Poor Agreement on Health-Related Quality of Life Between Children With Congenital Hand Differences and Their Parents

被引:14
|
作者
Ardon, Monique S. [1 ,2 ]
Selles, Ruud W. [1 ,2 ]
Roebroeck, Marij E. [1 ]
Hovius, Steven E. [2 ]
Stam, Henk J. [1 ]
Janssen, Wim G. [1 ]
机构
[1] Erasmus MC, Univ Med Ctr Rotterdam, Dept Rehabil Med & Phys Therapy, NL-3000 CA Rotterdam, Netherlands
[2] Erasmus MC, Univ Med Ctr Rotterdam, Dept Plast & Reconstruct Surg & Hand Surg, NL-3000 CA Rotterdam, Netherlands
来源
关键词
Child; Female; Hand deformities; congenital; Male; Quality of life; Questionnaires; Rehabilitation; GENERIC CORE SCALES; AGE SUBGROUPS; SELF-REPORT; PROXY-REPORTS; PEDSQL(TM)-4.0; RELIABILITY; DEFICIENCY; VALIDITY;
D O I
10.1016/j.apmr.2011.11.023
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Ardon MS, Selles RW, Roebroeck ME, Hovius SE, Stain Hi, Janssen WG. Poor agreement on health-related quality of life between children with congenital hand differences and their parents. Arch Phys Med Rehabil 2012;93: 641-6. Objectives: To determine agreement between children with congenital hand differences (CHDs) and their parents on health-related quality of life (HRQOL) and to explore whether characteristic variables were associated with this agreement on different domains of HRQOL. Design: Survey. Setting: University hospital, outpatient clinic. Participants: Children with CHD (age range, 10-14y; N=106). Interventions: Not applicable. Main Outcome Measure: Agreement on HRQOL was determined by comparing child self-reports and parent proxy-reports of the Pediatric Quality of Life Inventory 4.0 generic core scales, in Dutch. Agreement was examined both at group level and individual level. Results: On a group level, children scored the same as their parents on a scale of 0 to 100 (physical health, 89.1 +/- 14.1 vs 88.0 +/- 15.6; psychosocial health, 80.6 +/- 13.4 vs 79.0 +/- 14.5; and total HRQOL, 83.5 +/- 12.3 vs 82.0 +/- 13.6). On an individual level, however, scoring was subject to high variation, with children reporting both higher and lower scores than their parent proxy. There were no major determinants for agreement; we only found that agreement was higher on emotional functioning in children with more affected fingers and on social functioning in bilaterally involved children. Conclusions: In terms of mean group scores, 10- to 14-year-old children with CHD agree with their parents or proxy on the child's HRQOL. However, on an individual level, they disagree; on some subdomains limits of agreement are as large as 30 points on the 0 to 100 scale. Therefore, care should be taken in cases where children are unable to complete the questionnaire in choosing the parents' score as a representative substitute for the child's score.
引用
收藏
页码:641 / 646
页数:6
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