Anomalous origin and distribution of coronary arteries. Review of 38 patients who underwent operation.

Abstract

Between October 1961 and December 1973, 38 patients with an anomaly in origin (15 patients) or distribution (23 patients) of the main coronary artery or one of its branches underwent operation at the Texas Heart Institute. The left coronary artery originating from the pulmonary artery occurred most frequently-in 13 of 15 patients. An aortocoronary artery bypass was performed in 12 patients with the saphenous vein used in ten of the 12, initially in 1965; and a Dacron tube graft in the other two. Of the 15 patients, only one died during the early period after operation. A follow-up of ten years revealed 11 asymptomatic patients; to date the longest period of patency of a saphenous vein graft is seven years in an 11-year-old girl. Of 23 patients with an unusual coronary artery distribution, 22 had tetralogy of Fallot, 20 of whom underwent total correction. In 21 of the 23 patients the left anterior descending coronary artery originated from the right coronary artery and crossed the right ventricular outflow tract. In two patients this abnormally distributed artery was injured through a vertical right ventriculotomy; both patients died from myocardial failure during the early postoperative period. Subsequently a transverse right ventriculotomy, either alone or combined with a right ventricular outflow and/or pulmonary artery patch enlargement was performed in 16 patients, and a double outlet right ventricle was created through insertion of a Dacron tube graft in two patients. With this method injury to the abnormal left anterior descending coronary artery was avoided and all 18 patients survived the operation. On the basis of our experience and today's advanced techniques, it is believed that most patients, including some under two years of age, can undergo correction of a left coronary artery originating from the pulmonary artery through insertion of a saphenous vein graft between the aorta and left coronary artery. During the surgical correction of cardiac anomalies necessitating a right ventriculotomy, a transverse or double incision in the right ventricular outflow tract in most patients will prevent injury to an abnormally distributed coronary artery branch; sometimes insertion of a Dacron tube graft between the right ventricular outflow tract and pulmonary artery is necessary.

• Authors: J Meyer, G J Peul Jr, L Chiarello, G L Hallman, D A Cooley
• Journal: The Journal of cardiovascular surgery (J Cardiovasc Surg (Torino)) 1975 Sep-Oct Vol. 16 Issue 5 Pg. 500-5 ISSN: 0021-9509 [Print] Italy
• PMID: 1194335 (Publication Type: Journal Article)

Topics

• Adolescent
• Adult
• Aortic Valve Insufficiency (complications, surgery)
• Blood Vessel Prosthesis
• Child
• Child, Preschool
• Coronary Vessel Anomalies (complications, surgery)
• Evaluation Studies as Topic
• Female
• Heart Septal Defects, Ventricular (complications, surgery)
• Humans
• Infant
• Male
• Methods
• Postoperative Complications
• Pulmonary Artery (abnormalities)
• Tetralogy of Fallot (complications, surgery)
• Transposition of Great Vessels (complications, surgery)