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Abstract Number: 298

Long-Term Impact of Juvenile Idiopathic Arthritis in the Greek adults’ Psychosocial Life

Despoina Dimopoulou1, Maria Trachana2, Polyxeni Pratsidou-Gertsi3, George Garyfallos4, Prodromos Sidiropoulos5, Athina Theodoridou6 and Alexandros Garyfallos6, 1Nikolaou Manou Str. 20, 4th Department of Internal Medicine, Aristotle University, Hippocratio Hospital, Thessaloniki, Greece, 2Aristotle University, Thessaloniki, Greece, 31st Department of Pediatrics, Aristotle University, 1st Department of Pediatrics, Aristotle University, Thessaloniki, Greece, 42nd Department of Psychiatry Aristotle University, 2nd Department of Psychiatry Aristotle University, Thessaloniki, Greece, 5Rheumatology, Clinical Immunology, and Allergy, University of Crete, Heraklion, Greece, 64th Department of Internal Medicine, Aristotle University, Hippocratio Hospital, 4th Department of Internal Medicine, Aristotle University, Hippocratio Hospital, Thessaloniki, Greece

Meeting: 2014 ACR/ARHP Annual Meeting

Keywords: Juvenile Arthritis, outcomes and psychosocial

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Session Information

Title: Pediatric Rheumatology - Clinical and Therapeutic Aspects: Juvenile Idiopathic Arthritis

Session Type: Abstract Submissions (ACR)

Background/Purpose Juvenile idiopathic arthritis (JIA) seems to have a negative impact on patients’ life style mostly due to the disease chronicity. No relevant data have been published for Greek young adults so far. /To capture the impact of disease burden in the psychosocial profile of adults with JIA, 17.2 years after disease onset. 

Methods A total of 96 (66 females) patients were enrolled. Psychosocial distress was assessed by the Greek version of the self-completed paper-based General Health Questionnaire (GHQ-28). A second questionnaire regarding marital status, education level and employment status was completed by all patients. Disease activity status at the last follow-up visit was assessed according to the Wallace’s criteria while the level of disease activity by the Disease Activity Score-28 (DAS-28). The patient’s assessment of global disease activity was measured on a Visual Analogue Scale (VAS) 0 to 10. Structural damage was scored by the the Juvenile Arthritis Damage Index-Articular (JADI-A) and by the Total modified Sharp/van der Heijde Score (TmSvdHS). Physical ability was assessed by the Health Assessment Questionnaire-Disability Index (HAQ-DI).

Results The GHQ-28 case score depicted impaired psychosocial status in 18 patients (18.7%). The level of psychosocial distress was significantly correlated with DAS28 at the last follow up visit (r=0.446, p<0.001). The presence of disease activity was correlated with higher degree of depression (p=0.032) and social dysfunction (p=0.008). Interestingly, patients without or with mild physical disability (HAQ-DI=0-0.49) differed from those with moderate-to-severe disability (HAQ-DI=0.5-3) in the fields of somatization (p=0.004) and social dysfunction (p<0.001), but not of depression. Higher degree of depression was recorded in the unemployed patients (p=0.018) and in those with mandatory education (p=0.018). In contrast, structural damage (JADI-A, TmSvdHS), marital status and current use or duration of corticosteroid treatment didn’t find to influence patients’ psychosocial profile. Global disease activity rated by the patient was found to be the only significant predictor of psychosocial distress in the multivariate analysis [B=0.057 95%CI (0.017, 0.097), P=0.005].

Conclusion Psychosocial distress is evident in a considerable proportion of the patients (~19%), indicating a constant impact of the disease on every-day life. The tight control of disease activity is therefore crucial in order to prevent symptoms of depression in these JIA adults.


Disclosure:

D. Dimopoulou,
None;

M. Trachana,
None;

P. Pratsidou-Gertsi,
None;

G. Garyfallos,
None;

P. Sidiropoulos,
None;

A. Theodoridou,
None;

A. Garyfallos,
None.

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