JTCS Tips for Better Browsing
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):
Sachin Talwar
Arkalgud Sampath Kumar
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 Talwar, S.
Right arrow Articles by Kumar, A. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Talwar, S.
Right arrow Articles by Kumar, A. S.
Related Collections
Right arrow Valve disease

J Thorac Cardiovasc Surg 2005;129:875-879
© 2005 The American Association for Thoracic Surgery


Surgery for Acquired Cardiovascular Disease

Mitral valve repair in children with rheumatic heart disease

Sachin Talwar, MCh, Manithara Raman Rajesh, MS, Anandaraja Subramanian, DM, Anita Saxena, DM, Arkalgud Sampath Kumar, MCh*

Cardiothoracic Centre, All India Institute of Medical Sciences, New Delhi, India.

Received for publication August 25, 2004; revisions received November 1, 2004; accepted for publication November 9, 2004.

* Address for reprints: A. Sampath Kumar, MCh, Professor, Department of Cardiothoracic & Vascular Surgery, Cardiothoracic Centre, All India Institute of Medical Sciences, Ansari Nagar, New Delhi-110 029, India. (E-mail: asampath_kumar{at}hotmail.com).


    Abstract
 Top
 Abstract
 Patients and methods
 Results
 Discussion
 Conclusion
 References
 
OBJECTIVE: The purpose of this study was to assess the long-term results of mitral valve repair in children with chronic rheumatic heart disease.

METHODS: From January 1988 through December 2003, 278 children (153 male children) underwent mitral valve repair. Mean age was 11.7 ± 2.9 years (range, 2–15 years). One hundred seventy-three children (62%) were in the New York Heart Association functional class III or IV. Congestive heart failure was present in 24 (8.6%). Reparative procedures included posterior collar annuloplasty (n = 242), commissurotomy (n = 187), cusp-level chordal shortening (n = 94), cusp thinning (n = 71), cleft suture (n = 65), and cusp excision or plication (n = 10). Associated procedures included atrial septal defect closure (n = 22), aortic valve repair/replacement (n = 13), and tricuspid valve repair (n = 3).

RESULTS: Early mortality was 2.2% (6 patients). Preoperative left ventricular dysfunction was associated with greater mortality. Median follow-up was 56.5 months (mean, 58.9. ± 32.3 months; range, 5 to 180 months). One hundred seventy-seven survivors (65%) had no or trivial mitral regurgitation. Sixteen patients (6%) required reoperation for valve dysfunction. There were 7 late deaths (2.6%). Actuarial, reoperation-free, and event-free survivals at a median follow-up of 56.5 months were 95.2% ± 1.5%, 91.6% ± 2.2%, and 55.9% ± 3.5%, respectively; at 15 years, they were 95.2% ± 1.5%, 85.9% ± 5.9%, and 46.7% ± 4.7%, respectively.

CONCLUSION: Mitral valve repair in children with chronic rheumatic heart disease is feasible and provides acceptable long-term results.



Figure 1
Saxena, Rajesh, Kumar, Talwar, Subramanian (left to right)


Experience with mitral valve repair in the rheumatic population is limited.1–6 Major hindrances to the less-frequent repairs in this population have been the unpredictability of long-term results and, more important, the complexity of the disease process, which make it difficult to choose the appropriate procedure for any given patient.7

In 1995, we reported our initial experience with mitral valve reconstruction in 125 children operated on between 1988 and 1994.8 We now present detailed results with long-term follow-up.


    Patients and methods
 Top
 Abstract
 Patients and methods
 Results
 Discussion
 Conclusion
 References
 
From January 1988 through December 2003, 1022 patients underwent mitral valve reconstruction at our institution. We studied 278 (27.2%) of these patients who were 15 years of age or younger. Of these 278 patients, 153 (55%) were male. The mean age at surgery was 11.7 ± 2.9 years (range, 2–15 years). All patients had evidence of rheumatic heart disease. Pure mitral regurgitation (MR) was present in 123 (44%) patients, and combined mitral stenosis (MS) and MR was present in 155 (56%) patients. Atrial fibrillation (AF) was present in 143 patients (51.4%). The predominant presenting symptom was dyspnea on exertion. One hundred seventy-three patients (62%) were in New York Heart Association (NYHA) functional class III or IV. Congestive heart failure (CHF) was present in 24 (8.6%) patients.

