Department of Physiotherapy, Western Health, Sunshine Hospital, Melbourne, VIC, Australia.
Department of Critical Care, School of Medicine, The University of Melbourne, Melbourne, VIC, Australia.
Crit Care Med. 2022 Dec 1;50(12):1778-1787. doi: 10.1097/CCM.0000000000005681. Epub 2022 Oct 7.
To engage critical care end-users (survivors and caregivers) to describe their emotions and experiences across their recovery trajectory, and elicit their ideas and solutions for health service improvements to improve the ICU recovery experience.
End-user engagement as part of a qualitative design using the Framework Analysis method.
The Society of Critical Care Medicine's THRIVE international collaborative sites (follow-up clinics and peer support groups).
Patients and caregivers following critical illness and identified through the collaboratives.
None.
Eighty-six interviews were conducted. The following themes were identified: 1) Emotions and experiences of patients-"Loss of former self; Experiences of disability and adaptation"; 2) Emotions and experiences of caregivers-"Emotional impacts, adopting new roles, and caregiver burden; Influence of gender roles; Adaptation, adjustment, recalibration"; and 3) Patient and caregiver-generated solutions to improve recovery across the arc of care-"Family-targeted education; Expectation management; Rehabilitation for patients and caregivers; Peer support groups; Reconnecting with ICU post-discharge; Access to community-based supports post-discharge; Psychological support; Education of issues of ICU survivorship for health professionals; Support across recovery trajectory." Themes were mapped to a previously published recovery framework (Timing It Right) that captures patient and caregiver experiences and their support needs across the phases of care from the event/diagnosis to adaptation post-discharge home.
Patients and caregivers reported a range of emotions and experiences across the recovery trajectory from ICU to home. Through end-user engagement strategies many potential solutions were identified that could be implemented by health services and tested to support the delivery of higher-quality care for ICU survivors and their caregivers that extend from tertiary to primary care settings.
让重症监护的终端用户(幸存者和护理人员)参与进来,描述他们在康复过程中的情绪和体验,并征求他们对改善卫生服务的意见和建议,以改善重症监护恢复体验。
作为使用框架分析方法的定性设计的一部分,让终端用户参与进来。
重症监护医学会 THRIVE 国际合作地点(随访诊所和同伴支持小组)。
通过合作确定的重病后患者和护理人员。
无。
共进行了 86 次访谈。确定了以下主题:1)患者的情绪和体验——“失去从前的自我;残疾和适应的经历”;2)护理人员的情绪和体验——“情绪影响、新角色的采用和护理人员负担;性别角色的影响;适应、调整、重新校准”;以及 3)患者和护理人员提出的改善整个护理过程中恢复的解决方案——“面向家庭的教育;期望管理;患者和护理人员的康复;同伴支持小组;与 ICU 出院后重新联系;获得出院后基于社区的支持;心理支持;对 ICU 幸存者问题的健康教育;在整个恢复过程中的支持”。主题被映射到一个以前发表的恢复框架(Timing It Right),该框架捕捉了患者和护理人员在从事件/诊断到出院回家后的适应阶段的体验和支持需求。
患者和护理人员报告了从 ICU 到家庭的康复过程中的一系列情绪和体验。通过终端用户参与策略,确定了许多潜在的解决方案,这些解决方案可以由卫生服务部门实施,并进行测试,以支持为 ICU 幸存者及其护理人员提供更高质量的护理,从三级护理扩展到初级护理。