Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-19T22:47:10.391Z Has data issue: false hasContentIssue false
  • English
  • Français

Anatomic correction of congenitally corrected transposition and its close cousins

Published online by Cambridge University Press:  13 October 2006

Edward L. Bove ,
Richard G. Ohye ,
Eric J. Devaney ,
Hiromi Kurosawa ,
Toshiharu Shin'oka ,
Aki Ikeda  and
Toshio Nakanishi
Edward L. Bove
Affiliation:
The Division of Pediatric Cardiovascular Surgery, Section of Cardiac Surgery, The University of Michigan School of Medicine, Ann Arbor, Michigan, United States of America
Richard G. Ohye
Affiliation:
The Division of Pediatric Cardiovascular Surgery, Section of Cardiac Surgery, The University of Michigan School of Medicine, Ann Arbor, Michigan, United States of America
Eric J. Devaney
Affiliation:
The Division of Pediatric Cardiovascular Surgery, Section of Cardiac Surgery, The University of Michigan School of Medicine, Ann Arbor, Michigan, United States of America
Hiromi Kurosawa
Affiliation:
The Department of Cardiovascular Surgery and Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical University, Tokyo, Japan
Toshiharu Shin'oka
Affiliation:
The Department of Cardiovascular Surgery and Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical University, Tokyo, Japan
Aki Ikeda
Affiliation:
The Department of Cardiovascular Surgery and Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical University, Tokyo, Japan
Toshio Nakanishi
Affiliation:
The Department of Cardiovascular Surgery and Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical University, Tokyo, Japan
Get access Rights & Permissions [Opens in a new window]

Abstract

The congenital cardiac malformation characterized by discordant connections between the atriums and ventricles, as well as those between the ventricles and the arterial trunks, has been given many names. The terms atrioventricular discordance, l-transposition of the great arteries, ventricular inversion, and congenitally corrected transposition have all been used. Regardless of terminology, this complex congenital anomaly has only recently been studied to analyze the long-term effects of its natural history and outcomes following traditional surgical repair of the associated malformations which serve to uncorrect the circulatory pathways. As more patients survive into adulthood, the effects of this condition are now better understood, and the surgical approaches used in the past are being re-examined in light of longer-term follow up.

