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Kardiochirurgia i Torakochirurgia Polska/Polish Journal of Thoracic and Cardiovascular Surgery
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Congenital heart disease in children and adults
Comparison of the Mid-term Results of Pulmonary Valve-sparing Strategy and Transannular Patch Repair in Tetralogy of Fallot

Ozgur Arslan
,
Taylan Adademir
,
Ahmet Elibol
,
Oguz Ugur
,
Ebuzer Aydın
,
Mehmet Kalender
,
Kamil Boyacıoğlu
,
Numan Ali Aydemir

Kardiochirurgia i Torakochirurgia Polska 2013; 10 (4): 352–356
Online publish date: 2013/12/27
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Introduction

Tetralogy of Fallot (TOF) is the most common cause of cyanotic congenital heart disease. Improved operative techniques resulting in reduced operative mortality and the chance of surgical repair in early childhood prior to the development of cardiac compromise from chronic hypoxia have both contributed to improved survival. In this study, early postoperative and mid-term results of two techniques (transannular patch versus pulmonary valve-sparing strategy) for total repair of TOF were compared.

Material and methods

Screening of operative protocols, patient records, and the department database revealed a total of 148 surgically treated patients with TOF without pulmonary atresia from January 2006 to October 2009. All patients (n = 148) were evaluated in the Department of Pediatric Cardiology and echocardiography was performed in all patients. In addition to echocardiography, angiography was done in 140 patients before surgery.

In addition to the status of pulmonary annulus and valvular structures and the clinical status of the patient, the McGoon ratio calculated from angiographic and echocardiographic measurements was used to establish the surgical indication and the need for a shunting operation. The McGoon ratio of the patients ranged from 1.7 to 2.4, with a mean value of 2.06. In patients with a McGoon ratio < 1.6, a Blalock-Taussig (BT) shunt was placed prior to total repair (n = 13), whereas in the remaining patients with a McGoon ratio ≥ 1.7, total repair was the initial procedure.

Selection of the right ventricular outflow tract (RVOT) reconstruction technique was based on preoperative angio­cardiographic and echocardiographic data, as well as the assessment of pulmonary valve structure and body surface area-specific pulmonary annulus diameter during the operation. If a Hegar dilator with a diameter 2-3 mm larger than the normal body surface area-specific pulmonary annulus size could easily pass through the annulus, then the patient was accepted as a candidate for valve-sparing surgery. A transannular patch (TAP) was indicated for patients with a smaller annulus size, hypoplastic annulus, or inappropriate valve structure.

A TAP repair was performed in 127 patients (85.8%), and the pulmonary valve-sparing strategy was used in 21 patients (14.2%). None of the patients required re-operation for a residual ventricular septal defect (VSD) or residual RVOT systolic gradient. In all patients, resection of the infundibular muscle band and VSD closure were done using a transatrial-transpulmonary approach.

A pericardial infundibular patch was used for RVOT reconstruction in 16 of 21 patients who were operated on using the pulmonary valve-sparing strategy. In five patients from the valve-sparing group, pulmonary arterial stenosis was evident after band resection, which was treated with pulmonary artery patch reconstruction.

Echocardiographic evaluation of the right ventricle was done at postoperative 12 months and patients were followed for approximately 4 years. Patients with a > 30% increase in age-specific RV end-diastolic parasternal long axis (M-mode) wall thickness were considered to have a dilated RV due to pulmonary failure.



Surgical technique



A median sternotomy was done under general anes­thesia to access the mediastinum. Previously created aorto-pulmonary shunts were identified and prepared for closure to prevent ventricular distension due to the flow from the systemic circulation to the pulmonary bed during the early periods of cardiopulmonary bypass. Pericardium that would be used in the reconstruction of the right ventricular outflow tract was removed and processed in 0.6% glutaraldehyde for 10 minutes.

