JTCS Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Personal Folders
Right arrow Download to citation manager
Right arrow Author home page(s):
Piroze M. Davierwala
Michael A. Borger
Tirone E. David
Vivek Rao
Terrence M. Yau
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Davierwala, P. M.
Right arrow Articles by Yau, T. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Davierwala, P. M.
Right arrow Articles by Yau, T. M.
Related Collections
Right arrow Valve disease

J Thorac Cardiovasc Surg 2006;131:329-335
© 2006 The American Association for Thoracic Surgery


Surgery for Acquired Cardiovascular Disease

Reoperation is not an independent predictor of mortality during aortic valve surgery

Piroze M. Davierwala, MD, Michael A. Borger, MD, PhD, Tirone E. David, MD, Vivek Rao, MD, PhD, Manjula Maganti, MSc, Terrence M. Yau, MD, MSc *

Division of Cardiovascular Surgery, Toronto General Hospital, University Health Network, Department of Surgery, University of Toronto, Toronto, Ontario, Canada.

Received for publication March 10, 2005; revisions received August 14, 2005; accepted for publication September 9, 2005.

* Address for reprints: Terrence M. Yau, MD, MSc, FRCSC, Toronto General Hospital, 4N-470, 200 Elizabeth St, Toronto, Ontario M5G 2C4, Canada. (Email: terry.yau{at}utoronto.ca).


    Abstract
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 References
 
OBJECTIVE: Reoperations on aortic valves are associated with increased mortality, which may affect valve prosthesis selection at the time of initial aortic valve replacement. We analyzed our experience to determine whether reoperation itself independently predicts mortality during aortic valve surgery.

METHODS: Demographic, intraoperative, and outcome data were collected prospectively on patients undergoing primary or redo aortic valve replacement or Bentall procedures after previous aortic valve replacement with or without concomitant coronary bypass grafting at a single institution from 1990 through 2002. Logistic regression analyses validated by means of bootstrap methodology identified the predictors of hospital mortality and the independent effect of reoperation.

RESULTS: Of 2673 patients undergoing aortic valve surgery, 2375 were primary operations, 216 were reoperations, and 82 were Bentall–after–aortic valve replacement procedures. Of 298 reoperations, 32 were third and 5 were fourth procedures. Mortality was 2.3% for primary operations, 4.6% for redo aortic valve replacement, and 2.4% for Bentall–after–aortic valve replacement procedures. Most patients underwent elective procedures, with mortalities of 1.6%, 1.7%, and 2.5%, respectively. Hospital mortality was independently predicted by peripheral vascular disease (odds ratio, 3.6), active endocarditis (odds ratio, 2.9), worsening New York Heart Association class (odds ratio, 2.3), and need for annular enlargement (odds ratio, 2.1). Reoperation itself did not predict hospital mortality.

CONCLUSIONS: The risk of mortality during aortic valve surgery is due mostly to active endocarditis, New York Heart Association class, and comorbidity. We failed to find a significant effect of reoperation on perioperative mortality. Mechanical valves, with their attendant anticoagulation-related morbidity, should not be implanted solely because of anticipated high mortality associated with bioprosthetic rereplacement.



Abbreviations and Acronyms AVR = aortic valve replacement; CABG = coronary artery bypass grafting; CI = confidence interval; LV = left ventricular; LVEF = left ventricular ejection fraction; NYHA = New York Heart Association



    Introduction
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 References
 
Reoperative aortic valve surgery has traditionally been associated with significant mortality and morbidity. 1 Go Mechanical valves have a long record of excellent durability 2 Go but significant morbidity and sometimes mortality related to anticoagulant-related hemorrhage and other factors. 3-5 Go Bioprosthetic aortic valves have excellent freedom from thromboembolism 3,4 Go but are subject to primary tissue failure and may therefore require rereplacement. 6,7 Go

Factors like advanced age, left ventricular (LV) dysfunction, and an acute presentation with structural valve failure or infective endocarditis may make reoperations on the aortic valve a challenging proposition. Scarring, distortion, and calcification of the aortic annulus and root present increased technical difficulties, which may require reconstruction of the aortic root. However, because surgical results have improved over time, reoperations on the aortic valve may no longer carry the same increase in risks as in the past. We therefore evaluated our experience with aortic valve surgery to determine whether redo aortic valve replacement (AVR) or Bentall-after-AVR procedures are independent predictors of perioperative mortality.


