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. Author manuscript; available in PMC: 2019 Mar 1.
Published in final edited form as: Pediatr Cardiol. 2018 Jan 3;39(3):610–616. doi: 10.1007/s00246-017-1801-8

Table 1.

Patient demographics, pre-operative characteristics, and follow-up status in pediatric Turner syndrome patients undergoing heart transplantation; Hypoplastic left heart syndrome (HLHS), total anomalous pulmonary venous return (TAPVR), pulmonary artery (PA), endocardial fibroelastosis (EFE)

Patient
#
Age at
transplant
Race Transplant
indication
Prior
Surgery
Mechanical
ventilation
Ventricular
assist
device
Listingstatus Follow-
up
statusb
Follow-
up
time
1 0m
a10y 6m
Caucasian HLHS
Cardiac allograft vasculopathy
-
Y
N
N
N
N
1A
1A
R
A
10y 179d
3y 364d
2 1m Hispanic HLHS N N N 1A D 110d
3 2m Caucasian HLHS, TAPVR, PA anomaly Y Y N 1A A 4y 350d
4 3m Caucasian HLHS Y N N 1A A 10y 323d
5 7m Hispanic HLHS, PAPVR, EFE Y N N 1A A 7y 351d
6 10m Caucasian HLHS Y Y N 1A A 5y 333d
7 10m Caucasian HLHS, coronary anomaly Y Y N 1A A 365d
8 10m
a4y 11m
Caucasian HLHS
Cardiac allograft vasculopathy
Y
Y
Y
N
N
N
1A
1B
R
D
4y 40d
20d
9 3y Caucasian Other single ventricle Y N N 1A D 16d
10 5y 1m African American HLHS Y N N 2 D 11d
11 6y 1m Caucasian HLHS Y N N 1A D 12d
12 8y 7m Caucasian Idiopathic dilated cardiomyopathy - N N 1A D 27d
13 10y 9m Caucasian Congenital heart defect with prior surgery Y N Y 1A D 14d
14 17y 2m Caucasian Idiopathic dilated cardiomyopathy Y N Y 1A A 10y 4d
a

Re-transplantation in same patient,

b

Alive (A), died (D), re-transplanted (R)