|
|
||||||||
J Thorac Cardiovasc Surg 2000;119:210-220
© 2000 Mosby, Inc.
SURGERY FOR ACQUIRED CARDIOVASCULAR DISEASE |
From the Divisions of Cardiovascular Surgery and Cardiology of Toronto General Hospital and University of Toronto, Toronto, Ontario, Canada.
Address for reprints: Tirone E. David, MD, 200 Elizabeth St13EN219, Toronto, Ontario, Canada M5G 2C4 (E-mail: tdavid{at}torhosp.toronto.on.ca) .
| Abstract |
|---|
|
|
|---|
| Introduction |
|---|
|
|
|---|
A referral of an outside patient in whom a pulmonary autograft aneurysm and severe AI developed after the Ross procedure prompted us to review our experience to determine the magnitude of this problem and the factors that may play a role in dilation of the pulmonary autograft.
| Patients and methods |
|---|
|
|
|---|
|
The pulmonary autograft was implanted inside the aortic root in the subcoronary position in 2 patients. The root inclusion technique was used in 45 and root replacement in 71. A strip of Teflon felt was not used in the annular or distal anastomoses of the pulmonary autograft with the aortic anulus or the ascending aorta.
The right ventricular outflow tract was reconstructed with a pulmonary valve homograft in all but the first patient of this series, who had an aortic valve homograft. Table II summarizes the operative data.
|
All operations were performed with transesophageal Doppler echocardiography. All patients had a transthoracic echocardiogram 1 week after the operation, and 82 patients had an echocardiogram at our hospital during the last follow-up visit for the purpose of this study. The diameters of the aortic anulus, sinotubular junction, and sinuses of Valsalva were measured. Echocardiographic examinations from other institutions were also reviewed but only used for measurement of the diameter of the sinuses of Valsalva.
It is not possible to accurately measure the diameters of the aortic anulus and sinotubular junction with echocardiography soon after the Ross procedure because of edema, hematoma, and other factors related to the trauma of the operation. An experienced sonographer measured both the internal and external diameters of the aortic anulus and of the sinotubular junction. These diameters were compared with those obtained by direct measurement during the operation. The external diameters were larger and the internal diameters were smaller than those obtained during the operation. The mean values between the internal and external diameters were 1 to 3 mm smaller than those obtained during the operation. For this reason, the mean values were used as early diameters of the aortic anulus and sinotubular junction. Only the internal diameters were measured in the late echocardiographic studies.
Statistical analysis.
Data were managed in dBASEIV data sets and analyzed with the SAS for PC statistical program (SAS Language Guide for Personal Computers, SAS Institute Inc, Cary, NC, 1988).
Data are presented as means ± standard errors in text and figures and as mean ± standard deviation in tables. The early and late diameters of the pulmonary autograft were evaluated by two methods. Analysis of covariance was used to evaluate the main effects of operative technique (aortic root inclusion vs aortic root replacement), time, and the interaction of technique versus time. PROC MIXED was also used as corroborating longitudinal analysis. Statistical significance was set at
= .05.
Time-related events such as late survival, reoperations, and development of AI were calculated by the Kaplan-Meier method.
| Results |
|---|
|
|
|---|
The diameter of the sinuses of Valsalva increased from 31.4 ± 0.4 mm to 33.7 ± 0.5 mm (P = .01), as illustrated in the upper panel of Fig 1. Analysis of covariance showed a significant change over time in the diameter of the sinus of Valsalva, as well as a significant difference between operative techniques, with replacement associated with a higher risk of dilation as shown in the lower panel of Fig 1
. The diameter of the sinuses of Valsalva increased from 32.2 ± 0.5 mm to 35.0 ± 0.6 mm in patients who had the technique of aortic root replacement and from 30.2 ± 0.5 mm to 31.5 ± 0.8 mm in those who had the technique of aortic root inclusion. Table III shows the results of the mixed linear model.
|
|
|
|
The diameter of the aortic anulus decreased from 26.2 ± 0.3 mm to 23.6 ± 0.4 mm (P < .01). The upper panel of Fig 2 shows the changes in diameter of the aortic anulus in all patients, and the lower panel shows the changes in patients who had the Ross procedure (done by two different operative techniques). There was no significant time or operative difference in the change in the aortic anulus diameter by PROC MIXED (Table IV
), but there was a significant time effect by analysis of covariance (P = .004, lower panel of Fig 2
).