Heparin was given at a dose of 3 mg/kg before a standard aortic and bicaval cannulation was done. The patient was cooled following the establishment of partial bypass. Simultaneously, if present, aorto-pulmonary shunt or patent ductus arteriosus was either ligated or a hemostatic clip was applied. The patient was cooled to 30°C and then a cross-clamp was placed to establish total bypass. Cardiac arrest was induced by injection of 20 mL/kg of blood cardioplegic solution from the aortic root. Cardioplegia was repeated every 15-20 mi­nutes with a dose of 10 mL/kg. The VSD was explored and transatrial closure of the VSD was performed by gore-tex patch using a continuous suture technique. First, a transatrial septal and parietal band resection was performed. A ventriculotomy was performed using a vertical incision in the absence of a coronary anomaly crossing the right ventricular outlet, or an incision parallel to the coronary artery was made in the presence of such an anomaly. Septoparietal bands and VSD were explored. Following the septal and parietal band resections, the sizes of the main pulmonary artery and its branches were measured using Hegar dilators.

The pulmonary valve-sparing strategy was used in patients with a well-developed pulmonary valve annulus (n = 21). In order to eliminate pulmonary valve stenosis, if necessary, a pulmonary commissurotomy was performed through ventriculotomy incision. RVOT of 21 patients with a normal annulus diameter in whom valvular stenosis was relieved was reconstructed using a glutaraldehyde-treated pericardium. The pulmonary artery was reconstructed with pulmonary arteriotomy and a pericardial patch in five of these 21 patients. Intraoperative pressure measurements revealed that the RV/LV pressure ratio was < 0.7 in all patients.

In patients with a less developed pulmonary annulus (n = 127), transannular patch repair was done during RVOT reconstruction. When peripheral pulmonary stenosis was present, the patch was extended to the distal part of the stenosis unilaterally or in a T-shape extending the pulmonary arteries bilaterally, whichever was compatible with the anatomy. Intraoperative pressure measurements revealed that the RV/LV ratio was < 0.7 in all patients.

Additional cardiac repairs were carried out during the warming period. Hemofiltration was routinely performed for all patients during weaning from cardiopulmonary bypass. Following de-airing through the left atrial and aortic cannula, the clamp was removed. Extracorporeal circulation was terminated after sufficient pump support.



Statistical analysis



Statistical analysis of data was done using SPSS 11.0 statistical software (SPSS Inc, Chicago, IL, USA). Descriptive data are presented as mean and standard deviation for continuous variables, and categorical data are presented as frequency and percentage. The Kolmogorov-Smirnov test was used to test the normality of distribution. The parametric Student-t test or non-parametric Mann-Whitney U test was used for inter-group comparison of continuous variables. Inter-group comparisons of categorical data were done using the chi-square test or Fisher exact test, where appropriate. A p value < 0.05 was considered as an indication of statistical significance.

Results

Of the 148 patients included in the study, the pulmonary valve-sparing strategy was used in 21 patients. A BT shunt was done in 13 of 148 patients before total repair (TAP or pulmonary valve-sparing strategy). Of these 13 patients, TAP was performed for 12 patients and pulmonary valve-sparing strategy was used for one patient. All 21 patients who were operated on using the valve-sparing stra­tegy had a well-developed annulus.

Details of demographic and clinical characteristics of the patients are given in Table I. There was no significant difference between the two groups in terms of age. However, the mean weight in the valve-sparing group was significantly lower and in that group the male-to-female ratio was significantly higher. Regarding clinical data, hypoplastic annulus and RV diastolic dilatation (corrected for age, at follow-up) were more frequent among the patients in the TAP group. In addition, the follow-up residual RVOT systolic gradient was higher and the RV diastolic parasternal long axis wall thickness was shorter in the valve-sparing group, whereas groups did not differ with regard to intraope­rative RV/LV pressure ratio. During follow-up, moderate-to-severe free pulmonary insufficiency occurred in 80% of the patients treated by TAP, whereas mild-to-moderate pulmonary insufficiency was present in 30% of the patients treated by the pulmonary valve-sparing strategy.