    Methods
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 References
 
Data Source
From January 1990 through December 2002, 2673 patients underwent AVR with or without concomitant coronary artery bypass grafting (CABG) at our institution. Of these, 2375 patients underwent primary (first-time) AVR, and 298 patients (11.1%) underwent redo aortic valve surgery. Clinical, operative, and outcome data were collected prospectively in a computerized database on all patients undergoing cardiac surgery. Patients who underwent operations on other valves, ventricular aneurysm resection, arrhythmia surgery, or extracardiac procedures were excluded from this study.

Outcome and Explanatory Variables
Our primary outcome in this study was hospital mortality, which was defined as any postoperative death in the hospital. We also recorded age, sex, LV grade (based on left ventricular ejection fraction [LVEF] obtained by means of ventriculography or echocardiography as follows: grade 1, LVEF ≥60%; grade 2, LVEF 40%-59%; grade 3, LVEF 20%-39%; grade 4, LVEF <20%), previous AVR, urgency of operation (elective; semiurgent, indicating an operation during the same admission as a cardiac catheterization or a cardiac event; urgent, indicating an operation within 72 hours of an event; or emergency, indicating an operation within 12 hours of an event), New York Heart Association (NYHA) class, native and prosthetic aortic valve lesion (stenotic, regurgitant, or mixed, as determined by means of echocardiography) and infective endocarditis (active endocarditis, active endocarditis with abscess formation, remote endocarditis, or none), recent (within 30 days) myocardial infarction, congestive heart failure, diabetes, hyperlipidemia, peripheral vascular disease, hypertension, and preoperative stroke or transient ischemic attack.

Analysis
Statistical analyses were performed with SAS (Version 8.2) software. 8 Go Univariate analyses were performed with {chi}2 analyses or the Fisher exact test for categoric variables and analysis of variance for continuous variables. Variables that had a univariate P value of less than .25 or those judged to be clinically important were submitted to a logistic regression model by means of stepwise selection. Multivariate logistic regression methods, validated by means of bootstrap methodology, were used to calculate factor-adjusted odds ratios. Model discrimination was evaluated by using the area under the receiver operating characteristic curve, 9,10 Go and calibration was assessed with the Hosmer-Lemeshow goodness-of-fit statistic.


    Results
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 References
 
Demographics
Two thousand three hundred seventy-five (88.9%) patients underwent first-time AVR (primary AVR), 216 (8.1%) patients underwent an aortic valve rereplacement (redo AVR), and 82 (3.1%) patients underwent a modified Bentall procedure or complete aortic root replacement with reimplantation of coronary buttons after a previous AVR (Bentall-after-AVR, Table 1). For patients in the redo AVR group, the median duration between operations was 10.3 years (mean, 10.6 ± 5.4 years). For patients in the Bentall-after-AVR group, the median duration was 11.2 years (mean, 11.0 ± 6.2 years).


View this table:
[in this window]
[in a new window]
 
TABLE 1. Number of previous aortic valve operations in patients undergoing redo operations
 
Patients undergoing reoperations were younger than those undergoing primary AVR (P < .0001, Table E1). Patients in the primary AVR group had predominantly aortic stenosis, whereas patients in the redo AVR and Bentall-after-AVR groups had predominantly aortic regurgitation (P < .0001). Infective endocarditis and the need for urgent or emergency operation were more common in the redo AVR and Bentall-after-AVR groups (P < .0001).


View this table:
[in this window]
[in a new window]
 
TABLE E1. Distribution of preoperative variables
 
Valvular Pathology
Eighty-three percent of patients in the redo AVR group and 71% in the Bentall-after-AVR group had received a bioprosthetic valve during their previous operation. Most explanted bioprostheses demonstrated cusp tears, calcification, and/or fusion, with many showing pannus ingrowth (Figure 1). Seventeen percent of patients in the redo AVR group and 29% in the Bentall-after-AVR group had received a mechanical valve during their previous operation. Most patients in the redo AVR group had significant pannus ingrowth, whereas patients undergoing Bentall-after-AVR procedures chiefly had paravalvular leaks or dehiscences (Figure 2). One valve in the redo AVR group and 11 in the Bentall-after-AVR group were found to be normal at pathologic review. These patients required reoperation predominantly because of abnormalities of the aortic root or proximal ascending aorta.


