Istanboulian Laura, Gilding Anthony J, Hamilton Lorrie, Master Tasneem, Bingler Sarah, Soldatic Karen, Smith Kelly M
Daphne Cockwell School of Nursing Toronto Metropolitan University, Toronto, Canada.
Michael Garron Hospital, Toronto, Canada.
BMC Nurs. 2024 Sep 6;23(1):625. doi: 10.1186/s12912-024-02300-5.
Patients with persistent critical illness experience prolonged multi-system morbidity, functional impairments, and chronic conditions. As a result, these patients have prolonged intensive care unit admissions. If discharged, they return home with long-term medical dependencies. Care partners take on a variety of physical, mental health, cognitive, and social roles to support the provision of care for these patients. There is limited evidence, however, of the impact of being a care partner for this patient population during hospitalization.
A qualitative descriptive study was conducted to explore the impact care provision on care partners for patients experiencing persistent critical illness. Patients who have or have had persistent critical illness and care partners were recruited from two inpatient units in a single community academic hospital in Toronto, Canada to participate in semi-structured interviews. Data was analyzed using a team-based inductive content analysis.
Seven (43.8%) participants were patient survivors, and nine (56.3%) were care partners. Patients and care partners reported physical, socio-emotional, and social stress as impacts of care provision during persistent critical illness hospitalization. Care partners identified several protective strategies that they used to mitigate the impacts of care provision on them such as seeking external mental health support and boundary setting. Features of formalized and care partner programs were also identified and suggest that these programs can be protective of care partner values, mitigate feelings of helplessness and stress, and may improve relationships between the family members who are in the care partner role and the healthcare team.
This study identified physical, socio-emotional, and social stress related impacts of care provision on care partners of patients with persistent critical illness during hospitalization. Additionally, this study identified protective factors initiated by care partners to mitigate the reported stresses of the role, as well as protective features of a care partner program. The results provide a better understanding supportive features of care partner programs that are specific to the experiences and needs of persistent critical illness and add to the growing body of evidence about how to provide equitable access to care during and post hospitalization.
患有持续性危重症的患者会经历长期的多系统疾病、功能障碍和慢性病。因此,这些患者在重症监护病房的住院时间延长。如果出院,他们回家后会有长期的医疗依赖。护理伙伴承担着各种身体、心理健康、认知和社会角色,以支持对这些患者的护理。然而,关于在住院期间作为这类患者的护理伙伴所产生的影响,证据有限。
进行了一项定性描述性研究,以探讨为患有持续性危重症的患者提供护理对护理伙伴的影响。从加拿大多伦多一家社区学术医院的两个住院科室招募了患有或曾患有持续性危重症的患者及其护理伙伴,参与半结构化访谈。使用基于团队的归纳性内容分析法对数据进行分析。
七名(43.8%)参与者是患者幸存者,九名(56.3%)是护理伙伴。患者和护理伙伴报告称,在持续性危重症住院期间提供护理产生的影响包括身体、社会情感和社会压力。护理伙伴确定了几种他们用来减轻护理对自身影响的保护策略,如寻求外部心理健康支持和设定界限。还确定了正式护理伙伴项目的特点,表明这些项目可以保护护理伙伴的价值观,减轻无助感和压力,并可能改善担任护理伙伴角色的家庭成员与医疗团队之间的关系。
本研究确定了在住院期间为患有持续性危重症的患者提供护理对护理伙伴产生的与身体、社会情感和社会压力相关的影响。此外,本研究确定了护理伙伴启动的保护因素,以减轻所报告的角色压力,以及护理伙伴项目的保护特点。这些结果有助于更好地理解针对持续性危重症患者的经验和需求的护理伙伴项目的支持性特点,并为如何在住院期间和出院后提供公平的护理服务增添了越来越多的证据。