Anomalous origin of the left coronary artery from the pulmonary trunk. Clinical features and midterm results after surgical treatment

Detalhes bibliográficos
Autor(a) principal: Amaral,Fernando
Data de Publicação: 1999
Outros Autores: Carvalho,Julene S., Granzotti,João A., Shinebourne,Elliot A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Arquivos Brasileiros de Cardiologia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X1999000300004
Resumo: OBJECTIVE: To report the authors' experience with the anomalous origin of the left coronary artery (AOLCA) from the pulmonary trunk, emphasizing preoperative data, surgical aspects and midterm results of the follow-up. METHODS: Retrospective analysis of 11 patients operated upon at the Royal Brompton Hospital from October, 84 to April, 97. RESULTS: Nine infants had heart failure (HF) and two other children presented with dyspnea and chest pain. All had ECG changes. The echocardiogram identified the anomalous origin of the coronary artery in 7 (64%) patients and hemodynamic studies were performed in 7 patients. All infants were operated upon between the 2nd and 10th month of life. Six patients were treated with aortic reimplantation of the left coronary artery, whereas five were operated upon according to the Takeuchi technique. All patients are alive, with clear improvement of the ECG changes and ventricular function, as evaluated by echocardiography. Two patients operated upon according to the Takeuchi technique required additional surgery due to severe supravalvular pulmonary stenosis. CONCLUSION: AOLCA is a rare disease. Most patients show early signs of severe HF associated with ECG findings. Surgical therapy must be instituted early in the disease, preferentially through aortic implantation of the anomalous coronary artery, with a high possibility of success. Shortly after surgery, clinical and ECG improvement, as well as normalization of left ventricular function, should be expected.
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spelling Anomalous origin of the left coronary artery from the pulmonary trunk. Clinical features and midterm results after surgical treatmentanomalous left coronary arteryBland-White-Garland syndromeleft ventricular functionOBJECTIVE: To report the authors' experience with the anomalous origin of the left coronary artery (AOLCA) from the pulmonary trunk, emphasizing preoperative data, surgical aspects and midterm results of the follow-up. METHODS: Retrospective analysis of 11 patients operated upon at the Royal Brompton Hospital from October, 84 to April, 97. RESULTS: Nine infants had heart failure (HF) and two other children presented with dyspnea and chest pain. All had ECG changes. The echocardiogram identified the anomalous origin of the coronary artery in 7 (64%) patients and hemodynamic studies were performed in 7 patients. All infants were operated upon between the 2nd and 10th month of life. Six patients were treated with aortic reimplantation of the left coronary artery, whereas five were operated upon according to the Takeuchi technique. All patients are alive, with clear improvement of the ECG changes and ventricular function, as evaluated by echocardiography. Two patients operated upon according to the Takeuchi technique required additional surgery due to severe supravalvular pulmonary stenosis. CONCLUSION: AOLCA is a rare disease. Most patients show early signs of severe HF associated with ECG findings. Surgical therapy must be instituted early in the disease, preferentially through aortic implantation of the anomalous coronary artery, with a high possibility of success. Shortly after surgery, clinical and ECG improvement, as well as normalization of left ventricular function, should be expected.Sociedade Brasileira de Cardiologia - SBC1999-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X1999000300004Arquivos Brasileiros de Cardiologia v.72 n.3 1999reponame:Arquivos Brasileiros de Cardiologia (Online)instname:Sociedade Brasileira de Cardiologia (SBC)instacron:SBC10.1590/S0066-782X1999000300004info:eu-repo/semantics/openAccessAmaral,FernandoCarvalho,Julene S.Granzotti,João A.Shinebourne,Elliot A.eng2002-01-08T00:00:00Zoai:scielo:S0066-782X1999000300004Revistahttp://www.arquivosonline.com.br/https://old.scielo.br/oai/scielo-oai.php||arquivos@cardiol.br1678-41700066-782Xopendoar:2002-01-08T00:00Arquivos Brasileiros de Cardiologia (Online) - Sociedade Brasileira de Cardiologia (SBC)false
dc.title.none.fl_str_mv Anomalous origin of the left coronary artery from the pulmonary trunk. Clinical features and midterm results after surgical treatment
title Anomalous origin of the left coronary artery from the pulmonary trunk. Clinical features and midterm results after surgical treatment
spellingShingle Anomalous origin of the left coronary artery from the pulmonary trunk. Clinical features and midterm results after surgical treatment
Amaral,Fernando
anomalous left coronary artery
Bland-White-Garland syndrome
left ventricular function
title_short Anomalous origin of the left coronary artery from the pulmonary trunk. Clinical features and midterm results after surgical treatment
title_full Anomalous origin of the left coronary artery from the pulmonary trunk. Clinical features and midterm results after surgical treatment
title_fullStr Anomalous origin of the left coronary artery from the pulmonary trunk. Clinical features and midterm results after surgical treatment
title_full_unstemmed Anomalous origin of the left coronary artery from the pulmonary trunk. Clinical features and midterm results after surgical treatment
title_sort Anomalous origin of the left coronary artery from the pulmonary trunk. Clinical features and midterm results after surgical treatment
author Amaral,Fernando
author_facet Amaral,Fernando
Carvalho,Julene S.
Granzotti,João A.
Shinebourne,Elliot A.
author_role author
author2 Carvalho,Julene S.
Granzotti,João A.
Shinebourne,Elliot A.
author2_role author
author
author
dc.contributor.author.fl_str_mv Amaral,Fernando
Carvalho,Julene S.
Granzotti,João A.
Shinebourne,Elliot A.
dc.subject.por.fl_str_mv anomalous left coronary artery
Bland-White-Garland syndrome
left ventricular function
topic anomalous left coronary artery
Bland-White-Garland syndrome
left ventricular function
description OBJECTIVE: To report the authors' experience with the anomalous origin of the left coronary artery (AOLCA) from the pulmonary trunk, emphasizing preoperative data, surgical aspects and midterm results of the follow-up. METHODS: Retrospective analysis of 11 patients operated upon at the Royal Brompton Hospital from October, 84 to April, 97. RESULTS: Nine infants had heart failure (HF) and two other children presented with dyspnea and chest pain. All had ECG changes. The echocardiogram identified the anomalous origin of the coronary artery in 7 (64%) patients and hemodynamic studies were performed in 7 patients. All infants were operated upon between the 2nd and 10th month of life. Six patients were treated with aortic reimplantation of the left coronary artery, whereas five were operated upon according to the Takeuchi technique. All patients are alive, with clear improvement of the ECG changes and ventricular function, as evaluated by echocardiography. Two patients operated upon according to the Takeuchi technique required additional surgery due to severe supravalvular pulmonary stenosis. CONCLUSION: AOLCA is a rare disease. Most patients show early signs of severe HF associated with ECG findings. Surgical therapy must be instituted early in the disease, preferentially through aortic implantation of the anomalous coronary artery, with a high possibility of success. Shortly after surgery, clinical and ECG improvement, as well as normalization of left ventricular function, should be expected.
publishDate 1999
dc.date.none.fl_str_mv 1999-03-01
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dc.language.iso.fl_str_mv eng
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Cardiologia - SBC
publisher.none.fl_str_mv Sociedade Brasileira de Cardiologia - SBC
dc.source.none.fl_str_mv Arquivos Brasileiros de Cardiologia v.72 n.3 1999
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