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J Thorac Cardiovasc Surg 1999;118:483-490
© 1999 Mosby, Inc.
SURGERY FOR ACQUIRED CARDIOVASCULAR DISEASE |
From the Department of Cardiothoracic and Vascular Surgery,a Department of Cardiology,b and the Department of Pathology,c All India Institute of Medical Sciences, New Delhi, India.
Address for reprints: A. Sampath Kumar, Professor, Department of Cardiothoracic and Vascular Surgery, All India Insitute of Medical Sciences, Ansari Nagar, New Delhi-110029, India.
| Abstract |
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| Introduction |
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| Patients and methods |
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Operative technique.
Intraoperative transesophageal echocardiography was performed for all patients. Surgical procedures were performed under moderately hypothermic (28°C) cardiopulmonary bypass. Antegrade cold blood cardioplegia (4°C) and topical cooling with ice slush was used for myocardial protection. If required, the mitral valve procedure was done first before the Ross procedure was begun.
The technique of autograft harvesting and insertion was essentially the same as mentioned by Oury and associates
11 and as described previously by us.
12 After the pulmonary artery was separated from the aorta, the pulmonary artery was opened transversely and the pulmonary valve was inspected. If found suitable, it was harvested and kept in the right ventricular cavity for further use. The diseased aortic valve was excised, and the right coronary ostium was separated as a button. The aortotomy incision was extended posteriorly on both sides to meet below the left coronary ostium. Thus the aorta was divided completely, leaving the left coronary ostium attached to a tongue of distal aortic wall. The autograft was inserted as in a root replacement. Proximally, the autograft was sutured to the aortic anulus with a triangulated running polypropylene suture. The left coronary sinus of the autograft was slit open to within 3 to 4 mm of the cusp to receive the tongue of the distal aorta containing the left coronary ostium. Distal aortic anastomosis was performed with running polypropylene suture. The right coronary button was implanted in the autograft. The right ventriclepulmonary artery continuity was re-established with either an antibiotic preserved (n = 47 patients) or cryopreserved pulmonary/aortic homograft (n = 55 patients).
In addition, 31 patients had 33 associated procedures: open mitral commissurotomy (n = 15 patients), mitral valve repair (n = 15 patients), tricuspid valve repair (n = 2 patients), and homograft mitral valve replacement (n = 1 patient). The technique of mitral valve repair has been described earlier.
13,14
The mean aortic crossclamp and cardiopulmonary bypass times for the isolated Ross procedure were 119.3 ± 24.6 minutes (range, 84-190 minutes) and 145.8 ± 26.3 minutes (range, 123-220 minutes), respectively. The mean ischemic and bypass times for the Ross procedure combined with mitral procedure were 134.3 ± 28.5 minutes (range, 110-228) minutes) and 167.3 ± 31.4 minutes (range, 141-276 minutes), respectively.
The autograft function was assessed intraoperatively by transesophageal echocardiography and subsequently by transthoracic/transesophageal echocardiography before discharge from the hospital. Echocardiographic assessment was performed subsequently at intervals of 6 months.
None of the patients with the isolated Ross procedure received anticoagulants or antiplatelet agents. Patients who had undergone mitral valve annuloplasty with a Teflon collar received antiplatelet therapy for 6 months.
All patients under 45 years of age and with rheumatic involvement were treated with antibiotic prophylaxis to prevent recurrence of rheumatic fever, using long-acting benzathine penicillin delivered intramuscularly every 3 weeks.
Statistical analysis.
For the purpose of analysis, patients have been divided into rheumatic and nonrheumatic groups, based on the cause of the aortic lesion. All the interval/ratio parameters are expressed as mean ± standard deviation, and the categoric variables are expressed as percentages. Acturial estimates have been calculated with the Kaplan-Meier technique
15 and are reported with standard error of the estimate. Comparison of these estimates among subgroups has been performed with the Mantel-Cox (log-rank) test.
16 Prognostic factors for late failure have been identified by Coxs proportional hazard model. All statistical analysis has been performed with the SPSS for Windows 6.0 software package (SPSS Inc, Chicago, Ill).
| Results |
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Early echocardiographic results.
In all patients, intraoperative transesophageal echocardiography revealed no or trivial AR. Two patients had mild (2/4+) mitral regurgitation. Transthoracic echocardiography performed before discharge from the hospital showed mild (2/4+) AR in 1 patient.
Late deaths.
