Sun Carolyn, Cheung Wing, Corpuz Kathryn, Shang Jingjing, Stone Patricia W
Hunter College, Hunter-Bellevue School of Nursing, 425 E 25th St., New York, NY 10065, USA.
New York University, 726 Broadway, 4th Floor, Suite 403, New York, NY 10003, USA.
Nurs Res Pract. 2024 Oct 11;2024:2280296. doi: 10.1155/2024/2280296. eCollection 2024.
To assess the acceptability of a symptom self-management booklet among older Chinese Americans receiving kidney replacement therapy.
In previous work, we identified commonly occurring, bothersome symptoms and strategies used in this population to ameliorate symptoms. We used these data to develop a symptom self-management booklet in English, traditional, and simplified Chinese.
In the United States, the prevalence of kidney disease is 1.5 times higher in Asians compared to whites. With the many symptoms associated with this disease, self-management of symptoms would be particularly helpful.
Seven older Chinese Americans receiving kidney replacement therapy and their caregivers were interviewed to assess the acceptability of the booklets. We reviewed participant feedback on content, graphics, and design, reading experience, suggestions for improvement, and health information sources using the inductive thematic method.
Overall, patients confirmed acceptability of these self-management booklets across all domains. . This study validated the booklet as a source of health information for older Chinese American patients with kidney disease, which some studies suggest are preferred to electronic materials or methods in this population. Health care providers can use the resultant booklets when caring for these patients to provide culturally sensitive information on self-management of symptoms. . These booklets provide a free resource tailored to an underserved population and may help nurses and nurse practitioners provide care with cultural humility. . Embracing community-based participatory research, as was done in this study, can help create culturally appropriate patient education materials that empower patient symptom self-management and promote informative and culturally sensitive conversations between patients, families, and providers.
评估一本症状自我管理手册在美国华裔老年肾脏替代治疗患者中的可接受性。
在之前的研究中,我们确定了该人群中常见的、令人困扰的症状以及用于缓解症状的策略。我们利用这些数据编写了一本英文、繁体中文和简体中文的症状自我管理手册。
在美国,亚洲人的肾病患病率是白人的1.5倍。鉴于这种疾病伴有多种症状,症状的自我管理会特别有帮助。
对7名接受肾脏替代治疗的美国华裔老年人及其护理人员进行访谈,以评估手册的可接受性。我们采用归纳主题法,回顾了参与者对内容、图表、设计、阅读体验、改进建议以及健康信息来源的反馈。
总体而言,患者确认这些自我管理手册在所有方面都具有可接受性。 本研究验证了该手册可作为美国华裔老年肾病患者的健康信息来源,一些研究表明,在这一人群中,他们更喜欢手册而非电子材料或方法。医疗保健提供者在护理这些患者时可以使用编写好的手册,以提供关于症状自我管理的具有文化敏感性的信息。 这些手册为服务不足的人群提供了免费资源,可能有助于护士和执业护士以文化谦逊的态度提供护理。 正如本研究中所做的那样,采用基于社区的参与性研究有助于创建适合文化背景的患者教育材料,从而增强患者对症状的自我管理能力,并促进患者、家庭和提供者之间提供信息且具有文化敏感性的对话。