Five patients died in the TAP group (3.9%), whereas no deaths were recorded in the pulmonary valve-sparing group. However, the difference was not significant (p = 0.49). Detailed postoperative morbidity and mortality data are given in Table II.

Discussion

The original surgical repair of TOF involves closure of the VSD through a large right ventriculotomy and enlargement of the RVOT with a large TAP [1]. Later, advanced techniques including transatrial closure of the VSD and resection of the RVOT [2-3], and transatrial-transpulmonary repair and enlargement of the pulmonary artery with a patch [4-5] were developed. The most promising techniques avoid ventriculotomy and adopt a pulmonary valve-sparing strategy. In addition, pre- and peri-operative evaluations together with the use of a Z-value, defined by Kirklin et al. [6], and the pulmonary index, introduced by Nakata [7], led to a significant reduction in mortality and morbidity rates, and offered the chance to perform early primary repair during infancy.

Although satisfactory results have been obtained by surgery performed in the neonatal period and infancy together with the use of TAP with well-tolerated free pulmonary insufficiency [8-12], some studies have demonstrated that free pulmonary insufficiency induced by the TAP procedure is not well tolerated; and RV dysfunction [13-14], low functional status [15], arrhythmia, and sudden death [16-17] have been reported in the long-term follow-up of these patients. Gatzoulis et al. reported that occurrence of free pulmonary insufficiency after TAP repair was associated with ventricular tachycardia and sudden death in the long-term follow-up period [17]. On the other hand, several long-term studies have demonstrated improvement in ventricular function and symptoms by placement of the pulmonary valve following TOF repair [18-19].

Several studies have compared TAP with other strategies. Bacha et al. evaluated the long-term results of 45 patients with TOF who were operated on in the infantile period and reported successful outcomes without any significant difference between the valve-sparing strategy and TAP in terms of functional status [10]. On the other hand, Kirklin et al. retrospectively evaluated 814 patients (aged between 2 months and 57 years) with TOF who had been treated by total repair [11]: 255 were treated by TAP, 538 by RVOT patch with or without pulmonary valvotomy, and 21 by valved conduit. The mortality rate was 4% in the TAP group, whereas it was 1.4% in the patients who did not undergo TAP. Based on their 20 years of experience and considering the potential RV dysfunction problems and pulmonary insufficiency in the early and late periods, Kirklin et al. recommended preservation of the pulmonary artery annulus in patients with TOF where possible and they suggested that TAP should be reserved for patients with an expected RV/LV pressure ratio > 0.65 after repair. In support of these suggestions, findings of this study were in favor of the pulmonary valve sparing strategy. During follow-up, the mean RV diastolic parasternal long axis wall thickness on echocardiography was significantly higher and RV dia­stolic dilation (corrected for age) was significantly more frequent in the TAP group, when compared to the valve-sparing strategy group. In addition, moderate-to-severe free pulmonary insufficiency was evident in a substantial proportion of patients (80%) in the TAP group.

None of the patients in this study required re-operation for residual VSD and/or RVOT obstruction during follow-up. Despite higher residual RVOT systolic gradient in the valve-sparing group, no significant difference was found between groups with regard to re-operation for residual RVOT gradient. Aggressive resection of the muscle bands within the right ventricle seems to account for the absence of re-operation requirement in either of the groups. Besides muscle band resection, commissurotomy was performed when pulmonary stenosis was present. If a residual gra­dient is suspected despite valvotomy, and there is obstruction in the RVOT and/or pulmonary artery and/or its distal parts, reconstruction should be performed with two separate patches preserving the annulus.