There were 8 late deaths (7.8%). Infective endocarditis was the cause of death in 4 patients (2 patients underwent reoperation). One patient, who had undergone associated homograft mitral valve replacement, died after 6 months of mitral homograft failure. In another patient, the initial mitral valve repair failed; at reoperation, a partial mitral homograft replacement was performed. However, the mitral homograft failed and the patient died after 2 months. In an additional 2 patients (patients 1 and 13, Table II), the autograft failed and the patients died of congestive heart failure 24 and 5 months after the operation, respectively.
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Recurrent rheumatic fever.
Two boys (patients 1 and 4,Table II
), 11 and 13 years old, who had initially undergone the Ross procedure associated with mitral valve repair were admitted 8 and 12 months, respectively, after the operation with acute rheumatic activity and congestive heart failure. There was no history of joint pains in either of the patients. Erythrocyte sedimentation rate and antistreptolysin titers were raised significantly in both the cases. Both patients had experienced the development of severe AR and moderate-to-severe mitral regurgitation. The first patient had not complied with penicillin prophylaxis after the operation. The second patient was receiving regular penicillin prophylaxis. Both patients underwent decongestion and were discharged with advice for reoperation. Patient 1 died after 6 months; patient 4 underwent reoperation, and both the aortic and mitral valves were replaced with prosthetic valves.
In addition, 2 other patients (14 and 17 year olds, male) also had a history of joint pains and fever during their follow-up but did not have laboratory or clinical evidence of recurrent rheumatic activity at the time of examination.
Late echocardiographic follow-up.
Follow-up was 98% complete. Two patients in the rheumatic group were lost to follow-up. The remaining 93 patients (68 in the rheumatic group; 25 in the nonrheumatic group) underwent regular echocardiographic assessment. Follow-up ranged from 1 to 60 months (mean, 25.3-15.4 months).
Autograft function.
In the rheumatic group, 13 patients experienced the development of moderate (3/4+) or severe (4/4+) AR 8 to 48 months after the operation(Fig 1). This included the 2 patients who had recurrent rheumatic fever. In most, the significant (3-4/4+) AR developed 12 to 24 months after the operation. Two of these patients died, and 2 of the patients underwent reoperation. In addition, 7 other patients in the rheumatic group experienced the development of mild (2/4+) AR. Characteristically, all these patients were young (<30 years of age), and 10 of them also had multivalvular lesions at the time of the initial operation. Demographic and clinical profiles of patients with significant AR after operation and their echocardiographic findings are shown inTable II
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In the rheumatic group, various risk factors for late failure were analyzed separately and included age (<30 years vs >30 years), sex, chronologic order of surgery, associated mitral disease, associated tricuspid disease, previous cardiac procedure, and presence of congestive heart failure. Age less than 30 years (P = .001) and associated mitral valve disease (P = .04) were independent predictors of autograft failure. The Cox proportional hazard analysis was also used to predict the risk with age as continuous variable. The hazard function equation
h (t,xt) = ho(t) e0.114 x age
yielded a hazard risk of 0.89 (95% confidence limit, 0.81-0.98), suggesting a progressive decrease in the risk of autograft failure with advancement of age.
Mitral valve function.
In the rheumatic group, 29 survivors who had undergone an associated mitral valve procedure, 11 patients experienced significant mitral regurgitation; 3 patients underwent mitral valve replacement with a prosthetic valve, and 1 patient underwent a partial homograft mitral valve replacement. In 1 patient, the mitral homograft was inserted initially and failed after an interval of 6 months, leading to death.
Homograft function.
Significant right-sided homograft valve dysfunction (gradient, >40 mm Hg) was present in 3 patients. In 2 patients, gradients were located at the distal pulmonary anastomosis; in 1 patient it was located at the level of valve. One additional patient experienced moderate pulmonary regurgitation. In all 4 patients, a pulmonary homograft was used. All these patients are free of symptoms.
| Morphologic features of failed autografts |
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Microscopic examination.
Microscopic examination of explanted autograft cusps revealed valvular thickening, fibrosis, and an active chronic inflammation with remarkable small vessel and intimal proliferation(Fig 4). The neovascularization was most marked near the base of the cusps. The picture was compatible with valvulitis of rheumatic involvement.
