Table 2.
Baseline Characteristics and Congenital Heart Disease diagnosis
| 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 |
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