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MMCTS (February 20, 2008). doi:10.1510/mmcts.2006.002337
Copyright © 2008 European Association for Cardio-thoracic Surgery


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Procedure


Nikaidoh operation for transposition of the great arteries with a ventricular septal defect and pulmonary stenosis

Victor O. Morell* and Peter D. Wearden

Section of Pediatric Cardiothoracic Surgery of the Heart, Lung and Esophageal Surgical Institute, University of Pittsburgh Medical School, Children's Hospital of Pittsburgh, Room 2820, 3705 Fifth Avenue, Pittsburgh, PA 15213, USA

* Corresponding author: * Tel.: +1-412-692 5218; fax: +1-412-692 5817 E-mail:victor.morell{at}chp.edu


    Summary
 Top
 Summary
 Introduction
 Surgical technique
 Results
 Discussion
 Acknowledgements
 References
 
The optimal surgical management of patients with transposition of the great arteries with a ventricular septal defect and pulmonary stenosis remains challenging. When compared to other surgical options, the Nikaidoh procedure results in a ‘more normal’ anatomic result, with better alignment of the right and left ventricular outflow tracts. Also, the pulmonary outflow is less likely to be compressed by the sternum, a major issue associated with the Rastelli repair. This technique is especially useful in the presence of an inlet or restrictive ventricular septal defect, a hypoplastic right ventricle, a straddling atrioventricular valve and/or anomalous coronary anatomy interfering with a distal right ventricular outflow tract incision.

Key Words: Aortic translocation • Nikaidoh procedure • Rastelli repair • Transposition of the great arteries


    Introduction
 Top
 Summary
 Introduction
 Surgical technique
 Results
 Discussion
 Acknowledgements
 References
 
In 1980, Bex and associates [1] were the first to introduce the concept of aortic translocation for the management of transposition of the great arteries (TGA) but it was Nikaidoh [2], in 1984, who popularized the technique for the treatment of TGA with a ventricular septal defect (VSD) and pulmonary stenosis (PS). The repair consists of harvesting the aortic root from the right ventricle, relieving the left ventricular outflow tract obstruction by dividing the outlet septum and excising the pulmonary valve, reconstructing the left ventricular outflow tract (LVOT) with the translocated aortic root and the VSD patch, and the right ventricular outflow tract (RVOT) with a pericardial patch. Modifications to the original technique include individual coronary transfer during translocation (to avoid the possibility of coronary ischemia), the use of the Lecompte maneuver, and RVOT reconstruction with a pulmonary homograft or direct right ventricle to pulmonary artery anastomosis. Although technically challenging, aortic translocation combines elements of commonly performed surgical techniques including the Ross, Konno and Jatene procedures.


    Surgical technique
 Top
 Summary
 Introduction
 Surgical technique
 Results
 Discussion
 Acknowledgements
 References
 
Via a standard median sternotomy incision cardiopulmonary bypass is established with a single right atrial cannula or with bicaval cannulation and a left ventricular vent. The patient is cooled to 28–30 °C. A piece of pericardium is harvested and placed in glutaraldehyde for the reconstruction of the right ventricular outflow tract. The branch pulmonary arteries are extensively mobilized to allow for the Lecompte maneuver.

With a beating heart, or under cardiac arrest, the aorta is harvested from the right ventricle (Videos 1 and 2, Schematic 1). Importantly, the proximal aspects of the coronary arteries need to be extensively mobilized in order to safely separate the aortic root from the right ventricle and to allow for the translocation of the aorta without undo tension and/or torsion on the coronaries. Alternatively, under cardiac arrest, the coronary buttons are harvested before the aortic root is separated from the right ventricle (Schematics 2Go4).


Figure 1
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Video 1 The anterior aspect of the aortic root has been partially dissected from the right ventricle.
 

Figure 2
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Video 2 The aortic root has been completely separated from the right ventricle with the coronary arteries attached. Note the distended and competent aortic valve.
 