Figure 1
View larger version (15K):
[in this window]
[in a new window]
 
Figure 1. Pathology of explanted bioprosthetic valves. AVR, Aortic valve replacement.

 

Figure 2
View larger version (13K):
[in this window]
[in a new window]
 
Figure 2. Pathology of explanted mechanical valves. AVR, Aortic valve replacement.

 
Of the 82 patients in the Bentall-after-AVR group, the indication for a root replacement was a type A acute or chronic dissection in 10% of patients, dilation of the aortic root in 20%, ascending aortic aneurysm in 12%, periannular abscess in 18%, partial or complete excision of the annulus during excision of the prosthesis in 16%, and a calcified, friable, or abnormal aortic root in 20%. Seven patients undergoing Bentall-after-AVR procedures had a Dacron or pericardial patch enlargement or reconstruction of the aortic root at the time of the previous operation.

Sixteen patients who had undergone primary AVR with Toronto SPV bioprostheses required a reoperation. Eight underwent a redo AVR, and 8 underwent a modified Bentall or root replacement procedure. Eight patients who had undergone primary AVR with a homograft required a reoperation. One patient underwent a redo AVR, and 7 underwent a modified Bentall or root replacement procedure. There were 2 more patients (one with a previous Medtronic Freestyle valve in situ and the other who had undergone a Ross procedure) who underwent redo AVR. Other commonly explanted tissue valves were Carpentier Edwards Porcine, Ionescu-Shiley, and Hancock II Porcine valves (24%, 21%, and 20% of all tissue valves explanted, respectively).

Intraoperative Data
The proportion of patients who received mechanical valves was significantly higher in the redo AVR and Bentall-after-AVR groups than in the primary AVR group (P < 0.0001, Table 2). A greater percentage of patients in the redo AVR group required enlargement of the aortic annulus or one of the sinuses (P < .05). Aortic crossclamp and cardiopulmonary bypass times were longer in patients in the Bentall-after-AVR group (P < .0001).


View this table:
[in this window]
[in a new window]
 
TABLE 2. Distribution of intraoperative variables
 
Outcomes
Hospital mortality was 2.3% for primary AVR, 4.6% for redo AVR, and 2.4% for Bentall-after-AVR (Table 3). In the redo AVR group, mortality was 3.7% for second operations, 13% for third operations, and 0% for fourth operations. In the Bentall-after-AVR group mortality was 2.9% for second operations and 0% for third, fourth, or fifth operations.


View this table:
[in this window]
[in a new window]
 
TABLE 3. Distribution of postoperative outcomes
 
Univariate analyses showed that mortality was high in patients undergoing emergency primary or redo AVR (Table E2). Preoperative cardiogenic shock and congestive heart failure increased mortality to a greater degree for redo AVR than for primary AVR. In all groups the presence of diabetes or active endocarditis or the requirement for patch enlargement of the aortic root were associated with increased mortality. Peripheral vascular disease and preoperative renal failure increased mortality for primary or redo AVR but not for Bentall-after-AVR.


View this table:
[in this window]
[in a new window]
 
TABLE E2. Influence of preoperative and intraoperative variables on hospital mortality by univariate analysis
 
Postoperative low cardiac output syndrome, myocardial infarction, or stroke did not differ between groups (Table 3), but postoperative renal failure was more common after reoperations (P = .04), as were re-exploration for bleeding (P < .0001) and permanent pacemaker insertion (P = .02). The durations of intensive care unit and hospital stay were longer in patients undergoing reoperations (P = .02).

Predictors of Hospital Mortality for Aortic Valve Operations and Reoperations
The independent predictors of mortality were determined by multivariable logistic regression analysis (Figure 3) and included increasing NYHA class (odds ratio, 2.3; 95% confidence interval [CI], 1.5-3.4), infective endocarditis (odds ratio, 2.9; 95% CI, 1.4-5.9), peripheral vascular disease (odds ratio, 3.6; 95% CI, 1.9-6.8), and the requirement for aortic root enlargement (odds ratio, 2.1; 95% CI, 1.2-3.7). However, reoperative aortic valve surgery was not a significant predictor of hospital mortality.


