Literature DB >> 21803785

A study on caregiver burden: stressors, challenges, and possible solutions.

Laura Nelson Bialon1, Sallie Coke.   

Abstract

PURPOSE: The purpose of this qualitative study was to explore factors impacting caregiver burden and to explore possible solutions for family caregivers of terminally ill patients.
RESULTS: The majority of caregivers reported experiencing role conflict and inadequate stress management. Caregivers who worked outside the home, those who cared for two parents concurrently, those with the least amount of outside assistance, and caregivers who spent a longer period of time caregiving reported the highest levels of health problems and overall burden. Caregivers stated a need for more support from Hospice agencies, more education on caregiver training, and more public education about Hospice services. Faith played a positive role in alleviating caregiver burden.
CONCLUSION: Early identification, intervention, education and coordination of services may help to alleviate caregiver burden, which will improve quality of life for both patient and caregiver.

Entities:  

Mesh:

Year:  2011        PMID: 21803785     DOI: 10.1177/1049909111416494

Source DB:  PubMed          Journal:  Am J Hosp Palliat Care        ISSN: 1049-9091            Impact factor:   2.500


  17 in total

Review 1.  Informal caregiving of hospice patients.

Authors:  Colin G Pottie; Karen A Burch; Lori P Montross Thomas; Scott A Irwin
Journal:  J Palliat Med       Date:  2014-07       Impact factor: 2.947

2.  RDOS-family: a guided learning tool for layperson assessment of respiratory distress.

Authors:  Margaret L Campbell; Thomas N Templin
Journal:  J Palliat Med       Date:  2014-08-12       Impact factor: 2.947

3.  Emotional vitality in family caregivers: content validation of a theoretical framework.

Authors:  Skye P Barbic; Nancy E Mayo; Carole L White; Susan J Bartlett
Journal:  Qual Life Res       Date:  2014-05-23       Impact factor: 4.147

4.  Exploring the collective hospice caregiving experience.

Authors:  Elaine Wittenberg-Lyles; Robin L Kruse; Debra Parker Oliver; George Demiris; Greg Petroski
Journal:  J Palliat Med       Date:  2013-12-18       Impact factor: 2.947

5.  Caregiver perceptions about the impact of caring for patients with wet age-related macular degeneration.

Authors:  M Vukicevic; J Heraghty; R Cummins; B Gopinath; P Mitchell
Journal:  Eye (Lond)       Date:  2015-11-27       Impact factor: 3.775

6.  Caregiving for patients in vegetative and minimally conscious states: perceived burden as a mediator in caregivers' expression of needs and symptoms of depression and anxiety.

Authors:  M Pagani; A M Giovannetti; V Covelli; D Sattin; M Leonardi
Journal:  J Clin Psychol Med Settings       Date:  2014-09

7.  "A True Human Interaction": Comparison of Family Caregiver and Hospice Nurse Perspectives On Needs of Family Hospice Caregivers.

Authors:  Kristin G Cloyes; Joan G Carpenter; Patricia H Berry; Maija Reblin; Margret Clayton; Lee Ellington
Journal:  J Hosp Palliat Nurs       Date:  2014-07       Impact factor: 1.918

8.  A qualitative study on perceptions of changes reported by caregivers of patients in vegetative state and minimally conscious state: the "time gap experience".

Authors:  Venusia Covelli; Milda Cerniauskaite; Matilde Leonardi; Davide Sattin; Alberto Raggi; Ambra Mara Giovannetti
Journal:  ScientificWorldJournal       Date:  2014-11-06

9.  Critically examining diversity in end-of-life family caregiving: implications for equitable caregiver support and Canada's Compassionate Care Benefit.

Authors:  Melissa Giesbrecht; Valorie A Crooks; Allison Williams; Olena Hankivsky
Journal:  Int J Equity Health       Date:  2012-11-01

10.  The development of an online intervention (Care Assist) to support male caregivers of women with breast cancer: a protocol for a mixed methods study.

Authors:  Janelle V Levesque; Martha Gerges; Afaf Girgis
Journal:  BMJ Open       Date:  2018-02-17       Impact factor: 2.692

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