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Published on: January 16, 2019
Navigating post-ICU care: understanding family members' experiences - a qualitative study
Matteo Danielis1, Alessandro Garau2, Dina Molaro2
1Laboratory of Studies & Evidence Based Nursing, Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova, Padova, Italy.
Family members caring for loved ones post-intensive care unit (ICU) experience transformed quality of life (QoL). Addressing caregiver needs and fostering positive emotions enhances their resilience and fulfillment during this challenging transition.
Area of Science:
- Critical Care Medicine
- Nursing Research
- Psychosocial Support
Background:
- Supporting family members (FMs) after intensive care unit (ICU) discharge is crucial for patient and caregiver well-being.
- The post-ICU phase presents unique challenges impacting the quality of life (QoL) for caregivers.
Purpose of the Study:
- To explore the experiences of family members (FMs) three months after intensive care unit (ICU) discharge.
- To assess the quality of life (QoL) of family members (FMs) during the post-intensive care unit (ICU) transition.
Main Methods:
- Qualitative, descriptive study involving telephonic interviews with 24 family members (FMs).
- Data collected from two Italian Academic Hospital ICUs over two months.
- Thematic analysis using a hybrid deductive and inductive coding approach facilitated by Atlas.ti software.
Main Results:
- Four themes emerged: transformed QoL, significant positive emotions, the caregiver's supporting role, and meaning-making of the illness event.
- Caregiving experiences are multifaceted, influenced by emotional and practical aspects.
- Family members (FMs) demonstrated adaptation and resilience in their caregiving roles.
Conclusions:
- Findings highlight the importance of addressing environmental challenges and emotional needs of family members (FMs) post-ICU.
- Strengthening caregiver-patient relationships is key to improving overall QoL.
- Family members (FMs) can achieve resilience and fulfillment by adapting to the caregiver role and finding meaning in the illness experience.
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