Figure 3
View larger version (6K):
[in this window]
[in a new window]
 
Figure 3. Independent predictors of hospital mortality for primary or redo aortic valve replacement. NYHA, New York Heart Association.

 
When reoperation was forced into the model, its odds ratio (odds ratio, 1.4; 95% CI, 0.7-2.9) was considerably lower than those associated with NYHA class, endocarditis, peripheral vascular disease, and root enlargement (P = .34).

The multivariable model for mortality was robust, with an area under the receiver operating characteristic curve of 0.735 and a Hosmer-Lemeshow goodness-of-fit P value of .7, indicating good model calibration and discrimination. We further validated the model with bootstrap methodology (Table 4). The logistic regression analysis was repeated 100 times in subsets of 2000 patients randomly selected from the entire dataset for each analysis, with replacement. There was excellent correlation of the predictors selected in the 100 bootstrap analyses with those identified in the original model. As Table 4 indicates, NYHA class was identified as a significant predictor of mortality in 98% of these multivariable models and peripheral vascular disease in 96%, but only 4% of models identified reoperation as a predictor. The finding that reoperation was not a significant predictor of hospital mortality was therefore robust.


View this table:
[in this window]
[in a new window]
 
TABLE 4. Bootstrap analysis for validation of the multivariate regression model
 

    Discussion
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 References
 
Reoperative valvular surgery is often performed in higher-risk patients rather than those undergoing primary procedures and is more technically demanding. Reoperative aortic valvular surgery after previous AVR 1 Go or CABG 11 Go has therefore been associated with increased morbidity and mortality compared with that seen with primary procedures. Although some series have reported that prior CABG is not a significant risk factor for mortality during subsequent AVR, 12,13 Go the incremental risk of aortic valvular reoperation caused specifically by prior aortic valve surgery has been difficult to quantify.

The desire to avoid subsequent high-risk reoperations may encourage the implantation of mechanical valves because late freedom from structural failure is excellent. 2 Go However, mechanical valves are subject to endocarditis and paravalvular leaks, similar to bioprostheses, and valve thrombosis and pannus ingrowth are not infrequent causes for reoperation. Primary tissue failure is therefore the only indication for reoperation that is specific to bioprostheses. The risk of reoperation for bioprosthetic tissue failure varies by patient age, with excellent valve durability in patients aged 65 years or older. 6,7,14-16 Go The likelihood of reoperation for bioprosthetic failure may also be reduced by coronary artery disease, which represents a competing risk. 14 Go Bioprosthetic aortic valves typically fail gradually, with an increasing incidence of reoperation beginning after 7 to 8 years. In our series we noted median intervals of 10.3 years between operations in the redo AVR group and 11.2 years in the Bentall-after-AVR group, which are very similar to those reported by Vogt and colleagues. 17 Go

When aortic valvular rereplacement was carried out electively, mortality in our series was low (1.6% for elective primary AVR vs 1.7% for elective redo AVR). Vogt and colleagues 17 Go noted a similarly low risk (1.4%) of elective rereplacement of degenerated aortic bioprostheses, and Akins and associates 18 Go reported a 4.8% mortality in similar patients. Jamieson and coworkers 19 Go reported an overall mortality of 6.8% in 322 reoperations for failed aortic bioprostheses.

In the current series reoperative surgery was associated with a nonsignificantly increased risk of mortality (4.6% vs 2.3%). This difference may be due to the increased prevalence of other risk factors in patients undergoing reoperations. For instance, patients presenting with active endocarditis underwent urgent or emergency operations more often in the redo AVR (10.8%) and Bentall-after-AVR (9.1%) groups than in the group undergoing primary AVR (6.4%). Timing of the operation is important because nonelective operation was also reported to be a predictor of death by Akins and associates, 18 Go with an odds ratio of 2.5.

We also found that worsening NYHA class was a significant predictor of hospital mortality, as did Jamieson and coworkers. 19 Go Reoperations may therefore involve greater risk not just because of increased technical difficulties but also because such patients often present urgently with endocarditis, congestive heart failure, or shock or with renal failure related to sepsis. These conclusions were also reached by Potter and colleagues, 20 Go who recently analyzed their institutional experience with reoperative aortic valve surgery and concluded that mortality was related to endocarditis, advanced NYHA symptom class, peripheral vascular disease, preserved LV function, and male sex but not to reoperation itself.

