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Agreement between Proxy and Adolescent Assessment of Disability, Pain, and Well-Being in Juvenile Idiopathic Arthritis - 02/08/11

Doi : 10.1016/j.jpeds.2010.08.003 
Sham D. Lal, MD a, Janet McDonagh, MD b, Eileen Baildam, MD c, Lucy R. Wedderburn, MD d, Janet Gardner-Medwin, MD e, Helen E. Foster, MD f, Alice Chieng, MD g, Joyce Davidson, MD e, Navid Adib, MD a, Wendy Thomson, MD a, Kimme L. Hyrich, MD a,
a Arthritis Research UK Epidemiology Unit, University of Manchester, Manchester Academic Health Sciences Centre, Manchester, United Kingdom 
b Institute of Child Health, Birmingham Children’s Hospital, Birmingham, United Kingdom 
c Alder Hey Children’s NHS Foundation Trust, Department of Rheumatology, Liverpool, United Kingdom 
d Rheumatology Unit, UCL, Institute of Child Health, London, United Kingdom 
e Department of Child Health, Glasgow University, Royal Hospital for Sick Children, Glasgow, United Kingdom 
f Department of Rheumatology, Medical School, Newcastle Upon Tyne, United Kingdom 
g Royal Manchester Children’s Hospital, Manchester, United Kingdom 

Reprint requests: Dr Kimme Hyrich, Arthritis Research UK Epidemiology Unit, University of Manchester, Manchester Academic Health Sciences Centre Stopford Building, Oxford Road, Manchester, United Kingdom M13 9PT.

Abstract

Objectives

Adolescents with juvenile idiopathic arthritis have demonstrated substantial disagreement with their proxy’s assessment of their disability, pain, and well-being. Our objective was to describe the clinical and psychological factors associated with discordance.

Study design

This analysis included 204 proxy-adolescent (median age, 13 years) dyads that completed a Childhood Health Assessment Questionnaire for disability with 100-mm visual analogue scales for pain and well-being. Depressive symptoms in adolescents were measured by the Mood and Feelings Questionnaire and in proxies the General Health Questionnaire. Disagreement was assessed using Bland-Altman plots. Associations with discordance were identified using logistic regression analyses.

Results

There was higher agreement for disability (84%) than for pain (71%) and well-being (66%). Regression analyses found no association between age, sex, or disease duration and disagreement. However, relationships between disease activity and disagreement in outcomes were identified. Independent associations were found between increasing Mood and Feelings Questionnaire scores and disagreement in pain and well-being.

Conclusions

Proxy and adolescent reports of pain and well-being are more likely to disagree in those with severe disease. Adolescents who report depressive symptoms are also more likely to disagree with their proxy. The reasons for these are multifactorial, and considerations of both reports are important when assessing outcomes in juvenile idiopathic arthritis.

El texto completo de este artículo está disponible en PDF.

Mots-clés : AHAQ, CAPS, HRQOL, JIA, MFQ-C, PGA, VAS


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 Supported by Arthritis Research UK. The authors declare no conflicts of interest.


© 2011  Mosby, Inc. Reservados todos los derechos.
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Vol 158 - N° 2

P. 307-312 - février 2011 Regresar al número
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