SEVERE KAWASAKI HEART-DISEASE TREATED WITH AN INTERNAL MAMMARY ARTERY GRAFT IN PEDIATRIC-PATIENTS - A 1ST SUCCESSFUL REPORT
- 1 January 1985
- journal article
- research article
- Vol. 89 (6) , 860-866
Abstract
Two Japanese boys, 6 and 10 yr old, required operation for severe Kawasaki heart disease. Both had multiple coronary arterial aneurysms and stenoses, and one had mitral regurgitation as well. The operations consisted of anastomosis between the left internal mammary arterial and the left anterior descending artery and insertion of an autologous saphenous vein between the aorta and the posterior descending artery in both patients. The mitral valve was replaced in the one with mitral regurgitation. Angina pectoris was completely relieved as confirmed by postoperative angiocardiography. Late results of coronary bypass grafting with the saphenous vein in pediatric patients with Kawasaki disease were less satisfactory because of the high occlusion rate of the graft. The internal mammary artery may be superior, at least theoretically, to the saphenous vein graft because it is a living graft with a high possibility of growing and with less susceptibilty to degeneration. This is the first report of successful operation utilizing an internal mammary artery graft in coronary bypass for Kawasaki disease.This publication has 5 references indexed in Scilit:
- Early and late postoperative studies in coronary arterial lesions resulting from Kawasaki’s disease in childrenThe Journal of Thoracic and Cardiovascular Surgery, 1982
- Internal Mammary–Anomalous Left Anterior Descending Coronary Artery Graft in 16-Month-Old Infant with Tetralogy of Fallot: 30-Month Follow-upThe Annals of Thoracic Surgery, 1980
- Severe mitral regurgitation due to coronary arteritis of mucocutaneous lymph node syndrome A new surgical entityThe Journal of Thoracic and Cardiovascular Surgery, 1980
- Mucocutaneous Lymph Node SyndromeChest, 1980
- Aortocoronary bypass grafting in a child with coronary artery obstruction due to mucocutaneous lymphnode syndrome: report of a case.Circulation, 1976