In this series an aggressive institutional practice of annular enlargement was reflected in a prevalence of annular enlargement of 20% in patients undergoing primary operations, 36% in patients undergoing redo AVR, and 6% in patients undergoing Bentall procedures after prior AVR. The nominal mean size of valve implanted at reoperation was identical in patients undergoing primary AVR versus redo AVR, whereas those undergoing Bentall procedures received valves with larger sizes. It is likely that without the greater prevalence of annular enlargement during redo AVR, the mean size of prostheses reimplanted would have been significantly lower. The requirement for annular enlargement was associated, however, with a significant increase in hospital mortality. Whether an increased operative risk caused by annular enlargement is counterbalanced by improved late survival related to a larger prosthesis and improved hemodynamics remains controversial and cannot be addressed by our current study.

Of the 298 patients who underwent reoperations, 82 patients required a Bentall procedure or aortic root replacement for acute or chronic aortic dissections, aneurysmal disease of the aortic root or ascending aorta, annular or subannular abscess cavities, excision of the annulus with the prosthesis, or a calcified or friable aortic root. Patients in this group were younger but had a higher prevalence of active and remote endocarditis and thus required more emergency procedures. Despite this, the overall hospital mortality for this group of patients was only 2.4%, which compares favorably with the 11.5% mortality reported by Vallely and associates 21 Go for elective root replacement after previous AVR and the 8.3% mortality noted by Dougenis and coworkers 22 Go for root replacement after prior AVR or CABG. We attribute the low mortality in this series to a number of factors, including concentration of cases to a small number of experienced surgeons, ensuring safe sternal reentry, careful myocardial protection, aggressive debridement of all suspicious infected tissues, and reconstruction of the heart with pericardium in patients with aortic root abscesses. 23 Go

Because aortic bioprostheses do not require anticoagulation with warfarin, they are indicated in young patients whose physical activity increases the risk of anticoagulant-related hemorrhage, women who wish to bear children, 24 Go and those in whom anticoagulation cannot be safely monitored and maintained. They are also indicated in elderly patients undergoing AVR (>65 years of age) because of excellent durability and limited patient life expectancy. In addition, some middle-aged patients (40-65 years) choose bioprosthetic valves because of the desire to avoid warfarin therapy. Our results suggest that the median interval between operations and the time course over which symptoms of bioprosthetic tissue failure develop might support this approach in carefully selected patients. When reoperation to replace a failing tissue valve can be carried out on an elective basis, the associated mortality is low.

The strategy of increased use of bioprosthetic valves must be tempered by other mitigating factors. Patients who already have another indication for lifelong warfarin anticoagulation usually have a mechanical valve implanted. In addition, in patients with a small annulus at the time of the initial operation, the necessity of an annular enlargement procedure at future reoperation might be anticipated to be greater, thereby increasing the mortality of reoperation. A mechanical prosthesis, stentless bioprosthesis, or composite root replacement may be better choices for such patients. However, reoperations in patients who have undergone previous stentless valve implantation or root replacement may be technically more complex. Because patients who underwent aortic root replacement at their initial operation were not included in this series, we are unable to comment on mortality at reoperation in this more challenging patient subgroup.

In conclusion, our experience suggests that the mortality of AVR is strongly related to peripheral vascular disease, endocarditis, NYHA symptom class, and the requirement for annular enlargement. Reoperation itself is not significantly associated with mortality. Bioprostheses implanted to avoid anticoagulation can often be replaced electively with low mortality. Although bioprostheses are not indicated in all patients, the anticipated risk of reoperation may be a less significant consideration in preoperative valve selection in the future.


    References
 Top
 Abstract
 Introduction
 Methods
 Results
 Discussion
 References
 

