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Table 1 Demographic and clinical patient’s characteristics by baseline, follow-up and lost to follow-up groups

From: Quality of life in children with infrequent congenital heart defects: cohort study with one-year of follow-up

 

Baseline (n = 157)

Follow-up (n = 112)

Lost to follow-up (n = 45)

Age years, median (IQR)

6.0 (3.0–11.0)

7.0 (4.0–11.7)

6.0 (3.0–10.5)

Sex female, n (%)

85 (54.1)

62 (55.4)

23 (51.1)

I-CHD distribution, n (%)

 EA

56 (35.7)

40 (35.7)

16 (35.5)

 HTX

9 (5.7)

4 (3.6)

5 (11.1)

 IAA

15 (9.6)

11 (9.8)

4 (8.9)

 PVS

71 (45.2)

51 (45.5)

20 (44.4)

 WS

6 (3.8)

6 (5.4)

Prenatal diagnosis, n (%)

25 (15.9)

13 (11.6)

12 (26.7)

Previous surgical or percutaneous intervention, n (%)

100 (63.7)

74 (66.1)

26 (57.8)

  1. IQR Interquartile range, EA Ebstein’s Anomaly, HTX Heterotaxy Syndrome, IAA Interrupted Aortic Arch, PVS Pulmonary Valve Stenosis, WS Williams’ Syndrome