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nursing
1,013 studies tagged nursing, dated 1986-10-01 to 2026-09-17 (1 undated). Bibliography: BibTeX (.bib) · RIS (.ris)
Newest in this topic
- Is there a role for artificial intelligence in end-of-life care for persons with dementia? Perspectives of and recommendations by caregivers and hospice staff 2026-09-17
- Online Peer Support Use Among Informal Caregivers of People Living With Alzheimer Disease or Related Dementias: National Cross-Sectional Web-Based Survey 2026-09-07
- Interconnected Challenges in Dementia Caregiving: A Co-occurrence Network Analysis of Burden, Unmet Needs, and System Failures Among Caregivers 2026-08-17
Studies
1,013 studies carry this tag; 1,012 of them have a date.
Date range
1986 to 2026
Top journals
- Journal of the American Geriatrics Society 63
- The Gerontologist 48
- Alzheimer s & Dementia 28
- International psychogeriatrics 28
- Journal of the American Medical Directors Association 26
339 journals in all.
Newest first, then by address. Each study has a usefulness score out of 100 (rubric version 4.0); tap a score to see what makes it up. Tags were assigned automatically from each study's title and summary. The same studies as a filter in the library.
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It has been suggested that there are several societal and cultural demands on women to adopt the role of a family-caregiver.
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Contextual factors regarding the care home environment may be obdurate and tend to negatively impact on the quality of end of life dementia care.
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Advance care planning can assist patients to achieve a sense of control and 'peace of mind' and facilitates important family discussion.
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Twelve studies were identified.
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Although multi-component social support interventions may improve caregiver well-being, there is insufficient evidence to conclude whether a change in social support is the underlying mediating factor.
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When an individual has dementia, family members are involved in many care transitions in their roles as caregivers.
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This study followed a national sample of Medicare beneficiaries who died and compared total health and long-term care spending in their final five years of life.
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Nursing homes generally met three quarters of the pre-defined criteria for advance care planning policy.
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The results of the study identified that professionals across Europe have different opinions regarding the time point when to consider a person with dementia in need of palliative care.
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Health care expenditures among persons with dementia were substantially larger than those for other diseases, and many of the expenses were uncovered (uninsured).
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There is emerging evidence that physical exercise significantly benefits individuals living with a dementia in nursing homes.
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For people with dementia living and dying in care homes, EoL interventions need to provide strategies that can accommodate or "hold" the inevitable and often unresolvable uncertainties of providing and receiving care in these settings.
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This paper provides an overview of the evidence on the perspective of health care professionals (HCPs) in relation to advance care planning (ACP) for people with dementia, residing in long-term care settings.
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Use of in-depth data, consensus methods and theoretical understanding of the intervention components produced an evidence-based intervention for further testing in end-of-life care in advanced dementia.
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ACP is a multifactorial process, which may lean on professional caregivers' guidance.
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Nurses play a key role in the effective management of pain through the use of pain assessment tools, behavioural observation, and analgesic choice.
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The preferences of end-of-life issues differed greatly between dementia patients and their caregivers.
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Community-based services are important for improving outcomes for individuals with dementia and their caregivers.
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Benefits of palliative care in dementia are acknowledged by experts worldwide, but there is some controversy around its early introduction.
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Factors of caregiver burden in regard to people with dementia living in the community were clarified in this review study.
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In this study, quantitative results were inconclusive owing to small sample size.
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Optimal timing of ACP discussions should be determined by the readiness of the patient and family carer to face end of life.
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We recommend development and testing of decision aids targeting the decisions carers report finding most distressing, including those around where people should live, accessing services, and end of life treatments.
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Physicians should consider advanced dementia as a terminal disease for which there is a continuum of care that goes from palliative care with life-extending measures to symptomatic interventions only.
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Community-based palliative care of people who die with or of dementia is relatively infrequent but associated with significant reductions in hospital emergency department use in the last year of life.
