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Table 2 Summary of QoL survey results by % of area of involvement in vitiligo participants

From: Childhood vitiligo impacts emotional health of parents: a prospective, cross-sectional study of quality of life for primary caregivers

Patient/parent grouping (area of involvement)

N (%) for each survey (FLDQI and QLCCDQ)

Mean FDLQI overall score ± SD

Mean QLCCDQ per-item score ± SD

Mean QLCCDQ social domain score ± SD

Mean QLCCDQ occupational roles domain score ± SD

Mean QLCCDQ symptom domain score ± SD

Mean QLCCDQ emotional roles domain ± SD score

Mean QLCCDQ family perception domain score ± SD

0–25%

78 (66.1%, FLDQI);

77 (65.3%, QLCCDQ)

12.3 ± 2.7

6.1 ± 1.2

6.7 ± 1.2

6.5 ± 1.2

6.0 ± 1.5

5.4 ± 1.5

6.6 ± 1.2

25–50%

26 (22.0% FLDQI; 22.2% QLCCDQ)

14.0 ± 4.3

5.7 ± 1.2

6.6 ± 1.1

6.3 ± 1.5

5.0 ± 1.4

4.8 ± 1.6

6.7 ± 1.1

50–75%

8 (6.8% for both FLDQI and QLCCDQ)

15.3 ± 3.5

5.7 ± 0.7

6.9 ± 0.3

6.7 ± 0.4

4.7 ± 1.6

4.1 ± 2.0

6.9 ± 0.2

75–100%

6 (5.1% for both FLDQI and QLCCDQ)

15.8 ± 6.5

5.3 ± 1.0

6.4 ± 1.0

5.7 ± 1.7

4.7 ± 1.4

4.2 ± 1.1

6.3 ± 1.1

Overall

118 (FLDQI);

117 (QLCCDQ)

13.1 ± 3.5

5.9 ± 1.1

6.6 ± 1.3

6.4 ± 1.5

5.6 ± 1.6

5.1 ± 1.6

6.6 ± 1.1