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J Thorac Cardiovasc Surg 1997;114:766-772
© 1997 Mosby, Inc.
SURGERY FOR ACQUIRED HEART DISEASE |
Received for publication May 6, 1997 accepted for publication June 5, 1997. Address for reprints: T. E. David, MD, 200 Elizabeth St., 13EN219, Toronto, Ontario, Canada M5G 2C4.
Abstract
Objective: The intervalvular fibrous body between the aortic and mitral valves can be damaged by infective endocarditis, degenerative calcification, or multiple previous heart valve operations, making double valve replacement difficult. We have managed this problem by approaching the aortic and mitral valves through the aortic root and the dome of the left atrium. After excising the aortic valve, the diseased fibrous body, and the mitral valve, we suture a properly tailored patch of Dacron fabric or bovine pericardium to the lateral and medial fibrous trigones and to the aortic root, reestablishing the aortic and mitral anuli. A prosthetic mitral valve is implanted and a separate patch is used to close the left atriotomy before implantation of a prosthetic aortic valve. This study was undertaken to determine the efficacy of this operation. Methods: Forty-three patients underwent reconstruction of the intervalvular fibrous body during aortic and mitral valve replacement because of infective endocarditis with abscess in 14 patients, extensive calcification in 9, lack of fibrous tissue because of multiple previous operations in 10, and to enlarge the aortic and mitral anuli in 10. The group comprised 18 men and 25 women with a mean age of 58 ± 12 years. Thirty-two patients had had one or more previous heart valve replacements. All patients were in New York Heart Association functional classes III and IV, and 9 patients were in shock before the operation. Results: Seven operative deaths occurred (16%). Early prosthetic valve endocarditis developed in two patients and necessitated reoperation. Follow-up extended from 4 to 108 months, with a mean of 38 months. No patient was lost to follow-up. Six late deaths occurred. The actuarial survival at 6 years was 56% ± 6%. A Doppler echocardiographic study revealed normal prosthetic valve function and anatomically intact anuli in all 30 long-term survivors. Conclusions: Reconstruction of the intervalvular fibrous body during aortic and mitral valve replacement is a satisfactory operative approach in patients with complex valve annular pathology.
The aortic and mitral valves are connected by a fibrous body that extends from the lateral to the medial fibrous trigones. This fibrous structure is seldom more than 1 cm in height, and from the ventricular side it is indistinguishable from the anterior leaflet of the mitral valve until the point where the noncoronary cusp of the aortic valve begins. From the atrial side, the dome of the left atrium is attached to it, separating the anterior leaflet of the mitral valve from the aortic root. This fibrous body may be damaged by infective endocarditis, degenerative calcification, or previous mitral valve replacement, making combined aortic and mitral valve replacement difficult.
1-8
Patients with rheumatic heart valve disease may have small aortic and mitral anuli partially as a consequence of inadequate growth or fibrotic contraction of the fibrous body. Double valve replacement in these patients is often complicated by patient-valve size mismatch.
9,10
This article describes our experience with aortic and mitral valve replacement in patients who needed reconstruction of the intervalvular fibrous body.
Patients and methods
From 1985 to 1996, 43 patients who needed aortic and mitral valve surgery were found to have a diseased intervalvular fibrous body.
Table I shows the clinical profile of these patients. The principal indication for operation was infective endocarditis in 14 patients (native valve in 3 and prosthetic valve in 11) and symptoms of congestive heart failure in 29. The offending microorganisms in patients with active infective endocarditis were staphylococci in 6 patients, streptococci in 5, and other bacteria in 3. The indication for reconstruction of the intervalvular fibrous body was abscess in 14 patients, extensive calcification of the mitral anulus and fibrous body in 9, lack of tissue to secure the prosthetic valves because of previous valve replacements in 10, and small aortic and mitral anuli in 10. Eleven patients had more than one of the aforementioned indications.
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Seven operative deaths occurred (16%), 2 caused by technical problems, 2 by myocardial infarction, 2 by multiorgan failure, and 1 by hemorrhagic stroke. Three of 14 patients with infective endocarditis died, and 5 of 9 patients in preoperative shock died. Postoperative complications included reexploration of the mediastinum for bleeding in 3 patients, insertion of a permanent transvenous pacemaker for heart block in 6, and early prosthetic valve endocarditis in 2 patients who did not have endocarditis before the operation. In both patients the patches and valves were successfully changed.
