Evaluation of advanced home care (AHC). The next-of-kin's experiences

European Journal of Oncology Nursing

Volumn 6, Issue 2, 2002, Pages 100-106

  Rollison, Britta ^a   Carlsson, Maria ^b  

^a Kronparkens Sjukhem   (Sweden)

^b UPPSALA UNIVERSITY   (Sweden)

Author keywords

Cancer; Emotional support; Evaluation; Next of kin; Palliative care; Symptom relief

Indexed keywords

ADULT; ARTICLE; CANCER PALLIATIVE THERAPY; CAREGIVER; COMPETENCE; CONTROLLED STUDY; DEATH; DYING; EMOTION; EXPERIENCE; FEMALE; HEALTH CARE COST; HEALTH CARE QUALITY; HOME CARE; HUMAN; INTERPERSONAL COMMUNICATION; MALE; MEDICAL DECISION MAKING; MEDICAL INFORMATION; NURSE ATTITUDE; NURSING; QUESTIONNAIRE; RELATIVE; SATISFACTION; SEX DIFFERENCE; SLEEP DISORDER; SYMPTOM;

EID: 0036617561     PISSN: 14623889     EISSN: None     Source Type: Journal    
DOI: 10.1054/ejon.2001.0172     Document Type: Article

References (27)

1. Quality of life of cancer patients and their spouses in palliative home care
2. Hospital-based home care of terminally ill cancer patients. The Motala model
3. The organisation of hospital-based home care for terminally ill cancer patients: The Motala model
4. The family in hospital-based home care with special reference to terminally ill cancer patients
5. Need for overnight respite for primary caregivers of hospice clients
6. Effect of home care on the plate of death of advanced cancer patients
7. Can the experience of caring at home affect carers' retrospective evaluation of community care services?
8. Carers' health status: Is it associated with their evaluation of the quality of palliative care?
9. An evaluation of palliative care services for cancer patients in the Southern Health and Social Services Board of Northern Ireland
10. Palliative care at home: A reality or mission impossible?
11. Support needs in the last year of life: Patient and carer dilemmas
12. Identifying the needs of home caregivers of patients with cancer
13. Anhöriga som omsorgsgivare och omsorgsbehövande
14. Death from cancer at home: The carers' perspective
15. Family members' perceptions of palliative cancer care: Predictors of family functioning and family members' health
16. Needs of family caregivers of persons with cancer: A review
17. The impact of hospice services on the quality of life of primary caregivers
18. Quality of final care for terminal cancer patients in a comprehensive cancer centre from the point of view of patients' families
19. The impact of cancer on the family: An overview
20. Qualitative evaluation methods
21. Anhörigvårdare i hemsjukvården-behov av stödåtgärder
22. Quality of care of the terminally ill: The carers perspective
23. Hustruns hjälp eller hemtjänstens?
24. The needs of family members of cancer patients
25. Carers and services: A review of research
26. Cancer patient satisfaction with care
27. Cancer pain relief and palliative care: Report of a WHO expert committee