Coronary artery bypass grafting for Kawasaki disease / 中华医学杂志(英文版)
Chin. med. j
; Chin. med. j;(24): 1533-1536, 2010.
Article
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| WPRIM
| ID: wpr-352547
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WPRO
ABSTRACT
<p><b>BACKGROUND</b>Kawasaki disease (KD) is the leading cause of pediatric ischemic heart disease. The incidence of serious coronary sequelae is low and about 2% - 3% of patients with KD, but once myocardial infarction occurs in children, the mortality is quite high and 22% at the first infarction.This study aimed to evaluate the efficacy of coronary artery bypass grafting (CABG) in patients with KD.</p><p><b>METHODS</b>Eight patients with a history of KD underwent CABG between October 1997 and July 2005. The number of bypass grafts placed was 2 to 4 per patient (mean 2.5 +/- 0.8). Various bypass grafts were used in patients, i.e. the left internal mammary artery (LIMA) in 3 patients, bilateral internal mammary artery (IMA) in 2 patients, LIMA plus gastroepiploic artery (GEA) in 1 patient and total saphenous vein grafts (SVGs) in 2 patients. The combined procedures included ventricular aneurysmectomy in 1 patient, mitral valve plasty in 1 and right coronary aneurysmectomy in 1. One patient was not able to wean from cardiopulmonary bypass (CPB), after being supported with intra-aortic balloon pump (IABP), the patient was weaned from CPB successfully.</p><p><b>RESULTS</b>One patient died of low cardiac output syndrome and acute renal failure 19 days after operation. Other patients recovered and were discharged uneventfully. During the follow-up that ranged from 3 to 57 months (mean 27 months), clincal angina disappeared or improved. Cardiac function was in Class I - II (NYHA).</p><p><b>CONCLUSION</b>CABG is a safe and effective procedure for Kawasaki coronary artery disease. However long-term results need to be followed up.</p>
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Assunto principal:
Patologia
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Cirurgia Geral
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Aneurisma Coronário
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Ponte de Artéria Coronária
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Resultado do Tratamento
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Métodos
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Síndrome de Linfonodos Mucocutâneos
Limite:
Adolescent
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Adult
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Child
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Child, preschool
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Female
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Humans
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Male
Idioma:
En
Revista:
Chin. med. j
Ano de publicação:
2010
Tipo de documento:
Article