Preoperative transthoracic echocardiography was performed in all patients. Cardiac catheterization and cineangiography were performed on suspicion of associated aortic valve disease. MR was graded by Doppler echocardiography or angiography or by both according to previously published criteria.9,10 After January 1994, intraoperative transesophageal echocardiography was performed with a Hewlett- Packard Sonos 1500, 2500, or 5500 ultrasonography system. (Hewlett-Packard Co, Andover, Mass). Echocardiographic assessment included the annulus, leaflet thickness and mobility, commissural and chordal fusion, presence of calcification, regurgitant jet, thickness of the chordae tendineae, and the presence of clots in the left atrium or the left atrial appendage. Other valves were also assessed in a systematic fashion.

Surgical technique
Surgical approach was via a median sternotomy (n = 219) or, in female patients, a right anterolateral thoracotomy (n = 59) purely for cosmetic reasons. Aorto-bicaval cannulation was used in all patients. Before 1996, moderately hypothermic (32°C) cardiopulmonary bypass (CPB) was used. Since 1996, normothermic perfusion has been used in all patients. Antegrade cold blood cardioplegia and topical ice slush were used for myocardial production. The mitral valve was exposed through a standard incision in the left atrial wall behind the interatrial groove. In patients with an associated atrial septal defect (ASD), the approach was through the right atrium. After careful evaluation of the mitral valve, a variety of reparative procedures developed by us and described in detail in our previous publications5,8,11–13 was used. The procedures included posterior collar annuloplasty11 (n = 242), commissurotomy (n = 187), cusp-level chordal shortening (n = 94), cusp thinning (n = 71), cleft suture (n = 65), cusp excision or plication (n = 10), decalcification (n = 3), and chordal transfer (n = 3). No procedure was performed for correction of AF.

Associated procedures included atrial septal defect closure in 22 patients, aortic valve repair in 8, aortic valve replacement in 5, and tricuspid valve repair in 3. At the completion of repair, mitral valve competence was tested by using a bulb syringe to inject cold saline into the left ventricular cavity with the aortic root vent open, and coaptation of leaflets was observed. Since 1994, transesophageal echocardiography has been used for assessment of repairs.

Follow-up
Transthoracic echocardiography was carried out in all patients before discharge from the hospital and repeated at 6 monthly intervals. Before 1998, all patients undergoing posterior collar annuloplasty were prescribed acenocoumarin for 6 weeks and dipyridamole for 6 months. Since April 1998, this practice has been discontinued. All patients were seen in the outpatient clinic at our hospital. The results of their clinical status and echocardiograms between January 2004 and July 2004 were recorded and are reported in this study.

Statistical analysis
Data were analyzed with the SPSS 10.0 for Windows software package (SPSS Inc, Chicago Ill). Mean, median, and standard deviation were calculated for continuous variables. Univariate analysis was performed with the {chi}2 and Fisher exact tests. Actuarial estimates were calculated and compared by using the Kaplan-Meier analysis with Mantel-Cox log-rank tests. MR was considered to be significant if it was moderate or severe. Factors analyzed as predictors of early and late mortality and of development of significant MR included age, sex, type of lesion (MR or mixed), preoperative NYHA class, preoperative CHF, presence of AF, valve pathology (cusp prolapse, annular dilatation, chordal elongation, chordal rupture, calcification of valve leaflets), left ventricular dysfunction (ejection fraction < 50%, n = 24), associated aortic and tricuspid valve disease, CPB and aortic crossclamp time, and various reparative techniques. All factors were subjected to multiple logistic regression analysis to determine the independent predictors of early mortality. The Cox proportional hazards model was used to determine the prognostic factors for significant MR.


