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Palliative medicine · Jul 2017
ReviewA metasynthesis study of family caregivers' transition experiences caring for community-dwelling persons with advanced cancer at the end of life.
- Wendy Duggleby, Jamie Tycholiz, Lorraine Holtslander, Peter Hudson, Cheryl Nekolaichuk, Mehrnoush Mirhosseini, Jasneet Parmar, Thane Chambers, Angele Alook, and Jennifer Swindle.
- 1 Faculty of Nursing, University of Alberta, Edmonton, AB, Canada.
- Palliat Med. 2017 Jul 1; 31 (7): 602-616.
BackgroundFamily caregivers (broadly defined as family and friends) experience multiple concurrent transitions when caring for a person with advanced cancer.AimsTo (a) explore the transition experience of family caregivers caring for persons with advanced cancer living in the community, (b) describe potential triggers for transitions, (c) identify what influences this experience, and (d) develop a conceptual framework of their transition experience.DesignSandelowski and Barroso's methodology for synthesizing qualitative research included (a) a comprehensive search of empirical literature, (b) quality appraisal of qualitative studies, (c) classification of studies, and (d) synthesis of the findings.Data SourcesLiterature was sourced from six electronic data bases. Inclusion criteria were as follows: (a) published qualitative studies (and mixed-method designs) of the caregiving experience of family caregivers of community-living persons with advanced cancer at the end of life, (b) participants (caregivers and care recipients) of 18 years of age and above, (c) studies published in English in any country, and (d) studies published between 2004 and 2014.ResultsA total of 72 studies were included in the metasynthesis. Family caregivers experience a "life transition" whereby their lives are permanently altered. The participants described the process of redefining normal which consisted of coming to terms with their situation and connecting with others. Outcomes of these processes were as follows: (a) maintaining a sense of personhood, (b) reframing hope, (c) maintaining self-efficacy, (d) finding meaning, and (e) preparing for the death of their care recipient.ConclusionThe findings provide a framework to guide the development of supportive programs and future research.
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