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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