Problems to discuss with cancer patients in palliative care: A comprehensive approach

Patient Education and Counseling

Volumn 47, Issue 3, 2002, Pages 195-204

  Osse, Bart H P ^a   Vernooij Dassen, Myrra J F J ^a   Schadé, Egbert ^b   de Vree, Berna ^a   van den Muijsenbergh, Maria E T C ^a   Grol, Richard P T M ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

Health services needs and demands; Needs assessment; Palliative care; Qualitative studies; Quality of health care

Indexed keywords

ARTICLE; CANCER PATIENT; CLINICAL ARTICLE; CONTROLLED STUDY; DOCTOR PATIENT RELATION; FAMILY; FATIGUE; FEAR; HUMAN; PALLIATIVE THERAPY; PATIENT CARE; PRIORITY JOURNAL; QUALITY OF LIFE;

ADAPTATION, PSYCHOLOGICAL; HEALTH SERVICES NEEDS AND DEMAND; HUMANS; NEEDS ASSESSMENT; NEOPLASMS; PALLIATIVE CARE; QUALITY OF HEALTH CARE; SOCIAL SUPPORT;

EID: 0036090009     PISSN: 07383991     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0738-3991(02)00019-8     Document Type: Article

References (43)

1. Can home-care maintain an acceptable quality of life for patients with terminal cancer and their relatives?
2. Cancer patient satisfaction with care
3. Unmet needs of persons with cancer in Pennsylvania during the period of terminal care
4. An examination of the concrete service needs of advanced cancer patients
5. Need satisfaction in terminal care settings
6. Randomised controlled trial of effects of co-ordinating care for terminally ill cancer patients
7. Psychosocial problems: What do patients want? What do physicians want to provide?
8. Who should measure quality of life, the doctor or the patient?
9. Difficulty of symptom control and general practitioners' knowledge of patients' symptoms
10. ABC of palliative care: Communication with patients, families, and other professionals
11. Quality of life assessment in daily clinical oncology practice: A feasibility study
12. Assessment of the need for palliative care as perceived by individual cancer patients and their families: A review of instruments for improving patient participation in palliative care
13. Reaching the parts other methods cannot reach: An introduction to qualitative methods in health and health services research
14. Shared understanding of the qualitative research process. Guidelines for the medical researcher
15. Qualitative research methods in general practice and primary care
16. A critical appraisal of the role of triangulation in nursing research
17. Sampling for qualitative research using quantitative methods. Part 2. Characteristics of GPs who agree to video-taping of consultations
18. Rigour and qualitative research
19. Dying now
20. Kwalitan as an aid in qualitative analysis. University of Nijmegen, The Netherlands
21. Hoe oordelen chronisch zieken over de huisartsenzorg? (How do patients with chronic disease juge their general practitioner's care?)
22. The clinical meaning of Rankin handicap grades after stroke
23. The cancer inventory of problem situations, an instrument for assessing cancer patients' rehabilitation needs
24. The CARES: A generic measure of health-related quality of life for patients with cancer
25. Determinants of need and unmet need among cancer patients residing at home
26. Information needs of families of cancer patients: A literature review and recommendations
27. Effect of providing cancer patients with the audiotaped initial consultation on satisfaction, recall, and quality of life: A randomized, double-blind study
28. Care needs of home-based cancer patients
29. Helping cancer patients disclose their concerns
30. Terminally ill cancer patients: Their most important concerns
31. Needs of hospice and clinic patients with cancer
32. Needs of care-givers of clinic and hospice cancer patients
33. The needs of patients with cancer and their care-givers in rural areas
34. Measuring the unmet needs of people living with cancer
35. Defining a behavioral science curriculum for family physicians: What do patients think?
36. Behoeften en wensen van terminale patienten en hun naasten (Needs and desires of terminally ill patients and their next of kin)
37. Psychosocial issues in palliative care: The patient, the family, and the process and outcome of care
38. Self-identified needs of patients with cancer at home and their home-care-givers: A descriptive study
39. The end stage cancer patient: Terminal common pathway