2016
DOI: 10.1016/j.anr.2016.06.002
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Other Side of Breast Cancer: Factors Associated with Caregiver Burden

Abstract: Primary caregivers need to be financially supported by the relevant organizations. Care skills training and providing palliative care seem helpful in reducing the pain and the burden of family caregivers for patients with breast cancer.

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Cited by 62 publications
(99 citation statements)
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“…Caregiver burden is a subjective feeling of stress that occurs when the demands of caregiving overwhelm caregiver resources to cope with those demands [2,3]. Patient factors (such as advanced cancer stage [4], health status [5], increased symptom burden, and decreased quality of life [QOL] [6][7][8]), caregiver factors (such as female gender [6,7,[9][10][11], age [5,10,[12][13][14], comorbidity [5], relationship to patient [15], education [14], and employment status [10]), and caregiving characteristics (such as increased duration of caregiving [7] and more help required by the patient [6,10,14]) are associated with increased caregiver burden. This information is typically obtained from patients or their caregivers.…”
Section: Introductionmentioning
confidence: 99%
“…Caregiver burden is a subjective feeling of stress that occurs when the demands of caregiving overwhelm caregiver resources to cope with those demands [2,3]. Patient factors (such as advanced cancer stage [4], health status [5], increased symptom burden, and decreased quality of life [QOL] [6][7][8]), caregiver factors (such as female gender [6,7,[9][10][11], age [5,10,[12][13][14], comorbidity [5], relationship to patient [15], education [14], and employment status [10]), and caregiving characteristics (such as increased duration of caregiving [7] and more help required by the patient [6,10,14]) are associated with increased caregiver burden. This information is typically obtained from patients or their caregivers.…”
Section: Introductionmentioning
confidence: 99%
“…The patient's activity ability does indeed decrease during the disease process and treatment but still important to 'normalize' the patient to make sure they feel 'alive' and useful to others (Walshe et al, 2017). It certainly decreased the auxiliary load for ADL activity which is on the average increase in line with the improvement of conditions during the treatment process of the disease (Vahidi et al, 2016). Treatment time tends to be long since the diagnosis of disease has a positive correlation with the social burden and family life (Rha, Park, Song, Lee, & Lee, 2015).…”
Section: "But From Me I Couldn't Get It (Pay By Out Of Pocket Its Sementioning
confidence: 72%
“…Factors that affected the burden condition was the available resources such as daily activities competences, education level, gender, and financial status by the caregiver (Vahidi et al, 2016). This study found that level of education of participants was a range of elementary-senior high school level and equal, the condition of economic limitations and changes in daily activities experienced by all participants whose all male.…”
Section: Discussionmentioning
confidence: 99%
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