Allen, R.S., Haley, W.E. Haley, et al. (2002). Pain reports by older hospice cancer patients and family caregivers: The role of cognitive functioning. Gerontologist, 42(4), 507–514.
Anderson, G.F. & Squires, D.A. (2010). Measuring the U.S. health care system: A cross-national comparison. Issue Brief (Commonwealth Fund), 90, 1–10.
Breitbart, W., Rosenfeld, B., Roth, A., et al. (1997). The Memorial Delirium Assessment Scale. Journal of Pain and Symptom Management, 13(3), 128–137.
Bruera, E. & Hui, D. (2010). Integrating supportive and palliative care in the trajectory of cancer: Establishing goals and models of care. Journal of Clinical Oncology, 28(25), 4013–4017.
Bruera, E., Kuehn, N., Miller, M.J., et al. (1991). The Edmonton Symptom Assessment System (ESAS): A simple method for the assessment of palliative care patients. Journal of Palliative Care, 7(2), 6–9.
Bruera, E., Miller, L., McCallion, J., et al. (1992). Cognitive failure in patients with terminal cancer: A prospective study. Journal of Pain and Symptom Management, 7(4), 192–195.
Bruera, E., Hui, D., Dalal, S., et al. (2013). Parenteral hydration in patients with advanced cancer: A multicenter, double-blind, placebo-controlled randomized trial. Journal of Clinical Oncology, 31(1), 111–118.
Casarett, D.J. & Inouye, S.K. (2001). Diagnosis and management of delirium near the end of life. Annals of Internal Medicine, 135(1), 32–40.
Chang, V.T., Hwang, S.S. & Feuerman, M. (2000). Validation of the Edmonton Symptom Assessment Scale. Cancer, 88(9), 2164–2171.
Cheung, W.Y., Le, L.W. & Zimmermann, C. (2009). Symptom clusters in patients with advanced cancers. Supportive Care in Cancer, 17(9), 1223–1230.
Currow, D.C., Ward, A.M., Plummer, J.L., et al. (2008). Comfort in the last 2 weeks of life: Relationship to accessing palliative care services. Supportive Care in Cancer, 16(11), 1255–1263.
de Santiago, A., Portela, M.A., Ramos, L., et al. (2012). A new palliative care consultation team at the oncology department of a university hospital: An assessment of initial efficiency and effectiveness. Supportive Care in Cancer, 20(9), 2199–2203.
Donnelly, S. & Walsh, D. (1995). The symptoms of advanced cancer. Seminars in Oncology, 22(2, Suppl. 3), 67–72.
Fang, C.K., Chen, H.W., Liu, S.I., et al. (2008). Prevalence, detection and treatment of delirium in terminal cancer inpatients: A prospective survey. Japanese Journal of Clinical Oncology, 38(1), 56–63.
Gagnon, B., Lawlor, P.G., Mancini, I.L., et al. (2001). The impact of delirium on the circadian distribution of breakthrough analgesia in advanced cancer patients. Journal of Pain and Symptom Management, 22(4), 826–833.
Gaudreau, J.D., Gagnon, P., Harel, F., et al. (2005). Fast, systematic, and continuous delirium assessment in hospitalized patients: The nursing delirium screening scale. Journal of Pain and Symptom Management, 29(4), 368–375.
Greer, D.S., Mor, V., Sherwood, S., et al. (1983). National hospice study analysis plan. Journal of Chronic Diseases, 36(11), 737–780.
Hui, D., Parsons, H., Nguyen, L., et al. (2010). Timing of palliative care referral and symptom burden in phase 1 cancer patients: A retrospective cohort study. Cancer, 116(18), 4402–4409.
Hutcheson, A. (2011). Hospice care in the United States. Primary Care, 38(2), 173–182.
Lawlor, P.G. & Bruera, E.D. (2002). Delirium in patients with advanced cancer. Hematology/Oncology Clinics of North America, 16(3), 701–714.
Lawlor, P.G., Gagnon, B., Mancini, I.L., et al. (2000). Occurrence, causes, and outcome of delirium in patients with advanced cancer: A prospective study. Archives of Internal Medicine, 160(6), 786–794.
McMillan, S.C. (1996 a). Pain and pain relief experienced by hospice patients with cancer. Cancer Nursing, 19(4), 298–307.
McMillan, S.C. (1996 b). The quality of life of patients with cancer receiving hospice care. Oncology Nursing Forum, 23(8), 1221–1228.
McMillan, S.C. & Small, B.J. (2002). Symptom distress and quality of life in patients with cancer newly admitted to hospice home care. Oncology Nursing Forum, 29(10), 1421–1428.
Nekolaichuk, C.L., Maguire, T.O., Suarez-Almazor, M., et al. (1999). Assessing the reliability of patient, nurse, and family caregiver symptom ratings in hospitalized advanced cancer patients. Journal of Clinical Oncology, 17(11), 3621–3630.
Rodriguez, K.L., Hanlon, J.T., Perera, S., et al. (2010). A cross-sectional analysis of the prevalence of undertreatment of non-pain symptoms and factors associated with undertreatment in older nursing home hospice/palliative care patients. American Journal of Geriatric Pharmacotherapy, 8(3), 225–232.
Sessler, C.N., Gosnell, M.S., Grap, M.J., et al. (2002). The Richmond Agitation–Sedation Scale: Validity and reliability in adult intensive care unit patients. American Journal of Respiratory and Critical Care Medicine, 166(10), 1338–1344.
Steinhauser, K.E., Christakis, N.A., Clipp, E.C., et al. (2000). Factors considered important at the end of life by patients, family, physicians, and other care providers. The Journal of the American Medical Association, 284(19), 2476–2482.
Watanabe, S.M., Nekolaichuk, C.L., Beaumont, C., et al. (2011). A multicenter study comparing two numerical versions of the Edmonton Symptom Assessment System in palliative care patients. Journal of Pain and Symptom Management, 41(2), 456–468.
Watanabe, S.M., Nekolaichuk, C.L. & Beaumont, C. (2012). The Edmonton Symptom Assessment System, a proposed tool for distress screening in cancer patients: Development and refinement. Psycho-Oncology, 21(9), 977–985.
Weitzner, M.A., Moody, L.N. & McMillan, S.C. (1997). Symptom management issues in hospice care. The American Journal of Hospice & Palliative Care, 14(4), 190–195.
Yang, F.M., Marcantonio, E.R., Inouye, S.K., et al. (2009). Phenomenological subtypes of delirium in older persons: Patterns, prevalence, and prognosis. Psychosomatics, 50(3), 248–254.
Yennurajalingam, S., Atkinson, B., Masterson, J., et al. (2012). The impact of an outpatient palliative care consultation on symptom burden in advanced prostate cancer patients. Journal of Palliative Medicine, 15(1), 20–24.
Yurk, R., Morgan, D., Franey, S., et al. (2002). Understanding the continuum of palliative care for patients and their caregivers. Journal of Pain and Symptom Management, 24(5), 459–470.