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Ann Thorac Surg 1998;65:1377-1380
© 1998 The Society of Thoracic Surgeons
a Department of Cardiovascular Surgery, National Cardiovascular Center, Osaka, Japan
Accepted for publication September 10, 1997.
Address reprint requests to Dr Yagihara, Department of Cardiovascular Surgery, National Cardiovascular Center, 2-5-1 Fujishirodai, Suita, Osaka, 565 Japan
| Abstract |
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Methods. Three patients with isolated congenital mitral regurgitation underwent mitral valve repair with use of expanded polytetrafluoroethylene sutures as artificial chordae.
Results. There have been no late deaths and no valve-related complications. Serial follow-up echocardiographic examinations have not revealed any increase in the severity of mitral regurgitation with continuing patient growth up to 39 months after the operation.
Conclusions. When combined with other conservative methods of mitral valve repair, chordal replacement with expanded polytetrafluoroethylene sutures in children undergoing mitral valve reconstruction produces good short-term results. We believe that it delays and possibly prevents the need for a mechanical prosthesis with its associated complications in this young patient population.
| Introduction |
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| Material and methods |
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Patient 2
A 4.6-year-old girl had a cleft on the anterior mitral valve leaflet. There was no chorda attached to this area. One elongated primary chorda was found on the anterolateral side of the cleft. The mitral valve annulus was dilated. The cleft was closed with interrupted sutures and 4-0 ePTFE suture was attached at the free margin of this area. Chordal shortening and bilateral mitral annuloplasty also was performed by Reed-type commissuroplasty, and the diameter of the mitral annulus was reduced from 27 mm to 19 mm, which was 119% of the normal mitral valve diameter calculated from the body surface area.
Patient 3
A 5.1-year-old boy had only one thickened dysplastic chorda on the anterolateral side of the anterior mitral valve leaflet, which restricted the motion of the leaflet. The anterolateral areas of both the anterior and posterior leaflets were sclerosed. Mobilization of the anterior leaflet was obtained by resection of the abnormal chorda, which was replaced with 4-0 ePTFE suture. Unilateral annuloplasty was performed, folding the sclerotic posterior leaflet by Reed-type commissuroplasty, and the diameter of the mitral annulus was reduced from 31 mm to 22 mm, which was 116% of the normal mitral valve diameter calculated from the body surface area.
| Results |
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Follow-up of the patients ranged from 17 to 39 months. There were no late deaths, no thromboemboli, no anticoagulant-related hemorrhages, and no cases of infective endocarditis. All the patients underwent cardiac catheterization before and 1 year after the operation. Left ventricular angiography showed a totally competent mitral valve in patient 2 and mild mitral insufficiency in patients 1 and 3. Left ventricular volume had returned to normal in all the patients. Serial follow-up echocardiographic examinations have revealed no increase in the severity of mitral regurgitation with continuing patient growth (Fig 2). All the patients have good activity levels without cardiac medication.
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| Comment |
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Chordal reconstruction with ePTFE sutures is a well-established technique for the correction of mitral insufficiency in adults [57]. We have used this technique in adult patients with mitral valve insufficiency with satisfactory intermediate results [8]. In this report, we describe the early results of this technique used in pediatric patients with various congenital malformations of the mitral valve.
The early postoperative results have been satisfactory. However, the long-term results have not yet been confirmed, particularly in terms of the reliability of ePTFE sutures as substitute chordae and their continued function as the patients grow.
Expanded polytetrafluoroethylene has been reported to be a reliable material for the replacement of mitral valve chordae [9]. In a clinical study, Zussa and associates [7] reported that ePTFE was not associated with either thromboembolic events or degeneration of the material. At reoperation 18 months and 2 years after the initial procedures, these investigators found the artificial chordae covered with fibrous tissue with no evidence of thrombi or calcification. Although the process of fibrous overgrowth has been reported to be slow in adults, the rates of fibrous overgrowth and calcification are not known in pediatric patients.
Theoretic concern exists over the possibility of relative shortening of chordae replaced with ePTFE as the patient grows, resulting in mitral regurgitation. In our limited experience over 3 years, no increase in the severity of mitral valve regurgitation has been detected in patients 1, 2, and 3, who have increased in body weight from 8.7 to 11.8 kg, 11.0 to 14.5 kg, and 22.5 to 35 kg, respectively (Fig 2). Two of our patients have shown dramatically decreased ventricular volume 1 year after the operation, but long-term changes in the longitudinal dimension of the left ventricle and their impact on mitral valve function after repair with the use of artificial chordae are uncertain. We would expect that the effect of relative shortening of the artificial chordae would be compensated for by growth or elongation of the papillary muscle or the mitral valve leaflet tissue, but further follow-up is needed to evaluate the long-term outcome.
We conclude that the short-term results of chordal replacement with ePTFE in children undergoing mitral valve reconstruction are satisfactory. We believe that when this technique is combined with other conservative methods of mitral valve repair, it delays and possibly prevents the need for a mechanical prosthesis with its associated complications in this young patient population.
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