There was no significant difference between the TAP and pulmonary valve-sparing strategy groups in terms of the RV/LV pressure ratio, and the mean ratio was 0.5. Kirklin et al. and Katz et al. reported that the mortality risk was increased by 2.5 and the re-operation risk was increased by 7.3-fold when RV/LV pressure ratio is > 0.85 [11, 20]. Hirch et al. also reported that the re-operation risk is increased when the RV/LV pressure ratio is > 0.7 [21]. In the present study, we aimed to keep the RV/LV pressure ratio < 0.7 in both treatment groups. In our study, the valve type of 21 patients treated using the pulmonary valve-sparing strategy was tricuspid in 20 patients and bicuspid in one patient. Besides the annulus diameter, the presence of a tricuspid pulmonary valve is also an important determinant for the pulmonary valve-sparing strategy since the tricuspid pulmonary valve has been reported to be associated with a low post-operative RV/LV pressure ratio and reduced prevalence of pulmonary insufficiency [22-24].

Karl et al. treated 366 patients with TOF between 1980 and 1991. The transatrial-transpulmonary approach was used and the hospital mortality rate was 0.5%. The surgery was postponed until the infant was 6-8 months of age. A palliative shunt was performed in 37% of these patients [4]. In this study including 148 patients with TOF, the mean age of 127 patients treated with TAP was 4.7 years and the mean age of 21 patients treated using the pulmonary valve-sparing strategy was 3.6 years. We believe that as the experience with the pulmonary valve-sparing strategy increases, the age of patients will decrease to the infant age.

Conclusion

In total correction of TOF, the pulmonary valve-sparing strategy seems to result in less perioperative mortality/morbidity and better long-term preservation of RV function, when compared to TAP. Thus, it would be wise to recom­mend avoiding TAP, particularly in patients with well-developed pulmonary valves, and to preserve pulmonary valve functions. TAP should be reserved for patients with insufficient annulus diameter or insufficient relief of RVOT obstruction despite resection.

References

1. Gott VL. C. Walton Lillehei and total correction of tetralogy of Fallot. Ann Thorac Surg 1990; 49: 328-332.

2. Hudspeth AS, Cordell AR, Johnston FR. Transatrial approach to total correction of tetralogy of Fallot. Circulation 1963; 27: 796-800.

3. Edmunds LH Jr., Saxena NC, Friedman S, Rashkind WJ, Dodd PF. Transatrial repair of tetralogy of Fallot. Surgery 1976; 80: 681-688.

4. Karl TR, Sano S, Pornviliwan S, Mee RB. Tetralogy of Fallot: favorable outcome of nonneonatal transatrial, transpulmonary repair. Ann Thorac Surg 1992; 54: 903-907.

5. Pacifico AD, Sand ME, Bargeron LM Jr., Colvin EC. Transatrial-transpulmonary repair of tetralogy of Fallot. J Thorac Cardiovasc Surg 1987; 93: 919-924.

6. Kirklin JK, Kirklin JW, Pacifico AD. Transannular outflow tract patching for tetralogy: indications and results. Semin Thorac Cardiovasc Surg 1990; 2: 61-69.

7. Nakata S, Imai Y, Takanashi Y, Kurosawa H, Tezuka K, Nakazawa M, Ando M, Takao A. A new method for the quantitative standardization of cross-sectional areas of the pulmonary arteries in congenital heart diseases with decreased pulmonary blood flow. J Thorac Cardiovasc Surg 1984; 88: 610-619.

8. Castaneda AR, Freed MD, Williams RG, Norwood WI. Repair of tetralogy of Fallot in infancy. Early and late results. J Thorac Cardiovasc Surg 1977; 74: 372-381.

9. Pigula FA, Khalil PN, Mayer JE, del Nido PJ, Jonas RA. Repair of tetralogy of Fallot in neonates and young infants. Circulation 1999; 100: II157-II161.

10. Bacha EA, Scheule AM, Zurakowski D, Erickson LC, Hung J, Lang P, Mayer JE Jr., del Nido PJ, Jonas RA. Long-term results after early primary repair of tetralogy of Fallot. J Thorac Cardiovasc Surg 2001; 122: 154-161.

11. Kirklin JK, Kirklin JW, Blackstone EH, Milano A, Pacifico AD. Effect of transannular patching on outcome after repair of tetralogy of Fallot. Ann Thorac Surg 1989; 48: 783-791.

