Paediatric respite care: A literature review from New Zealand

Palliative Medicine

Volumn 16, Issue 2, 2002, Pages 99-105

  Horsburgh, M ^a   Trenholme, A ^a   Huckle, T ^a  

^a UNIVERSITY OF AUCKLAND   (New Zealand)

Author keywords

Children; Culture; Family needs; New Zealand; Quality of health services; Respite care; Terminal illness

Indexed keywords

ARTICLE; CHILD; CHILD CARE; CHILD DEATH; CONTROLLED STUDY; CULTURAL FACTOR; FAMILY; HEALTH CARE NEED; HEALTH CARE POLICY; HEALTH CARE QUALITY; HEALTH SERVICE; HOME CARE; HUMAN; MEDICAL DOCUMENTATION; MEDICAL LITERATURE; MEDICAL RESEARCH; NEW ZEALAND; PALLIATIVE THERAPY; TERMINALLY ILL PATIENT;

ADOLESCENT; CHILD; FAMILY HEALTH; HEALTH PLANNING; HUMANS; NEW ZEALAND; PALLIATIVE CARE; QUALITY OF HEALTH CARE; RESPITE CARE; TERMINAL CARE;

EID: 0036223343     PISSN: 02692163     EISSN: None     Source Type: Journal    
DOI: 10.1191/0269216302pm515oa     Document Type: Article

References (46)

1. Assessment of need for a children's hospice program
2. A guide to the development of children palliative cares services. Report of a joint working party of the Association for Children with Life-Threatening or Terminal Conditions and Their Families and the Royal and Child Health
3. The role of the hospice for the dying
4. Facilitating the care of terminally ill children
5. Terminal care of the dying child psychosocial implications of care
6. Palliative care for children with cancer - Home, hospital or hospice
7. The interstellar cold: Parent's experiences of their child's palliative care
8. Expert opinions: A national survey of parents caring for a severely disabled child
9. Cornerstone care for families of children with life-threatening illness
10. Prevalence and impact of chronic childhood conditions in Auckland, New Zealand
11. The needs of parents of paediatric oncology patients during the palliative care phase
12. Review of respite services for children in the North Health Region
13. When a child dies. Caring for children with life-limiting/life-threatening conditions
14. The role and need of the children's hospice in the United Kingdom
15. Hospices for children?
16. Children and young people with terminal illness. Models of service delivery consumers prefer
17. Home care of the dying child
18. Review of palliative care services within the North Health Region
19. Home cares for children dependent on medical technology: The family perspective
20. Surviving death's grief
21. Practical issues
22. Cultural issues in palliative care
23. Helping to reach an understanding: Palliative care for ethnic minority groups
24. Cultural and spiritual issues in health care
25. Absent minorities? Ethnicity and the use of palliative care services in field D
26. Ethnic minorities and palliative care in Derby
27. Racial differences in attitudes toward hospice care
28. Identifying and meeting needs of ethnic minority patients
29. Ethnic minorities - Neglected by palliative care providers
30. Immigrants and the hospice
31. Deterrents to access and service for blacks and Hispanics: The Medicare hospice benefit, health care utilization and cultural barriers
32. Hospice and minorities: A national study of organizational access and practice
33. Patterns of provision in respite care and the children act
34. Bringing respite to your community
35. Palliative care for children
36. Standards of hospice care for children
37. Clinical governance: Implications for medical education
38. Evaluation of the pilot project for children with life-threatening illnesses
39. Support for the family
40. Provision of care
41. A study of the needs and provisions for families caring for children with life-limiting incurable disorders
42. An approach for studying the feasibility and desirability of home care for the child dying from cancer
43. The Rainbow Trust: A domiciliary crisis service
44. An evaluation of hospice care for children