Operative survivors have been followed up from 4 to 108 months (mean 38 ± 29 months). No patient was lost to follow-up. Six late deaths have occurred, caused by cerebral bleeding in 1, late prosthetic valve endocarditis in 1 (patient refused reoperation), congestive heart failure in 2, and noncardiac causes in 2. The actuarial survival is shown in Fig. 6; it was 56% ± 6% at 6 years.
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Discussion
The surgical disease described in this study is uncommon. At the Toronto Hospital, where approximately 650 patients with heart valve disease are operated on annually, only 3 to 5 patients with aortic and mitral valve disease are found to have a damaged intervalvular fibrous body. The most common cause of damaged intervalvular fibrous body is infective endocarditis of the aortic and mitral valve with paravalvular abscess.
1,2 Only a few reports on the surgical treatment of abscess of the intervalvular fibrous body have been published.
3-5 In the present study, 14 patients had endocarditis of the aortic and mitral valve with an abscess in the intervalvular fibrous body. Eleven of 14 patients had prosthetic valve endocarditis. The radical resection of the abscess and reconstruction of the base of the heart with glutaraldehyde-fixed bovine pericardium and valve replacement cured the infection, and 11 operative survivors had normally functioning prosthetic valves during the years of follow-up.
Another uncommon pathologic process that makes mitral valve surgery difficult and hazardous is the so-called "horseshoe" calcification of the mitral anulus, which occasionally extends into the fibrous trigones and intervalvular fibrous body.
6,7 Although mitral valve repair is feasible in some of these patients,
7,8 when the calcification extends into the fibrous trigones and aortic valve, combined aortic and itral valve replacement is usually necessary. Of 9 patients with this disease, 6 of them had already had at least one previous mitral valve replacement elsewhere and were referred because of prosthetic mitral valve dehiscence. The calcium had not been removed in any of these 6 patients at the previous operations. We managed these patients by excising all calcified tissues and reconstructing the entire base of the left ventricle with bovine pericardium. One of these 9 patients required reoperation for early prosthetic valve endocarditis. He had had 4 mitral valve replacements elsewhere and the reconstruction of the base of the heart had been his fifth heart operation. The postoperative course after the sixth operation was stormy, but he survived and eventually did very well. The remaining 8 patients had uneventful postoperative courses and had normally functioning prosthetic valves at the most recent examination.
Reoperations for failed prosthetic heart valves are usually associated with increased operative mortality and morbidity because of advanced symptoms or complex anatomic factors, or both. One of these anatomic factors is a damaged valve anulus. This problem is often seen after multiple previous valve replacements or when the prosthetic valves have been in place for a long time, usually one or two decades. The intervalvular fibrous body becomes rigid and sometimes calcified, and it fractures as the valve sutures are placed or tied down. Although it is possible to secure the aortic valve prosthesis in the sewing ring of the mitral valve prosthesis in that area, we do not believe this should be done when mechanical valves are used. Inadequate intervalvular fibrous body was the indication for reconstruction in 10 patients in our series. Two of these patients died; both were in cardiogenic shock before the operation because of thrombosed mechanical valves.
Prosthetic valvepatient mismatch has been documented after aortic valve replacement.
9,10 It has been suggested by Dusmenil and associates
11 that the indexed prosthetic aortic valve area should not be less than 0.9 cm2/m2. This type of information is not available for mitral valve replacement, but we estimate that the indexed prosthetic mitral valve area should be 1.3 to 1.5 cm2/m2. Smaller prosthetic mitral valves are usually associated with symptoms of pulmonary congestion during exercise.
In 1979 Manouguian, Abu-Aishah, and Neitzel
12 described an experimental procedure whereby both the aortic and mitral anuli were enlarged by increasing the width of the intervalvular fibrous body. In a report on patch enlargement of the aortic anulus in 8 patients, Manouguian and Seybold-Epting
13 described the case of 1 patient who had severe mitral regurgitation after aortic valve replacement with enlargement of the aortic anulus and required mitral valve replacement 4 days later. Because the fibrous body had been divided at the initial operation, a Dacron patch was used to close the gap and to enlarge both the mitral and aortic anuli. We have performed this procedure in 10 patients who required aortic and mitral valve replacement and were found to have small anuli. All patients had rheumatic heart disease; 5 had had previous valve surgery and had prosthesis-patient mismatch; no patient had an aortic anulus larger than 19 mm, and 3 patients had a mitral anulus of 23 mm or less. After reconstruction of the intervalvular fibrous body, the prosthetic mitral valve implanted was 27 or 29 mm in all patients and the prosthetic aortic valve was 21, 23, or 25 mm, depending on the patient's body surface area, to prevent prosthesis-patient mismatch. Two patients died after the operation; operative survivors have had normally functioning prosthetic valves and adequate effective valve areas.
