Community perspectives of end-of-life preparedness

被引:19
|
作者
Banner, Davina [1 ]
Freeman, Shannon [1 ]
Kandola, Damanpreet K. [1 ,2 ]
Meikle, Madeline [3 ]
Russell, Bridget K. M. [2 ]
Sommerfeld, E. Anne [2 ,4 ]
Flood, Donna [5 ]
Schiller, Catharine J. [1 ]
机构
[1] Univ Northern British Columbia, Sch Nursing, 3333 Univ Way, Prince George, BC V2N 4Z9, Canada
[2] Univ Northern British Columbia, Sch Hlth Sci, Prince George, BC, Canada
[3] Univ Northern British Columbia, Sch Social Work, Prince George, BC, Canada
[4] Prince George Rotary Hosp House, Prince George, BC, Canada
[5] Prince George Hosp Soc, Prince George, BC, Canada
关键词
QUALITATIVE DESCRIPTION; ADVANCE DIRECTIVES; CARE; DEATH; CONVERSATIONS; FAMILIES; HEALTH; COMMUNICATION; ASSOCIATIONS; DISCUSSIONS;
D O I
10.1080/07481187.2018.1446060
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
While death is a universal human experience, the process of planning for death can be difficult and may be avoided altogether. To understand community perspectives of end-of-life preparedness, we undertook a multimethod study exploring the experiences of 25 community members and 10 stakeholders engaged in end-of-life planning. In addition, card sorting activities and focused discussions with 97 older adults were undertaken to highlight perspectives and needs. Data were analyzed using descriptive statistics and qualitative description. Overall, the participants perceived many benefits to being end-of-life prepared, however, few community members had engaged in formal planning. Key barriers include concerns about the accessibility and accuracy of information, discomfort when engaging in end-of-life conversations, and perceptions about the cost associated with engaging in formal legal or financial preparations. Areas for further research include the need for studies that capture the cultural dimensions of end-of-life planning and explores the implementation and evaluation of community-based interventions to improve preparedness.
引用
收藏
页码:211 / 223
页数:13
相关论文
共 50 条
  • [41] Emotional Numbness Modifies the Effect of End-of-Life Discussions on End-of-Life Care
    Maciejewski, Paul K.
    Prigerson, Holly G.
    JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2013, 45 (05) : 841 - 847
  • [42] The Desires of Their Hearts: The Multidisciplinary Perspectives of African Americans on End-of-Life Care in the African American Community
    Rhodes, Ramona L.
    Elwood, Bryan
    Lee, Simon C.
    Tiro, Jasmin A.
    Halm, Ethan A.
    Skinner, Celette S.
    AMERICAN JOURNAL OF HOSPICE & PALLIATIVE MEDICINE, 2017, 34 (06) : 510 - 517
  • [43] A Pilot Study of the Effects of COMPLETE: A Communication Plan Early Through End of Life, on End-of-Life Outcomes in Children With Cancer
    Moody, Karen M.
    Hendricks-Ferguson, Verna L.
    Baker, Rebecca
    Perkins, Susan
    Haase, Joan E.
    JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2020, 60 (02) : 417 - 421
  • [44] Parent Perspectives of Neonatal Intensive Care at the End-of-Life
    Currie, Erin R.
    Christian, Becky J.
    Hinds, Pamela S.
    Perna, Samuel J.
    Robinson, Cheryl
    Day, Sara
    Meneses, Karen
    JOURNAL OF PEDIATRIC NURSING-NURSING CARE OF CHILDREN & FAMILIES, 2016, 31 (05): : 478 - 489
  • [45] Parental perspectives of initial end-of-life care communication
    Hendricks-Ferguson, Verna L.
    INTERNATIONAL JOURNAL OF PALLIATIVE NURSING, 2007, 13 (11) : 522 - 531
  • [46] Understanding community engagement in end-of-life care: developing conceptual clarity
    Sallnow, Libby
    Paul, Sally
    CRITICAL PUBLIC HEALTH, 2015, 25 (02) : 231 - 238
  • [47] Clinician Communication in Hospice: Constructions of Reality Throughout the End-of-Life Process
    Tenzek, Kelly E.
    Grant, Pei C.
    Depner, Rachel M.
    Levy, Kathryn
    Byrwa, David J.
    OMEGA-JOURNAL OF DEATH AND DYING, 2025, 90 (03) : 1109 - 1136
  • [48] Preference for initiation of end-of-life care discussion in Indonesia: a quantitative study
    Eng, Venita
    Hewitt, Victoria
    Kekalih, Aria
    BMC PALLIATIVE CARE, 2022, 21 (01)
  • [49] Characteristics of caregiver perceptions of end-of-life caregiving experiences in cancer survivorship: in-depth interview study
    Mori, Hiroko
    Fukuda, Risa
    Hayashi, Akitoshi
    Yamamoto, Kazunari
    Misago, Chizuru
    Nakayama, Takeo
    PSYCHO-ONCOLOGY, 2012, 21 (06) : 666 - 674
  • [50] Valuing end-of-life care in the United States: the case of newcancer drugs
    Sorenson, Corinna
    HEALTH ECONOMICS POLICY AND LAW, 2012, 7 (04) : 411 - 430