Higginson IJ, Sen-Gupta GJA (2000) Place of care in advanced cancer: a qualitative systematic literature review of patient preferences. J Palliat Med 3(3):287–300
PubMed
Article
CAS
Google Scholar
Given B, Wyatt G, Given C, Sherwood P, Gift A, DeVoss D, Rahbar M (2004) Burden and depression among caregivers of patients with cancer at the end of life. ONF 31(6):1105–1117
Article
Google Scholar
Grov EK, Dahl AA, Moum T, Fossa SD (2005) Anxiety, depression and quality of life in caregivers of patients with cancer in late palliative phase. Ann Oncol 16:1185–1191
PubMed
Article
CAS
Google Scholar
Payne S, Smith P, Dean S (1999) Identifying the concerns of informal carers in palliative care. Palliat Med 13(1):37–44
PubMed
Article
CAS
Google Scholar
Carter PA (2003) Family caregivers' sleep loss and depression over time. Cancer Nurs 26(4):253–259
PubMed
Article
Google Scholar
Carter PA, Chang BL (2000) Sleep and depression in cancer caregivers. Cancer Nurs 23(6):410–415
PubMed
Article
CAS
Google Scholar
Rossi-Ferrario S, Cardillo V, Vicaro F, Balzarini E, Zotti AM (2004) Advanced cancer at home: caregiving and bereavement. Palliat Med 18:129–136
PubMed
Article
Google Scholar
Carter PA (2001) A not-so-silent cry for help: older female cancer caregivers' need for information. J Holist Nurs 19(3):271–284. doi:10.1177/089801010101900307
PubMed
Article
CAS
Google Scholar
Rose K (1999) A qualitative analysis of the information needs of informal carers of terminally ill cancer patients. J Clin Nurs 8(1):81–88
PubMed
Article
CAS
Google Scholar
Grov EK, Dahl AA, Fossa SD, Wahl AK, Moum T (2006) Global quality of life in primary caregivers of patients with cancer in palliative phase staying at home. Support Care Cancer 14(9):943–951
PubMed
Article
Google Scholar
Juarez GP, Ferrell BP, Uman GP, Podnos Y, Wagman LD (2008) Distress and quality of life concerns of family caregivers of patients undergoing palliative surgery. Cancer Nurs 31(1):2–10
PubMed
Article
Google Scholar
Given BA, Given CW, Stommel M (1994) Family and out-of-pocket costs for women with breast cancer. Cancer Pract 2(3):187–193
PubMed
CAS
Google Scholar
Harding R, Higginson IJ, Donaldson N (2003) The relationship between patient characteristics and carer psychological status in home palliative cancer care. Support Care Cancer 11:638–643
PubMed
Article
Google Scholar
Hudson P (2004) Positive aspects and challenges associated with caring for a dying relative at home. Int J Palliat Nurs 10(2):58–65
PubMed
Google Scholar
Koop PM, Strang VR (2003) The bereavement experience following home-based family caregiving for persons with advanced cancer. Clin Nurs Res 12:127–144
PubMed
Article
Google Scholar
Nijboer C, Triemstra M, Tempelaar R, Mulder M, Sanderman S, van den Bos G (2000) Patterns of caregiver experience among partners of cancer patients. Gerontologist 40(6):738–746
PubMed
Article
CAS
Google Scholar
Funk L, Stajduhar K, Toye C, Aoun S, Grande G, Todd C (2010) Part 2: home-based family caregiving at the end of life: a comprehensive review of published qualitative research (1998–2008). Palliat Med 2(6):594–607
Article
Google Scholar
Stajduhar K, Funk L, Toye C, Grande G, Aoun S, Todd C (2010) Part 1: home-based family caregiving at the end of life: a comprehensive review of published quantitative research (1998–2008). Palliat Med 24(6):573–593
PubMed
Article
Google Scholar
Stenberg U, Ruland CM, Miaskowski C (2010) Review of the literature on the effects of caring for a patient with cancer. Psychooncology 19(10):1013–1025
