학술논문

Patient and Caregiver-Derived Health Service Improvements for Better Critical Care Recovery.
Document Type
Journal Article
Source
Critical Care Medicine. Dec2022, Vol. 50 Issue 12, p1778-1787. 10p.
Subject
*SERVICES for caregivers
*PATIENT-family relations
*MEDICAL care
*CRITICAL care medicine
*BURDEN of care
*MEDICAL personnel
*PATIENTS' attitudes
Language
ISSN
0090-3493
Abstract
Objectives: 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.Design: End-user engagement as part of a qualitative design using the Framework Analysis method.Setting: The Society of Critical Care Medicine's THRIVE international collaborative sites (follow-up clinics and peer support groups).Subjects: Patients and caregivers following critical illness and identified through the collaboratives.Interventions: None.Measurements and Main Results: 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.Conclusions: 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. [ABSTRACT FROM AUTHOR]