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Table 2 Baseline Characteristics and Congenital Heart Disease diagnosis

From: mDixon ECG-gated 3-dimensional cardiovascular magnetic resonance angiography in patients with congenital cardiovascular disease

Patient

Gender

Age

Diagnosis

#1

Female

4 mo

Scimitar syndrome, PAPVC, RPA branch supplying the left lower lung, ASD, VSD, dysplastic pulmonary valve

#2

Male

4 yrs

Heterotaxy, Right atrial isomerism, Complete AVSD, DORV, D-TGA, TAPVC, b/l SVC, s/ p TAPVC repair, b/l Glenn and pulmonary artery band

#3

Male

9 yrs

Loeys-Dietz Syndrome, s/p valve sparing aortic root replacement with coronary arteries re-implantation

#4

Female

13 yrs

TOF s/p VSD closure and transannular patch repair of the right ventricular outflow tract

#5

Female

13 yrs

TOF, AVSD, s/p patch repair, pulmonary valve regurgitation, b/l AVV regurgitation, ascending aorta dilation

#6

Female

14 yrs

TAPVC, Shone complex, hypoplastic MV, BAV, Coarctation of the aorta, s/p TAPVC repair, s/p coarctation repair with end to end anastomosis

#7

Female

14 yrs

TAPVC s/p repair with residual PAPVC

#8

Male

16 yrs

Hypoplastic Left Heart Syndrome, s/p Fontan procedure

#9

Female

16 yrs

DORV, subaortic VSD s/p patch VSD closure; s/p resection of subaortic membrane and RV muscle bundle

#10

Male

17 yrs

Congenital LPA hypoplasia

#11

Female

19 yrs

Pulmonary valve stenosis s/p balloon valvuloplasty

#12

Male

19 yrs

Down syndrome, Unrepaired Coarctation of aorta, congenital stenoses of the branch pulmonary arteries

#13

Male

20 yrs

TOF s/p VSD and transannular patch repair, mechanical pulmonary valve replacement, aortic root dilation

#14

Male

24 yrs

D-TGA s/p arterial switch; RPA narrowing, hypoplastic LPA, dilated aortic root, aortic valve regurgitation

#15

Male

24 yrs

TOF s/p complete repair, aortic root dilation, high LCA origin, pectus excavatum

#16

Male

27 yrs

Pulmonary vale atresia, VSD, discontinuous branch pulmonary arteries s/p repair

#17

Male

27 yrs

BAV, dilated aortic root

#18

Male

27 yrs

VSD, Coarctation of aorta s/p SCA flap repair, distal TAA pseudoaneurysm, dilated aortic root

#19

Female

27 yrs

Unrepaired PAPVC, BAV

#20

Male

30 yrs

BAV s/p repair with residual stenosis, ascending aorta dilation

#21

Male

31 yrs

BAV s/p bioprosthetic valve placement

#22

Male

38 yrs

TOF s/p RV-PA conduit replacement, with residual conduit stenosis and aortic root dilation

#23

Male

40 yrs

BAV, s/p mechanical valve placement, aortic root and ascending aorta dilation

#24

Female

40 yrs

Ehlers-Danlos syndrome s/p aortic root replacement; MRI-compatible Pacemaker

  1. Abbreviations: mo: months, yrs: years, PAPVC Partial Anomalous Pulmonary Venous Connection, RPA Right Pulmonary Artery, ASD Atrial Septal Defect, VSD Ventricular Septal Defect, AVSD Atrio-Ventricular Septal Defect, DORV Double Outlet Right Ventricle, D-TGA D-Transposition of the Great Arteries, TAPVC Total Anomalous Pulmonary Venous Connection, B/L Bilateral, SVC Superior Vena Cava, S/P Status Post, TOF Tetralogy of Fallot, AVV Atrioventricular Valve, MV Mitral Valve, BAV Bicuspid Aortic Valve, LPA Left Pulmonary Artery, SCA Subclavian Artery, TAA Transverse Aortic Arch, RV-PA Right Ventricle to Pulmonary Artery