| Literature DB >> 31832854 |
Rob J Fredericksen1,2, Emma Fitzsimmons3, Laura E Gibbons3, Stephanie Loo4, Sarah Dougherty5, Sonia Avendano-Soto6, Will A Anderson5, Cristina Gutierrez4, Sally Shurbaji5, Savannah Burleson5, Katerina Christopoulos7, Joanna Poceta7, Kenneth H Mayer4, Michael J Mugavero8, William C Mathews9, Paul K Crane3, Heidi M Crane3.
Abstract
Evidence suggests priorities differ between patients in HIV care and their providers regarding topics most important to address in care. At five U.S. sites, we asked patients and providers to prioritize 25 potential topic areas to address during routine visits, and invited patients to discuss selection rationale. Patients (n = 206) and providers (n = 17) showed high discordance in rank order priorities (X2 (24, 223) = 71.12; p < 0.0001). Patients ranked social domains such as HIV stigma highly; a higher proportion of providers prioritized substance use domains. HIV stigma was a higher priority for patients in care fewer than 6 years (Fisher's exact p = 0.0062), nonwhite patients (Fisher's exact p = 0.0114), and younger patients (Fisher's exact p = 0.0281). Patients' priorities differed between men and women (X2 (24, 188) = 52.89; p < 0.0001), white race vs. other races (X2 (24, 206) = 48.32; p = 0.0023), and Latinos vs. non-Latinos (X2 (24, 206) = 48.65; p = 0.0021). Interviews (n = 79) revealed perceived impact of social context on health and health behaviors.Entities:
Keywords: HIV care; Patient reported outcomes; Patient-provider communication
Mesh：
Year: 2020 PMID： 31832854 PMCID： PMC7950312 DOI： 10.1007/s10461-019-02746-8
Source DB: PubMed Journal: AIDS Behav ISSN： 1090-7165