    Results
 Top
 Abstract
 Patients and methods
 Results
 Discussion
 Conclusion
 References
 
Early mortality
All patients survived the operation. Mean aortic crossclamp time was 37.2 ± 12.8 minutes (range, 23–66 minutes), and the mean CPB time was 47.6 ± 11.9 minutes (range, 36–83 minutes) for patients who underwent mitral valve repair alone. Fifteen patients (5.4%) required inotropic support. Median duration of mechanical ventilation was 18 hours (range, 9–68 hours). Mean hospital stay was 5.8 ± 1.7 days (range, 4–29 days). There were 6 early deaths (2.2%), which were encountered in the first 125 patients and reported by us earlier.8 Of these deaths, 5 were due to persistent low cardiac output caused by severe left ventricular dysfunction, and 1was due to cerebral infarction. No in-hospital deaths occurred in the last 153 consecutive patients.

Late outcome
Follow-up was 98% complete (n = 266) and ranged from 5 to 180 months (mean, 58.9 ± 33.3 months; median, 56.5 months). Total follow-up was 1335 patient-years. Among survivors, 19 (7%) were followed up for 15 or more years, 25 (9%), for 10 or more years, 116 (43%), for more than 5 years, and 210 (77%), for more than 3 years. We followed standard published guidelines14 in reporting freedom from valve-related events.

Thromboembolic complications
Four patients (1.5%) had a thromboembolic complication (0.3 events per 100 patient-years) in the late postoperative period at a mean follow-up of 24 ± 24.4 months (range, 3–56 months). One of these patients died 3 months after surgery; the rest recovered uneventfully. Of the 4 patients, 3 had persistent AF.

Hemolysis
Sixteen patients had significant hemolysis (1.2 events per 100 patient-years) Nine of these had significant MR: two underwent MVR, 2 died without undergoing reoperation, and 5 are awaiting reoperation. Of the remaining 7 patients, 2 were lost to follow-up, and hemolysis gradually subsided in the other 5.

Infective endocarditis
One patient had subacute bacterial endocarditis. He was treated conservatively and is well 32 months after initial surgery.

Reoperation
Sixteen patients underwent reoperation for severe valve dysfunction (1.2 events per 100 patient-years) after a mean period of 39.13 ± 31.2 months (range, 3–132 months). Freedom from reoperation was 91.6% ± 2.2% at 56.5 months and 85.9% ± 5.9% at 15 years (Figure 1). One patient underwent repeat mitral valve repair within 3 months due to dehiscence of the annuloplasty ring. Another patient underwent mitral valve replacement (MVR) with a cryopreserved mitral homograft 18 months after initial surgery; however, 24 months after MVR, he continued to have recurrent attacks of rheumatic fever with severe aortic regurgitation and MR for which he underwent prosthetic double-valve replacement. Of the other 14 patients, 2 underwent repeat mitral valve repair, and the rest underwent MVR. Two of the latter died postoperatively of low cardiac output.


Figure 1
View larger version (11K):
[in this window]
[in a new window]
 
Figure 1. Freedom from reoperation (Kaplan-Meier) in children after mitral valve repair.
Time interval (mo) 0 12 36 60 120 180

Patients at risk 272 202 156 110 25 19
Freedom from reoperation (%) 100 96.7 92.7 91.7 85.9 85.9
Standard error 0 1.2 1.9 2.1 5.9 5.9

 
Apart from the patient in whom dehiscence of the annuloplasty felt developed, the remaining patients had evidence of progression of the disease, with new thickening of the cusps and subvalvular fusion. Twelve of these patients had mixed MR and MS as the initial lesion.

Valve function
Of the 272 survivors, 177 (65%) had no or trivial to mild MR at last follow-up. The remaining 95 patients (35%) had significant MR after a median period of 34 months (mean, 35.6 ± 34.5 months), which was moderate in 52 (19.1%) and severe in 43 patients (15.9%). Fourteen patients with severe MR underwent reoperation; 3 died as a result of persistent CHF. Freedom from development of significant MR was 55.9% ± 3.5% at a median of 56.5 months and 46.7% ± 4.7% at 15 years. Multivariate analysis of risk factors for significant MR showed a high probability in patients with mixed (regurgitant and stenotic) lesions (hazard ratio, 1.72; 95% confidence interval, 1.25–2.5; P = .006) and in patients with significant left ventricular dysfunction (hazard ratio, 4.9; 95% confidence interval, 2.65–9.2; P<.005.)

Severe MS developed in 3 patients: two underwent reoperation, and 1 was lost to follow-up.

