Pediatric Rheumatology Online Journal → June 2003 → Health-Related Quality of Life, Disease Activity and Outcome Assessments→ Abstract #32
PREDICTORS OF PAIN IN CHILDREN WITH ESTABLISHED JUVENILE RHEUMATOID ARTHRITIS
P. N. Malleson,1 K. Oen,2 D. A. Cabral,1 R. E. Petty,1 A. M. Rosenberg,3 M. Cheang.4
1Pediatrics, UBC, Vancouver, BC, Canada; 2Pediatrics, Univ. MB, Winnipeg, MB, Canada; 3Pediatrics, Univ. SK, Saskatoon, SK, Canada; 4Community Health Services, Univ. MB, Winnipeg, MB, Canada
Although pain is a major symptom in juvenile rheumatoid arthritis (JRA), it has not been extensively studied, and most reports include only a fairly small number of
children.
Objectives: To describe, in a large cohort of children with JRA followed at 3 Canadian centres,
the demographic, and disease-related variables which might affect pain. This
cohort has been previously reported (1).
Methods: All children with JRA (1977 ACR
criteria) with
Univariate analyses were performed and all significant variables were entered into a stepwise multiple regression
analysis.
Results: 388 subjects completed a VAS for pain, and had sufficient data for the
analyses.
Univariate Analyses:Active disease duration, active joint count, PGA, morning stiffness, age at study, race, and onset subtype, were significant
variables.
Multiple Regression Analyses: 301 subjects had enough data (excluding morning stiffness) for the analyses. Only 22% of the pain variation could be explained. Significant independent variables were disease activity by PGA,
disease duration, and age at study. When data on morning stiffness (195
subjects) were included, the proportion of variation explained increased to
27%.
Summary: Similar to the findings of other smaller studies only a relatively small proportion of pain variance can be explained by demographic or disease-related variables. These data emphasize the need to evaluate other factors including psychosocial variables to fully explain pain in
JRA.
(1)Oen K et al. Disease course and outcome of juvenile rheumatoid arthritis in a multicentre cohort. J Rheumatol
2002; 29:1989-1999.