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Congenitally corrected transposition of the great arteries: An update

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Congenitally corrected transposition of the great arteries is a rare condition in which systemic venous blood returns to normally positioned atria. However, the atria are connected to the opposite ventricle, right atrium to left ventricle, left atrium to right ventricle; so-called atrioventricular disordance. In addition, the ventricles are inverted (right to left change in position) and are connected to the opposite great artery, left ventricle to pulmonary artery, right ventricle to aorta; thus, forming ventricular-arterial discordance. The aorta is anterior and to the left of the pulmonary artery, L-transposed. Atrioventricular discordance plus ventricular-arterial discordance results in normal blood flow (ie, congenitally corrected). The right ventricle with the tricuspid valve is the systemic ventricle. Common associated conditions are ventricular septal defects (VSDs), pulmonary stenosis, and congenital heart block. Major issues related to management revolve around the status of the systemic right ventricle, which can develop dysfunction with increasing age and tricuspid regurgitation, which can increase in severity with age and contribute to ventricular dysfunction. One emerging treatment is the double switch operation. In patients with no pulmonary obstruction, it is possible to switch the systemic and pulmonary venous return using an atrial baffle procedure followed by an arterial switch procedure. This results in the anatomical left ventricle now functioning as the systemic ventricle. In those patients with associated pulmonary obstruction and a VSD, another type of double switch can be performed in which the left ventricle is tunneled through the VSD to the aorta, the right ventricle is connected to the pulmonary artery with a homograft or other conduit, and the atrial baffle procedure is performed. The most difficult challenge is choosing the patient who is a candidate for the double-switch operation and the timing of that operation, or the timing of a more classical operation for associated defects.

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References and Recommended Reading

  1. Graham TP: Congenitally corrected transposition. In Diagnosis and Management of Adult Congenital Heart Disease, edn. 1. Edited by Golzouli MA, et al. London: Churchill Livingstone; 2003:379–387.

    Google Scholar 

  2. Dabizzsi RP, Barletta GA, Caprioli G, et al.: Coronary artery anatomy in corrected transposition of the great arteries. J Am Coll Cardiol 1988, 12:486–491.

    Article  Google Scholar 

  3. Hornung TS, Bernard EJ, Jaeggi ET, et al.: Myocardial perfusion defects and associated systemic ventricular dysfunction in congenitally corrected transposition of the great arteries. Heart 1998, 80:322–326.

    PubMed  CAS  Google Scholar 

  4. Fischbach PS, Law JH, Serwer GS: Congenitally corrected transposition of the great arteries abnormalities of atrioventricular conduction. Prog Pediatr Cardiol 1999, 10:37–43.

    Article  Google Scholar 

  5. deLeval M, Bastos P, Stark J, et al.: Surgical technique to reduce risk of heart block following closure of ventricular septal defect in atrioventricular discordance. J Thorac Cardiovasc Surg 1979, 78:515–526.

    CAS  Google Scholar 

  6. Sano T, Riesenfeld T, Karl TR, Wilkinson JL: Intermediate-term outcome after intracardiac repair of associated defects with atrioventricular and ventriculoarterial discordance. Circulation 1995, 92(suppl II):II272–II278.

    PubMed  CAS  Google Scholar 

  7. Prieto L, Hordof AJ, Secic M, et al.: Progressive tricuspid valve disease in patients with congenitally corrected transposition of the great arteries. Circulation 1998, 98:997–1005.

    PubMed  CAS  Google Scholar 

  8. Acar P, Sidi D, Bonnet D, et al.: Maintaining tricuspid valve competence in double discordance; a challenge for the pediatric cardiologist. Heart 1998, 80:479–483.

    PubMed  CAS  Google Scholar 

  9. Yagihara T, Kishimoto H, Isobe F, et al.: Double switch operation in cardiac anomalies with atrioventricular and ventriculoarterial discordance. J Thorac Cardiovasc Surg 1994, 107:351–358.

    PubMed  CAS  Google Scholar 

  10. Yeh T, Connelly MS, Coles JG, et al.: Atrioventricular discordance: results of repair in 127 patients. J Thorac Cardiovasc Surg 1999, 117:1190–1203.

    Article  PubMed  Google Scholar 

  11. Imai Y, Sawatari K, Hoshkino S, et al.: Ventricular function after anatomic repair in patients with atrioventricular discordance. J Thorac Cardiovasc Surg 1994, 107:1272–1283.

    PubMed  CAS  Google Scholar 

  12. Forbess JM, Shah AS, St Louis JD, et al.: Cryopreserved homografts in the pulmonary position: determinants of durability. Ann Thorac Surg 2001, 71:54–60.

    Article  PubMed  CAS  Google Scholar 

  13. Ilbawi MN, DeLeon SY, Backer CL, et al.: An alternative approach to the surgical management of physiologically corrected transposition with ventricular septal defect and pulmonary stenosis or atresia. J Thorac Cardiovasc Surg 1990, 100:410–415.

    PubMed  CAS  Google Scholar 

  14. Graham TP, Driscoll DJ, Gersony WM, et al.: Task Force 2: congenital heart disease. Am Coll Cardiol 2005, 45:1326–1333.

    Article  Google Scholar 

  15. Reddy VM, McElhinney DB, Silverman NH, Hanley FL: The double switch procedure for anatomical repair of congenital corrected transposition of the great arteries in infants and children. Eur Heart J 1997, 18:1470–1477.

    PubMed  CAS  Google Scholar 

  16. Karl RT, Weintraub RG, Brizard CP, et al.: Senning plus arterial switch operation for discordant (congenital corrected) transposition. Ann Thorac Surg 1997, 64:493–502.

    Google Scholar 

  17. Yamagishi M, Imai Y, Hoshino S, et al.: Anatomic correction of atrioventricular discordance. J Thorac Cardiovasc Surg 1993, 105:1067–1976.

    PubMed  CAS  Google Scholar 

  18. Stumper O, Wright JGC, Giovanni JVD, et al.: Combined atrial and atrial switch procedure for congenital corrected transposition with ventricular septal defect. Br Heart J 1995, 73:470–482.

    Article  Google Scholar 

  19. DeVaney EJ, Charpie JR, Ohye RG, Bobe EL: Combined arterial switch procedure and Senning operation for congenitally corrected transposition of the great arteries: patient selection and intermediate results. J Thorac Cardiovasc Surg 2003, 125:500–507.

    Article  PubMed  Google Scholar 

  20. Duncan BW, Mee RB: Management of the failing systemic right ventricle. Semin Thorac Cardiovasc Surg 2005, 17:160–169.

    Article  PubMed  Google Scholar 

  21. Graham TP Jr, Bernard YD, Mellen BG, et al.: Long-term outcome in congenitally corrected transposition of the great arteries: a multi-institutional study. J Am Coll Cardiol 2000, 36:255–261.

    Article  PubMed  Google Scholar 

  22. Hraska V, Duncan BW, Mayer JE, et al.: Long-term outcome of surgically treated patients with corrected transposition of the great arteries. J Thorac Cardiovasc Surg 2005, 129:182–192.

    Article  PubMed  Google Scholar 

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Correspondence to Thomas P. Graham Jr.

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Graham, T.P., Markham, L., Parra, D.A. et al. Congenitally corrected transposition of the great arteries: An update. Curr Treat Options Cardio Med 9, 407–413 (2007). https://doi.org/10.1007/s11936-007-0061-y

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