Literature DB >> 19939306

Palliative family caregivers' accounts of health care experiences: the importance of "security".

Laura M Funk1, Diane E Allan, Kelli I Stajduhar.   

Abstract

OBJECTIVE: When providing care for a loved one with a terminal illness, family members often look to health care providers for guidance and expertise. The objective of this study is to explore family caregiver accounts of their experiences within the health care system and with individual providers.
METHODS: A thematic analysis of secondary qualitative data was performed. Data are from a subsample of bereaved and current family caregivers (N = 31) in a prior study of coping in end-of-life cancer situations. Data from these participants referring to experiences with health care providers was thematically coded and the concept of "security" was used as an analytic lens to facilitate conceptual development and exploration.
RESULTS: Considered together, the findings can be viewed as manifestations of a need and desire for security in palliative family caregiving. Specifically, family caregivers' accounts illustrate the importance of feeling secure that health care services will be provided by competent professionals; feeling secure in their timely access to needed care, services, and information; and feeling secure in their own identity and self-worth as a caregiver and individual. In addition, the findings suggest a conceptualization of security that extends beyond trust in individuals to include a generalized sense of institutional trust in the health care system. SIGNIFICANCE OF
RESULTS: The concept of security moves beyond description of individual satisfaction or dissatisfaction with health care to identify a common, foundational need underlying such evaluations. Further empirical research is needed that explicitly focuses on caregivers' experiences of security and insecurity in the domains identified in this article. This will contribute to theory building as well as assist in identifying the causes and consequences of security.

Entities:  

Mesh:

Year:  2009        PMID: 19939306     DOI: 10.1017/S1478951509990447

Source DB:  PubMed          Journal:  Palliat Support Care        ISSN: 1478-9515


  7 in total

1.  Knowledge, beliefs, and concerns about opioids, palliative care, and homecare of advanced cancer patients: a nationwide survey in Japan.

Authors:  Miki Akiyama; Toru Takebayashi; Tatsuya Morita; Mitsunori Miyashita; Kei Hirai; Motohiro Matoba; Nobuya Akizuki; Yutaka Shirahige; Akemi Yamagishi; Kenji Eguchi
Journal:  Support Care Cancer       Date:  2011-06-10       Impact factor: 3.603

2.  Empowerment in outpatient care for patients with chronic kidney disease - from the family member's perspective.

Authors:  Annette Nygårdh; Kerstin Wikby; Dan Malm; Gerd Ahlstrom
Journal:  BMC Nurs       Date:  2011-10-28

3.  "Non-palliative care" - a qualitative study of older cancer patients' and their family members' experiences with the health care system.

Authors:  Marianne Fjose; Grethe Eilertsen; Marit Kirkevold; Ellen Karine Grov
Journal:  BMC Health Serv Res       Date:  2018-09-29       Impact factor: 2.655

4.  The experience of family caregivers of patients with cancer in an Asian country: A grounded theory approach.

Authors:  Martina Sinta Kristanti; Christantie Effendy; Adi Utarini; Myrra Vernooij-Dassen; Yvonne Engels
Journal:  Palliat Med       Date:  2019-03-27       Impact factor: 4.762

5.  A sense of security in palliative homecare in a Norwegian municipality; dyadic comparisons of the perceptions of patients and relatives - a quantitative study.

Authors:  Reidun Hov; Bente Bjørsland; Bente Ødegård Kjøs; Bodil Wilde-Larsson
Journal:  BMC Palliat Care       Date:  2020-01-11       Impact factor: 3.234

6.  A qualitative study of bereaved family caregivers: feeling of security, facilitators and barriers for rural home care and death for persons with advanced cancer.

Authors:  Anne Sæle Barlund; Beate André; Kari Sand; Anne-Tove Brenne
Journal:  BMC Palliat Care       Date:  2021-01-08       Impact factor: 3.234

7.  Family caregivers' advocacy in voluntary stopping of eating and drinking: A holistic multiple case study.

Authors:  Jasmin Eppel-Meichlinger; Sabrina Stängle; Hanna Mayer; André Fringer
Journal:  Nurs Open       Date:  2021-11-09
  7 in total

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