Eliciting patient past experiences of healthcare discrimination as a potential pathway to reduce health disparities: A qualitative study of primary care staff

• Published in: Health services research 2024-08, p.e14373
• Main Authors: Cortés, Dharma E, Progovac, Ana M, Lu, Frederick, Lee, Esther, Tran, Nathaniel M, Moyer, Margo A, Odayar, Varshini, Rodgers, Caryn R R, Adams, Leslie, Chambers, Valeria, Delman, Jonathan, Delman, Deborah, de Castro, Selma, Sánchez Román, María José, Kaushal, Natasha A, Creedon, Timothy B, Sonik, Rajan A, Rodriguez Quinerly, Catherine, Nakash, Ora, Moradi, Afsaneh, Abolaban, Heba, Flomenhoft, Tali, Nabisere, Ruth, Mann, Ziva, Shu-Yeu Hou, Sherry, Shaikh, Farah N, Flores, Michael W, Jordan, Dierdre, Carson, Nicholas, Carle, Adam C, Cook, Benjamin Lé, McCormick, Danny
• Format: Article
• Language: English
• ISSN: 0017-9124; 1475-6773; 1475-6773
• DOI: 10.1111/1475-6773.14373

To understand whether and how primary care providers and staff elicit patients' past experiences of healthcare discrimination when providing care. Twenty qualitative semi-structured interviews were conducted with healthcare staff in primary care roles to inform future interventions to integrate data about past experiences of healthcare discrimination into clinical care. Qualitative study. Data were collected via semi-structured qualitative interviews between December 2018 and January 2019, with health care staff in primary care roles at a hospital-based clinic within an urban safety-net health system that serves a patient population with significant racial, ethnic, and linguistic diversity. Providers did not routinely, or in a structured way, elicit information about past experiences of healthcare discrimination. Some providers believed that information about healthcare discrimination experiences could allow them to be more aware of and responsive to their patients' needs and to establish more trusting relationships. Others did not deem it appropriate or useful to elicit such information and were concerned about challenges in collecting and effectively using such data. While providers see value in eliciting past experiences of discrimination, directly and systematically discussing such experiences with patients during a primary care encounter is challenging for them. Collecting this information in primary care settings will likely require implementation of multilevel systematic data collection strategies. Findings presented here can help identify clinic-level opportunities to do so.