Vanderbilt Center for Kidney Disease, Nashville, Tennessee.
Division of Nephrology, Vanderbilt University Medical Center, Nashville, Tennessee.
Clin J Am Soc Nephrol. 2018 Apr 6;13(4):551-559. doi: 10.2215/CJN.07580717. Epub 2018 Mar 15.
Incidence of ESKD is three times higher in black Americans than in whites, and CKD prevalence continues to rise among black Americans. Community-based kidney disease screening may increase early identification and awareness of black Americans at risk, but it is challenging to implement. This study aimed to identify participants' perspectives of community kidney disease screening. The Health Belief Model provides a theoretic framework for conceptualization of these perspectives and optimization of community kidney disease screening activities.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Researchers in collaboration with the Tennessee Kidney Foundation conducted three focus groups of adults in black American churches in Nashville, Tennessee. Questions examined views on CKD information, access to care, and priorities of kidney disease health. Content analysis was used. Guided by the Health Belief Model, themes were generated, and additional themes were derived from the data using an inductive approach.
Thirty-two black Americans completed the study in 2014. Participants were mostly women (79%) with a mean age of 56 years old (range, 24-78). Two major categories of barriers to kidney disease screening were identified: () participant factors, including limited kidney disease knowledge, spiritual/religious beliefs, emotions, and culture of the individual; and () logistic factors, including lack of convenience and incentives and poor advertisement. Potential facilitators of CKD screening included provision of CKD education, convenience of screening activities, and use of culturally sensitive and enhanced communication strategies. Program recommendations included partnering with trusted community members, selecting convenient locations, tailored advertising, and provision of compensation.
Findings of this study suggest that provider-delivered culturally sensitive education and stakeholder engagement are critical to increase trust, decrease fear, and maximize participation and early identification of kidney disease among black Americans considering community screening.
在美国黑人中,终末期肾病(ESKD)的发病率比白人高三倍,且慢性肾脏病(CKD)的患病率仍在上升。基于社区的肾脏疾病筛查可能会增加高危美国黑人的早期识别和意识,但实施起来具有挑战性。本研究旨在确定参与者对社区肾脏疾病筛查的看法。健康信念模型(Health Belief Model)为概念化这些观点和优化社区肾脏疾病筛查活动提供了理论框架。
设计、地点、参与者和测量:研究人员与田纳西州肾脏基金会合作,在田纳西州纳什维尔的黑人美国教堂进行了三次成人焦点小组讨论。问题探讨了对 CKD 信息、获得护理的看法,以及肾脏病健康的优先事项。采用内容分析法。在健康信念模型的指导下,生成了主题,并使用归纳法从数据中得出其他主题。
2014 年,32 名美国黑人完成了这项研究。参与者主要是女性(79%),平均年龄为 56 岁(范围为 24-78 岁)。确定了两个主要的肾脏疾病筛查障碍类别:()参与者因素,包括有限的肾脏疾病知识、精神/宗教信仰、情绪和个人文化;和()逻辑因素,包括缺乏便利性和激励措施以及广告宣传不佳。CKD 筛查的潜在促进因素包括提供 CKD 教育、筛查活动的便利性,以及使用文化敏感和增强的沟通策略。项目建议包括与值得信赖的社区成员合作、选择方便的地点、量身定制的广告宣传以及提供补偿。
本研究结果表明,提供者提供文化敏感的教育和利益相关者的参与对于增加信任、减少恐惧以及最大限度地提高美国黑人对社区筛查的参与和早期识别至关重要。