Figure 1
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Schematic 1 The aortic root is harvested from the RV and the proximal pulmonary artery divided.

 

Figure 2
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Schematic 2 With a posterior and leftward pulmonary trunk (A) only the right coronary button is harvested (B) and reimplanted (C). Note the clockwise rotation of the aortic root.

 

Figure 3
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Schematic 3 With a posterior and rightward pulmonary trunk (A) only the left coronary button is harvested (B) and reimplanted (C). Note the counterclockwise rotation of the aortic root during translocation.

 

Figure 4
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Schematic 4 When the pulmonary trunk is located posterior to the aortic root (A) both coronaries are harvested (B) and reimplanted (C).

 
The main pulmonary artery is transected proximally and the pulmonary valve leaflets excised (Videos 3 and 4).


Figure 3
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Video 3 The proximal pulmonary artery is partially transected.
 

Figure 4
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Video 4 The proximal pulmonary artery has been completely transected allowing for resection of the pulmonary valve leaflets and visualization of the morphologic left ventricular outflow tract.
 
The outlet septum is then opened into the VSD (Videos 5 and 6); then, the aortic root is translocated posteriorly, suturing the posterior aspect of the aortic root to the opened pulmonary annulus (Videos 7 and 8, Schematic 5).


Figure 5
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Video 5 The outlet septum is clearly identified.
 

Figure 6
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Video 6 The outlet septum is divided.
 

Figure 7
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Video 7 The posterior suture-line between the proximal aortic root and the pulmonary annulus is performed with a running suture. In this case, the right coronary button was separated from the aorta before moving the aortic root.
 

Figure 8
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Video 8 With a beating heart, the aortic root is sutured to the posterior pulmonary annulus.
 

Figure 5
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Schematic 5 The outlet septum has been opened into the VSD and the aortic root is sutured to the pulmonary annulus. Note the harvested right coronary button.

 
The ventricular septal defect is closed with a patch and the anterior aspect of the aortic root is sutured to the superior aspect of the VSD patch (Videos 9 and 10, Schematic 6). In some patients the anterior aspect of the aortic root can be sutured directly to the crest of the VSD, eliminating the need of a VSD patch (Video 11).


Figure 9
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Video 9 The ventricular septal defect is clearly seen after the aortic translocation.
 

Figure 10
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Video 10 The VSD has been closed with a patch; the right ventricular outflow tract is inspected.
 

Figure 6
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Schematic 6 The VSD is closed with a patch.

 

Figure 11
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Video 11 The proximal root is sutured directly to the crest of the VSD with interrupted-pledgeted-mattress sutures, avoiding the need of a patch.
 
Under cardiac arrest, the ascending aorta is transected thus allowing for the Lecompte maneuver. A small section of the aorta is excised in order to prevent or minimize the anterior bowing of the ascending aorta, which could contribute to proximal branch pulmonary artery stenosis (Videos 12 and 13).


Figure 12
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Video 12 After aortic transection the Lecompte maneuver is performed and a segment of ascending aorta excised.
 

Figure 13
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Video 13 With the ascending aorta back together, we are now ready to establish RV to PA continuity.
 
Finally, the proximal main pulmonary artery is connected directly to the right ventricle with an anterior patch of pericardium (Videos 14 and 15, Schematics 7 and 8). Also, the pericardial patch is used to augment the main pulmonary artery, which is usually hypoplastic. A monocup valve could be used in the pulmonary position. Alternatively, a pulmonary homograft could be used to establish right ventricle to pulmonary artery continuity.


Figure 14
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Video 14 The main pulmonary artery is sutured to the RVOT. Note that the anterior wall of the PA has been opened longitudinally to the level of the bifurcation.
 

Figure 15
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Video 15 An anterior autologous pericardial patch is utilized to augment the main pulmonary artery and complete the RV to PA connection.
 

Figure 7
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Schematic 7 The pulmonary artery is directly sutured to the distal right ventricular outflow tract opening.

 

Figure 8
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Schematic 8 An anterior pericardial patch is used to complete the RV to PA anastomosis.

