Literature DB >> 21665229

Repair of anomalous origin of the left coronary artery from the pulmonary artery in infants and children.

Vladimir Alexi-Meskishvili1, Boris A Nasseri, Sarah Nordmeyer, Boris Schmitt, Yu-Guo Weng, Wolfgang Böttcher, Michael Hübler, Felix Berger, Roland Hetzer.   

Abstract

OBJECTIVE: Although mortality after direct aortic reimplantation for anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) has significantly decreased, many questions remain unanswered.
METHODS: Between 1986 and June 2010, we operated on 27 consecutive pediatric patients with anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA). All patients underwent reestablishment of a dual coronary system with direct aortic reimplantation of the left coronary artery into the aorta. Postoperative extracorporeal mechanical circulatory support was necessary in 7 cases. In all 7 patients, hemodynamic stability was achieved after 4 to 10 days of support. Mitral valve repair was performed in 9 patients with severe mitral valve incompetence and resulted in stable mitral valve function during follow-up as long as 19 years.
RESULTS: There were no early or late deaths. During follow-up (3 months-17.5 years), both early and late improvement of myocardial function was observed in all patients. Reduced left ventricular regional function late after successful surgical correction of ALCAPA was related to the presence of left ventricular myocardial scar tissue, as detected by magnetic resonance imaging.
CONCLUSIONS: Despite the absence of early and late mortality, the long-term prognosis for patients after reimplantation of ALCAPA into the aorta is not clear. Scars and perfusion deficits of the left ventricle may not be detected by standard echocardiographic evaluation of global left ventricular function and therefore may be underestimated. We therefore recommend lifelong surveillance of these patients, including magnetic resonance imaging.
Copyright © 2011 The American Association for Thoracic Surgery. Published by Mosby, Inc. All rights reserved.

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Year:  2011        PMID: 21665229     DOI: 10.1016/j.jtcvs.2011.04.006

Source DB:  PubMed          Journal:  J Thorac Cardiovasc Surg        ISSN: 0022-5223            Impact factor:   5.209


  17 in total

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Authors:  Rita Schuck; Mohamed Y Abd El Rahman; Axel Rentzsch; Wei Hui; Yuguo Weng; Vladimir Alexi-Meskishvili; Peter E Lange; Felix Berger; Hashim Abdul-Khaliq
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5.  Anomalous Left Coronary Artery Arising from Right Pulmonary Artery and Giant Left Atrium.

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7.  Repair of anomalous origin of the left coronary artery from the pulmonary artery in infants.

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8.  Anomalous left coronary artery connected to the pulmonary artery associated with other cardiac defects: a difficult joint diagnosis.

Authors:  Daniela Laux; Claire Bertail; Fanny Bajolle; Lucile Houyel; Younes Boudjemline; Damien Bonnet
Journal:  Pediatr Cardiol       Date:  2014-06-05       Impact factor: 1.655

9.  Cardiovascular magnetic resonance assessment of ventricular function and myocardial scarring before and early after repair of anomalous left coronary artery from the pulmonary artery.

Authors:  Heiner Latus; Kerstin Gummel; Stefan Rupp; Matthias Mueller; Christian Jux; Gunter Kerst; Hakan Akintuerk; Juergen Bauer; Dietmar Schranz; Christian Apitz
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10.  Midterm outcome after surgical correction of anomalous left coronary artery from the pulmonary artery.

Authors:  Yunfei Ling; Sandeep Bhushan; Qiang Fan; Menglin Tang
Journal:  J Cardiothorac Surg       Date:  2016-08-26       Impact factor: 1.637

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