Interact CardioVasc Thorac Surg 2009;9:814-818. doi:10.1510/icvts.2009.208215 © 2009 European Association of Cardio-Thoracic Surgery
Institutional report - Congenital |
Anomalous left coronary artery from the pulmonary artery: intermediate results of coronary elongation
William M. Novicka,g*,
Xiao F. Lib,
Darko Anicc,g,
Alexander Baskevitchd,
Nestor Sandovale,g,
Christian L. Gilbertg and
Thomas G. Di Sessaf,g
a Departments of Surgery and Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA
b Department of Cardiac Surgery, Beijing Children's Hospital, Beijing, China
c Department of Cardiac Surgery, KBC-Rijeka, Rijeka, Croatia
d Department of Neonatal and Infant Cardiac Surgery, National Center for Children's Cardiac Surgery, Minsk, Belarus
e Department of Cardiac Surgery, Cardio-Infantile, Bogotá, Colombia
f Department of Pediatrics, University of Kentucky, Lexington, KY, USA
g International Children's Heart Foundation, Memphis, TN, USA
*Corresponding author. 1750 Madison Ave., Suite 500, Memphis, TN 38104, USA. Tel.: +1 901-8694243; fax: +1 901-4324243.
E-mail address: ichfno{at}aol.com (W.M. Novick).
A two coronary system is preferred for correcting anomalous left coronary artery from the pulmonary artery (ALCAPA); however, translocation is not always possible. In countries where neonatal arterial switch operations have not been perfected coronary transfer can be difficult. The purpose of this report is to describe the intermediate results using the coronary elongation and translocation technique in developing countries. Records of patients undergoing operation by the International Children's Heart Foundation team were reviewed (April 1993–October 2008) for those undergoing ALCAPA repair. All patients received a 2-D echocardiographic–color Doppler examination prior to discharge and at follow-up. A total of 13 patients were identified, age ranged from 9 days to 41 years. All but one patient were operated upon at one of our affiliate hospitals in Croatia, Belarus, China and Colombia. All patients presented with moderate to severe mitral regurgitation and cardiac failure. Follow-up ranged from six months to 9.5 years postoperatively. Color Doppler showed a patent left coronary artery; echocardiography estimated a normal left ventricular ejection fraction and improved mitral regurgitation in all patients. The technique provides an alternative approach to translocation for ALCAPA in countries where routine neonatal coronary transfer techniques may not be perfected. Intermediate results are comparable to translocation.
Key Words: Anomalous left coronary artery; Surgical correction; Congenital
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