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Validation of the self-administered comorbidity questionnaire adjusted for spondyloarthritis: results from the ASAS-COMOSPA study.

Authors
  • Stolwijk, Carmen1, 2, 3
  • Essers, Ivette1, 2
  • van den Bosch, Filip4
  • Dougados, Maxime5
  • Etcheto, Adrien5
  • van der Heijde, Désirée6
  • Landewé, Robert7
  • Molto, Anna5
  • van Tubergen, Astrid1, 2
  • Boonen, Annelies1, 2
  • 1 Department of Rheumatology, Maastricht University Medical Center.
  • 2 Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht.
  • 3 Department of Rheumatology, Erasmus Medical Center, Rotterdam, The Netherlands. , (Netherlands)
  • 4 Department of Rheumatology, Ghent University Hospital and University of Ghent, Ghent, Belgium. , (Belgium)
  • 5 Department of Rheumatology, Paris Descartes University and Cochin Hospital, Assistance Publique Hôpitaux de Paris, Paris, France. , (France)
  • 6 Department of Rheumatology, Leiden University Medical Center, Leiden.
  • 7 Department of Clinical Immunology and Rheumatology, Amsterdam Rheumatology & Immunology Centre, Amsterdam, The Netherlands. , (Netherlands)
Type
Published Article
Journal
Rheumatology (Oxford, England)
Publication Date
Jul 01, 2020
Volume
59
Issue
7
Pages
1632–1639
Identifiers
DOI: 10.1093/rheumatology/kez482
PMID: 31665462
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

To confirm validity of the Self-administered Comorbidity Questionnaire modified for patients with SpA (mSCQ), and assess whether validity improves when adding items on extra-articular manifestations (EAMs), i.e. uveitis, psoriasis, and IBD, and osteoporosis and fractures. Data from the Assessment in SpondyloArthritis international Society COMOrbidities in SPondyloArthritis study were used. Criterion validity of presence of EAMs, osteoporosis and fractures was assessed as agreement (kappa) between patients' self-reported and physician-confirmed disease. Construct validity of the mSCQ including EAMs, osteoporosis and/or fractures (SpA-SCQ) was assessed by testing hypotheses about correlations with demographics, physical function, work ability, health utility and disease activity, and was compared with construct validity of the rheumatic disease comorbidity index. In total, 3984 patients contributed to the analyses. Agreement between patient-reported and physician-reported EAMs was substantial to almost perfect (uveitis ĸ = 0.81, IBD ĸ = 0.73, psoriasis ĸ = 0.86). Agreement for osteoporosis (ĸ = 0.38) and fractures (ĸ = 0.39) was fair. As hypothesized, the mSCQ correlated moderately to weakly with age, physical function, work limitations and health utility, and very weakly with disease activity. In contrast to our hypothesis, adding EAMs, osteoporosis and/or fractures to the mSCQ decreased correlations with several external constructs, especially among patients with peripheral SpA. Correlations with the different constructs were stronger for the both mSCQ and SpA-SCQ (rBASFI = 0.34; rEQ-5D = -0.33) compared with the rheumatic disease comorbidity index (rBASFI = 0.24; rEQ-5D = -0.21). The mSCQ is a valid self-report instrument to assess the influence of comorbidities on health outcomes in patients with SpA. Adding EAMs and/or osteoporosis or fractures does not improve validity of the mSCQ. © The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Rheumatology.

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