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THU0482 PAIN CATASTROPHIZING AND DISEASE PERCEPTION DIFFERS BETWEEN NORWEGIAN AND FINNISH OUTPATIENT CLINIC PSORIATIC ARTHRITIS PATIENTS DESPITE COMPARABLE OUTCOMES ON OBJECTIVE MEASURES OF DISEASE

Authors :
T. Sokka-Isler
Brigitte Michelsen
K. Paalanen
I. J. Widding Hansen
H. Berner Hammer
A. Kavanaugh
Glenn Haugeberg
Source :
Annals of the Rheumatic Diseases. 79:478.1-479
Publication Year :
2020
Publisher :
BMJ, 2020.

Abstract

Background:Pain catastrophizing (the tendency to describe a pain experience in more exaggerated terms than the average person, to ruminate on it more, or to feel more helpless about it), has been associated with reduced likelihood of achieving remission in rheumatoid arthritis patients (1). Cultural and societal differences between countries may have an impact on outcome such as patients’ perceptions of disease.Objectives:To compare patient pain catastrophizing, patient perception of disease, objective measures of disease and treatment in psoriatic arthritis (PsA) patients between a Norwegian and a Finnish outpatient clinic. Further, to explore for associations with pain catastrophizing.Methods:All PsA patients followed at the outpatient clinics are routinely monitored using a structured medical support system (GoTreatIT® Rheuma). Data collection, done in 2018-19 is listed in the table.Patients reported their pain catastrophizing answering the two questions, “When I feel pain it is terrible and I feel it is never going to get any better. When I feel pain, I can’t stand it anymore.” Each question is scored 0-6 and mean value of both is calculated. Pain catastrophizing was defined if mean score ≥4.Categorical variables were presented as numbers (%) and continuous variables as mean (SD) and associates explored using univariate and multivariate analysis.Results:A total of 302 Finnish and 363 Norwegian PsA patients were examined. Pain catastrophizing was reported significantly less commonly among the Finnish as compared to the Norwegian PsA clinic patients, both expressed as mean (SD) values (1.48 (1.42) vs 2.05 (1.42), pFinland (n=302)Norway (n=363)PAge, years54.0 (13.3)54.7 (12.5)0.49Females153 (50.7%)181 (49.9%)0.84BMI. Kg/m228.8 (5.6)28.1(5.1)0.06Current smoking44 (14.6%)51 (14.1%)0.86Education, years13.6 (3.5)12.7 (3.8)0.001Disease duration, years4.7 (4.3)9.9 (8.9)CRP, mg/L4.3 (6.8)4.0 (8.8)0.69MDglobal assessment, VAS 0-100 mm6.84 (1.29)5.71 (8.50)0.1928 swollen joint count0.48 (1.35)0.31 (1.16)0.1428 tender joint count1.01 (2.83)1.37 (2.80)0.14DAPSA9.66 (8.95)11.33 (9.60)0.06Pain, VAS 0-100 mm30.73 (25.92)35.55 (25.76)0.023Fatigue, VAS 0-100 mm29.96 (29.24)42.56 (31.94)MHAQ, 0-30.39 (0.44)0.43 (0.41)0.24Body surface area for psoriasis2.45 (8.15)2.66 (6.15)0.17Current b-tsDMARDs121 (40.1%)139 (38.3%)0.64In univariate analyses female gender, higher BMI, less years of education, Dr. global, tender joint count, DAPSA, pain, fatigue, MHAQ and psoriasis body surface area were found to be associated with more pain catastrophizing.In multivariate analysis (mandatory adjusting for age, gender, BMI, years of education and disease duration) fewer years of education, higher scores for pain, fatigue and MHAQ and being patient at the Norwegian center were independently associated with more pain catastrophizing.Conclusion:Our data indicate that cultural differences across countries may have a significant impact on outcomes that reflecting patients’ perceptions of disease. This may have an implication when merging heterogeneous databases across countries.References:[1]Hammer HB et al. Arthritis Care Res 2018;70:703-12.Disclosure of Interests: :Glenn Haugeberg: None declared, Inger Johanne Widding Hansen: None declared, Hilde Berner Hammer: None declared, Arthur Kavanaugh Grant/research support from: Abbott, Amgen, AstraZeneca, BMS, Celgene Corporation, Centocor-Janssen, Pfizer, Roche, UCB – grant/research support, Brigitte Michelsen: None declared, Kirsi Paalanen: None declared, Tuulikki Sokka-Isler: None declared

Details

ISSN :
14682060 and 00034967
Volume :
79
Database :
OpenAIRE
Journal :
Annals of the Rheumatic Diseases
Accession number :
edsair.doi...........5f34f5d133dbe66a98c32e94807e533e