Systematic review and meta-analysis of racial and ethnic differences in dementia caregivers' well-being

C Liu, ANS Badana, J Burgdorf, CD Fabius… - The …, 2021 - academic.oup.com
Abstract Background and Objectives Studies comparing racial/ethnic differences on
measures of psychological and physical well-being for dementia caregivers have reported …

Dementia care: mental health effects, intervention strategies, and clinical implications

S Sörensen, P Duberstein, D Gill… - The Lancet Neurology, 2006 - thelancet.com
Caring for elderly people with dementia is associated with well-documented increases in
burden, distress, and decrements in mental health and wellbeing. More severe behavioural …

[图书][B] Caregiving in the illness context

T Revenson, K Griva, A Luszczynska, V Morrison… - 2016 - books.google.com
How does caregiving affect health and well-being and what resources help caregivers? This
book provides a synthesis of psychological research on caregiver stress and brings attention …

Feeling like a burden: Exploring the perspectives of patients at the end of life

CJ McPherson, KG Wilson, MA Murray - Social science & medicine, 2007 - Elsevier
The issue of caregiver burden within the context of end-of-life care has received
considerable attention. Less focus has been directed at the corresponding issue of care …

Unmet needs of caregivers of individuals referred to a dementia care program

LA Jennings, DB Reuben, LC Evertson… - Journal of the …, 2015 - Wiley Online Library
Objectives To characterize caregiver strain, depressive symptoms, and self‐efficacy for
managing dementia‐related problems and the relationship between these and referring …

Dying with dementia: what we know after more than a decade of research

JT Van der Steen - Journal of Alzheimer's Disease, 2010 - content.iospress.com
Death with dementia is increasingly common. Although prognostication is difficult, it is an
incurable life-limiting illness for which palliative care for the patient is often appropriate …

Feeling like a burden to others: a systematic review focusing on the end of life

CJ McPherson, KG Wilson, MA Murray - Palliative medicine, 2007 - journals.sagepub.com
Research into the burden of illness has focused predominantly on family caregivers, with
little consideration of the other side of the caregiving relationship-care recipients' …

晚期癌症患者自我感受负担的研究进展

田秀丽, 刘化侠, 柴士美 - 中华护理杂志, 2008 - cqvip.com
在疾病照护研究中, 有关接受照护个体及照护效果的研究越来越多[1-3], 逐渐成为研究热点,
在照护关系中作为照护行为的接收者, 逐渐显示出其重要性[4-7]. 过去的研究多重于照护者负担 …

[图书][B] Handbook of thanatology: The essential body of knowledge for the study of death, dying, and bereavement

DK Meagher, DE Balk - 2013 - books.google.com
If ever there was an area requiring that the research-practice gap be bridged, surely it occurs
where thanatologists engage with people dealing with human mortality and loss. The field of …

Pediatric resident education in palliative care: a needs assessment

RC Kolarik, G Walker, RM Arnold - Pediatrics, 2006 - publications.aap.org
OBJECTIVE. The goal was to characterize pediatric residents' perceived educational needs
for pediatric palliative care. The data generated from this study will facilitate the planning of …