Determinants of Child-Parent Agreement in Quality-of-Life Reports: A European Study of Children With Cerebral Palsy

Author:

White-Koning Melanie12,Arnaud Catherine123,Dickinson Heather O.4,Thyen Ute5,Beckung Eva6,Fauconnier Jerome7,McManus Vicki8,Michelsen Susan I.9,Parkes Jackie10,Parkinson Kathryn11,Schirripa Giorgio12,Colver Allan13

Affiliation:

1. Institut National de la Santé et de la Recherche Médicale, U558, Toulouse, France

2. Université Toulouse III Paul Sabatier, Département d’Epidémiologie Economie de la santé et Santé publique, Toulouse, France

3. Centre Hospitalier Universitaire de Toulouse, Service d'Epidémiologie, Toulouse, France

4. Newcastle University, School of Population and Health Sciences, Newcastle-upon-Tyne, United Kingdom

5. Universitatsklinikum Schleswig-Holstein, Klinik fur Kinder, Lubeck, Germany

6. Göteborg University, Queen Silvia Children's Hospital, Göteborg, Sweden

7. Université Joseph Fourier, Laboratoire Techniques de l’Ingénierie Médicale et de la Complexité, Grenoble, France

8. Enable Ireland, Lavanagh Centre, Cork, Ireland

9. National Institute of Public Health, Copenhagen, Denmark

10. School of Nursing & Midwifery, Queen's University Belfast, Belfast, United Kingdom

11. School of Clinical Medical Sciences

12. Azienda Sanitaria Locale Viterbo, Viterbo, Italy

13. Sir James Spence Institute, Newcastle University, Newcastle-upon-Tyne, United Kingdom

Abstract

OBJECTIVES. The differences between child self-reports and parent proxy reports of quality of life in a large population of children with cerebral palsy were studied. We examined whether child characteristics, severity of impairment, socioeconomic factors, and parental stress were associated with parent proxy reports being respectively higher or lower than child self-reports of quality of life. METHODS. This study was conducted in 2004–2005 and assessed child quality of life (using the Kidscreen questionnaire, 10 domains, each scored 0–100) through self-reports and parent proxy reports of 500 children aged 8 to 12 years who had cerebral palsy and were living in 7 countries in Europe. RESULTS. The mean child-reported scores of quality of life were significantly higher than the parent proxy reports in 8 domains, significantly lower for the finances domain, and similar for the emotions domain. The average frequency of disagreement (child-parent difference greater than half an SD of child scores) over all domains was 64%, with parents rating their child's quality of life lower than the children themselves in 29% to 57% of child-parent pairs. We found that high levels of stress in parenting negatively influenced parents’ perception of their child's quality of life, whereas the main factor explaining parents’ ratings of children's quality of life higher than the children themselves is self-reported severe child pain. CONCLUSIONS. This study shows that the factors associated with disagreement are different according to the direction of disagreement. In particular, parental well-being and child pain should be taken into account in the interpretation of parent proxy reports, especially when no child self-report of quality of life is available. In the latter cases, it may be advisable to obtain additional proxy reports (from caregivers, teachers, or clinicians) to obtain complementary information on the child's quality of life.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

Reference66 articles.

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3. World Health Organization. Measurement of Quality of Life in Children. Geneva, Switzerland: Division of Mental Health, World Health Organization; 1993

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5. Juniper EF, Guyatt GH, Feeny DH, Griffith LE, Ferrie PJ. Minimum skills required by children to complete health-related quality of life instruments for asthma: comparison of measurement properties. Eur Respir J. 1997;10:2285–2294

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