Caregivers' insights on the dying trajectory in hematology oncology

Cancer Nursing

Volumn 24, Issue 5, 2001, Pages 413-421

  McGrath, Pam ^a  

^a UNIVERSITY OF QUEENSLAND   (Australia)

Author keywords

Caregivers; End of life care; Hematologic malignancies; Information provision; Nursing; Palliative care

Indexed keywords

ARTICLE; CANCER THERAPY; CAREGIVER; CONTROLLED STUDY; DYING; FEMALE; HEMATOLOGIC DISEASE; HOSPICE; HUMAN; INTENSIVE CARE UNIT; MALE; MEDICAL RESEARCH; NURSING; PALLIATIVE THERAPY; PRIORITY JOURNAL; TERMINAL CARE;

EID: 0034780717     PISSN: 0162220X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00002820-200110000-00014     Document Type: Article

References (37)

1. Defense mechanisms in patients with bone marrow transplantation: A retrospective study
2. Leukaemia: Bone marrow transplantation
3. Two-year adjustment of bone marrow transplant survivors
4. Psychosocial preparation and follow-up for pediatric bone marrow transplant patients
5. Role retention and quality of life of bone marrow transplant survivors
6. Long-term psychological adjustment of acute leukemia survivors: Impact of bone marrow transplantation versus conventional chemotherapy
7. QOL Assessment in patients with AML
8. Informed consent to peripheral blood stem cell transplantation
9. New directions in leukaemia research; a focus on psychosocial issues from a consumer's perspective
10. Update on psychosocial research on leukaemia for social work practitioners
11. Quality of life in adult patients with acute myeloid leukaemia receiving intensive and prolonged chemothetapy - A longitudinal study
12. Experience versus expectations of B.M.T.: A case report [abstract]
13. Quality of life issues in patients dying from hematological diseases
14. Hematology and palliative care: An account of shared care for a patient undergoing bone marrow transplantation for chronic myeloid leukemia
15. Palliative care for patients with hematological malignancies - If not, why not?
16. End-of-life care for hematological malignancies: The "technological imperative" and palliative care
17. Transforming end-of-life care for the 21st century: The hospice vision
18. Care Pathways development implementation
19. Introducing anticipated recovery Pathways: A teaching hospital experience
20. Clinical protocols are key to quality in healthcare
21. Planning individual care with protocols
22. The multidisciplinary mandate of clinical pathways
23. Hospice, entropy, and the 1990s: Toward a hospice world view
24. Returning to normal following bone marrow transplantation: Outcomes, expectations and informed consent
25. Mood and memory
26. Emotional stress and eyewitness memory: A critical review
27. Survivors of acute leukemia and highly malignant lymphoma - Retrospective views of daily life problems during treatment and when in remission
28. Remembering emotional events: The fate of detailed information
29. Respecting the autonomy of patients with cancer when talking with their families: Qualitative analysis of semi-structured interviews with patients
30. Cancer patients' information needs and information seeking behaviour: In-depth interview study
31. How are you feeling? Who wants to know? Patients' and oncologists' preferences for discussing health-related quality-of-life issues
32. Collusion in doctor-patient communication about imminent death: An ethnographic study