Comparison of disease activity measures in early psoriatic arthritis in usual care

Author:

Wervers Kim1,Luime Jolanda J1,Tchetverikov Ilja2,Gerards Andreas H3,Kok Marc R4,Appels Cathelijne W Y5,van der Graaff Wiebo L6,van Groenendael Johannes H L M7,Korswagen Lindy-Anne8,Veris-van Dieren Josien J7,Hazes Johanna M W1,Vis Marijn1,

Affiliation:

1. Department of Rheumatology, Erasmus University Medical Centre, Rotterdam, The Netherlands

2. Department of Rheumatology, Albert Schweitzer Hospital, Dordrecht, The Netherlands

3. Department of Rheumatology, Vlietland Hospital, Schiedam, The Netherlands

4. Department of Rheumatology, Maasstad Hospital, Rotterdam, The Netherlands

5. Department of Rheumatology, Amphia Hospital, Breda, The Netherlands

6. Department of Rheumatology, Rivas Hospital, Gorinchem, The Netherlands

7. Department of Rheumatology, Reumazorg Zuid West Nederland, Roosendaal, The Netherlands

8. Department of Rheumatology, Sint Franciscus Gasthuis, Rotterdam, The Netherlands

Abstract

Abstract Objectives To compare responsiveness and longitudinal validity of Disease Activity Score 28 (DAS28), Disease Activity index for PSoriatic Arthritis (DAPSA), Composite Psoriatic Disease Activity Index (CPDAI), Psoriatic ArthritiS Disease Activity Score (PASDAS), GRAppa Composite scorE (GRACE) and Minimal Disease Activity (MDA) in usual care PsA patients, within 1 year after diagnosis. Methods Data collected in the Dutch southwest early PsA cohort (DEPAR) were used. Responsiveness was assessed using effect size (ES), standardized response mean (SRM), and discrimination between different general health states. Longitudinal validity was tested using mixed models with outcomes health-related quality of life (HRQOL), productivity and disability. Results Responsiveness was highest for PASDAS, with ES 1.00 and SRM 0.95, lowest for DAPSA, with ES 0.73 and SRM 0.71, and in between for DAS28, CPDAI and GRACE. Differences in general health were best discriminated with PASDAS and GRACE. Patients reporting stable or worsening general health could not be distinguished by DAS28 or CPDAI. Discrimination was better using DAPSA, but worse than when using PASDAS and GRACE. Longitudinal evolvement of HRQOL and productivity had the highest association with low disease activity according to GRACE, followed by PASDAS, MDA, DAPSA, DAS28, with the lowest association for CPDAI. Conclusion PASDAS and GRACE were superior with respect to responsiveness, and together with MDA best related to longitudinal evolvement of HRQOL, productivity and disability. Responsiveness and longitudinal validity of most outcomes were inferior for DAS28, DAPSA and CPDAI. As alternatives to the continuous measure DAPSA, use of PASDAS or GRACE should be considered.

Funder

Pfizer

ASPIRE

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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