Tilnærming til pasienter som trenger palliativ behandling
- 1.
Jordhøy MS, Fayers P, Loge JH et al. Quality of life in advanced cancer patients: the impact of sociodemographic and medical characteristics. Br J Cancer 2001; 85: 1478 – 85.
- 2.
Kaasa S, red. Palliativ behandling og pleie. Nordisk lærebok. Oslo: Ad Notam Gyldendal, 1998.
- 3.
Vaglum P. Pasienten din har også en familie. I: Vaglum P, Ekeberg Ø, Finset A et al. Innføring i medisinske atferdsfag. Oslo: Cappelen Akademisk, 2000: 69 – 85.
- 4.
Jordhøy MS, Saltvedt I, Fayers P et al. Which cancer patients die in nursing homes? Quality of life, medical and sociodemographic characteristics. Palliat Med 2003; 17: 433 – 44.
- 5.
Ringdal GI, Ringdal K, Jordhøy MS et al. Health-related quality of life (HRQOL) in family members of cancer victims: results from a longitudinal intervention study in Norway and Sweden. Palliat Med 2004; 18: 108 – 20.
- 6.
Lederberg MS. The family of the cancer patient. I: Holland JC, red. Psycho-oncology. New York: Oxford University Press, 1998: 981 – 3.
- 7.
Kissane DW. A challenge for palliative medicine: bereavement care. Eur J Pall Care 2005; 12: 19 – 23.
- 8.
The AM, Hak T, Koeter G et al. Collusion in doctor-patient communication about imminent death: an ethnographic study. BMJ 2000; 321: 1376 – 81.
- 9.
Vaglum P. Pasienten din har en personlighet. I: Vaglum P, Ekeberg Ø, Finset A et al. Innføring i medisinske atferdsfag. Oslo: Cappelen Akademisk, 2000: 55 – 67.
- 10.
Finset A. Hvordan reagerer pasienten din på sykdomstegn? I: Vaglum P, Ekeberg Ø, Finset A et al. Innføring i medisinske atferdsfag. Oslo: Cappelen Akademisk, 2000: 103 – 14.
- 11.
Johansen S, Holen JC, Kaasa S et al. Attitudes towards, and wishes for, euthanasia in advanced cancer patients at a palliative medicine unit. Palliat Med 2005; 19: 454 – 60.
- 12.
Miaskowski C, Dodd MJ, West C et al. Lack of adherence with the analgesic regimen: a significant barrier to effective cancer pain management. J Clin Oncol 2001; 19: 4275 – 9.
- 13.
Norsk forening for palliativ medisin. Standard for palliasjon. Oslo: Den norske lægeforening, 2004. www.legeforeningen.no/?id=53750 (30.11.2005).
- 14.
Kaasa S, Loge JH. Quality of life in palliative medicine: principles and practice. I: Doyle D, Cherny N, Hanks G et al, red. Oxford textbook of palliative medicine. 3. utg. Oxford: Oxford University Press, 2004: 196 – 210.
- 15.
Detmar SB, Muller MJ, Schornagel JH et al. Role of health-related quality of life in palliative chemotherapy treatment decisions. J Clin Oncol 2002; 20: 1056 – 62.
- 16.
Detmar SB, Muller MJ, Wever LD et al. The patient-physician relationship: patient-physician communication during outpatient palliative treatment visits: an observational study. JAMA 2001; 285: 1351 – 7.
- 17.
Detmar SB, Muller MJ, Schornagel JH et al. Health-related quality-of-life assessments and patient-physician communication: a randomized controlled trial. JAMA 2002; 288: 3027 – 34.
- 18.
Emanuel EJ, Fairclough DL, Wolfe P et al. Talking with terminally ill patients and their caregivers about death, dying, and bereavement: is it stressful? Is it helpful? Arch Intern Med 2004; 164: 1999 – 2004.
- 19.
Fallowfield L, Jenkins V. Communicating sad, bad, and difficult news in medicine. Lancet 2004; 363: 312 – 9.
- 20.
Chochinov HM. Dignity and the eye of the beholder. J Clin Oncol 2004; 22: 1336 – 40.
- 21.
Butow PN, Kazemi JN, Beeney LJ et al. When the diagnosis is cancer: patient communication experiences and preferences. Cancer 1996; 77: 2630 – 7.
- 22.
Bruera E, Kuehn N, Miller MJ et al. The Edmonton Symptom Assessment System (ESAS): a simple method for the assessment of palliative care patients. J Palliat Care 1991; 7: 6 – 9.
- 23.
Caraceni A, Cherny N, Fainsinger R et al. Pain measurement tools and methods in clinical research in palliative care: recommendations of an Expert Working Group of the European Association of Palliative Care. J Pain Symptom Manage 2002; 23: 239 – 55.
- 24.
Chochinov HM, Wilson KG, Enns M et al. «Are you depressed?» Screening for depression in the terminally ill. Am J Psychiatry 1997; 154: 674 – 6.
- 25.
Nekolaichuk CL, Bruera E, Spachynski K et al. A comparison of patient and proxy symptom assessments in advanced cancer patients. Palliat Med 1999; 13: 311 – 23.
- 26.
Sprangers MA, Aaronson NK. The role of health care providers and significant others in evaluating the quality of life of patients with chronic disease: a review. J Clin Epidemiol 1992; 45: 743 – 60.
- 27.
Songe-Møller S, Saltvedt I, Hølen JC et al. Smertemålinger hos eldre med kognitiv svikt Tidsskr Nor Lægeforen 2005; 125: 1838 – 40.
- 28.
Ingham J, Portenoy RK. The measurement of pain and other symptoms. I: Doyle D, Hanks GW, Cherny N et al, red. Oxford textbook of palliative medicine. 3. utg. Oxford: Oxford University Press, 2004: 167 – 84.
- 29.
Centeno C, Sanz A, Bruera E. Delirium in advanced cancer patients. Palliat Med 2004; 18: 184 – 94.
- 30.
Fayers PM, Hjermstad MJ, Ranhoff AH et al. Which Mini-Mental State Exam (MMSE) items can be used to screen for delirium and cognitive impairment? J Pain Symptom Manage 2005; 30: 41 – 50.
- 31.
Lickiss JN, Turner KS, Pollock ML. The interdisciplinary team. I: Doyle D, Hanks G, Cherny N et al, red. Oxford textbook of palliative medicine. 3. utg. Oxford: Oxford University Press, 2004: 42 – 6.
- 32.
Bruera E, Neumann CM. The uses of psychotropics in symptom management in advanced cancer. Psychooncology 1998; 7: 346 – 58.