Woodard Lechauncy D, Hernandez Marie T, Lees Emily, Petersen Laura A
Houston Center for Quality of Care and Utilization Studies, Department of Veterans Affairs, Health Services Research and Development Center of Excellence, Houston Veterans Affairs Medical Center, Houston, TX 77030, USA.
Patient Educ Couns. 2005 May;57(2):225-31. doi: 10.1016/j.pec.2004.06.004.
The objective of this study was to explore coronary heart disease (CHD) health care experiences and beliefs of African-American and white patients to elicit potential causes of racial disparities in CHD outcomes. Twenty-four patients (14 white, 10 African-American) with established CHD participated in one of four focus groups. Using qualitative methods, verbatim transcripts of the groups were analyzed by independent investigators to identify key themes. We identified four themes: risk factor knowledge, physician--patient relationship, medical system access, and treatment beliefs. Racial differences were apparent in the experience of racism as a stress, knowledge of specifics of CHD risk factors, and assertiveness in the physician--patient relationship. These findings suggest that strategies to improve risk factor knowledge and to enable African-American patients to become active partners in their medical care may lead to improved CHD morbidity and mortality in this population. The efficacy of such interventions would need to be tested in further work.
本研究的目的是探究非裔美国人和白人患者在冠心病(CHD)医疗保健方面的经历和信念,以找出冠心病治疗结果中种族差异的潜在原因。24名确诊为冠心病的患者(14名白人,10名非裔美国人)参加了四个焦点小组中的一个。采用定性方法,独立研究人员对各小组的逐字记录进行分析,以确定关键主题。我们确定了四个主题:危险因素知识、医患关系、医疗系统准入和治疗信念。在将种族主义视为一种压力的体验、对冠心病危险因素细节的了解以及医患关系中的自信方面,种族差异很明显。这些发现表明,提高危险因素知识以及使非裔美国患者能够积极参与其医疗护理的策略,可能会改善该人群的冠心病发病率和死亡率。此类干预措施的效果需要在进一步的研究中进行检验。