Responsiveness and Minimum Clinically Important Difference in Patient‐Reported Outcome Measures Among Patients With Psoriatic Arthritis: A Prospective Cohort Study

Author:

Karmacharya Paras1ORCID,Stull Courtney2,Stephens‐Shields Alisa3,Husni M. Elaine4ORCID,Scher Jose U.5,Craig Ethan3,Fitzsimmons Robert3,Reddy Soumya M.5,Magrey Marina N.6,Ogdie Alexis3ORCID,Walsh Jessica A.7ORCID

Affiliation:

1. Vanderbilt University Medical Center Nashville Tennessee

2. University of Pittsburgh Medical Center Pittsburgh Pennsylvania

3. University of Pennsylvania Philadelphia

4. Cleveland Clinic Cleveland Ohio

5. New York University New York

6. University Hospitals Cleveland Medical Center Cleveland Ohio

7. University of Utah Salt Lake City

Abstract

ObjectiveTo determine the responsiveness to therapy and minimum clinically important improvement (MCII) for patient‐reported outcome measures in psoriatic arthritis (PsA) and to examine the impact of baseline disease activity on the ability to demonstrate change.MethodsA longitudinal cohort study was performed within the PsA Research Consortium. Patients completed several patient‐reported outcomes, including the Routine Assessment of Patient Index Data, the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), the Psoriatic Arthritis Impact of Disease 12‐item (PsAID12) questionnaire, and others. The mean change in the scores between visits and standardized response means (SRMs) were calculated. The MCII was calculated as the mean change in score among patients who reported minimal improvement. SRMs and MCIIs were compared among subgroups with moderate to highly active PsA and those with lower disease activity.ResultsAmong 171 patients, 266 therapy courses were included. The mean ± SD age was 51 ± 13.8 years, 53% were female, and the mean swollen and tender joint counts were 3 and 6, respectively, at baseline. SRMs and MCII for all measures were small to moderate, although greater among those with higher baseline disease activity. BASDAI had the best SRM overall and for less active PsA, and the clinical Disease Activity of PsA (cDAPSA) and PsAID12 were best for those with higher disease activity.ConclusionSRMs and MCII were relatively small in this real‐world population, particularly among those with lower disease activity at baseline. BASDAI, cDAPSA, and PsAID12 had good sensitivity to change, but selection for use in trials should consider the baseline disease activity of patients to be enrolled.

Funder

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Rheumatology Research Foundation

Spondyloarthritis Research and Treatment Network

Publisher

Wiley

Subject

Rheumatology

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