|
The upper panel of Fig 3 shows the diameters of the sinotubular junction of all 82 patients studied. It measured 29.1 ± 0.3 mm early and 29.1 ± 0.6 mm in the late postoperative period. The lower panel of Fig 3
shows the diameters of the sinotubular junction in patients who had the technique of aortic root replacement (29.5 ± 0.4 mm early and 30.6 ± 0.8 mm late) and the technique of aortic root inclusion (28.7 ± 0.5 mm early and 26.7 ± 0.8 mm late). There was a significant interaction between time and operative technique for the change in the diameters of the sinotubular junction (Table V
and lower panel of Fig 3
). The technique of aortic root replacement was associated with increased dilation over time.
|
Reoperations on the pulmonary autograft.
Four patients have required reoperation on the pulmonary autograft. In the first patient, moderate AI developed as a result of acute dilation of the entire pulmonary autograft 2 weeks after aortic root replacement. He underwent re-replacement of the aortic root with an aortic homograft.
In the second patient, who had had aortic root replacement, a false aneurysm developed between the mitral valve and the pulmonary autograft without AI. This was diagnosed on a routine echocardiographic examination. The false aneurysm was successfully repaired with preservation of the pulmonary autograft.
A third patient had partial detachment of the proximal suture line of the pulmonary autograft and moderate AI, which were detected on a routine echocardiographic study 3 years after the operation. The technique of aortic root inclusion had been used. Dilation of the aortic anulus was thought to be the cause of this complication. This patient had aortic valve replacement with a mechanical valve.
A fourth patient needed mitral valve repair for mitral regurgitation resulting from advanced myxomatous disease of both leaflets 5 years after aortic root replacement with a pulmonary autograft. The mitral valve repair failed and since he had moderate AI and a dilated pulmonary autograft at 45 mm, both the mitral and the aortic valves were replaced.
These 4 patients survived reoperation. The freedom from reoperation on the pulmonary autograft was 91% ± 5% at 6 years.
AI.
Transthoracic Doppler echocardiography in 117 patients before hospital discharge revealed no AI in 24 patients, trivial AI in 81, mild AI in 11, and moderate in 1. At the most recent study in 116 patients, including those echocardiograms done before reoperations on the pulmonary autograft, there was no AI in 18 patients, trivial in 59, mild AI in 32, and moderate in 7. Three of the 7 patients with moderate AI have undergone replacement of the pulmonary autograft (described earlier).
All patients with moderate AI had dilation of the aortic anulus and/or sinotubular junction. We could not establish a relation between the degree of dilation and the development of AI.
The freedom from moderate AI including patients who had reoperations was 92% ± 3% at 6 years.
Functional status.
At the latest follow-up visit, 113 patients were alive with their pulmonary autograft in place. Of those, 110 had no cardiac symptoms and were in New York Heart Association functional class I, and 3 patients were in functional class II.
| Discussion |
|---|
|
|
|---|
Our study indicates that the pulmonary autograft dilates in certain patients with bicuspid and other congenital aortic valve anomalies. We found that the technique of aortic root replacement was associated with a higher risk of dilation of the sinuses of Valsalva and sinotubular junction than the technique of aortic root inclusion. As expected, the operative technique had no effect on annular dilation. Unfortunately, our patients had only one early and one late measurement of the pulmonary autograft and it was not possible to determine other predictors of dilation. For the same reason, Figs 1
through 3
showed linear changes in the diameters of the pulmonary autograft, which in fact may be nonlinear.
Hokken and associates
13 measured the diameters of the pulmonary autograft with echocardiography at various time intervals after the Ross procedure and found a significant increase in the diameters of the aortic anulus and sinuses of Valsalva. In most cases, dilation occurred during the first 10 postoperative days. During a mean follow-up of 2.3 years, the aortic anulus increased from 26.4 mm to 31.5 mm in 22 patients, and the diameter of the sinuses of Valsalva increased from 36.5 mm to 43.9 mm in 17 patients.
13 Although those investigators claimed that no patient had severe AI develop (they did not address the issue of dilation of the sinotubular junction) and none required a reoperation, some of their patients had a pulmonary autograft with a transverse diameter of 55 mm. By most surgeons criterion, an aortic root of 55 mm is an aneurysm that warrants surgical repair.
10
Dilation of the pulmonary autograft is probably the most common cause of failure of the Ross procedure.
