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Table 3 Binary logistic regression analysis in EA patients and their parents using the generic PedsQL core module

From: Parent–child-agreement on health-related quality of life and its determinants in patients born with Esophageal Atresia: a Swedish–German cross-sectional study

 

PedsQL total score

 

PR < CR versus agreementa (n = 51)

PR > CR versus agreementb (n = 45)

 

B

Wald

p

[95% CI]

B

Wald

p

[95% CI]

Child genderc

− 1.12

2.24

.13

[.08, 1.41]

1.57

3.51

.06

[.93, 24.87]

Child age

.02

.03

.87

[.81, 1.29]

.13

1.24

.27

[.91, 1.43]

EA severity leveld

.59

.56

.45

[.39, 8.36]

.02

.00

.98

[.21, 5.01]

Parental HRQOL

.01

.06

.80

[.95, 1.07]

.00

.01

.92

[.93, 1.08]

Family functioning

− .04

2.15

.14

[.91, 1.01]

− .04

1.31

.25

[.90, 1.03]

Countrye

− 1.08

2.26

.13

[.08, 1.39]

− .56

.44

.51

[.11, 3.00]

Model summary

R2 = .24

R2 = .23

χ2(6) = 9.887, p = .13

χ2(6) = 8.016, p = .24

  1. PR = Parent-report, CR = Child-report, B = regression coefficient, Wald = Wald-value, p = p-value, CI = confidence interval, R2 = Nagelkerkes R-square, EA = Esophageal atresia, HRQOL = Health-related quality of life
  2. a 0 = agreement, 1 = PR < CR, defined using a threshold of ½ SD
  3. b 0 = agreement, 1 = PR > CR, defined using a threshold of ½ SD
  4. c Child gender: 0 = male, 1 = female
  5. d EA severity level: 0 = mild moderate, 1 = severe (Dellenmark–Blom, Dingemann, Witt, Quitmann, Jönsson et al. 2018)
  6. e Country: 0 = Germany; 1 = Sweden
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Orphanet Journal of Rare Diseases

ISSN: 1750-1172