Sledge Renata, Concepcion Beatrice P, Witten Beth, Klicko Kristi, Schatell Dori
Department of Social Work, Fontbonne University, Saint Louis, Missouri.
Division of Nephrology and Hypertension, Vanderbilt University Medical Center, Nashville, Tennessee.
Kidney Med. 2023 Jan 21;5(4):100603. doi: 10.1016/j.xkme.2023.100603. eCollection 2023 Apr.
RATIONALE & OBJECTIVE: Patients with kidney failure who have used multiple treatment modalities are a unique source of information for how different options may best fit values. We aimed to understand how people interpret their health and kidney failure treatment experience to inform providers who facilitate shared decision-making conversations.
This qualitative, interpretive phenomenological study explores how patients with kidney failure interpret health throughout their treatment trajectory.
SETTING & PARTICIPANTS: We recruited a purposive sample of patients who had used 3 or more kidney failure treatment options, including transplant and dialysis from transplant clinics and online support groups, for semi-structured interviews. Eligible participants were over 18 and spoke English for a total of 7 current transplant, 10 current home dialysis, and 1 current in-center patient.
A 6-step iterative process of data analysis occurred concurrently with data collection.
Half of the 18 participants were Black; 67% were women. Three interrelated themes emerged from interviews: ability to engage in meaningful activities; working for balance; and living in context. Participants evaluated health according to their ability to engage in meaningful activities while balancing their emotional and physical needs with their life goals. When their social and treatment environments supported their autonomy, participants also considered themselves healthy.
The inclusion of only English-speaking patients limits the transferability of findings. A longitudinal design, repeated interviews, observation, and dyadic interviews would increase the health care providers' understanding and interpretation of health.
The themes demonstrated patients evaluated health based on ability to engage in meaningful activities while maintaining balance. The treatment context, particularly how health care providers responded to patients' physiological experience, autonomy, and power, influenced interpretation of patient treatment experiences. Integrating patient interpretations of health with quantitative measures of treatment effectiveness can help health care providers better partner with patients to provide effective care for kidney failure.
使用过多种治疗方式的肾衰竭患者是了解不同治疗方案如何最佳契合价值观的独特信息来源。我们旨在了解人们如何解读自身健康状况及肾衰竭治疗经历,以为促进共同决策对话的医疗服务提供者提供参考。
这项定性的解释现象学研究探讨了肾衰竭患者在整个治疗过程中如何解读健康状况。
我们从移植诊所和在线支持小组中,有目的地选取了曾使用过3种或更多肾衰竭治疗方案(包括移植和透析)的患者样本,进行半结构化访谈。符合条件的参与者年龄在18岁以上,说英语,共有7名当前正在接受移植治疗的患者、10名当前正在进行家庭透析的患者和1名当前正在中心透析的患者。
数据分析的6步迭代过程与数据收集同时进行。
18名参与者中有一半是黑人;67%为女性。访谈中出现了三个相互关联的主题:参与有意义活动的能力;努力实现平衡;以及结合具体情况生活。参与者根据自己参与有意义活动的能力来评估健康状况,同时在情感和身体需求与生活目标之间寻求平衡。当他们的社会和治疗环境支持他们的自主权时,参与者也会认为自己是健康的。
仅纳入说英语的患者限制了研究结果的可推广性。采用纵向设计、重复访谈、观察和二元访谈将增进医疗服务提供者对健康的理解和解读。
这些主题表明,患者基于参与有意义活动并保持平衡的能力来评估健康状况。治疗环境,尤其是医疗服务提供者对患者生理体验、自主权和权力的反应,影响了对患者治疗经历的解读。将患者对健康的解读与治疗效果的定量指标相结合,有助于医疗服务提供者更好地与患者合作,为肾衰竭患者提供有效的治疗。