8,14,15 Moritz and associates
14 reduced the diameter of the aortic anulus and wrapped the pulmonary autograft with an absorbable mesh in a few patients as an attempt to prevent postoperative AI. Pacifico and colleagues
15 described an operative technique whereby the entire pulmonary autograft was wrapped with glutaraldehyde-fixed bovine pericardium to prevent dilation. Elkins, Lane, and McCue
8 reported a freedom from reoperation on the pulmonary autograft of 92% ± 3% at 5 years. Eleven of 206 patients who had the Ross procedure required reoperation on the pulmonary autograft from 2 to 62 months after the operation.
8 Those investigators believed that annular dilation was the principal cause of AI in 6 of their patients.
We initially believed that dilation of the pulmonary autograft occurred because of mismatch between the diameters of the anulus and sinotubular junction of the aortic root and those of the pulmonary root.
12 This happened early on in our experience with the Ross procedure when a fairly acute dilation of the pulmonary autograft and AI developed in a patient.
12 We solved the problem of early dilation of the annular and sinotubular junction and AI by surgically reducing the diameters of the aortic anulus and ascending aorta to that of the pulmonary root.
12 However, continued follow-up of our patients revealed that these surgical maneuvers did not prevent late dilation of the pulmonary autograft in certain patients with bicuspid and other congenital aortic valve disease.
It has been demonstrated that dilation of the sinuses of Valsalva without concomitant dilation of the sinotubular junction does not cause AI.
9,10 That is why patients with isolated sinus of Valsalva aneurysm do not have AI. Dilation of the sinotubular junction causes AI because it pulls the commissures of the aortic valve away from the center of the aortic root, preventing coaptation of the cusps.
9,10 Dilation of the aortic anulus can also cause AI because it flattens the scalloped shape of the aortic anulus, preventing coaptation of the cusps.
10
The diameters of the sinotubular junction and of the aortic anulus are related to the size of the aortic valve cusps.
10,11 The components of the pulmonary root have the same geometric relationships as the aortic root.
10-12 Thus the diameter of the sinotubular junction and the diameter of the pulmonary anulus are related to the size of the pulmonary cusps. Although it is difficult to measure the diameter of the pulmonary anulus because it is attached to distensible right ventricular muscle, the diameter of the sinotubular junction can be easily measured with metric sizers. The geometric relationship between these two components in a semilunar valve indicates that the diameter of the anulus is approximately 10% to 20% larger than the diameter of the sinotubular junction.
10,12 The diameter of the aortic root should also be measured during the performance of the Ross procedure. We firmly believe that mismatch between the diameters of the aortic root and of the pulmonary root causes AI.
12 For this reason, the aortic anulus should be reduced to the diameter of the pulmonary anulus if it is larger, and the same principle applies to the sinotubular junction.
We have not used a Teflon strip to buttress the proximal or distal anastomoses of the pulmonary autograft. However, our data suggest that it may be safer to do so to prevent dilation of the aortic anulus, as well as of the sinotubular junction. This maneuver would prevent dilation of the aortic anulus and sinotubular junction but would not prevent dilation of the sinuses of Valsalva when the Ross procedure is performed by the technique of aortic root replacement. We showed that the technique of aortic root inclusion prevents or at least retards dilation of the sinuses of Valsalva and sinotubular junction. This operative technique is more complex than the one of aortic root replacement because the autograft has to be perfectly aligned within the aortic root to prevent AI. In addition, fixation of the aortic anulus with a strip of Teflon is not advisable because it alters the geometry of the anulus of the pulmonary valve when the inclusion technique is used. The aortic anulus can be fixed with a strip of Dacron fabric applied on the outside of its fibrous component.
12 These are probably the reasons why Elkins and associates
5 found the technique of aortic root inclusion to be associated with a higher risk of AI than the technique of aortic root replacement, which they recommended. Presently, most surgeons prefer the technique of aortic root replacement when performing the Ross procedure.
6
Bicuspid aortic valve is the most common cause of aortic valve disease in children and young adults in North America.
16-19 Young patients with bicuspid aortic valve frequently have a dilated aortic root because of premature degenerative disease of the aortic root and ascending aorta.
16,20 Erdheims cystic medial necrosis has been described in the arterial wall of the ascending aorta and pulmonary artery in these patients.