Functional class
One hundred seventy-seven patients with insignificant MR are in NYHA class I. Of the 52 patients with moderate MR, 46 are free of symptoms, 4 are in NYHA class II-III due to development of aortic valve disease, and 2 are in NYHA class III due to left ventricular dysfunction. Of the 43 patients with severe MR, 19 were in NYHA class III or IV: fourteen of the latter underwent reoperation, and 5 died due to persistent CHF. The remaining 24 patients are in either NYHA class I or II. Of the 3 patients with severe MS, 2 were in NYHA class IV and underwent reoperation, and 1 was lost to follow-up. A total of 160 patients (60%) are in normal sinus rhythm.

Late deaths and survival
There were 7 late deaths (2.6%) after a median period of 18 months (mean, 31 ± 41.2 months; range, 2.2 to 118 months). Two patients died at reoperation: 3 due to persistent CHF while awaiting reoperation, 1 due to cerebrovascular accident, and 1 due to acute viral hepatitis.

Actuarial survival in the 278 patients was 95.2% ± 1.5% at 56.5 months and was similar at 15 years. In patients with left ventricular dysfunction, the survival at 56.5 months was 63.8% ± 14.9% compared with 99% ± 0.1% in patients with normal left ventricular function. Left ventricular function was an independent predictor of late death (P = .017). Event-free survival in survivors was 55.9% ± 3.5% at 56.5 months and 46.7% ± 4.7% at 15 years (Figure 2).


Figure 2
View larger version (12K):
[in this window]
[in a new window]
 
Figure 2. Event-free survival (Kaplan-Meier) in children after mitral valve repair.
Time interval (mo) 0 12 >36 60 120 180

Patients at risk 272 195 95 67 25 15
Actuarial survival (%) 100 80.4 58.7 55.7 46.7 46.7
Standard error 0 2.4 3.3 3.5 4.7 4.7

 

    Discussion
 Top
 Abstract
 Patients and methods
 Results
 Discussion
 Conclusion
 References
 
Two thirds of patients with rheumatic heart disease in developing countries are of school age.15 Because of recurrent rheumatic fever, a large proportion of these patients have chronic rheumatic mitral valve disease requiring surgery. Valve replacement is not the best option in these patients because of (1) higher mortality compared with adults; (2) small size of the implanted valve due to smaller heart size; (3) problems of long-term anticoagulation, thromboembolism, and bleeding; (4) rapid degeneration of the available bioprosthesis in the young population; (5) higher risk of endocarditis; and (6) suboptimal preservation of ventricular function and reduced long-term survival.5–8,16,17 Because of these problems, mitral valve repair is the procedure of choice for MR in the young.5–8,16–21

Repair is technically more difficult in this group of patients, and the failure rates are higher, with reoperation rates between 5% to 27% compared with the 8% to 10% rate in the adult population at 5 years of follow-up.6–8,17–20 In one large series, it was found that the rate of repair was inversely related to the age of the patient: At maximum follow-up of 52 months, the reoperation rate in this series was 23.6% in patients 20 years of age or younger compared with 9.6% in older patients.5 In our early experience, the reoperation rate was 5.98%8 in this study, it was 6% at a longer follow-up. Rheumatic etiology, mixed lesions, thickened cusps, and younger age have been associated with an early rate of valve failure.4–6,16,18–20 In an earlier study of more than 800 patients of all age groups undergoing mitral valve repair at our institution, we found that only younger age, left ventricular dysfunction, mixed lesions, and the need for cuspal thinning were independent risk factors for development of significant MR;5 however, in the present study, only left ventricular dysfunction and mixed lesions were independent risk factors in the younger population. The instantaneous hazard for developing significant MR was higher (Figure 3) in the immediate postoperative phase and remained constant for the first 18 months of follow-up. This plateau was followed by a gradual rise up to 6 years, followed by intermittent peaks and a plateau after 10 years of follow-up. This finding correlates with our previous observation that the early peak could be due to suboptimal repair.5 The later peaks may be due to recurrence and progression of rheumatic activity.


Figure 3
View larger version (13K):
[in this window]
[in a new window]
 
Figure 3. Instantaneous risk (hazard function) for development of significant mitral regurgitation across time after mitral valve repair.

