Borasio, G.D. (2011). Translating the World Health Organization definition of palliative care into scientific practice. Palliative & Supportive Care, 9, 1–2.
Creamer, M., Bell, R. & Failla, S. (2003). Psychometric properties of the impact of Event Scale–Revised. Behavioural Research and Therapy, 41, 1489–1496.
Cummins, R.A. (2003). Normative life satisfaction: Measurement issues and a homeostatic model. Social Indicators Research, 64, 225–256.
Deeken, J.F., Taylor, K.L., Mangan, P., et al. (2003). Care for the caregivers: A review of self-report instruments developed to measure the burden, needs, and quality of life of informal caregivers. Journal of Pain and Symptom Management, 26, 922–953.
Fridriksdottir, N., Sigurdardottir, V. & Gunnarsdottir, S. (2006). Important needs of families in acute and palliative care settings assessed with the family inventory of needs. Palliative Medicine, 20, 425–432.
Friethriksdottir, N., Saevarsdottir, T., Halfdanardottir, S.I., et al. (2011). Family members of cancer patients: Needs, quality of life and symptoms of anxiety and depression. Acta Oncologica, 50, 252–258.
Hannon, B., O'Reilly, V., Bennett, K., et al. (2012). Meeting the family: Measuring effectiveness of family meetings in a specialist inpatient palliative care unit. Palliative & Supportive Care, 10, 43–49.
Henriksson, A., Benzein, E., Ternestedt, B.-M., et al. (2011). Meeting needs of family members of persons with life-threatening illness: A support group program during ongoing palliative care. Palliative & Supportive Care, 9, 263–271.
Herrmann, C. (1997). International experiences with the Hospital Anxiety and Depression Scale: A review of validation data and clinical results. Journal of Psychosomatic Research, 42, 17–41.
Hirdes, J.P., Freeman, S., Smith, T.F., et al. (2012). Predictors of caregiver distress among palliative home care clients in Ontario: Evidence based on the interRAI Palliative Care. Palliative & Supportive Care, 10, 155–163.
Horowitz, M., Wilner, N. & Alvarez, W. (1979). Impact of Event Scale: A measure of subjective stress. Psychosomatic Medicine, 41, 209–218.
Hudson, P. (2013). Improving support for family carers: Key implications for research, policy and practice. Palliative Medicine, 27, 581–582.
Hudson, P.L., Trauer, T., Graham, S., et al. (2010). A systematic review of instruments related to family caregivers of palliative care patients. Palliative Medicine, 24, 656–668.
Hwang, S.S., Chang, V.T., Alejandro, Y., et al. (2003). Caregiver unmet needs, burden, and satisfaction in symptomatic advanced cancer patients at a Veterans Affairs (VA) medical center. Palliative & Supportive Care, 1, 319–329.
Kim, Y., Kashy, D.A., Spillers, R.L., et al. (2010). Needs assessment of family caregivers of cancer survivors: Three cohorts comparison. Psycho-Oncology, 19, 573–582.
Kogan, N.R., Dumas, M. & Cohen, S.R. (2013). The extra burdens patients in denial impose on their family caregivers. Palliative & Supportive Care, 11, 91–99.
Kristjanson, L.J., Atwood, J. & Degner, L.F. (1995). Validity and reliability of the family inventory of needs (FIN): Measuring the care needs of families of advanced cancer patients. Journal of Nursing Measurement, 3, 109–126.
Kubinger, K.D. (2009). Psychologische diagnostik: Theorie und praxis psychologischen diagnostizierens. Göttingen: Hogrefe-Verlag.
Lee, G.L., Woo, I.M.H. & Goh, C. (2013). Understanding the concept of a “good death” among bereaved family caregivers of cancer patients in Singapore. Palliative & Supportive Care, 11, 37–46.
Molassiotis, A., Wilson, B., Blair, S., et al. (2011). Unmet supportive care needs, psychological well-being and quality of life in patients living with multiple myeloma and their partners. Psycho-Oncology, 20, 88–97.
Park, S.M., Kim, Y.J., Kim, S., et al. (2010). Impact of caregivers' unmet needs for supportive care on quality of terminal cancer care delivered and caregiver's workforce performance. Supportive Care in Cancer, 18, 699–706.
Sanderson, C., Lobb, E.A., Mowll, J., et al. (2013). Signs of post-traumatic stress disorder in caregivers following an expected death: A qualitative study. Palliative Medicine, 27, 625–631.
Schrank, B., Woppmann, A., Sibitz, I., et al. (2011). Development and validation of an integrative scale to assess hope. Health Expectations, 14, 417–428.
Scott, G., Whyler, N. & Grant, G. (2001). A study of family carers of people with a life-threatening illness, 1: The carers' needs analysis. International Journal of Palliative Nursing, 7, 290–291.
Sharpe, L., Butow, P., Smith, C., et al. (2005). The relationship between available support, unmet needs and caregiver burden in patients with advanced cancer and their carers. Psycho-Oncology, 14, 102–114.
Stenberg, U., Ruland, C.M. & Miaskowski, C. (2010). Review of the literature on the effects of caring for a patient with cancer. Psycho-Oncology, 19, 1013–1025.
Wanzer, S.H., Federman, D.D., Adelstein, S.J., et al. (1989). The physician's responsibility toward hopelessly ill patients: A second look. The New England Journal of Medicine, 320, 844–849.
Wen, K.-Y. & Gustafson, D. (2004). Needs assessment for cancer patients and their families. Health and Quality of Life Outcomes, 2, 11.
Williams, A.-L. & McCorkle, R. (2011). Cancer family caregivers during the palliative, hospice, and bereavement phases: A review of the descriptive psychosocial literature. Palliative & Supportive Care, 9, 315–325.