Literature DB >> 28618898

A metasynthesis study of family caregivers' transition experiences caring for community-dwelling persons with advanced cancer at the end of life.

Wendy Duggleby1, Jamie Tycholiz2, Lorraine Holtslander3,4, Peter Hudson5,6,7, Cheryl Nekolaichuk8, Mehrnoush Mirhosseini8, Jasneet Parmar9,10, Thane Chambers11, Angele Alook12, Jennifer Swindle1.   

Abstract

BACKGROUND: Family caregivers (broadly defined as family and friends) experience multiple concurrent transitions when caring for a person with advanced cancer. AIMS: To (a) explore the transition experience of family caregivers caring for persons with advanced cancer living in the community, (b) describe potential triggers for transitions, (c) identify what influences this experience, and (d) develop a conceptual framework of their transition experience.
DESIGN: Sandelowski and Barroso's methodology for synthesizing qualitative research included (a) a comprehensive search of empirical literature, (b) quality appraisal of qualitative studies, (c) classification of studies, and (d) synthesis of the findings. DATA SOURCES: Literature was sourced from six electronic data bases. Inclusion criteria were as follows: (a) published qualitative studies (and mixed-method designs) of the caregiving experience of family caregivers of community-living persons with advanced cancer at the end of life, (b) participants (caregivers and care recipients) of 18 years of age and above, (c) studies published in English in any country, and (d) studies published between 2004 and 2014.
RESULTS: A total of 72 studies were included in the metasynthesis. Family caregivers experience a "life transition" whereby their lives are permanently altered. The participants described the process of redefining normal which consisted of coming to terms with their situation and connecting with others. Outcomes of these processes were as follows: (a) maintaining a sense of personhood, (b) reframing hope, (c) maintaining self-efficacy, (d) finding meaning, and (e) preparing for the death of their care recipient.
CONCLUSION: The findings provide a framework to guide the development of supportive programs and future research.

Entities:  

Keywords:  Caregivers; community-living; metasynthesis; palliative care; transitions

Mesh:

Year:  2016        PMID: 28618898     DOI: 10.1177/0269216316673548

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  13 in total

1.  What contextual factors account for anxiety and depressed mood in hospice family caregivers?

Authors:  Djin L Tay; Eli Iacob; Maija Reblin; Kristin G Cloyes; Miranda Jones; Megan C Thomas Hebdon; Kathleen Mooney; Anna C Beck; Lee Ellington
Journal:  Psychooncology       Date:  2021-09-12       Impact factor: 3.894

2.  Factors influencing adult carer support planning for unpaid caregiving at the end of life in Scotland: Qualitative insights from triangulated interviews and focus groups.

Authors:  Susan Swan; Richard Meade; Debbie Cavers; Barbara Kimbell; Anna Lloyd; Emma Carduff
Journal:  Health Soc Care Community       Date:  2021-08-24

3.  Building a new life: a qualitative study of how family carers deal with significant changes.

Authors:  Wendy Duggleby; Hannah M O'Rourke; Pamela Baxter; Cheryl Nekolaichuk; Genevieve Thompson; Shelley Peacock; Sunita Ghosh; Jayna Holroyd-Leduc; Carrie McAiney; Véronique Dubé; Jennifer Swindle; Madeleine Pagnucco-Renaud; Samina Sana
Journal:  BMC Geriatr       Date:  2022-07-01       Impact factor: 4.070

4.  Engaging Carers in Co-Design: Development of the Carer Readiness Tool.

Authors:  Sian White; Natalie Hart; Suzanne Lewis
Journal:  Int J Integr Care       Date:  2021-03-15       Impact factor: 5.120

5.  Addressing cancer patient and caregiver role transitions during home hospice nursing care.

Authors:  Janella Hudson; Maija Reblin; Margaret F Clayton; Lee Ellington
Journal:  Palliat Support Care       Date:  2019-10

Review 6.  Self-efficacy in caregivers of adults diagnosed with cancer: An integrative review.

Authors:  Megan C Thomas Hebdon; Lorinda A Coombs; Pamela Reed; Tracy E Crane; Terry A Badger
Journal:  Eur J Oncol Nurs       Date:  2021-03-10       Impact factor: 2.588

7.  Stress, Coping, and Lived Experiences among Caregivers of Cancer Patients on Palliative Care: A Mixed Method Research.

Authors:  Lovely Antony; Linu Sara George; Tessy Treesa Jose
Journal:  Indian J Palliat Care       Date:  2018 Jul-Sep

8.  Web-Based Intervention for Family Carers of Persons with Dementia and Multiple Chronic Conditions (My Tools 4 Care): Pragmatic Randomized Controlled Trial.

Authors:  Wendy Duggleby; Jenny Ploeg; Carrie McAiney; Shelley Peacock; Kathryn Fisher; Sunita Ghosh; Maureen Markle-Reid; Jennifer Swindle; Allison Williams; Jean Ac Triscott; Dorothy Forbes; Kathya Jovel Ruiz
Journal:  J Med Internet Res       Date:  2018-06-29       Impact factor: 5.428

Review 9.  Disparities in Palliative and Hospice Care and Completion of Advance Care Planning and Directives Among Non-Hispanic Blacks: A Scoping Review of Recent Literature.

Authors:  Mohsen Bazargan; Shahrzad Bazargan-Hejazi
Journal:  Am J Hosp Palliat Care       Date:  2020-12-08       Impact factor: 2.500

10.  Dignity of older home-dwelling women nearing end-of-life: Informal caregivers' perception.

Authors:  Katrine Staats; Ellen Karine Grov; Bettina S Husebø; Oscar Tranvåg
Journal:  Nurs Ethics       Date:  2020-10-28       Impact factor: 2.874

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.