Clinical Implications for Supporting Caregivers at the End-of-Life: Findings and from a Qualitative Study

被引:0
作者
Forbat, Liz [1 ]
McManus, Elaine [2 ]
Haraldsdottir, Erna [3 ]
机构
[1] Univ Stirling, Canc Care Res Ctr, Stirling FK9 4LA, Scotland
[2] Strathcarron Hosp, Dept Palliat Care, Denny FK6 5HJ, Stirling, Scotland
[3] Strathcarron Hosp, Dept Educ, Denny FK6 5HJ, Stirling, Scotland
关键词
Palliative care; Death; Medical family therapy; Grief;
D O I
10.1007/s10591-012-9194-6
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Despite families providing considerable care at end of life, there are substantial gaps in the provision of supportive care. A qualitative interview study was conducted with 17 caregivers of people supported by an adult hospice to explore the support needs of families. Family members readily identified the ways in which the diagnosis of a life-limiting illness impacted on them and the family as a whole, not just the patient. Implications for practice demonstrate the need to intervene at a family and relational level prior to bereavement, in order to mitigate complicated grief for the surviving family members. Such an approach offers a fruitful prospective alternative to supporting caregivers post-bereavement.
引用
收藏
页码:282 / 292
页数:11
相关论文
共 50 条
  • [1] Clinical Implications for Supporting Caregivers at the End-of-Life: Findings and from a Qualitative Study
    Liz Forbat
    Elaine McManus
    Erna Haraldsdottir
    Contemporary Family Therapy, 2012, 34 (2) : 282 - 292
  • [2] Supporting family caregivers to identify their own needs in end-of-life care: Qualitative findings from a stepped wedge cluster trial
    Aoun, Samar
    Deas, Kathleen
    Toye, Chris
    Ewing, Gail
    Grande, Gunn
    Stajduhar, Kelli
    PALLIATIVE MEDICINE, 2015, 29 (06) : 508 - 517
  • [3] Family caregivers' experiences of end-of-life care in the acute hospital setting. A qualitative study
    Robertson, Svala Berglind
    Hjorleifsdottir, Elisabet
    Sigurdardottir, Porhalla
    SCANDINAVIAN JOURNAL OF CARING SCIENCES, 2022, 36 (03) : 686 - 698
  • [4] Design-Related Impacts on End-of-Life Experience: A Brief Report of Findings from an Exploratory Qualitative Study
    Knox, Michelle
    AMERICAN JOURNAL OF HOSPICE & PALLIATIVE MEDICINE, 2023, 40 (07) : 753 - 760
  • [5] End-of-life priorities of older adults with terminal illness and caregivers: A qualitative consultation
    Lewis, Ebony T.
    Harrison, Reema
    Hanly, Laura
    Psirides, Alex
    Zammit, Alexandra
    McFarland, Kathryn
    Dawson, Angela
    Hillman, Ken
    Barr, Margo
    Cardona, Magnolia
    HEALTH EXPECTATIONS, 2019, 22 (03) : 405 - 414
  • [6] Family caregivers' conceptualisation of quality end-of-life care for people with dementia: A qualitative study
    Davies, Nathan
    Rait, Greta
    Maio, Laura
    Iliffe, Steve
    PALLIATIVE MEDICINE, 2017, 31 (08) : 726 - 733
  • [7] Perceptions of a psychoeducation program for caregivers of persons with dementia at end of life: a qualitative study
    Durepos, Pamela
    Kaasalainen, Sharon
    Carroll, Sandra
    Papaioannou, Alexandra
    AGING & MENTAL HEALTH, 2019, 23 (02) : 263 - 271
  • [8] Bereaved caregivers' satisfaction with end-of-life care
    Frame, Abbey
    Grant, Janie Busby
    Layard, Elizabeth
    Scholz, Brett
    Law, Elly
    Ranse, Kristen
    Mitchell, Imogen
    Chapman, Michael
    PROGRESS IN PALLIATIVE CARE, 2022, 30 (04) : 212 - 220
  • [9] Supporting family carers providing end-of-life home care: a qualitative study on the impact of a hospice at home service
    Jack, Barbara A.
    O'Brien, Mary R.
    Scrutton, Joyce
    Baldry, Catherine R.
    Groves, Karen E.
    JOURNAL OF CLINICAL NURSING, 2015, 24 (1-2) : 131 - 140
  • [10] "Whatever happens, happens" challenges of end-of-life communication from the perspective of older adults and family caregivers: a Qualitative study
    Im, Jennifer
    Mak, Susanna
    Upshur, Ross
    Steinberg, Leah
    Kuluski, Kerry
    BMC PALLIATIVE CARE, 2019, 18 (01)