Specialized palliative care services are associated with improved short- and long-term caregiver outcomes. - Wikidata - awgldk - TriplyDB

Specialized palliative care services are associated with improved short- and long-term caregiver outcomes.

Specialized palliative care services are associated with improved short- and long-term caregiver outcomes.

http://www.wikidata.org/entity/Q36700005

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The value of data collection within a palliative care program Bereavement help-seeking following an 'expected' death: a cross-sectional randomised face-to-face population survey Quality of life, psychological burden, needs, and satisfaction during specialized inpatient palliative care in family caregivers of advanced cancer patients.Smokers' recall of Australian graphic cigarette packet warnings & awareness of associated health effects, 2005-2008.Caregivers' perceived adequacy of support in end-stage lung disease: results of a population survey.Referral patterns and proximity to palliative care inpatient services by level of socio-economic disadvantage. A national study using spatial analysis The caregiving perspective in heart failure: a population based study.Palliative care needs of patients with cancer living in the community Association Between Hospice Use and Depressive Symptoms in Surviving Spouses.Family Caregivers Who Would Be Unwilling to Provide Care at the End of Life Again: Findings from the Health Survey for England Population Survey.Spousal Characteristics and Older Adults' Hospice Use: Understanding Disparities in End-of-Life Care Physical well-being of oncology caregivers: an important quality-of-life domain Caregivers for people with end-stage lung disease: characteristics and unmet needs in the whole population.Research priorities in geriatric palliative care: informal caregiving An overview and evaluation of the oncology family caregiver project: improving quality of life and quality of care for oncology family caregivers."Not the 'grim reaper service'": an assessment of provider knowledge, attitudes, and perceptions regarding palliative care referral barriers in heart failure.Acute hospital-based services utilisation during the last year of life in New South Wales, Australia: methods for a population-based study.Palliative care for Parkinson's disease: has the time come?Background and design of the symptom burden in end-stage liver disease patient-caregiver dyad study.Quality of life and burden in family caregivers of patients with advanced cancer in active treatment settings and hospice care: A comparative study.Primary palliative care for heart failure: what is it? How do we implement it?Time for better integration of oncology and palliative care.Early integration of palliative care into standard oncology care: evidence and overcoming barriers to implementation Who provides care for people dying of cancer? A comparison of a rural and metropolitan cohort in a South Australian bereaved population study.Family Caregiver Depressive Symptom and Grief Outcomes From the ENABLE III Randomized Controlled Trial [What influences end-of-life decisions? Results of a representative German survey].A comparison between end-of-life home care clients with cancer and heart failure in Ontario.Defining distinct caregiver subpopulations by intensity of end-of-life care provided.Caring for persons with schizophrenia at home:examining the link between family caregivers’ role distress and quality of life.Palliative care in neonatal intensive care, effects on parent stress and satisfaction: a feasibility study.Improving support for family carers: key implications for research, policy and practice.Infrequent Provision of Palliative Care to Patients with Dialysis-Requiring AKI.Can assessing caregiver needs and activating community networks improve caregiver-defined outcomes? A single-blind, quasi-experimental pilot study: community facilitator pilot.An Observational Study to Explore the Feasibility of Assessing Bereaved Relatives' Experiences Before and After a Quality Improvement Project to Improve Care of Dying Medical Inpatients.A point prevalence survey of hospital inpatients to define the proportion with palliation as the primary goal of care and the need for specialist palliative care.Uncovering an invisible network of direct caregivers at the end of life: a population study.Moving on: Factors associated with caregivers' bereavement adjustment using a random population-based face-to-face survey.What is the role of friends when contributing care at the end of life? Findings from an Australian population study.Caring at the end of life: do cancer caregivers differ from other caregivers?Impact of In-Hospital Death on Spending for Bereaved Spouses.

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P2860

Specialized palliative care services are associated with improved short- and long-term caregiver outcomes.

http://www.wikidata.org/entity/Q36700005

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Supportive Care in Cancer

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Belinda S Fazekas

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Jane L Wheeler

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Maragatha Kuchibhatla

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P2860

Development and validation of a core outcome measure for palliative care: the palliative care outcome scale. Palliative Care Core Audit Project Advisory Group

Psychiatric disorders among bereaved persons: the role of perceived circumstances of death and preparedness for death.

Is there evidence that palliative care teams alter end-of-life experiences of patients and their caregivers?

Searching for meaning in loss: are clinical assumptions correct.

Complicated grief as a disorder distinct from bereavement-related depression and anxiety: a replication study.

Do hospital-based palliative teams improve care for patients or families at the end of life?

Judging the quality of care at the end of life: can proxies provide reliable information?

Use of family proxies in quality of life research for cancer patients at the end of life: a literature review.

The quality of medical care at the end-of-life in the USA: existing barriers and examples of process and outcome measures.

Terminal care: evaluation of effects on surviving family of care before and after bereavement

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