12. Murphy JG, Gersh BJ, Mair DD, Fuster V, McGoon MD, Ilstrup DM, McGoon DC, Kirklin JW, Danielson GK. Long-term outcome in patients undergoing surgical repair of tetralogy of Fallot. N Engl J Med 1993; 329: 593-599.

13. Frigiola A, Redington AN, Cullen S, Vogel M. Pulmonary regurgitation is an important determinant of right ventricular contractile dysfunction in patients with surgically repaired tetralogy of Fallot. Circulation 2004; 110: II153-II157.

14. Singh GK, Greenberg SB, Yap YS, Delany DP, Keeton BR, Monro JL. Right ventricular function and exercise performance late after primary repair of tetralogy of Fallot with the transannular patch in infancy. Am J Cardiol 1998; 81: 1378-1382.

15. Carvalho JS, Shinebourne EA, Busst C, Rigby ML, Redington AN. Exercise capacity after complete repair of tetralogy of Fallot: deleterious effects of residual pulmonary regurgitation. Br Heart J 1992; 67: 470-473.

16. Marie PY, Marcon F, Brunotte F, Briancon S, Danchin N, Worms AM, Robert J, Pernot C. Right ventricular overload and induced sustained ventricular tachycardia in operatively “repaired” tetralogy of Fallot. Am J Cardiol 1992; 69: 785-789.

17. Gatzoulis MA, Balaji S, Webber SA, Siu SC, Hokanson JS, Poile C, Rosenthal M, Nakazawa M, Moller JH, Gillette PC, Webb GD, Redington AN. Risk factors for arrhythmia and sudden cardiac death late after repair of tetralogy of Fallot: a multicentre study. Lancet 2000; 356: 975-981.

18. Discigil B, Dearani JA, Puga FJ, Schaff HV, Hagler DJ, Warnes CA, Danielson GK. Late pulmonary valve replacement after repair of tetralogy of Fallot. J Thorac Cardiovasc Surg 2001; 121: 344-351.

19. Eyskens B, Reybrouck T, Bogaert J, Dymarkowsky S, Daenen W, Dumoulin M, Gewillig M. Homograft insertion for pulmonary regurgitation after repair of tetralogy of fallot improves cardiorespiratory exercise performance. Am J Cardiol 2000; 85: 221-225.

20. Katz NM, Blackstone EH, Kirklin JW, Pacifico AD, Bargeron LM Jr. Late survival and symptoms after repair of tetralogy of Fallot. Circulation 1982; 65: 403-410.

21. Hirsch JC, Mosca RS, Bove EL. Complete repair of tetralogy of Fallot in the neonate: results in the modern era. Ann Surg 2000; 232: 508-514.

22. Stewart RD, Backer CL, Young L, Mavroudis C. Tetralogy of Fallot: results of a pulmonary valve-sparing strategy. Ann Thorac Surg 2005; 80: 1431-1438; discussion 1438-1439.

23. Parry AJ, McElhinney DB, Kung GC, Reddy VM, Brook MM, Hanley FL. Elective primary repair of acyanotic tetralogy of Fallot in early infancy: overall outcome and impact on the pulmonary valve. J Am Coll Cardiol 2000; 36: 2279-2283.

24. Boudjemline Y, Agnoletti G, Bonnet D, Sidi D, Bonhoeffer P. Percutaneous pulmonary valve replacement in a large right ventricular outflow tract: an experimental study. J Am Coll Cardiol 2004; 43: 1082-1087.

25. Sousa Uva M, Lacour-Gayet F, Komiya T, Serraf A, Bruniaux J, Touchot A, Roux D, Petit J, Planche C. Surgery for tetralogy of Fallot at less than six months of age. J Thorac Cardiovasc Surg 1994; 107: 1291-1300.
Copyright: © 2013 Polish Society of Cardiothoracic Surgeons (Polskie Towarzystwo KardioTorakochirurgów) and the editors of the Polish Journal of Cardio-Thoracic Surgery (Kardiochirurgia i Torakochirurgia Polska). This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
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