Literature DB >> 12886117

Family experience caring for terminally ill patients with cancer in Hong Kong.

Esther Mok1, Faye Chan, Vivian Chan, Ellen Yeung.   

Abstract

In this study, 24 family caregivers of terminally ill patients participated in in-depth interviews regarding their experiences of giving care. The data were analyzed using grounded theory qualitative method. Commitment emerged as the precondition of the caregiving process. The caregivers did not perceive the work of caring as a burden. Rather, they felt that despite any personal hardships, what they were doing was important to their loved ones and therefore meaningful to them as caregivers. The components of commitment can be described as relational commitment, the act of showing love, and determination. The process of caregiving includes four phases: 1) holding onto hope for a miracle, 2) taking care, 3) preparing for death, and 4) adjusting to another phase of life. A patient-caregiver relationship, Confucian concepts of yi (appropriateness or rightness), and filial duty are reflected in the process of caregiving. Consequences of the process include finding meaning in life and peace of heart and mind. The emotional aspect of the caregiving experience can be described as an intense emotional experience filled with feelings of hope and hopelessness, guilt, fear, and regret. As a result of the caregiving experience, most participants found they have had a change of worldviews and treasure their lives. Findings show a significant need for interventions at each phase of the caregiving process designed to provide effective and culturally sensitive support and affirmation to family members as they care for their loved ones with terminal illnesses.

Entities:  

Mesh:

Year:  2003        PMID: 12886117     DOI: 10.1097/00002820-200308000-00003

Source DB:  PubMed          Journal:  Cancer Nurs        ISSN: 0162-220X            Impact factor:   2.592


  14 in total

Review 1.  The cancer family caregiving experience: an updated and expanded conceptual model.

Authors:  Barbara Swore Fletcher; Christine Miaskowski; Barbara Given; Karen Schumacher
Journal:  Eur J Oncol Nurs       Date:  2011-10-14       Impact factor: 2.398

Review 2.  Cultural aspects of communication in cancer care.

Authors:  Antonella Surbone
Journal:  Support Care Cancer       Date:  2008-01-15       Impact factor: 3.603

3.  Psychosocial care for patients and their families is integral to supportive care in cancer: MASCC position statement.

Authors:  Antonella Surbone; Lea Baider; Tammy S Weitzman; Mary Jacqueline Brames; Cynthia N Rittenberg; Judith Johnson
Journal:  Support Care Cancer       Date:  2009-07-17       Impact factor: 3.603

4.  Caregivers needing care: the unmet needs of the family caregivers of end-of-life cancer patients.

Authors:  Maryam Hashemi; Alireza Irajpour; Fariba Taleghani
Journal:  Support Care Cancer       Date:  2017-09-27       Impact factor: 3.603

5.  The relatives' perspective on advanced cancer care in Denmark. A cross-sectional survey.

Authors:  Anna T Johnsen; Lone Ross; Morten A Petersen; Line Lund; Mogens Groenvold
Journal:  Support Care Cancer       Date:  2012-04-15       Impact factor: 3.603

6.  Food meanings in HIV and AIDS caregiving trajectories: ritual, optimism and anguish among caregivers in Lesotho.

Authors:  Mokhantso G Makoae
Journal:  Psychol Health Med       Date:  2011-03       Impact factor: 2.423

7.  Care-giving as a Canadian-Vietnamese tradition: 'it's like eating, you just do it'.

Authors:  Rhonda Donovan; Allison M Williams
Journal:  Health Soc Care Community       Date:  2014-10-20

Review 8.  The preferences and perspectives of family caregivers towards place of care for their relatives at the end-of-life. A systematic review and thematic synthesis of the qualitative evidence.

Authors:  Caroline Woodman; Jessica Baillie; Stephanie Sivell
Journal:  BMJ Support Palliat Care       Date:  2015-05-19       Impact factor: 3.568

Review 9.  Methodological challenges in cross-language qualitative research: a research review.

Authors:  Allison Squires
Journal:  Int J Nurs Stud       Date:  2008-09-13       Impact factor: 6.612

10.  Caregivers' active role in palliative home care - to encourage or to dissuade? A qualitative descriptive study.

Authors:  Anna Weibull; Frede Olesen; Mette Asbjoern Neergaard
Journal:  BMC Palliat Care       Date:  2008-09-16       Impact factor: 3.234

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.