PubMed
Google Scholar
Bodnar JC, Kiecolt-Glaser JK (1994) Caregiver depression after bereavement: chronic stress isn't over when it's over. Psychol Aging 9(3):372–380
PubMed
Article
CAS
Google Scholar
Robinson-Whelen S, Tada Y, MacCallum RC, McGuire L, Kiecolt-Glaser JK (2001) Long-term caregiving: what happens when it ends? J Abnorm Psychol 110(4):573–584
PubMed
Article
CAS
Google Scholar
Nijboer C, Tempelaar R, Triemstra M, van den Bos GA, Sanderman R (2001) The role of social and psychologic resources in caregiving of cancer patients. Cancer 91(5):1029–1039
PubMed
Article
CAS
Google Scholar
Weitzner MA, McMillan SC (1999) The Caregiver Quality of Life Index-Cancer (CQOLC) Scale: revalidation in a home hospice setting. J Palliat Care 15(2):13–20
PubMed
CAS
Google Scholar
Goldstein NE, Concato J, Fried TR, Kasl SV, Johnson-Hurzeler R, Bradley EH (2004) Factors associated with caregiver burden among caregivers of terminally ill patients with cancer. J Palliat Care 20(1):38–43
PubMed
Google Scholar
Siegel K, Raveis VH, Houts P, Mor V (1991) Caregiver burden and unmet patient needs. Cancer 68(5):1131–1140
PubMed
Article
CAS
Google Scholar
Stetz KM, Hanson WK (1993) Alterations in perceptions of caregiving demands in advanced cancer during and after the experience. Hosp J 8(3):21–34
Article
Google Scholar
Strang VR, Koop PM, Peden J (2002) The experience of respite during home-based family caregiving for persons with advanced cancer. J Palliat Care 18(2):97–104
PubMed
Google Scholar
Harding R, Higginson I (2001) Working with ambivalence: informal caregivers of patients at the end of life. Support Care Cancer 9(8):642–645
PubMed
Article
CAS
Google Scholar
Harding R, Higginson I (2003) What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness. Palliat Med 17(1):63–74
PubMed
Article
CAS
Google Scholar
Rossi Ferrario S, Zotti AM, Massara G, Nuvolone G (2003) A comparative assessment of psychological and psychosocial characteristics of cancer patients and their caregivers. Psychooncology 12(1):1–7
PubMed
Article
CAS
Google Scholar
Simmons S (1995) From paradigm to method in interpretive action research. J Adv Nurs 21:837–844
PubMed
Article
CAS
Google Scholar
Denzin N (1978) The research act: a theoretical introduction to sociological methods. McGraw-Hill, New York
Google Scholar
Blumer H (1969) Symbolic interactionism: perspective and method. University of California Press, Berkeley
Google Scholar
Gysels M, Shipman C, Higginson IJ (2008) Is the qualitative research interview an acceptable medium for research with palliative care patients and carers? BMC Med Ethics 9:7
PubMed
Article
Google Scholar
Glaser B, Strauss A (1967) The discovery of grounded theory: strategies for qualitative research. Aldine, Chicago
Google Scholar
Glaser B (1992) Basics of grounded theory analysis: emergence vs forcing. Sociology Press, California
Google Scholar
O'Connor DL (2007) Self-identifying as a caregiver: exploring the positioning process. J Aging Stud 21(2):165–174
Article
Google Scholar
Tishelman C, Sachs L (1998) The diagnostic process and the boundaries of normality. Qual Health Res 8(1):48–60
PubMed
Article
CAS
Google Scholar
Kleinman A (1988) The illness narratives: suffering, healing and the human condition. Basic Books, New York
Google Scholar
Pinnock H, Kendall M, Murray SA, Worth A, Levack P, Porter M, MacNee W, Sheikh A (2011) Living and dying with severe chronic obstructive pulmonary disease: multi-perspective longitudinal qualitative study. BMJ 342:d142
PubMed
Article
Google Scholar