Family caregivers and palliative care: current status and agenda for the future.
about
Minor children of palliative patients: a systematic review of psychosocial family interventionsVariances in family carers' quality of life based on selected relationship and caregiving indicators: A quantitative secondary analysis.The Melbourne Family Support Program: evidence-based strategies that prepare family caregivers for supporting palliative care patients.An examination of the research priorities for a hospice service in New Zealand: A Delphi study.Quality of life, psychological burden, needs, and satisfaction during specialized inpatient palliative care in family caregivers of advanced cancer patients.Why is high-quality research on palliative care so hard to do? Barriers to improved research from a survey of palliative care researchers.Delivering and participating in a psycho-educational intervention for family caregivers during palliative home care: a qualitative study from the perspectives of health professionals and family caregiversEvaluating the effects of mindfulness-based interventions for informal palliative caregivers: A systematic literature review.Psychometric properties of carer-reported outcome measures in palliative care: A systematic reviewBenefits and resource implications of family meetings for hospitalized palliative care patients: research protocolGuidelines for the psychosocial and bereavement support of family caregivers of palliative care patients.Applying Risk Society Theory to findings of a scoping review on caregiver safety.Balance artistry: the healthy parent's role in the family when the other parent is in the palliative phase of cancer--challenges and coping in parenting young children.Psychosocial, educational and communicative interventions for patients with cachexia and their family carers.The end of life and the family: hospice patients' views on dying as relational.Background and design of the symptom burden in end-stage liver disease patient-caregiver dyad study.Leading an intervention for family caregivers-a part of nursing in palliative care.Communication differences when patients and caregivers are seen separately or together.The influence of psychological factors on the burden of caregivers of patients with advanced cancer: Resiliency and caregiver burden.Relational experiences of family caregivers providing home-based end-of-life care.Predictors of caregiver burden across the home-based palliative care trajectory in Ontario, Canada.Experiences of carers supporting dying renal patients managed without dialysis.Maintaining ordinariness around food: partners' experiences of everyday life with a dying person.Physician-assisted suicide and/or euthanasia: Pragmatic implications for palliative care [corrected].Exploring dimensions of coping in advanced colorectal cancer: implications for patient-centered care.Health care professionals' perspectives of the experiences of family caregivers during in-patient cancer care.Translation and Testing of the Italian Version of FAMCARE-2: Measuring Family Caregivers' Satisfaction With Palliative Care."Never at ease" - family carers within integrated palliative care: a multinational, mixed method study.
P2860
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P2860
Family caregivers and palliative care: current status and agenda for the future.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 20 May 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Family caregivers and palliative care: current status and agenda for the future.
@en
Family caregivers and palliative care: current status and agenda for the future.
@nl
type
label
Family caregivers and palliative care: current status and agenda for the future.
@en
Family caregivers and palliative care: current status and agenda for the future.
@nl
prefLabel
Family caregivers and palliative care: current status and agenda for the future.
@en
Family caregivers and palliative care: current status and agenda for the future.
@nl
P356
P1476
Family caregivers and palliative care: current status and agenda for the future.
@en
P2093
Peter Hudson
Sheila Payne
P304
P356
10.1089/JPM.2010.0413
P577
2011-05-20T00:00:00Z