Patient perceptions of health-related quality of life in giant cell arteritis: international development of a disease-specific patient-reported outcome measure

Author:

Robson Joanna C12ORCID,Almeida Celia12,Dawson Jill3,Bromhead Alison2,Dures Emma12,Guly Catherine2,Hoon Elizabeth4,Mackie Sarah56ORCID,Ndosi Mwidimi12ORCID,Pauling John78ORCID,Hill Catherine4910

Affiliation:

1. Centre for Health and Clinical Research, University of the West of England

2. Bristol Royal Infirmary, University Hospitals and Weston Bristol NHS Foundation Trust, Bristol

3. Nuffield Department of Population Health (HSRU), University of Oxford, Oxford, UK

4. School of Public Health, University of Adelaide, Adelaide, SA, Australia

5. Leeds Institute of Rheumatic and Musculoskeletal Medicine, NIHR (National Institute for Health Research) Leeds Biomedical Research Centre, University of Leeds

6. Leeds Teaching Hospitals NHS (National Health Service) Trust, Leeds

7. Department of Rheumatology, Royal National Hospital for Rheumatic Diseases

8. Department of Pharmacy & Pharmacology, University of Bath, Bath, UK

9. Rheumatology Unit, The Queen Elizabeth Hospital, Woodville

10. Rheumatology Unit, The Royal Adelaide Hospital, Adelaide, SA, Australia

Abstract

Abstract Objectives GCA is a large vessel vasculitis (LVV) presenting with headache, jaw claudication, musculoskeletal and visual involvement. Current treatment is glucocorticoids and anti-IL-6 tocilizumab in refractory disease. The objective of this study was to explore the impact of GCA and its treatment on people’s health-related quality of life (HRQoL), to inform the development of a disease-specific patient-reported outcome measure (PROM) for use in clinical trials and practice. Methods Participants from the UK and Australia, with biopsy- or imaging-confirmed GCA, were interviewed to identify salient aspects of HRQoL in relation to GCA and its treatment. Purposive sampling included a range of demographic and disease features (cranial, LVV-GCA and visual involvement). Inductive analysis identified individual themes of importance, then domains. Candidate questionnaire items were developed from the individual themes, refined by piloting, cognitive interviews and a linguistic translatability assessment. Results Thirty-six interviews were conducted to saturation with participants with GCA from the UK (25) and Australia (11). Mean age was 74 years, 23 (63.9%) were female, 13 (36.1%) had visual loss and 5 (13.9%) had LVV-GCA. Thirty-nine individual themes within five domains were identified: physical symptoms; activity of daily living and function; participation; psychological impact; and impact on sense of self and perception of health. Sixty-nine candidate items were developed from individual themes; piloting and refinement resulted in a 40-item draft questionnaire. Conclusion This international qualitative study underpins the development of candidate items for a disease-specific PROM for GCA. The draft questionnaire is now ready for psychometric testing.

Funder

Above and Beyond Grant University Hospitals Bristol NHS Foundation Trust and QR Funding

University of the West of England

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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