Literature DB >> 22275212

Factors associated with positive consequences of serving as a family caregiver for a terminal cancer patient.

Jina Kang1, Dong Wook Shin, Ji Eun Choi, Makiko Sanjo, Soo Jin Yoon, Hwan Kyun Kim, Myoung Suk Oh, Hyang Suk Kwen, Hae Young Choi, Wook Hee Yoon.   

Abstract

BACKGROUND: We examined factors associated with positive consequences for family members who served as caregivers of terminal cancer patients.
METHODS: We conducted a nationwide cross-sectional survey of 501 bereaved family members who served as caregivers for terminal cancer patients. The main outcomes were measured by the previously developed Caregiving Consequences Inventory, which assesses perceived rewards and burdens of caregiving.
RESULTS: Bereaved family caregivers reported high levels of perceived rewards and burden. Among the characteristics of bereaved family members, older age, female gender, and having a religion were associated with some domains of perceived rewards, but being a spouse of a patient was negatively associated with some domains of perceived rewards. Caregiver depression or perceived burden did not affect positive consequences of caregiving. However, receiving bereavement care was significantly associated with positive outcome in all four perceived reward domains (sense of mastery [adjusted odds ratio {aOR} = 1.69; 95% CI, 1.05-2.70]; appreciation for others [aOR = 2.19; 95% CI, 1.27-3.76]; meaning in life [aOR = 1.80; 95% CI, 1.13-2.89]; and reprioritization about his/her life [aOR = 2.02; 95% CI, 1.27-3.19]).
CONCLUSIONS: Family caregivers of terminal cancer patients experience burdens, but caregiving also has positive consequences. This study has important implications for the development of bereavement interventions that aim to encourage positive outcomes and reduce negative outcomes for caregivers.
Copyright © 2012 John Wiley & Sons, Ltd.

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Year:  2012        PMID: 22275212     DOI: 10.1002/pon.3033

Source DB:  PubMed          Journal:  Psychooncology        ISSN: 1057-9249            Impact factor:   3.894


  15 in total

1.  Measuring caregiver outcomes in palliative care: a construct validation study of two instruments for use in economic evaluations.

Authors:  Renske Hoefman; Hareth Al-Janabi; Nikki McCaffrey; David Currow; Julie Ratcliffe
Journal:  Qual Life Res       Date:  2014-11-08       Impact factor: 4.147

2.  Informal caregiver quality of life in a palliative oncology population.

Authors:  Adele Duimering; Jill Turner; Karen Chu; Fleur Huang; Diane Severin; Sunita Ghosh; Don Yee; Ericka Wiebe; Nawaid Usmani; Zsolt Gabos; Samir Patel; Brita Danielson; John Amanie; Wilson Roa; Alysa Fairchild
Journal:  Support Care Cancer       Date:  2019-07-10       Impact factor: 3.603

3.  Cancer family caregiver depression: are religion-related variables important?

Authors:  Anna-Leila Williams; Jane Dixon; Richard Feinn; Ruth McCorkle
Journal:  Psychooncology       Date:  2014-08-11       Impact factor: 3.894

4.  Examining the role of subjective and objective burden in carer health-related quality of life: the case of colorectal cancer.

Authors:  Paul Hanly; Rebecca Maguire; Philip Hyland; Linda Sharp
Journal:  Support Care Cancer       Date:  2014-12-12       Impact factor: 3.603

5.  The Prevalence and Risks for Depression and Anxiety in Hospice Caregivers.

Authors:  Debra Parker Oliver; Karla Washington; Jamie Smith; Aisha Uraizee; George Demiris
Journal:  J Palliat Med       Date:  2016-12-02       Impact factor: 2.947

6.  Anxiety, Depression, Quality of Life, Caregiver Burden, and Perceptions of Caregiver-Centered Communication among Black and White Hospice Family Caregivers.

Authors:  Lauren T Starr; Karen Bullock; Karla Washington; Subhash Aryal; Debra Parker Oliver; George Demiris
Journal:  J Palliat Med       Date:  2021-11-18       Impact factor: 2.947

Review 7.  Application of psychological theories on the role of gender in caregiving to psycho-oncology research.

Authors:  Youngmee Kim; Hannah-Rose Mitchell; Amanda Ting
Journal:  Psychooncology       Date:  2018-12-27       Impact factor: 3.894

8.  Quality of dying and death with cancer in Israel.

Authors:  Michal Braun; Ilanit Hasson-Ohayon; Sarah Hales; Camilla Zimmermann; Anne Rydall; Tamar Peretz; Gary Rodin
Journal:  Support Care Cancer       Date:  2014-03-05       Impact factor: 3.603

9.  Caring for a spouse with advanced cancer: similarities and differences for male and female caregivers.

Authors:  Dana Ketcher; Ryan Trettevik; Susan T Vadaparampil; Richard E Heyman; Lee Ellington; Maija Reblin
Journal:  J Behav Med       Date:  2019-12-16

10.  Multiple Roles of Parental Caregivers of Children with Complex Life-Threatening Conditions: A Qualitative Descriptive Analysis.

Authors:  Amie Koch; Arthi S Kozhumam; Erika Seeler; Sharron L Docherty; Debra Brandon
Journal:  J Pediatr Nurs       Date:  2021-03-26       Impact factor: 2.145

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