 Shinanomachi, Shinjuku, Tokyo 160, Japan
e-mail: (katogi{at}mc.med.keio.ac.jp)

Background. Isolated congenital tricuspid regurgitation without downward displacement of the leaflet is a rare clinical entity. Degenerative cusps and lack of chordae may preclude valvuloplasty and require valve replacement.

Methods. Three consecutive patients with isolated congenital tricuspid regurgitation underwent surgical repair between May 1995 and April 1997. Their ages were 23, 15, and 8 years old. Tricuspid valvuloplasty was feasible in all of them, with use of a gathering suture of the anterior leaflet, artificial chordae implantation, and ring annuloplasty.

Results. All 3 patients survived and recovered well after the operation. The cardiothoracic ratios on their chest roentgenograms decreased from 0.64 to 0.52 in patient 1, from 0.58 to 0.48 in patient 2, and from 0.60 to 0.44 in patient 3. Postoperative echocardiograms showed competent tricuspid valves and the disappearance of regurgitation in all cases.

Conclusions. Although malformation of the valve is extensive in isolated congenital tricuspid regurgitation, application of artificial chordae with conventional valvuloplasty technique can avoid the use of prosthetic valves by establishing the competence of the tricuspid valve.




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