 

    Results
 Top
 Summary
 Introduction
 Surgical technique
 Results
 Discussion
 Acknowledgements
 References
 
Since 1996, 21 patients have undergone aortic translocation at Children's Hospital of Pittsburgh and at the Congenital Heart Institute of Florida. There was one (4.7%) early death and one patient required cardiac transplantation because of severe postoperative left ventricular dysfunction. The late mortality consists of three patients, two of which were preventable (one patient died from an unrecognized pericardial effusion and one from cardiac injury during sternal reentry).

On his latest report, Nikaidoh [2] describes no intervention for left ventricular outflow tract problems and five interventions for right ventricular outflow tract problems (two for conduit stenosis and three for pulmonary insufficiency) in a group of eighteen patients with a mean follow-up of 13 years. His early mortality was of 5.2%, and there were no late deaths. Interestingly, half the patients have developed mild aortic insufficiency. In our series, three patients have required right ventricle to pulmonary artery conduit replacement because of conduit stenosis and one underwent aortic valve replacement because of severe aortic insufficiency. Table1 summarizes several institutional experiences with the aortic translocation procedure.


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Table 1 Summary of institutional experiences with the aortic translocation procedure

 

    Discussion
 Top
 Summary
 Introduction
 Surgical technique
 Results
 Discussion
 Acknowledgements
 References
 
The Nikaidoh procedure results in a more ‘normal’ anatomic repair; the right and left ventricular outflow tracts are better aligned, avoiding the right angle turns created by the Rastelli repair. Also, the right ventricle to pulmonary artery connection is less susceptible to sternal compression (Schematic 9), which should decrease the incidence of reoperations for right ventricular outflow obstruction, especially when using a direct pulmonary artery to right ventricle connection [4].


Figure 9
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Schematic 9 The right ventricle to pulmonary artery connection is more susceptible to sternal compression in the Rastelli (A) than in the Nikaidoh (B) because of the non-anatomical origin of the conduit from the distal right ventricular outflow tract in the Rastelli repair.

 
In our experience, the only contraindication to the Nikaidoh procedure has been the presence of anomalous coronary anatomy. The epicardial course of a major coronary artery could preclude the safe harvesting of the aortic root from the right ventricle (i.e. right coronary artery originating from the left main). Also, the coronary anatomy could affect the ability to safely move the aorta posteriorly, into the pulmonary annulus (i.e. posterior intramural coronary artery course); this anatomy may also not be amenable to coronary reimplantation in conjunction with aortic translocation. In these patients the Rastelli procedure appears to be a better option.

Aortic translocation is a complex operation that has an acceptable early and late mortality, and should be considered for patients undergoing repair of transposition of the great arteries with a ventricular septal defect and pulmonary stenosis. Although the overall ‘published experience’ [1, 2, 3, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17] with this technique is somewhat limited, the early and midterm results are encouraging, suggesting improved outcomes when compared to the Rastelli. Certainly, in patients with ‘inadequate anatomy’ for a Rastelli repair the Nikaidoh procedure becomes an attractive alternative.



    Acknowledgements
 Top
 Summary
 Introduction
 Surgical technique
 Results
 Discussion
 Acknowledgements
 References
 
We would like to thank Dr. Angelo Rutty for the beautiful illustrations.


    References
 Top
 Summary
 Introduction
 Surgical technique
 Results
 Discussion
 Acknowledgements
 References
 

