Associated coronary and cardiac anomalies in the tetralogy of Fallot. An angiographic study
R P Dabizzi1, G Teodori, G A Barletta
1Istituto di Clinica Medica 1a, University of Florence, Italy.
Insights
Tetralogy of Fallot (TF) often co-occurs with other heart defects, particularly coronary artery anomalies. Preoperative coronary angiography is crucial for identifying these associated anomalies in complex congenital heart disease patients.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Congenital Heart Disease
Background:
- Tetralogy of Fallot (TF) is frequently associated with other cardiovascular anomalies.
- Coronary artery anomalies are common in patients with TF.
Purpose of the Study:
- To investigate the prevalence and types of cardiac defects and coronary tree anomalies associated with Tetralogy of Fallot.
- To evaluate the utility of preoperative coronary angiography in managing TF patients.
Main Methods:
- Retrospective analysis of 265 patients with Tetralogy of Fallot.
- Cardiac catheterization and selective coronary angiography were performed.
- Detailed documentation of associated cardiac and coronary anomalies.
Main Results:
- 181 (68%) patients had associated cardiac defects; 96 (36%) had coronary artery anomalies.
- Prevalence of coronary anomalies increased with the number of associated defects.
- Common anomalies included single coronary ostium, anomalous coronary artery origins, fistulas, and large conus arteries.
Conclusions:
- Coronary artery anomalies are a significant component of cardiac defects associated with Tetralogy of Fallot.
- Routine preoperative coronary angiography is essential for comprehensive assessment and management of TF patients.
Abstract:
Numerous studies have pointed out the frequent association of tetralogy of Fallot (TF) with other cardiovascular defects and coronary tree anomalies. We found cardiac defects in 181 (68%) out of 265 patients with TF investigated by catheterization and selective coronary angiography. These anomalies were isolated in 88 cases (49%) and associated with others in 93 patients. In the case of an isolated anomaly associated with TF, the coronary tree was involved in 37.5% and the cardiovascular system in the remaining 62.5%; in the case of two anomalies, the coronary system was involved in 66% of the patients and the cardiovascular apparatus in 34%; in the case of three or more anomalies, the coronary arteries were involved in 71% and the cardiovascular system in 29%. Anomalies in the course and/or distribution of coronary arteries were present in 96 patients (36%): 10 had a single coronary ostium, 13 a left anterior descending artery arising from the right coronary artery, one a circumflex artery arising from the right coronary artery. Small fistulas between coronary arteries and the pulmonary artery were found in 20 cases; anastomoses between coronary and bronchial arteries or right atrium in 42. In 39 patients we observed a large conus artery or large anterior ventricular branches crossing the right ventricle. A right aortic arch was found in 56 patients (21%), a stenosis of the trunk and/or the peripheral pulmonary artery in 35 (13%) and pulmonary artery atresia in five. Four patients showed a complete atrioventricular canal, three an atrial septal defect (primum type) with cleft of the mitral valve, 61 (23%) an atrial septal defect (ostium secundum). Eleven patients had anomalies of the systemic venous return, 26 (10%) a patent ductus arteriosus. Four patients had valvular abnormalities. In our series, a large proportion of cardiac defects associated with TF consists of anomalies of coronary arteries. Our data confirm the usefulness of performing preoperatively routine coronary angiography in patients with complex congenital heart disease.
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