Keywords

Discordant atrioventricular connectionsdouble discordanceatrioventricular dissociationcongenital heart disease
Type
Discordant Atrioventricular Connections
Information
Cardiology in the Young , Volume 16 , Supplement S3: Controversies and Challenges of the Atrioventricular Junctions and Other Challenges Facing Paediatric Cardiovascular Practitioners and their Patients , September 2006 , pp. 85 - 90
Copyright
© 2006 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Allwork S, Bentall HH, Becker AE, et al. Congenitally corrected transposition of the great arteries. Morphologic study of 32 cases. Am J Cardiol 1976; 38: 910–923.Google Scholar
Becker AE, Anderson RH. Conditions with discordant atrioventricular connections – Anatomy and conductive tissues. In: Anderson RH, Shinebourne EA (eds). Pediatric Cardiology 1977, Churchill Livingstone, London, 1978, p 184.
Kurosawa H, Imai Y, Becker AE. Congenitally corrected transposition with normally positioned atria, straddling mitral valve, and isolated posterior atrioventricular node bundle. J Thorac Cardiovasc Surg 1990; 99: 312–313.Google Scholar
Mahle WT, Marx GR, Anderson RH. Anatomy and echocardiography of discordant atrioventricular connections. Cardiol Young, 2006; 16: this suppl.Google Scholar
Anderson RH, Becker AE, Arnold R, Wilkinson JL. The conducting tissues in congenitally corrected transposition. Circulation 1974; 50: 911–923.Google Scholar
Uher V. Zur pathologie des reizleietungssystem bei congenital herzanomalien. Frank Z Pathol 1936; 347–365.Google Scholar
Monckeberg JG. Zur entwicklungsgeschicte des atrioventricular-systems. Verhandl d Deutsch path Gesellsch 1913; 18: 228–249.Google Scholar
Hosseinpour AR, McCarthy KP, Griselli M, Sethia B, Ho SY. Congenitally corrected transposition: size of the pulmonary trunk and septal malalignment. AnnThor Surg 2004; 77: 2163–2166.Google Scholar
Lundstrom U, Bull C, Wyse RK, Somerville J. The natural and “unnatural” history of congenitally corrected transposition. Am J Cardiol 1990; 65: 1222–1229.Google Scholar
Graham Jr TP, 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.Google Scholar
Prieto LR, Hordof AJ, Secic M, Rosenbaum MS, Gersony WM. Progressive tricuspid valve disease in patients with congenitally corrected transposition of the great arteries. Circulation 1998; 98: 997–1005.Google Scholar
Connelly MS, Liu PP, Williams WG, Webb GD, Robertson P, McLaughlin PR. Congenitally corrected transposition of the great arteries in the adult: functional status and complications. J Am Coll Cardiol 1996; 27: 1238–1243.Google Scholar
Presbitero P, Somerville J, Rabajoli F, Stone S, Conte MR. Corrected transposition of the great arteries without associated defects in adult patients: clinical profile and follow up. Br Heart J 1995; 74: 57–59.Google Scholar
van Son JA, Danielson GK, Huhta JC, et al. Late results of systemic atrioventricular valve replacement in corrected transposition. J Thorac Cardiovasc Surg 1995; 109: 642–652.Google Scholar
Termignon JL, Leca F, Vouhe PR, et al. “Classic” repair of congenitally corrected transposition and ventricular septal defect. Ann Thorac Surg 1996; 62: 199–206.Google Scholar
Hraska V, Duncan BW, Mayer Jr JE, et al. Long-term outcome of surgically treated patients with corrected transposition of the great arteries. J Thorac Cardiovasc Surg 2005; 129: 182–191.Google Scholar
de Leval MR, Bastos P, Stark J, Taylor JFN, Macartney FJ, Anderson RH. Surgical technique to reduce the risks of heart block following closure of ventricular septal defect in atrioventricular discordance. J Thorac Cardiovasc Surg 1979; 78: 515.Google Scholar
Bove EL. Congenitally corrected transposition of the great arteries: options for biventricular repair. Prog Ped Cardiol 1999; 10: 45–49.Google Scholar
Szufladowicz M, Horvath P, de Leval M, Elliott M, Wyse R, Stark J. Intracardiac repair of lesions associated with atrioventricular discordance. Eur J Cardiothorac Surg 1996; 10: 443–448.Google Scholar
Biliciler-Denktas G, Feldt RH, Connolly HM, Weaver AL, Puga FJ, Danielson GK. Early and late results of operations for defects associated with corrected transposition and other anomalies with atrioventricular discordance in a pediatric population. J Thorac Cardiovasc Surg 2001; 122: 234–241.Google Scholar
Imai Y, Seo K, Aoki M, Shin'oka T, Hiramatsu K, Ohta A. Double-Switch operation for congenitally corrected transposition. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu 2001; 4: 16–33.Google Scholar
Devaney EJ, Charpie JR, Ohye RG, Bove EL. Combined arterial switch and Senning operation for congenitally corrected transposition of the great Arteries: patient selection and intermediate-term results. J Thorac Cardiovasc Surg 2003; 125: 500–507.Google Scholar
Imamura M, Drummond-Webb JJ, Murphy Jr DJ, et al. Results of the double switch operation in the current era. Ann Thorac Surg 2000; 70: 100–105.Google Scholar
Yamagishi M, Imai Y, Hoshino S, et al. Anatomic correction of atrioventricular discordance. J Thorac Cardiovasc Surg 1993; 105: 1067–1076.Google Scholar
Karl TR, Weintraub RG, Brizard CP, Cochrane AD, Mee RB. Senning plus arterial switch operation for discordant (congenitally corrected) transposition. Ann Thorac Surg 1997; 64: 495–502.Google Scholar
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.Google Scholar
Ilbawi MN, Ocampo CB, Allen BS, et al. Intermediate results of the anatomic repair for congenitally corrected transposition. Ann Thorac Surg 2002; 73: 594–599.Google Scholar
Sharma R, Bhan A, Juneja R, Kothari SS, Saxena A, Venugopal P. Double switch for congenitally corrected transposition of the great arteries. Eur J Cardiothorac Surg 1999; 15: 276–281.Google Scholar
Tanaka K, Kurosawa H, Morita K, Nomura K. Double switch with reversed Patrick-McGoon for corrected transposition of the great arteries with double outlet right ventricle. Jpn J Thorac Cardiovasc Surg 2004; 52: 300–304.Google Scholar