A Qualitative Analysis of Patient Perspectives and Preferences in Lupus Management to Guide Lupus Guidelines Development

作者：Shivani Garg, Izzy Hartel, Lisa R. Sammaritano, Anca Askanase, Bonnie L. Bermas, Maria Dall’Era, Alí Duarte‐García, Victoria P. Werth, Brad H. Rovin, Reem A. Mustafa, Amy S. Turner, Bené Williams, Brian Ung, Hiya Bhavsar, Monique Gore‐Massy, Nahirannette Pulido, N Hernandez Guerrero, Natalie Smith, Wambui Machua, Linda T. Hiraki, Mary Beth F. Son · 发表于：Arthritis Care & Research · 年份：2025 · DOI：10.1002/acr.25693 · 被引用次数：1 · 研究领域：Systemic Lupus Erythematosus Research、Diabetes Management and Education、Mental Health and Patient Involvement

OBJECTIVE: A patient-centered approach for chronic disease management, including systemic lupus erythematosus (SLE), aligns treatment with patients' values and preferences, leading to improved outcomes. This paper summarizes how patient experiences, perspectives, and priorities informed the American College of Rheumatology (ACR) 2024 Lupus Nephritis (LN) and 2025 SLE screening, treatment guidelines. METHODS: We completed a cross-sectional qualitative study using content analysis of two Patient Panel meetings for the ACR LN and SLE guidelines. Key themes were presented by Patient Panel representatives during Voting Panel Meetings along with evidence for each recommendation, to ensure comprehensive discussions and align treatment recommendations with patients' priorities and values. RESULTS: Nineteen people (90% women) with diagnoses of SLE and/or LN participated in the Patient Panels and 17 consented to use their feedback for analysis. Thematic analysis of their discussions revealed nine patient-reported key themes in three domains: (1) treatment and monitoring of LN and SLE: medication side effects, daily function, treatment goals, and monitoring and screening; (2) clinical communication: strategies to optimize communication and provider and structural impediments to effective communication; and (3) improving transparency and information sharing: clinical trial participation, and medical costs and insurance coverage. These themes were actively incorporated into discussions du...