 
The results of MVR in children are inferior to those of mitral valve repair. In a report of 90 children undergoing MVR, the in-hospital mortality was 19% with 6 thromboembolic events and 9 bleeding complications on follow-up.7 In a large study of the long-term results of mitral valve repair in 254 young patients with chronic rheumatic MR, the operative mortality was 2.6%, late mortality was 15%, and the reoperation rate was 27% at 5 years of follow-up.4 In contrast, we observed an operative mortality of 2.2% and a late mortality of only 2.6%. Mitral valve repair is thus clearly superior to MVR. A large number of these young patients enjoy a carefree childhood and adolescence and have children before returning for reoperation. The reoperation rates in patients undergoing initial repair or replacement are similar, which favors repair as an option.


    Conclusion
 Top
 Abstract
 Patients and methods
 Results
 Discussion
 Conclusion
 References
 
Mitral valve repair in children with rheumatic heart disease is feasible and provides acceptable long-term results.


    Acknowledgments
 
We thank Dr Rajvir Singh, PhD (Biostatistics), for statistical analysis.


    References
 Top
 Abstract
 Patients and methods
 Results
 Discussion
 Conclusion
 References
 

  1. Loop FD. Long-term results of mitral valve repair. Semin Thorac Cardiovasc Surg. 1989;1:203-210.[Medline]
  2. Antunes MJ, Magalhaes MP, Colsen PR, Kinsley RH. Valvuloplasty for rheumatic mitral valve disease. A surgical challenge. J Thorac Cardiovasc Surg. 1987;94:44-56.[Abstract]
  3. Duran CM, Gometza B, Saad E. Valve repair in rheumatic mitral disease. an unsolved problem. J Card Surg. 1994;9(2 suppl):282-285.[Medline]
  4. Skoularigis J, Sinovich V, Joubert G, Sareli P. Evaluation of the long-term results of mitral valve repair in 254 young patients with rheumatic mitral regurgitation. Circulation. 1994;90(5 pt 2):II167-II174.
  5. Choudhary SK, Talwar S, Dubey B, Chopra A, Saxena A, Kumar AS. Mitral valve repair in a predominantly rheumatic population. Long-term results. Tex Heart Inst J. 2001;28:8-15.[Medline]
  6. Duran CG, Revuelta JM, Gaite L, Alonso C, Fleitas MG. Stability of mitral reconstructive surgery at 10–12 years for predominantly rheumatic valvular disease. Circulation. 1988;78(3 pt 2):I91-I96.
  7. Erez E, Kanter KR, Isom E, Williams WH, Tam VK. Mitral valve replacement in children. J Heart Valve Dis. 2003;12:25-29.[Medline]
  8. Kumar AS, Rao PN, Saxena A. Results of mitral valve reconstruction in children with rheumatic heart disease. Ann Thorac Surg. 1995;60:1044-1047.[Abstract/Free Full Text]
  9. Helmcke F, Nanda NC, Hsiung MC, Soto B, Adey CK, Goyal RG, et al. Color Doppler assessment of mitral regurgitation with orthogonal planes. Circulation 1987;75:175-183.[Abstract/Free Full Text]
  10. Grossman W. Profiles in valvular heart disease. In: Baim DS, Grossman W, editors. Cardiac catheterization, angiography, and intervention. 5th ed.. Baltimore: Willams & Wilkins; 1996. pp. 742-744.
  11. Kumar AS, Kumar RV, Shrivastava S, Venugopal P, Sood AK, Gopinath N. Mitral valve reconstruction. early results of a modified cooley technique. Tex Heart Inst J. 1992;19:107-111.[Medline]
  12. Kumar AS, Rao PN. Restoration of pliability to the mitral leaflets during reconstruction. J Heart Valve Dis. 1995;4:251-253.[Medline]
  13. Kumar AS, Bhan A, Kumar RV, Shrivastava S, Sood AK, Gopinath N. Cusp-level chordal shortening for rheumatic mitral regurgitation. early results. Tex Heart Inst J. 1992;19:47-50.[Medline]
  14. Edmunds LH, Clark Re, Cohn LH, Grunkemeier GL, Miller DC, Weisel RD. Guidelines for reporting morbidity and mortality after cardiac valvular operations. J Thorac Cardiovasc Surg. 1996;112:708-711.[Free Full Text]
  15. Chockalingam A, Prabhakar D, Dorairajan S, Priya C, Gnanavelu G, Venkatesan S. Rheumatic heart disease. occurrence, patterns, and clinical correlates in children aged less than five years. J Heart Valve Dis. 2004;13:11-14.[Medline]
  16. Enriquez-Sarano M, Schaff HV, Orszulak TA, Tajik AJ, Bailey KR, Frye RL. Valve repair improves the outcome of surgery for mitral regurgitation. a multivariate analysis. Circulation. 1995;91:1022-1028.[Abstract/Free Full Text]
  17. Galloway AC, Colvin SB, Baumann FG, Grossi EA, Ribakove GH, Harty S, et al. A comparison of mitral valve reconstruction with mitral valve replacement. intermediate-term results. Ann Thorac Surg. 1989;47:655-662.[Abstract]
  18. Aharon AS, Laks H, Drinkwater DC, Chugh R, Gates RN, Grant PW, et al. Early and late results of mitral valve repair in children. J Thorac Cardiovasc Surg. 1994;107:1262-1270.[Abstract/Free Full Text]
  19. Duran CM, Gometza B, De Vol EB. Valve repair in rheumatic mitral disease. Circulation. 1991;84(5 suppl):III125-III132.
  20. Prabhakar G, Kumar N, Gometza B, Galal O, Al-Halees Z, Duran CM. Triple-valve operation in the young rheumatic patient. Ann Thorac Surg. 1993;55:1492-1496.[Abstract]
  21. Duran CM, Gometza B, Saad E. Valve repair in rheumatic mitral disease. an unsolved problem. J Card Surg. 1994;9(2 suppl):282-285.



