Anomalous origin and distribution of coronary arteries. Review of 38 patients who underwent operation
- PMID: 1194335
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.
Similar articles
-
Coronary artery anomalies in patients with tetralogy of Fallot.J Thorac Cardiovasc Surg. 1975 Mar;69(3):373-6. J Thorac Cardiovasc Surg. 1975. PMID: 123291
-
Primary repair minimizing the use of conduits in neonates and infants with tetralogy or double-outlet right ventricle and anomalous coronary arteries.J Thorac Cardiovasc Surg. 2000 Feb;119(2):314-23. doi: 10.1016/S0022-5223(00)70187-5. J Thorac Cardiovasc Surg. 2000. PMID: 10649207
-
Conduit reconstruction of right ventricular outflow tract. Experience with 17 patients.Ann Thorac Surg. 1975 Mar;19(3):277-88. doi: 10.1016/s0003-4975(10)64018-0. Ann Thorac Surg. 1975. PMID: 123441
-
Tetralogy of Fallot with pulmonary atresia, coronary artery-pulmonary artery fistula, and origin of left pulmonary artery from descending aorta: total correction in infancy.J Thorac Cardiovasc Surg. 1993 Jan;105(1):186-8. J Thorac Cardiovasc Surg. 1993. PMID: 8419704 Review. No abstract available.
-
Rare associations of tetralogy of Fallot with anomalous left coronary artery from pulmonary artery and totally anomalous pulmonary venous connection.Cardiol Young. 2016 Jun;26(5):1017-20. doi: 10.1017/S1047951116000342. Epub 2016 Apr 8. Cardiol Young. 2016. PMID: 27056487 Review.
Cited by
-
Reconstruction of coronary artery anomaly in an infant using the internal mammary artery: 10-year follow-up.Pediatr Cardiol. 1987;8(4):257-9. doi: 10.1007/BF02427538. Pediatr Cardiol. 1987. PMID: 3432115