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| Discussion |
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What could have led to autograft failure in patients with rheumatic conditions? Obviously, in patients where rheumatic valvulitis was demonstrated at reoperation, recurrence of the rheumatic activity was the cause of autograft failure. In some of the reported cases,
5,6,8,9 there was history and laboratory evidence suggesting recurrence of rheumatic fever. Two of our patients in whom the autograft failed also had recurrent rheumatic fever. One of these patients showed evidence of rheumatic valvulitis at reoperation. In underdeveloped countries, a typical history suggestive of rheumatic fever may not always be present, and the patient may directly have features of carditis.
18 This was also observed in patient 2. The patient had demonstrable rheumatic valvulitis at reoperation but never gave a history suggestive of rheumatic fever after the initial Ross procedure. The involvement of the pulmonary valve in the chronic rheumatic process is rare.
19-21 Involvement in the chronic rheumatic process appears to be related to the mechanical force the valve faces during its closed state. This is the highest in the mitral valve and the lowest in the pulmonary valve. Somehow, when the pulmonary autograft is transplanted to the aortic position, it becomes susceptible to chronic rheumatic involvement. However, when there is severe pulmonary hypertension, the pulmonary valve is still free from rheumatic involvement in its native position.
In 1 of the reported cases,
5,6 recurrence of rheumatic activity was attributed to the cessation of penicillin prophylaxis. This was the case with 1 of our patients also. But another 3 of our patients who received regular prophylaxis also experienced recurrent rheumatic activity. Halees and colleagues
8 have also questioned the compliance to and efficacy of penicillin prophylaxis. This may be partly due to the failure of penicillin prophylaxis as a result of higher infection rates in a malnourished population who live in very over-crowded conditions.
18,22,23
Characteristically, among the rheumatic group, all the patients with a failed autograft were young (<30 years of age). Because rheumatic fever is more prevalent in a younger population,
18,22-24 this further supports the possibility of recurrent rheumatic activity in this subgroup of patients. However, if all the failures are related to recurrent rheumatic activity, the incidence of relapse becomes unacceptably high. There may be some other mechanism by which autografts fail in patients with rheumatic etiology. It is possible that pulmonary valves that appear grossly normal at operation and echocardiographically may have been affected microscopically during recent rheumatic activity; and when subjected to higher stress in the aortic position, these valves develop pathologic changes and fail.
Most of the investigators have attributed the autograft failure mainly to technical errors during the learning curve.
25,26 This does not appear to be the case in our series. In all the patients except 1, who experienced the development of significant AR, there was no or trivial regurgitation at the time of discharge from the hospital. Only 1 patient had mild AR. It was only in the subsequent time course that these patients experienced the development of progressively significant AR. In our series, autograft failure is exclusively limited to the rheumatic population and is evenly distributed chronologically. These facts suggest that technical errors during the learning curve were not responsible for autograft failure in our patients.
We have used a root replacement technique for pulmonary autograft insertion in which a tongue of the posterior wall of the aorta with the left main coronary artery was left behind while the aorta was divided posteriorly. This tongue of aortic wall was sutured to the left pulmonary sinus. This technique carries a potential risk of altering the geometry of the sinotubular junction of the pulmonary root and may predispose to subsequent AR. In our experience, patients with both rheumatic and nonrheumatic etiology had identical technique, and thus the use of this technique could not explain the occurrence of significant AR in the patients with rheumatic etiology alone.
Investigators
8,9 have found that preoperative AR is a common accompaniment to subsequent autograft failure. Although, in all our patients with a failed autograft, AR was the predominant physiologic lesion, we failed to attach any significance to it. This may be because of the fact that in our experience all young patients with rheumatic pathogenesis had predominant AR.
Coexisting mitral valve pathologic feature is a serious concern in the rheumatic population. Associated mitral valve disease that requires a surgical procedure at the time of the initial procedure was a strong predictor of autograft failure. Among 29 survivors who underwent an associated mitral valve procedure, 10 patients (35%) experienced autograft failure. Similarly, of 13 patients with a failed autograft, 10 patients (76%) had undergone a concomitant mitral valve procedure. The high incidence of failed mitral valve procedure in these patients, in itself, is an important cause of morbidity and reoperation and thus limits the usefulness of the Ross procedure in this subgroup.
Considering the poor results in young patients with rheumatic etiology (<30 years of age), we have abandoned the use of the Ross procedure in this subgroup of patients. Similarly, coexisting mitral disease, usually present in the younger subgroup, also disfavors the Ross procedure.
| Acknowledgments |
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| References |
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