19,20 We found that degenerative changes in the media of the pulmonary artery are common in normal subjects, but they are more severe in patients with bicuspid aortic valve disease than in those with normal or diseased tricuspid aortic valve.
20 The pulmonary root may have inadequate elastic fibers and fibrillin in its media to adapt itself to the mechanical stress of the aortic root. For these reasons, it may be more appropriate to use subcoronary implantation to perform the Ross procedure when the pulmonary and the aortic roots have similar geometry and the aortic root inclusion technique in patients in whom the aortic root is larger than the pulmonary root. In these patients, a band of Dacron fabric should probably be used on the outside of the aortic anulus and the sinotubular junction to prevent late dilation. Fixation of these structures with Dacron fabric may be inappropriate in children.
| Limitations of the study |
|---|
|
|
|---|
Most of our patients had congenital aortic valve disease, an entity that is often associated with premature degenerative changes of the ascending aorta and pulmonary artery,
19,20 and our conclusions are valid only for this patient population. Finally, all operations were performed by a single surgeon who has a certain bias regarding the functional anatomy of the aortic and pulmonary roots and may have introduced confounding factors that could not be assessed.
| Appendix: Discussion |
|---|
|
|
|---|
In a presentation before this Association 3 years ago, Dr David postulated that correction of any substantial geometric mismatch between the aortic and pulmonary valves would prevent AI. He and his colleagues reduced the diameter of the aortic anulus, the sinotubular junction, or both, in approximately two thirds of their patients. Despite these reductions, further follow-up has demonstrated dilatation, which is defined as an increase in diameter of the sinotubular junction and/or sinuses of Valsalva by serial echocardiographic studies. In both of these locations the dilatation occurred with approximately equal frequency whether or not the patient had reduction of the aortic anulus and/or the sinotubular junction. Not surprisingly, use of the root inclusion technique was protective against dilatation of the sinotubular junction and the sinuses, and Dr David recommends use of this technique whenever possible. It is of interest, however, that one of the three reoperations for AI occurred in a patient in whom the root inclusion technique was used.
Our own experience differs somewhat from that of Dr David. We have performed sequential echocardiographic studies in our patients at 6- to 12-month intervals after the operation, and these have been interpreted by a single cardiologist. We perform annular reduction infrequently but in almost all cases tailor or replace the ascending aorta to conform to the size of the pulmonary artery and buttress the suture line between them with a felt strip. We do not perform the Ross operation in patients with an aortic anulus diameter of 30 mm or more.
Among 56 patients with serial measurements, 22 of whom have been followed up for more than 5 years, the sinotubular diameter increased by more than 20% in only 13% of the patients and the sinus diameter increased in 23%. We observed no significantly greater incidence of AI among these patients than among the remaining patients with no or lesser increases in these dimensions. Among the 22 patients with the longest follow-up, we have been unable to demonstrate a correlation between the severity or progression of AI and dilatation of the neo-aortic sinuses.
Histologic abnormalities of the ascending aorta are present in many patients with bicuspid aortic valves. In another study to be presented at this meeting, Dr David and his colleagues have demonstrated that similar structural abnormalities exist in the pulmonary arteries of many patients with bicuspid aortic valves, and they postulate that these abnormalities are most likely responsible for dilatation of the neo-aortic root and the development of AI. This is an intriguing hypothesis. However, a correlation between the severity of these changes in the pulmonary artery and the development of root dilatation and AI has not yet been demonstrated.
I have several questions. How did you determine that the value of 20% constituted a significant increase in the diameters of the sinotubular junction and of the sinuses of Valsalva?
What was the mean interval between the echocardiographic measurements? Is it possible that interobserver variability by your cardiologists could have produced errors in these measurements?
The great majority of patients currently undergoing the Ross operation have bicuspid aortic valves or congenital aortic valve disease. On the basis of your study, are you now recommending that the root replacement technique be abandoned in favor of the root inclusion technique in all of these patients? If not, in which patients should root replacement still be used?
If the root inclusion technique is used, is there not the potential for dilatation of the sinotubular junction and the development of AI as the native ascending aorta enlarges?
This important paper emphasizes the need for continuing critical evaluation of patients who have undergone the Ross operation to further refine the selection criteria and improve the late outcomes.
Dr David. Thank you, Dr Kouchoukos. I carefully stated that there could be bias that I could not detect in this study. All operations were performed by me, and we all have our own biases toward things we do. Perhaps these are the confounding factors that I could not detect in this study.
