Spondyloarthritis & psoriatic arthritis

The Patient Self-Administered Inflammatory Arthritis Detection Study

J RheumatolPublished Diagnostic accuracy study

Authors' conclusion

The results support the utility and feasibility of routine collection of EIAQ and CaFaSpA questionnaires for discriminating patients with IA from those with non-IA.

Study context

Population
Newly referred rheumatology patients in British Columbia, Canada
Participants
92 participants
Comparison
Early Inflammatory Arthritis Questionnaire (EIAQ) and Case Finding Axial Spondyloarthritis (CaFaSpA) questionnaire predictive scores vs rheumatologist diagnosis (reference standard)
Outcome
Discriminatory referral performance for inflammatory arthritis (IA) (AUC, sensitivity, specificity)

Performance

As reported in the abstract

Discrimination of IA vs non-IA
Test or modelAUCSensitivitySpecificity
EIAQ0.59 (95% CI 0.49-0.68)33% (95% CI 19-51%)84% (95% CI 73-91)

EIAQ

AUC0.59 (95% CI 0.49-0.68)
Sensitivity33% (95% CI 19-51%)
Specificity84% (95% CI 73-91)
Alternate algorithms based on EIAQ and CaFaSpA questions, AUC up to
0.80 (95% CI 0.68-0.90)

Further findings

Diagnosis distribution

OutcomeTS-IAOther IANon-IA
Time from referral to rheumatologist visit44 (IQR 28–83) days69 (IQR 40–102)65 (IQR 34–99)
Time from referral to rheumatologist visit — Longer for women
+ 9 days
Time from referral to rheumatologist visit — Longer in nonmetropolitan areas
+ 16 days

Original publication

The Patient Self-Administered Inflammatory Arthritis Detection Study. J Rheumatol. Published 1 December 2025. doi:10.3899/jrheum.2025-0428

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