  1. Bex JP, Lecompte Y, Baillot F, Hazan E. Anatomical correction of transposition of the great arteries. Ann Thorac Surg 1980;29:86–88.[Abstract]
  2. Nikaidoh H. Aortic translocation and biventricular outflow tract reconstruction. A new surgical repair for transposition of the great arteries associated with ventricular septal defect and pulmonary stenosis. J Thorac Cardiovasc Surg 1984;88:365–372.[Abstract]
  3. Yeh T, Ramaciotti C, Leonard SR, Roy L, Nikaidoh H. The aortic translocation (Nikaidoh) procedure: midterm results superior to the Rastelli procedure. J Thorac Cardiovasc Surg 2007;133:461–469.[Abstract/Free Full Text]
  4. Kreutzer C, De Vive J, Oppido G, Kreutzer J, Gauvreau K, Freed M, Mayer JE Jr, Jonas R, Del Nido PJ. Twenty-five-year experience with Rastelli repair for transposition of the great arteries. J Thorac Cardiovasc Surg 2000;120:211–223.[Abstract/Free Full Text]
  5. Morell VO, Jacobs JP, Quintessenza JA. Surgical management of transposition with ventricular septal defect and obstruction to the left ventricular outflow tract. Cardiol Young 2005;15:102–105.[CrossRef][Medline]
  6. Morell VO, Jacobs JP, Quintessenza JA. Aortic translocation in the management of transposition of the great arteries with ventricular septal defect and pulmonary stenosis: results and follow-up. Ann Thorac Surg 2005;79:2089–2093.[Abstract/Free Full Text]
  7. Morell VO. Aortic translocation for TGA with VSD and PS. Cardiothoracic surgery Network, Expert Techniques, Congenital Cardiac, November, 2005.
  8. Morell VO, Wearden PD. Aortic translocation for the management of transposition of the great arteries with a ventricular septal defect, pulmonary stenosis and hypoplasia of the right ventricle. Eur J Cardiothorac Surg 2007;31:552–554.[Abstract/Free Full Text]
  9. Morell VO, Jacobs JP, Quintessenza JA. The role of aortic translocation in the management of complex transposition of the great arteries. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu 2004;7:80–84.[CrossRef][Medline]
  10. Sayin OA, Ugurlucan M, Saltik L, Sungur Z, Tireli E. Modified Nikaidoh procedure for transposition of great arteries, ventricular septal defect and left ventricular outflow tract obstruction. Thorac Cardiovasc Surg 2006;54:558–560.[CrossRef][Medline]
  11. Bautista-Hernandez V, Marx GR, Bacha EA, del Nido PJ. Aortic root translocation plus arterial switch for transposition of the great arteries with left ventricular outflow tract obstruction: intermediate-term results. J Am Coll Cardiol 2007;49:485–490.[Abstract/Free Full Text]
  12. Hu S, Li S, Wang X, Wang L, Xiong H, Li L, Yan F, Wang X. Pulmonary and aortic root translocation in the management of transposition of the great arteries with ventricular septal defect and left ventricular outflow tract obstruction. J Thorac Cardiovasc Surg 2007;133:1090–1092.[Free Full Text]
  13. Hazekamp M, Portela F, Bartelings M. The optimal procedure for the great arteries and left ventricular outflow tract obstruction. An anatomical study. Eur J Cardiothorac Surg 2007;31:879–887.[Abstract/Free Full Text]
  14. Yamagishi M, Shuntoh K, Matsushita T, Fujiwara K, Shinkawa T, Miyazaki T, Kitamura N. Half-turned truncal switch operation for complete transposition of the great arteries with ventricular septal defect and pulmonary stenosis. J Thorac Cardiovasc Surg 2003;125:966–968.[Free Full Text]
  15. Kandeel M, Kumar N, Prabhakar G, Al-Halees Z, Duran CMG. Aortic translocation for D-TGA associated with LVOTO and VSD. Ann Thorac Surg 1995;59:515–517.[Abstract/Free Full Text]
  16. Haas GS. Advances in pediatric cardiovascular surgery: anatomic reconstruction of the left ventricular outflow tract in transposition of the great arteries with pulmonic valve abnormalities. Curr Opin Pediatr 2000;12:501–504.[CrossRef][Medline]
  17. Jacobs ML, Pelletier G, Wearden PD, Morell VO. The role of Fontan's procedure and aortic translocation in the surgical management of patients with discordant atrioventricular connections, interventricular communication, and pulmonary stenosis or atresia. Cardiol Young 2006;16:97–102.[Medline]



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