All echocardiograms included in this study were performed at the hospital and reviewed by two cardiologists, both very experienced sonographers. I chose 20% as the amount of dilation that is significant because of our work in functional anatomy of the aortic root and that of other investigators. An interesting study by Dr Furakawa and colleagues on the role of the sinotubular junction and sinuses of Valsalva on the development of AI is being published in The Annals of Thoracic Surgery . Those investigators showed that dilation of the sinotubular junction caused AI, whereas dilation of the sinuses of Valsalva does not.
I believe we should abandon the technique of aortic root replacement in patients with bicuspid aortic valve. I am convinced, and one of our fellows will be presenting his work on this subject at the Lillehei Forum,20 that most patients with bicuspid aortic valve have advanced degenerative changes in the arterial wall of the pulmonary trunk. By using the aortic inclusion technique, we may protect the pulmonary autograft from excessive dilation.
Finally, we should use a strip of Teflon felt on the inflow anastomosis between the left ventricular outflow tract and the pulmonary autograft and do the same or use a circumferential strip of Dacron graft at the level of its sinotubular junction, on the outside of the aorta.
Mr Donald N. Ross (London, United Kingdom). I enjoyed your paper very much. I was worried that you were going to shoot me down, but I am still here.
The first 251 patients in whom we did this operation had subcoronary implants. In fact, that was the original operation, and perhaps it has been misconstrued. However, the subcoronary operation was a big headache for us to achieve a competent valve both with it and the homograft. Once we had achieved that, those patients and their valves have withstood the test of time very well. My colleague, Dr Somerville in London, has followed them up over 30 years.
When the freestanding root was introduced with the homograft, everyone adopted it enthusiastically because of its competence and applied it automatically to the autograft. I wonder whether that was a mistake. From what you are saying, there may be some inherent disadvantages in using the root technique all the time. I am interested to hear that you are thinking in terms of inclusion roots in selected cases, in which the pathology progresses to aortic wall dilatation.
I think many people, and I am sure this does not apply to you, misapply the aortic root technique and put the valve in a supra-annular position quite unsupported. Even if it is technically correct, there are still cases in which the root perhaps should not be used. For instance, if there is a very small aortic root, we all agree that at least a relieving incision is necessary and perhaps also a Konno operation. In the presence of a satisfactory match, and this is usual, the root is probably appropriate, but what we still do not know is the effect of systemic pressure on the pulmonary artery wall. The problem arises when the root is markedly enlarged. I think we should abandon some of those operations and do a biopsy of the aortic root, retaining the pulmonary valve for a later day.
Would you recommend doing multicenter randomized studies of the freestanding root, subcoronary, and inclusion root techniques in this operation or for the series of diseases that are quite new to me, such as the bicuspid valve and its aortic wall pathology? I am grateful that you have brought this information to my attention.
Dr David. Thank you very much, Mr Ross. This study was not meant to show that the Ross procedure is a bad operation. I think it is a wonderful operation, and that is what I would choose for myself if I needed an aortic valve replacement, although I may be a bit too old for it. I believe it is an excellent option for children and young adults, and I will continue to do it.
The question I am raising is whether the pulmonary arterial wall is strong enough to endure systemic pressure for the duration of the patients life. The pulmonary root dilated in some. In my patients, I will do the Ross procedure by implanting the pulmonary autograft in the subcoronary position if the aortic and pulmonary roots have similar geometry and as an aortic inclusion technique in those in whom the aortic root is larger than the pulmonary root. In addition, the sinotubular junction of the pulmonary root should be fixed with a piece of Dacron graft to prevent dilation.
Dr Ronald C. Elkins (Oklahoma City, Okla). Dr David, you have raised an issue that concerns everyone who places the pulmonary valve in the systemic circulation. The dilatation that you have identified has been identified in patients who have undergone an arterial switch procedure, it has been identified in patients who have undergone a Damus-Kaye-Stansel procedure, and it clearly occurs in those patients who have a first-stage Norwood operation. The interesting thing about that is that the incidence of reoperation on the autograft is very low in all these groups of patients, including the Ross patients and those who have a root replacement.