This article has been cited by other articles:


Home page
Ann. Thorac. Surg.Home page
R. Hetzer, E. B. M. D. Walter, M. Hubler, V. Alexi-Meskishvili, Y. Weng, N. Nagdyman, and F. Berger
Modified surgical techniques and long-term outcome of mitral valve reconstruction in 111 children.
Ann. Thorac. Surg., August 1, 2008; 86(2): 604 - 613.
[Abstract] [Full Text] [PDF]


Home page
Ann. Thorac. Surg.Home page
A. Kalangos, J. T. Christenson, M. Beghetti, M. Cikirikcioglu, D. Kamentsidis, and Y. Aggoun
Mitral valve repair for rheumatic valve disease in children: midterm results and impact of the use of a biodegradable mitral ring.
Ann. Thorac. Surg., July 1, 2008; 86(1): 161 - 169.
[Abstract] [Full Text] [PDF]


Home page
HeartHome page
V Chaturvedi, S Talwar, B Airan, and B Bhargava
Interventional cardiology and cardiac surgery in India
Heart, March 1, 2008; 94(3): 268 - 274.
[Abstract] [Full Text] [PDF]


Home page
Asian Cardiovasc. Thorac. Ann.Home page
R. P Akhtar, A. R Abid, H. Zafar, S. S Sheikh, M. A Cheema, and J. S Khan
Prosthetic Valve Replacement in Adolescents with Rheumatic Heart Disease
Asian Cardiovasc Thorac Ann, December 1, 2007; 15(6): 476 - 481.
[Abstract] [Full Text] [PDF]


Home page
HeartHome page
V. T Nkomo
Epidemiology and prevention of valvular heart diseases and infective endocarditis in Africa
Heart, December 1, 2007; 93(12): 1510 - 1519.
[Abstract] [Full Text] [PDF]


Home page
ICVTSHome page
A. Sampath Kumar, S. Talwar, A. Saxena, R. Singh, and D. Velayoudam
Results of mitral valve repair in rheumatic mitral regurgitation
Interactive CardioVascular and Thoracic Surgery, August 1, 2006; 5(4): 356 - 361.
[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):
Sachin Talwar
Arkalgud Sampath Kumar
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 Talwar, S.
Right arrow Articles by Kumar, A. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Talwar, S.
Right arrow Articles by Kumar, A. S.
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