  1. Shemin RJ, Guadiani VA, Conkle DM, Morrow AG. Prosthetic aortic valves. Arch Surg. 1979;114:63-65.[Abstract/Free Full Text]
  2. Masters RG, Pipe AL, Walley VM, Keon WJ. Comparative results with the St. Jude Medical and Medtronic Hall mechanical valves. J Thorac Cardiovasc Surg. 1995;110:663-671.[Abstract/Free Full Text]
  3. Milano A, Guglielmi C, De Carlo M, Di Gregorio O, Borzoni G, Verunelli F, et al. Valve related complications in elderly patients with biological and mechanical aortic valves. Ann Thorac Surg. 1998;66(suppl):S82-S87.[Medline]
  4. Jamieson WRE, Munro AI, Burr LH, Germann E, Miyagishima RT, Ling H. Influence of coronary artery bypass and age on after aortic and mitral valve replacement with biological and mechanical prostheses. Circulation 1995;92(suppl II):101-106.[Abstract/Free Full Text]
  5. Jamieson WRE, Miyagishima RT, Grunkemeier GL, Germann E, Hendersen C, Lichtenstein SV, et al. Bileaflet mechanical prostheses for aortic valve replacement in patients younger than 65 years and 65 years of age or older. major thromboembolic and hemorrhagic complications. Can J Surg. 1999;42:27-36.[Medline]
  6. Glower DD, Landolfo KP, Cheruvu S, Cen YY, Harrison JK, Bashore TM, et al. Determinants of 15 year-outcome with 1,119 standard Carpentier Edward porcine valves. Ann Thorac Surg. 1998;66(suppl):S44-S48.[Medline]
  7. David TE, Armstrong S, Sun Z. The Hancock II bioprosthesis at 12 years. Ann Thorac Surg. 1998;66(suppl):S95-S98.[Medline]
  8. SAS Institute SAS/STAT user's guide, version 8. Cary, NC: SAS Institute Inc; 1988.
  9. Hanley JA, McNeil BJ. The meaning and the use of area under a receiver operating characteristic (ROC) curve. Radiology 1982;143:29-36.[Abstract/Free Full Text]
  10. Hanley JA, McNeil BJ. A method for comparing areas under receiver operating characteristic curves derived from the same cases. Radiology 1983;148:839-843.[Abstract/Free Full Text]
  11. Odell JA, Mullany CJ, Schaff HV, Orszulak TA, Daly RC, Morris JJ. Aortic valve replacement after previous coronary artery bypass grafting. Ann Thorac Surg. 1996;62:1424-1430.[Abstract/Free Full Text]
  12. Sundt III TM, Murphy SF, Barzilai B, Schuessler RB, Mendelhoff EN, Huddleston CB, et al. Previous coronary artery bypass grafting is not a risk factor for aortic valve replacement. Ann Thorac Surg. 1997;64:651-658.[Abstract/Free Full Text]
  13. Akins CW, Hilgenberg AD, Vlahakes GJ, Madsen JC, Macgillivray TE. Aortic valve replacement in patients with previous cardiac surgery. J Card Surg. 2004;19:308-312.[Medline]
  14. Cohen G, David TE, Ivanov J, Armstrong S, Feindel CM. The impact of age, coronary artery disease and cardiac comorbidity on late survival after bioprosthetic valve replacement. J Thorac Cardiovasc Surg. 1999;117:273-284.[Abstract/Free Full Text]
  15. David TE, Ivanov J, Armstrong S, Feindel CM, Cohen G. Late results of heart valve replacement with Hancock II bioprostheses. J Thorac Cardiovasc Surg. 2001;121:268-277.
  16. Rizzoli G, Bottio T, Thiene G, Toscano G, Casarotto D. Long term durability of Hancock II porcine bioprostheses. J Thorac Cardiovasc Surg. 2003;126:66-74.[Abstract/Free Full Text]
  17. Vogt PR, Brunner-LaRocca HP, Sidler P, Zund G, Truniger K, Lachat M, et al. Reoperative surgery for degenerated aortic bioprostheses. predictors for emergency surgery and reoperative mortality. Eur J Cardiothorac Surg. 2000;17:134-139.[Abstract/Free Full Text]
  18. Akins CW, Buckley MJ, Daggett WM, Hilgenberg AD, Vlahakes GJ, Torchiana DF, et al. Risk of reoperative valve replacement for failed mitral and aortic bioprostheses. Ann Thorac Surg. 1998;65:1545-1552.[Abstract/Free Full Text]
  19. Jamieson WRE, Burr LH, Miyagishima RT, Janusz MT, Fradet GJ, Ling H, et al. Reoperation for bioprosthetic aortic structural failure- risk assessment. Eur J Cardiothorac Surg. 2003;24:873-878.[Abstract/Free Full Text]
  20. Potter DD, Sundt 3rd TM, Zehr KJ, Dearani JA, Daly RC, Mullany CJ, et al. Operative risk of reoperative aortic valve replacement. J Thorac Cardiovasc Surg. 2005;129:94-103.[Abstract/Free Full Text]
  21. Vallely MP, Hughes CF, Bannon PG, Hendel PN, French BG, Bayfield MS. Composite graft replacement of the aortic root after previous cardiac surgery. a 20-year experience. Ann Thorac Surg. 2000;70:851-855.[Abstract/Free Full Text]
  22. Dougenis D, Daily BB, Kouchoukos NT. Reoperations on the aortic root and ascending aorta. Ann Thorac Surg. 1997;64:986-992.[Abstract/Free Full Text]
  23. Raanani E, David TE, Dellgren G, Armstrong S, Ivanov J, Feindel CM. Redo aortic root replacement. experience with 31 patients. Ann Thorac Surg. 2001;71:1460-1463.[Abstract/Free Full Text]
  24. Jamieson WRE, Miller DC, Akins CW, Munro AI, Glower DD, Moore KA, et al. Pregnancy and bioprostheses. influence on structural valve deterioration. Ann Thorac Surg. 1995;60(suppl):S282-S287.[Medline]



