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Methods Mothers or fathers of 143 children aged ≥ 5 with JIA, completed questionnaires about general beliefs regarding treatment (Treatment Representations Inventory, subscales – treatment value, concerns, cure and decision satisfaction) and specific beliefs regarding benefits and difficulties in taking MTX. Core outcome variables (COV), except ESR, were used to provide information on disease severity. Data were analysed by correlations followed by multiple linear regression with QoL, assessed by the Child Health Questionnaire (CHQ), as the dependent variable.

pediatric rheumatology online journal

Are parents' views about their child's treatment for juvenile idiopathic arthritis (JIA) related to evaluations of their child's quality of life (QoL)? – SPARKS CHARM study