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We found that family satisfaction with care is related to a comfort care goal shortly after admission, but quality of dying did not.
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Over the past 3 decades, more than 200 dementia caregiver interventions have been tested in randomized clinical trials and found to be efficacious.
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National dementia strategies cover part of the recent definition of palliative care in dementia, although they do not frequently label these references as "palliative care."
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The Internet course 'Mastery over Dementia' offers an effective treatment for family caregivers of people with dementia reducing symptoms of depression and anxiety.
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The uptake of advance care planning (ACP) is particularly low among people with dementia.
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36/100
Educating families and professionals about palliative care is important as many professionals and non-professionals believe that this approach intends to hasten death, instead of affirming life and regarding dying as a normal process.
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Place of death of older people who died from a dementia-related disease differs substantially between countries, which might point to organizational differences in end-of-life care provision.
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Most NH residents who use statins at the time of progression to advanced dementia continue use in follow-up.
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This paper reviews empirical findings concerning the decision-making process of persons with dementia and their family carers, with a particular focus on the extent and determinants of involvement of persons with dementia in the decision-making process.
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Of 5406 nursing home residents with advanced dementia, 2911 (53.9%) received at least 1 medication with questionable benefit (range, 44.7% in the Mid-Atlantic census region to 65.0% in the West South Central census region).
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A large proportion of patients with ECI decline ACP discussions and the reasons are influenced by personal values, coping behaviours and sociocultural norms.
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International experts selected a set of 23 QIs for the organisation of palliative care.
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Advance care planning can be facilitated with the family caregiver in the context of everyday practice within the nursing home environment for older people with dementia.
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We developed a mostly consensus-based practice guideline for patients with dementia and pneumonia and mapped controversial issues for future investigation.
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The ongoing change in long-term care from institutional care to housing services causes major challenges to the continuity of end-of-life care.
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The number of older adults with cognitive impairment is increasing, and such adults often require a surrogate to make decisions about health care.
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The journey for people with Alzheimer's disease or another dementia involves the need for increasing levels of support, with transitions across care settings.
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Family members of persons with advanced dementia may be asked to make complex treatment decisions without having adequate knowledge regarding the risks and benefits.
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Controlling for pretest, the benefit-finding group had lower depression than the psychoeducation group at post-test, despite the fact that some caregivers found benefit-finding challenging.
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We found 32 studies with burden models and 24 depression and mental health models.
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40/100
It is difficult to define what constitutes high-quality end-of-life care for people with dementia from the perspective of family carers.
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This JAMA clinical review synthesizes cohort studies and meta-analyses to give physicians practical guidance on recognizing, assessing, and treating caregiver burden.
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The percentage of psychological distress was similar between caregivers of cancer patients (77.6%) and caregivers of dementia patients (72.4%).
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We identified 101 deaths of residents with dementia in 69 nursing homes (58% response rate).
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Physicians have a responsibility to recognize caregiver burden.
From across this tag
10 of the 1,002 studies in this tag, picked by a fixed rule (a hash of each study's address), not by score or date; each page of this list shows a different 10. The same 10 appear here every time.
- Family caregivers of people with dementia
- Access to hospice programs in end-stage dementia: a national survey of hospice programs
- Suffering and loss in Lewy body dementia: Applying a palliative care lens to a longitudinal narrative study
- Cost–Benefit Analysis of the COPE Program for Persons Living With Dementia: Toward a Payment Model
- Burden and care time for dementia caregivers in the LIVE@Home.Path trial
- The Impact of Dementia Caregiving on the Health of the Spousal Caregiver
- Palliative Care Needs of Older Adults With and Without Dementia During Post-Acute Care in Skilled Nursing Facilities
- Level of Care Preferences Among Nursing Home Residents With Advanced Dementia
- Racial disparity in end-of-life hospitalizations among nursing home residents with dementia
- Advancing dementia care: a review of Italy’s public health response within the WHO Global Action Plan and European strategies