This article has been cited by other articles:


Home page
Ann. Thorac. Surg.Home page
P. Totaro, S. Carlini, M. Pozzi, F. Pagani, G. Zattera, A. M. D'Armini, and M. Vigano
Minimally invasive approach for complex cardiac surgery procedures.
Ann. Thorac. Surg., August 1, 2009; 88(2): 462 - 466.
[Abstract] [Full Text] [PDF]


Home page
ICVTSHome page
N. U. Khan and N. Yonan
Does preoperative computed tomography reduce the risks associated with re-do cardiac surgery?
Interactive CardioVascular and Thoracic Surgery, July 1, 2009; 9(1): 119 - 123.
[Abstract] [Full Text] [PDF]


Home page
Eur. J. Cardiothorac. Surg.Home page
N. Khaladj, M. Shrestha, S. Peterss, I. Kutschka, M. Strueber, L. Hoy, A. Haverich, and C. Hagl
Isolated surgical aortic valve replacement after previous coronary artery bypass grafting with patent grafts: is this old-fashioned technique obsolete?
Eur. J. Cardiothorac. Surg., February 1, 2009; 35(2): 260 - 264.
[Abstract] [Full Text] [PDF]


Home page
J. Thorac. Cardiovasc. Surg.Home page
A. Ali, Y. Abu-Omar, A. Patel, A. Y. Sheikh, Z. Ali, A. Saeed, A. Akhtar, T. Athanasiou, and J. Pepper
Propensity analysis of survival after subcoronary or root replacement techniques for homograft aortic valve replacement.
J. Thorac. Cardiovasc. Surg., February 1, 2009; 137(2): 334 - 341.
[Abstract] [Full Text] [PDF]


Home page
Eur. J. Cardiothorac. Surg.Home page
T. M. Joudinaud, F. Baron, R. Raffoul, B. Pagis, M. Vergnat, C. Parisot, U. Hvass, and P. R. Nataf
Redo aortic root surgery for failure of an aortic homograft is a major technical challenge
Eur. J. Cardiothorac. Surg., June 1, 2008; 33(6): 989 - 994.
[Abstract] [Full Text] [PDF]


Home page
Ann. Thorac. Surg.Home page
M. A. Borger, K. Prasongsukarn, S. Armstrong, C. M. Feindel, and T. E. David
Stentless Aortic Valve Reoperations: A Surgical Challenge
Ann. Thorac. Surg., September 1, 2007; 84(3): 737 - 744.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Personal Folders
Right arrow Download to citation manager
Right arrow Author home page(s):
Piroze M. Davierwala
Michael A. Borger
Tirone E. David
Vivek Rao
Terrence M. Yau
Right arrow Permission Requests
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Davierwala, P. M.
Right arrow Articles by Yau, T. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Davierwala, P. M.
Right arrow Articles by Yau, T. M.
Related Collections
Right arrow Valve disease


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ANN THORAC SURG ASIAN CARDIOVASC THORAC ANN EUR J CARDIOTHORAC SURG
J THORAC CARDIOVASC SURG ICVTS ALL CTSNet JOURNALS