If we look at the aortic valve diseaseunicuspid, bicuspid, or tricuspidwe are unable to show any difference in terms of our total experience of over 350 patients in the incidence of postoperative AI or changes involved in terms of the aortic sinus or the aortic anulus. We do strongly believe that if the root replacement technique is to be used, one must fix the size of the aortic anulus when it is appropriately dilated, except in the very young child, as well as the size of the sinotubular junction.
I have two questions for you. In a patient with significant sinus dilatation of the pulmonary artery and normal autograft valve function, at what size would you recommend reoperation on that autograft? I am presently observing one patient with significant dilatation of the sinus and I would like to know your recommendation about that.
Second, when you look at the improved early results (ie, freedom from acute intervention) and the late long-term results of the root replacement, do you really feel comfortable in recommending that we move backward in terms of 10-year success of the operation, where at 10 years there is a significant improvement of root replacement over intra-aortic implants in terms of freedom from autograft valve dysfunction?
Dr David. Thank you, Dr Elkins. You were the one who stimulated me to begin to do the Ross procedure in young patients.
The problem is that the autograft often dilates after the operation. Both the sinotubular junction and the sinuses of Valsalva dilate. Dilation of the sinotubular junction is more worrisome because it affects valve competence. Dilation of the sinuses of Valsalva simply causes an aneurysm. I have been aggressive in repairing aortic root and ascending aortic aneurysms and I believe these patients should be treated in the same fashion.
I have 3 patients with a neo-aortic root in excess of 50 mm in diameter, and I am planning to reoperate on them. I am hoping to be able to save the valves and perform an operation like the aortic valvesparing operations that I have described in the past. I think these patients should be reoperated on when the sinuses of Valsalva exceed 55 mm in transverse diameter.
I disagree with you that the technique of aortic root inclusion is associated with higher incidence of late AI. If you open the aortic root along the noncoronary aortic sinus, all the way down to the aortic anulus, it is possible to secure the pulmonary autograft inside the aortic root without disturbing its geometry. I used this technique early in my experience and almost exclusively during the past year, and AI is not more prevalent in those patients than in those who had aortic root replacement. The only difference is that aortic root dilation is more common in the group who had aortic root replacement.
Dr James H. Oury (Missoula, Mont). I think this paper could be taken as a caution or even possibly as a call to abandon the operation. I am glad to hear you say that you certainly would not abandon it. I think it is a very good operation.
My opinion is that we need to improve technique. Since that has already been discussed, I will not elaborate any further except to make one point: in our series of Ross procedures, which now numbers 147, we have used the root replacement on all but 3 patients. There was no hospital mortality in this series. We have had 3 explants of the autograft, so our actuarial survival is also 97%. In all of these cases we used annular plication and external support for the anulus, as well as the sinotubular junction. We initially did this because of some bleeding problems distally and quickly found that it not only eliminated the problem but also stabilized the sinotubular junction, as you have indicated. At follow-up, echocardiography showed progressive dilatation, mainly sinus dilatation, in about 10%.
I think your paper is very important in identifying a percentage of these operations that should be done as a subcoronary or as an inclusion technique. Could you further define what percentage of your cases you would now do as an inclusion or as a subcoronary procedure? Also, on the explanted cases, did you actually demonstrate viability of the explanted tissue?
Dr David. Stabilization of the sinotubular junction with a piece of Dacron graft is a new idea that we may have to incorporate in this operation. However, this technique could not be applied to children because it would prevent autograft growth.
In 3 patients who have been reoperated on, 2 of mine and 1 from another institution, the arterial wall of the autograft was viable but histologic examination revealed advanced elastic fragmentation and cystic medial necrosis; furthermore, both the gross and microscopic appearances were indistinguishable from that of degenerative aortic root aneurysm.
Like you, I do not plan to abandon the operation, but I will avoid performing it as a total root replacement. I started doing the Ross procedure by implanting the pulmonary valve in the subcoronary position, then changed to the aortic root inclusion technique, and later to aortic root replacement when Dr Elkins found a higher rate of AI with the two previous techniques. Last year I went back to the two initial techniques. If the aortic root cannot be used to wrap the pulmonary autograft, I use an autologous pericardial patch to close the aortotomy along the noncoronary sinus. I believe the pulmonary sinuses need some external support to prevent dilation.
