Doing our bit to ease the pain

Psychologist

Volumn 15, Issue 11, 2002, Pages 564-567

  Payne, Sheila ^a   Haines, Rebecca ^b  

^a UNIVERSITY OF SHEFFIELD   (United Kingdom)

^b ROYAL HALLAMSHIRE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0037562467     PISSN: 09528229     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (31)

1. Addington-Hall, J. & Higginson, I.J. (Eds.) (2001). Palliative care for non-cancer patients. Buckingham: Open University Press.
2. Barnett, M. (2001). Interviewing terminally ill people: Is it fair to take their time? Motive Medicine, 15, 157-158.
3. Bowlby, J. (1980). Attachment and loss:Vol. 3. Loss: Sadness and depression. London: Hogarth Press.
4. Brennan, J. (2001). Adjustment to cancer-coping or personal transition? Psychooncology, 10, 1-18.
5. Clark, D. (Ed.) (1993). The future for palliative care. Buckingham: Open University Press.
6. Clark, D. (1999). Cradled to the grave? Terminal care in the United Kingdom, 1948-67. Mortality, 4, 225-247.
7. Clark, D., Hockley, J. & Admedzai, S. (Eds.) (1997). New themes in palliative care. Buckingham: Open University Press.
8. Clark, D. & Seymour, J. (1999). Reflections on palliative care. Buckingham: Open University Press.
9. Crossley, M. (2000). Rethinking health psychology. Buckingham: Open University Press.
10. Department of Health (2000a). Manual of cancer service standards. London: HMSO.
11. Department of Health (2000b). The NHS Cancer Plan. London: HMSO.
12. de Reave, L. (1994). Ethical issues in palliative care research. Palliative Medicine, 8, 298-305.
13. Doyle, D., Hanks, W.C. & MacDonald, N. (Eds.) (1998). Oxford textbook of palliative medicine (2nd edn). Oxford: Oxford University Press.
14. Erikson, E.H. (1963). Childhood and society (2nd edn). New York: Norton.
15. Froggatt, K. (2001). Palliative care and nursing homes:Where next? Palliative Medicine, 15, 42-48.
16. Gott, M., Stevens, T., Small, N. & Ahmedzai, S.H. (2000). User involvement in cancer care. Bristol:The Policy Press.
17. Holmes, T.H. & Rahe, R.H. (1967). The Social Readjustment Scale. Journal of Psychosomatic Research, 11, 213-218.
18. Hospice Information Service (2001). Hospice directory. London: St Christopher's Hospice.
19. James, N. & Field, D. (1992). The routinization of hospice: Charisma and bureacratization. Social Science and Medicine, 34, 1363-1375.
20. Jordhoy, M.S., Kaassa, S., Fayers, P., Ovreness T., Underland G. & Ahlner-Elmqvist, M. (1999). Challenges in palliative care research: Recruitment, attrition and compliance. Palliative Medicine, 13, 299-310.
21. Lazarus, R.S. & Folkman, S. (1994). Stress, appraisal and coping. New York: Springer-Verlag.
22. Lloyd Williams, M. (2001). Screening for depression in palliative care patients:A review. European journal of Cancer Care 10, 1, 31-35.
23. Lloyd Williams, M. & Payne, S. (in press). A qualitative study of nurses' views on depression in palliative care patients. Palliative Medicine.
24. McNamara B. (2001). Fragile lives: Death dying and care. Buckingham: Open University Press.
25. National Council for Hospice and Specialist Palliative Care Services (1997). Feeling better: Psychosocial care in specialist palliative care. London:Author.
26. National Council for Hospice and Specialist Palliative Care Services (2001). What do we mean by palliative care? London: Author.
27. Parkes, CM. (1996). Bereavement (3rd edn). London: Routledge.
28. Payne, S., Horn, S. & Reif, M. (1999). Loss and bereavement. Buckingham: Open University Press.
29. Stroebe, M. & Schut, H. (1999). The dual process model of coping with bereavement. Death Studies, 23, 197-224.
30. Thorpe, G. (1993). Enabling more people to remain at home. British Medical Journal, 307, 915-918.
31. World Health Organization (1990). Technical report series 804, Geneva: Author.