Relatives in end-of-life care--part 1: a systematic review of the literature the five last years, January 1999-February 2004.
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Factors associated with feelings of reward during ongoing family palliative caregiving.How hospice staff members prepare family caregivers for the patient's final days of life: an exploratory study.Exploring factors and caregiver outcomes associated with feelings of preparedness for caregiving in family caregivers in palliative care: a correlational, cross-sectional study.Effects of a support group programme for patients with life-threatening illness during ongoing palliative care.Adaptation and psychometric evaluation of the Preparedness for Caregiving Scale, Caregiver Competence Scale and Rewards of Caregiving Scale in a sample of Swedish family members of patients with life-threatening illness.Guilt and shame--a semantic concept analysis of two concepts related to palliative care.Co-creating possibilities for patients in palliative care to reach vital goals--a multiple case study of home-care nursing encounters.How should we manage information needs, family anxiety, depression, and breathlessness for those affected by advanced disease: development of a Clinical Decision Support Tool using a Delphi design.Use of an Item Bank to Develop Two Short-Form FAMCARE Scales to Measure Family Satisfaction With Care in the Setting of Serious Illness.A systematic review of psychosocial interventions for family carers of palliative care patients.Challenges Facing Families at the End of Life in Three Settings.Performance of the Family Satisfaction with the End-of-Life Care (FAMCARE) measure in an ethnically diverse cohort: psychometric analyses using item response theory.Burden for family carers at the end of life; a mixed-method study of the perspectives of family carers and GPs.Family carers providing support to a person dying in the home setting: A narrative literature review.Living in the presence of death: an integrative literature review of relatives' important existential concerns when caring for a severely ill family member.Exploring access to care among older people in the last phase of life using the behavioural model of health services use: a qualitative study from the perspective of the next of kin of older persons who had died in a nursing homeNo Negative Impact of Palliative Sedation on Relatives' Experience of the Dying Phase and Their Wellbeing after the Patient's Death: An Observational Study.Guidelines for the psychosocial and bereavement support of family caregivers of palliative care patients.Family caregiver involvement for long-term care residents at the end of life.When expressions make impressions-nurses' narratives about meeting severely ill patients in home nursing care: a phenomenological-hermeneutic approach to understandingSupporting lay carers in end of life care: current gaps and future priorities.Conducting qualitative research with palliative care patients: applying Hammick's research ethics wheel.Review of patients' experiences with fungating wounds and associated quality of life.The State of the Science: Informing choices across the cancer journey with public health mechanisms and decision processes.Barriers and facilitators influencing death at home: A meta-ethnography.Older persons' existential loneliness, as interpreted by their significant others - an interview study.Between the patient and the next of kin in end-of-life care.Preparing for palliative caregiving as a transition in the awareness of death: family carer experiences.Struggling to find meaning in life among spouses of people with ALS.An Ecological Understanding of Caregiver Experiences in Palliative Care.Anxiety, depression and quality of life in family caregivers of palliative cancer patients during home care and after the patient's death.Family caregivers voice their needs: a photovoice study.Meanings of being a close relative of a family member treated with haemodialysis approaching end of life.What is a 'secure base' when death is approaching? A study applying attachment theory to adult patients' and family members' experiences of palliative home care.The perspectives of bereaved family members on their experiences of support in palliative care.Structural impact on gendered expectations and exemptions for family caregivers in hospice palliative home care.Relational experiences of family caregivers providing home-based end-of-life care.Ethical challenges related to next of kin - nursing staffs' perspective.'We're all carrying a burden that we're not sharing': a qualitative study of the impact of cutaneous T-cell lymphoma on the family.A family's beliefs about cancer, dying, and death in the end of life.
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P2860
Relatives in end-of-life care--part 1: a systematic review of the literature the five last years, January 1999-February 2004.
description
2006 nî lūn-bûn
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2006年の論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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2006年论文
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2006年论文
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2006年论文
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Relatives in end-of-life care- ...... s, January 1999-February 2004.
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Relatives in end-of-life care- ...... s, January 1999-February 2004.
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Relatives in end-of-life care- ...... s, January 1999-February 2004.
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Relatives in end-of-life care- ...... s, January 1999-February 2004.
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Relatives in end-of-life care- ...... s, January 1999-February 2004.
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Relatives in end-of-life care- ...... s, January 1999-February 2004.
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Relatives in end-of-life care- ...... s, January 1999-February 2004.
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P2093
Birgitta Andershed
P2860
P304
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10.1111/J.1365-2702.2006.01473.X
P577
2006-09-01T00:00:00Z