Deciphering difficult-to-treat psoriatic arthritis (D2T-PsA): a GRAPPA perspective from an international survey of healthcare professionals

Author:

Ribeiro Andre L1ORCID,Singla Shikha2,Chandran Vinod34,Chronis Nicholas5,Liao Wilson6,Lindsay Christine7,Soriano Enrique R8ORCID,Mease Philip J9ORCID,Proft Fabian10ORCID

Affiliation:

1. Division of Rheumatology, University of Toronto, Women’s College Hospital , Toronto, ON, Canada

2. Department of Rheumatology, Medical College of Wisconsin , Milwaukee, WI, USA

3. Division of Rheumatology, Department of Medicine, University of Toronto , Toronto, Canada

4. Psoriatic Arthritis Program, Schroeder Arthritis Institute, University Health Network , Toronto, Canada

5. Psoriatic Arthritis Program, Schroeder Arthritis Institute, University Health Network , Toronto, ON, Canada

6. Department of Dermatology, University of California San Francisco , San Francisco, USA

7. GRAPPA Patient Research Partner , Prosper, TX, USA

8. Rheumatology Section, Internal Medicine Service, Hospital Italiano de Buenos Aires , Buenos Aires, Argentina

9. Swedish Medical Center/Providence St, Joseph Health and University of Washington School of Medicine , Seattle, USA

10. Department of Gastroenterology, Infectiology and Rheumatology (including Nutrition Medicine), Charité—Universitätsmedizin Berlin , Berlin, Germany

Abstract

Abstract Objectives This study contributes to the Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA)’s effort to define ‘difficult-to-treat’ PsA (D2T-PsA), leveraging insights of healthcare professionals who are GRAPPA members. The primary objective is to inform GRAPPA’s D2T PsA project, ensuring the consensus definition reflects clinical experience and expertise. Methods An online survey was conducted among GRAPPA’s healthcare professionals managing PsA patients. The survey covered demographic details, structured questions, and open-ended queries to gather comprehensive insights into the experts’ viewpoints. Results About 223 physicians completed the survey, comprising 179 (80.2%) rheumatologists and 40 (17.9%) dermatologists. The majority, 184 (82.5%), favoured establishing distinct definitions for D2T-PsA and complex-to-manage PsA (C2M-PsA). Furthermore, 202 (90.5%) supported a definition that includes objective inflammation signs (clinical, laboratory, imaging, among others). However, opinions varied on the criteria for prior treatment failures, with most (93, 41.7%) favouring a definition that includes at least one conventional synthetic disease-modifying anti-rheumatic drug and two or more biological- or targeted-synthetic-DMARDs with different mechanisms of action. Conclusion The survey reveals a majority opinion among GRAPPA experts favouring the differentiation between D2T-PsA and C2M-PsA, and the inclusion of objective inflammatory markers in these definitions. However, there is less than 50% agreement on the specific treatment failure criteria, particularly regarding the number of therapies needed to classify PsA as D2T. These findings suggest a need for continued discussion to reach a more unified approach in defining D2T-PsA, reflecting the complexity of the condition.

Publisher

Oxford University Press (OUP)

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