Combined aortic and mitral valve replacement with reconstruction of the intervalvular fibrous body is a long operation, particularly in patients who have had multiple previous heart valve operations. Long operations are associated with an increased risk of intraoperative contamination and perioperative bacteremia. Early prosthetic valve endocarditis developed in two of our patients. We ordinarily give prophylactic antibiotics for 24 hours after cardiac operations, but because of this study we changed our policy and will give intravenous antibiotics for at least 2 days in patients who undergo complex and long cardiac valve operations.
The approach used to treat this small number of patients with aortic and mitral valve disease and complex annular abnormalities was associated with high mortality and morbidity, but we believe that most of these patients would not survive conventional heart valve replacement.
Although we have concerns about the durability of glutaraldehyde-treated bovine pericardium as heart valve anuli because it may degenerate and the prosthetic valve may dehisce, it has been an excellent material for use in reconstructing the heart in patients with paravalvular abscess and has given very satisfactory midterm results.
1,8
Appendix: Discussion
Dr. Alain F. Carpentier (Paris, France).
The authors must be congratulated for bringing to our attention a very difficult problem for construction of the aortic-mitral junction when destroyed by infection or calcification. The type of reconstructive operation depended in their series on the extension of the lesions. For lesions limited to the aortic-mitral triangle, a simple triangular patch can be used. For lesions extending to the aortic and the mitral anulus, they used a large single patch of bovine pericardium in which an opening is made through which to place and secure a mitral valve prosthesis.
The first of these techniques is known and widely used by most surgeons with good results. The second, however, is a significant improvement over a similar technique described some 10 years ago, in which a large oval patch was sutured to the left atrial wall in the supraannular position. The technique proposed by these authors has a lower incidence of patch and valve dehiscence.
The most important difference is the fact that the authors propose to secure the patch to the left ventricle itself. This approach allows the surgeon to use a smaller patch and to secure the patch in a stronger area; therefore the risk of displacement of the mitral prosthesis and dehiscence of the patch is reduced.
It is probably appropriate to mention another alternative that I prefer to use in this difficult situation, which is used often in a homograft aortic valve with the mitral leaflet left attached to the aortic homograft. This anterior leaflet is used to reconstruct the junction, and then the mitral valve anulus is reconstructed with a sliding plastic repair of the left atrium secured to the upper limit of the ventricle.
I have three questions for Dr. Kuo. First, is your patch reinforced with a layer of Dacron fabric? Second, how do you minimize the motion of the mitral valve between systole and diastole to reduce the incidence of dehiscence, patch dehiscence or valve dehiscence? Third, why do you not use the homograft valve more often and use the mitral valve as a living tissue, particularly in patients with bacterial endocarditis?
Dr. Ratna A. Magotra (Bombay, India).
I would like to share the sentiments regarding some patients with rheumatic heart disease with mitral stenosis, aortic stenosis, and gross left ventricular hypertrophy.
In our experience, even after double valve replacement, it was not infrequent to have less than satisfactory regression of the left ventricle. These patients continued to have symptoms, with normally functioning prosthetic heart valves but very high transvalvular gradients.
The technique described by the authors has been successfully used to enlarge the mitral and aortic anuli so that larger prosthetic valves can be implanted.
My only question for Dr. Kuo concerns heart block. He describes six patients requiring permanent pacemakers, and I presume they include the two patients who had permanent heart block before the operation. Were there any instances of temporary heart block and, if so, how long did it last?
Dr. Kuo.
I would like to thank Professor Carpentier for his kind remarks. In answer to his first question, we did not use Dacron fabric for reinforcement.
Regarding his second question, the rocking motion of the mitral valve during systole and diastole does worry us a bit. Dr. David modified his technique to try to reduce this rocking motion by not leaving too much patch between the sewing ring and the newly reconstructed mitral anulus. Obviously this is a worry, but we have not had any periprosthetic leak as a result of that in the 30 patients who survived the operation.
Third, we have not actually used a homograft in this situation.
Regarding Dr. Magotra's question, I suspect that the poor regression of the left ventricular hypertrophy in her group of patients may be the result of patient-valve size mismatch. If too small a valve is used, the left ventricular hypertrophy does not regress as much, as is shown very nicely in patients who previously had stentless valves.
The six patients who had pacemakers all had complete heart block after the operation. That did not include the two patients with complete heart block who had a pacemaker in place before the operation.
Footnotes
Read at the Seventy-seventh Annual Meeting of The American, Association for Thoracic Surgery, Washington, D.C., May 4-7, 1997. ![]()
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