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
Harvard Medical School, Boston, Massachusetts and Health Equity Research Lab, Cambridge Health Alliance, Cambridge, Massachusetts, USA.
Warren Alpert Medical School of Brown University, Brown University Health, Providence, Rhode Island, USA.
Health Serv Res. 2025 Apr;60(2):e14373. doi: 10.1111/1475-6773.14373. Epub 2024 Aug 27.
To understand whether and how primary care providers and staff elicit patients' past experiences of healthcare discrimination when providing care.
DATA SOURCES/STUDY SETTING: 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 COLLECTION/EXTRACTION METHODS: 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.
了解初级保健提供者及工作人员在提供医疗服务时是否以及如何引出患者过去遭受医疗歧视的经历。
数据来源/研究背景:对担任初级保健角色的医护人员进行了20次定性半结构化访谈,以为未来将医疗歧视既往经历的数据纳入临床护理的干预措施提供信息。
定性研究。
数据收集/提取方法:2018年12月至2019年1月期间,通过半结构化定性访谈收集数据,访谈对象是一个城市安全网医疗系统中一家医院门诊担任初级保健角色的医护人员,该系统服务的患者群体在种族、民族和语言方面具有显著多样性。
提供者没有常规地或以结构化方式引出有关过去医疗歧视经历的信息。一些提供者认为,有关医疗歧视经历的信息可以使他们更了解并回应患者需求,并建立更信任的关系。其他人则认为引出此类信息不合适或无用,并担心在收集和有效使用此类数据方面存在挑战。
虽然提供者认为引出过去的歧视经历有价值,但在初级保健就诊期间与患者直接且系统地讨论此类经历对他们来说具有挑战性。在初级保健环境中收集此类信息可能需要实施多层次的系统数据收集策略。此处呈现的研究结果有助于确定在诊所层面这样做的机会。