Smith Jamie, Shippee Nathan, Finnie Dawn, Killian Jill M, Montori Victor M, Redfield Margaret M, Dunlay Shannon
Mayo Clinic, Rochester, Minnesota, USA.
University of Minnesota Twin Cities, Minneapolis, Minnesota, USA.
BMJ Open. 2024 Dec 20;14(12):e088127. doi: 10.1136/bmjopen-2024-088127.
Patients with heart failure (HF) perform a variety of self-care activities to control symptoms and minimise the risk of HF decompensations. The objective of this study was to understand how patients build capacity and manage the work of living with HF.
A qualitative study using semi-structured telephone interviews. The interview guide was informed by the Cumulative Complexity Model, a conceptual framework that focuses on a patient's workload and their capacity to manage that work. Interview transcripts were analysed using a mixed inductive and deductive coding approach with organisation into larger thematic categories.
Southeastern Minnesota USA (11 counties) with capture of data from local community healthcare providers under the auspices of the Rochester Epidemiology Project.
Intentional sampling of local patients with HF (n=24, median age 69.5 years, 54% women, 63% rural, 54% preserved ejection fraction) who reported high treatment burden and/ or poor health status on a questionnaire.
Three major themes emerged: using capacity to manage workload, disruptions resulting in workload exceeding capacity and regaining workload-capacity balance. Participants described routinising the daily tasks associated with living with HF to minimise the associated burden and identified disruptions to their routines, including hospitalisations, emergency room visits, worsening health status and changes in healthcare access. To accommodate disruptions and regain workload-capacity balance, participants decreased workload and/or transferred tasks to others to maximise capacity.
Participants with HF described managing patient workload in times of stable health, but they sometimes struggled to accommodate disruptions and worsening health status. These findings can inform the design of interventions to minimise workload, maximise capacity and improve quality of life for patients with HF.
心力衰竭(HF)患者会进行各种自我护理活动,以控制症状并将HF失代偿的风险降至最低。本研究的目的是了解患者如何增强能力并应对与HF共存的生活负担。
一项采用半结构化电话访谈的定性研究。访谈指南基于累积复杂性模型,这是一个侧重于患者工作量及其管理该工作量能力的概念框架。访谈记录采用归纳与演绎相结合的编码方法进行分析,并组织成更大的主题类别。
美国明尼苏达州东南部(11个县),在罗切斯特流行病学项目的支持下,从当地社区医疗服务提供者处获取数据。
对当地HF患者进行立意抽样(n = 24,中位年龄69.5岁,54%为女性,63%为农村居民,54%射血分数保留),这些患者在问卷中报告了较高的治疗负担和/或较差的健康状况。
出现了三个主要主题:利用能力管理工作量、干扰导致工作量超过能力以及恢复工作量与能力的平衡。参与者描述了将与HF共存相关的日常任务常规化,以尽量减少相关负担,并确定了对其日常安排的干扰,包括住院、急诊就诊、健康状况恶化以及医疗服务获取的变化。为了适应干扰并恢复工作量与能力的平衡,参与者减少了工作量和/或将任务转移给他人以最大限度地提高能力。
HF患者描述了在健康状况稳定时如何管理患者工作量,但他们有时难以适应干扰和健康状况恶化。这些发现可为干预措施的设计提供参考,以尽量减少工作量、最大限度地提高能力并改善HF患者的生活质量。