1979
DOI: 10.1016/0002-8703(79)90248-5
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Surgical treatment of anomalous left coronary artery from pulmonary artery: Follow-up in teenagers and adults

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Cited by 68 publications
(33 citation statements)
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“…The high risk of sudden death, even in asymptomatic patients, warrants surgical correction of the anomaly when diagnosed (29,30). Many techniques for surgical correction have been utilized: ligation of the left main coronary artery (31,32), left main coronary ligation combined with bypass grafting (3 1,33), construction of a baffle from the left coronary artery to the aorta (34), left coronary artery to subclavian artery anastomosis (35), re-implantation of the coronary artery into the aorta (3 1,36), or tunneling from the aorta to left coronary artery using a tissue flap from the pulmonary artery (37,38). The type of surgical procedure may be dictated by the age of the patient and other…”
Section: Potentially Serious Coronary Anomaliesmentioning
confidence: 99%
“…The high risk of sudden death, even in asymptomatic patients, warrants surgical correction of the anomaly when diagnosed (29,30). Many techniques for surgical correction have been utilized: ligation of the left main coronary artery (31,32), left main coronary ligation combined with bypass grafting (3 1,33), construction of a baffle from the left coronary artery to the aorta (34), left coronary artery to subclavian artery anastomosis (35), re-implantation of the coronary artery into the aorta (3 1,36), or tunneling from the aorta to left coronary artery using a tissue flap from the pulmonary artery (37,38). The type of surgical procedure may be dictated by the age of the patient and other…”
Section: Potentially Serious Coronary Anomaliesmentioning
confidence: 99%
“…Bu anomali ile doğan çocukların %90'ı tedavi edilmezse ilk yıl içerisinde konjestif kalp yetmezliği (KKY) nedeniyle yaşamlarını yitirir. [1,2] İki yaşın altında KKY gelişen çocukların önemli bir kısmında nedenin ALCAPA olduğu, %80'den fazlasında semptomların yenidoğan ve erken bebeklik (infancy) döneminde ortaya çıktığı bildirilmiştir. [1][2][3][4][5] Bebeklik döneminde görülen dilate kardiyomiyopatilerin ayırıcı tanısında, tedavi edilebilir bir kardiyomiyopati nedeni olarak koroner arter anomalileri ve ALCAPA'nın dikkatle araştırılması büyük bir önem taşımaktadır.…”
Section: Discussionunclassified
“…[1,2] İki yaşın altında KKY gelişen çocukların önemli bir kısmında nedenin ALCAPA olduğu, %80'den fazlasında semptomların yenidoğan ve erken bebeklik (infancy) döneminde ortaya çıktığı bildirilmiştir. [1][2][3][4][5] Bebeklik döneminde görülen dilate kardiyomiyopatilerin ayırıcı tanısında, tedavi edilebilir bir kardiyomiyopati nedeni olarak koroner arter anomalileri ve ALCAPA'nın dikkatle araştırılması büyük bir önem taşımaktadır. [4,[6][7][8][9] Olguların çoğunda, sol ana koroner arter (sol ana KA), pulmoner arterin sol lateral sinüsünden çıkmaktadır.…”
Section: Discussionunclassified
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“…There seems to be a general consensus that establishing a two coronary artery system is preferable to assure adequate myocardial perfusion. [1][2][3][4][5][6][7] To aid in the evaluation of cardiac function of patients with anomalous origin of the left coronary from the pulmonary artery, this study evaluated the exercise performance of a group of patients who had undergone surgical repair of this defect. We evaluated both myocardial performance and, using thallium 201 scintigraphy, postoperative myocardial perfusion.…”
mentioning
confidence: 99%