PT - JOURNAL ARTICLE AU - Rebecca Williams-Hall AU - Pamela Berry AU - Nicola Williamson AU - Melissa Barclay AU - Anna Roberts AU - Adam Gater AU - Chloe Tolley AU - Helena Bradley AU - Amy Ward AU - Elizabeth Hsia AU - Qing Zuraw AU - Patricia DeLong AU - Zahi Touma AU - Vibeke Strand TI - Generation of evidence supporting the content validity of SF-36, FACIT-F, and LupusQoL, and novel patient-reported symptom items for use in patients with systemic lupus erythematosus (SLE) and SLE with lupus nephritis (LN) AID - 10.1136/lupus-2022-000712 DP - 2022 Aug 01 TA - Lupus Science & Medicine PG - e000712 VI - 9 IP - 1 4099 - http://lupus.bmj.com/content/9/1/e000712.short 4100 - http://lupus.bmj.com/content/9/1/e000712.full SO - Lupus Sci Med2022 Aug 01; 9 AB - Objective SLE and lupus nephritis (LN) have significant impacts on the health-related quality of life of patients living with the condition, which are important to capture from the patient’s perspective using patient-reported outcomes (PROs). The objectives of this study were to evaluate the content validity of PROs commonly used in SLE and LN (36-Item Short Form Health Survey (SF-36), Functional Assessment of Chronic Illness Therapy–Fatigue (FACIT-F) and Lupus Quality of Life (LupusQoL), as well as novel PRO symptom severity items measuring skin rash, joint pain, joint stiffness and swelling of the legs and/or feet, in both populations.Methods Qualitative, semi-structured, cognitive interviews were conducted with 48 participants (SLE=28, LN=20). Understanding and relevance of symptom and impact PRO concepts from existing PROs were assessed, alongside novel PRO symptom severity items with different recall periods (24 hours vs 7 days) and response scales (Numerical Rating Scale (NRS) vs Verbal Rating Scale). Interviews were conducted in multiple rounds to allow for modifications to the novel PRO items. Analysis of verbatim interview transcripts was performed.Results Symptom and impact concepts assessed by the SF-36, FACIT-F, and LupusQoL were well understood by both participants with SLE and LN (≥90.0%), with most considered relevant by over half of the participants asked (≥51.9%). All participants asked (100%) understood the novel PRO symptom severity items, and the majority (≥90.0%) considered the symptoms relevant. Minor modifications to the novel PRO items were made between rounds to improve clarity based on participant feedback. The selected 7-day recall period and NRS in the final iteration of the PRO items were understood and relevant. No differences in interview findings between the SLE and LN samples were identified.Conclusions Findings provide evidence of content validity for concepts assessed by the SF-36, FACIT-F, LupusQoL and the novel PRO symptom severity items, supporting use of these PROs to comprehensively assess disease impact in future SLE and LN clinical trials.All data relevant to the study are included in the article or uploaded as supplementary information.