| Footnotes |
|---|
| References |
|---|
|
|
|---|
This article has been cited by other articles:
![]() |
F. Ozaslan, T. Wittlinger, N. Monsefi, T. Bouhmidi, S. Theres, M. Doss, G. Wimmer-Greinecker, and A. Moritz Long-term follow-up of supra-annular pulmonary autograft aortic root replacement in patients with bicuspid aortic valve Eur. J. Cardiothorac. Surg., September 1, 2008; 34(3): 583 - 588. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. C. Elkins, D. M. Thompson, M. M. Lane, C. C. Elkins, and M. D. Peyton Ross operation: 16-year experience J. Thorac. Cardiovasc. Surg., September 1, 2008; 136(3): 623 - 630. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Frigiola, M. Ranucci, C. Carlucci, A. Giamberti, R. Abella, and M. Di Donato The ross procedure in adults: long-term follow-up and echocardiographic changes leading to pulmonary autograft reoperation. Ann. Thorac. Surg., August 1, 2008; 86(2): 482 - 489. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Ando, H. Kado, M. Masuda, T. Nakano, K. Hinokiyama, A. Shiose, and M. Kajimoto "Spiral-cuff" technique for repair of anomalous left coronary artery from the pulmonary artery. Ann. Thorac. Surg., August 1, 2008; 86(2): 667 - 668. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Carrel, M. Schwerzmann, F. Eckstein, T. Aymard, and A. Kadner Preliminary results following reinforcement of the pulmonary autograft to prevent dilatation after the Ross procedure. J. Thorac. Cardiovasc. Surg., August 1, 2008; 136(2): 472 - 475. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. M.A. Klieverik, J. A. Bekkers, J. W. Roos, M.J.C. Eijkemans, G. B. Raap, Ad. J.J.C. Bogers, and J. J.M. Takkenberg Autograft or allograft aortic valve replacement in young adult patients with congenital aortic valve disease Eur. Heart J., June 1, 2008; 29(11): 1446 - 1453. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kadner, O. Raisky, A. Degandt, D. Tamisier, D. Bonnet, D. Sidi, and P. R. Vouhe The Ross Procedure in Infants and Young Children Ann. Thorac. Surg., March 1, 2008; 85(3): 803 - 808. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. R. Hampton and E. D. Verrier Stentless Aortic Valve Replacement: Autograft/Homograft Card. Surg. Adult, January 1, 2008; 3(2008): 895 - 914. [Full Text] |
||||
![]() |
C. D. Etz, T. M. Homann, D. Silovitz, D. Spielvogel, C. A. Bodian, M. Luehr, G. DiLuozzo, K. A. Plestis, and R. B. Griepp Long-Term Survival After the Bentall Procedure in 206 Patients With Bicuspid Aortic Valve Ann. Thorac. Surg., October 1, 2007; 84(4): 1186 - 1194. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Hanke, U. Stierle, J. O. Boehm, C. A. Botha, J.F. Matthias Bechtel, A. Erasmi, M. Misfeld, W. Hemmer, J. G. Rein, D. R. Robinson, et al. Autograft Regurgitation and Aortic Root Dimensions After the Ross Procedure: The German Ross Registry Experience Circulation, September 11, 2007; 116(11_suppl): I-251 - I-258. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. M.A. Klieverik, J. J.M. Takkenberg, J. A. Bekkers, J. W. Roos-Hesselink, M. Witsenburg, and A. J.J.C. Bogers The Ross operation: a Trojan horse? Eur. Heart J., August 2, 2007; 28(16): 1993 - 2000. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. M. McMullan, G. Oppido, B. Davies, Y. Kawahira, A. D. Cochrane, Y. d'Udekem d'Acoz, D. J. Penny, and C. P. Brizard Surgical strategy for the bicuspid aortic valve: Tricuspidization with cusp extension versus pulmonary autograft J. Thorac. Cardiovasc. Surg., July 1, 2007; 134(1): 90 - 98. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Flynn, S. G. Little, E. H. Blackstone, and G. B. Pettersson Reversing the Ross operation: A new reoperation option for autograft failure J. Thorac. Cardiovasc. Surg., June 1, 2007; 133(6): 1645 - 1647. [Full Text] [PDF] |
||||
![]() |
J. W. Brown, M. Ruzmetov, M. D. Rodefeld, Y. Mahomed, and M. W. Turrentine Incidence of and Risk Factors for Pulmonary Autograft Dilation After Ross Aortic Valve Replacement Ann. Thorac. Surg., May 1, 2007; 83(5): 1781 - 1789. [Abstract] [Full Text] [PDF] |
||||
![]() |