Venetis Maria K, Hull Shawnika J, Nolan-Cody Haley, Austin Jorlanditha T, Salas M J, Jenny Mai ShuXian, Shields Lillianna, Alvarez Cimmiaron F
Department of Communication, Rutgers University, New Brunswick, USA.
Patient Educ Couns. 2025 May;134:108648. doi: 10.1016/j.pec.2025.108648. Epub 2025 Jan 11.
We conducted a systematic scoping review to characterize the landscape of communication scholarship within racial health equity in and through the patient-provider interaction.
We employed three waves of data collection to identify relevant articles (N = 454) about racial equity within provider-patient interactions. We iteratively developed a codebook concerning article characteristics, coding for journal names, data source, descriptive characteristics for the study samples, and presence of theory and equity in sections of the manuscripts.
This search identified studies (N = 206) that were published in 76 peer-reviewed scientific journals. The majority of studies reported primary data analyses and used survey and interview methodology. Many studies examined participants as patients generally rather than in reference to particular health conditions. Among those with a specific health condition, the largest proportion focused on cancer control. Very few studies included samples with Native American and Pacific Island heritage. Most studies included cisgender men and/or women, but none included transgender men or women. The vast majority of research focused on the patient experience; few centered on providers' and caregivers' experiences. The body of scholarship was largely atheoretical; the most frequently noted constructs were patient-provider communication (including patient-centered communication and patient-centered care), implicit/explicit racial bias, shared decision-making. There was wide variation in the extent to which equity was woven through the manuscripts. Equity is typically mentioned in the literature review, and racial identity in the sample may serve as a marker of racialized experiences.
This study demonstrates the need for the development of theory that elevates the centrality of health equity to attend to the bi- or multi-directional flow of communication that shapes the quality of these interactions.
These insights can serve as a strong foundation for the development of interventions to address equity in clinical interactions.
我们进行了一项系统的范围综述,以描述在医患互动中以及通过医患互动实现种族健康公平方面的沟通学术研究概况。
我们分三轮收集数据,以识别有关医患互动中种族公平的相关文章(N = 454)。我们反复制定了一个关于文章特征的编码手册,对期刊名称、数据源、研究样本的描述性特征以及手稿各部分中理论和公平性的存在情况进行编码。
此次检索确定了在76种同行评审科学期刊上发表的研究(N = 206)。大多数研究报告了原始数据分析,并使用了调查和访谈方法。许多研究将参与者总体上视为患者,而非针对特定健康状况。在那些针对特定健康状况的研究中,最大比例聚焦于癌症控制。极少有研究纳入有美国原住民和太平洋岛民血统的样本。大多数研究纳入了顺性别男性和/或女性,但没有一项研究纳入跨性别男性或女性。绝大多数研究聚焦于患者体验;很少有研究以提供者和护理者的体验为中心。学术研究主体在很大程度上缺乏理论性;最常提及的概念是医患沟通(包括以患者为中心的沟通和以患者为中心的护理)、隐性/显性种族偏见、共同决策。公平性在各手稿中的贯穿程度差异很大。公平性通常在文献综述中被提及,样本中的种族身份可能作为种族化经历的一个标志。
本研究表明需要发展理论,以提升健康公平的核心地位,关注塑造这些互动质量的双向或多向沟通流。
这些见解可为制定旨在解决临床互动中公平问题的干预措施提供坚实基础。