Skip to main content

Table 1 Patient Demographics and Clinical Indications for cardiac MRI

From: Dual-phase whole-heart imaging using image navigation in congenital heart disease

Age, (years, mean ± standard deviation): 16.7 ± 5.1
Male gender, N (%) 13 (43%)
Ethnicity, N (%)  
• Caucasian 22 (73%)
• Hispanic 5 (17%)
• Asian 2 (7%)
• African American 1 (3%)
Clinical indications for cardiac MRI, N (%)  
• Congenital heart disease post-surgical repair 16 (53%)
   Underlying cardiac disease:  
Tetralogy of Fallot  
Tetralogy of Fallot, absent pulmonary valve  
Total anomalous pulmonary venous return  
DORV, D-TGA, VSD, pulmonary stenosis  
DORV, D-TGA, VSD, aortic stenosis  
Coarctation of the aorta  
Coarctation of the aorta, VSD, bicuspid aortic valve  
Turner syndrome, partial anomalous pulmonary venous return  
Unbalanced AVCD, DORV, L-TGA, pulmonary stenosis  
AVCD, pulmonary stenosis, pulmonary regurgitation  
Ebstein’s malformation of the tricuspid valve  
Pulmonary atresia, intact ventricular septum  
Pulmonary valve regurgitation  
Pulmonary stenosis, sinus venosus defect  
Shone’s complex  
Partial anomalous pulmonary venous return, Atrial septal defect  
• Hypertrophic cardiomyopathy 4 (13%)
• Evaluation for arrhythmogenic right ventricular cardiomyopathy/dysplasia 2 (7%
• Bicuspid aortic valve; evaluation of aortic dilation 3 (10%)
• Loeys-Dietz syndrome 1 (3%)
• Evaluation for myocarditis 1 (3%)
• Suspected abnormal left coronary artery origin 1 (3%)
• Kawasaki disease with giant aneurysms 1 (3%)
• Ectopic atrial tachycardia; evaluate cardiac anatomy 1 (3%)
  1. DORV Double outlet right ventricle, TGA transposition of the great arteries, VSD ventricular septal defect, AVCD Atrioventricular canal defect