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  • Author, in press.
  • Author, in press.
  • Author, 2008.
  • Author, 06-08.
  • Author, 2005.
  • Author, 2005.
  • Aoun, S. M., & Kristjanson, L. J. (2005). Caregiving for the terminally ill: at what cost? Palliative Medicine, 19, 551555.
  • Bokhour, B. G. (2006). Communication in interdisciplinary team meetings: what are we talking about? Journal of Interprofessional Care, 20(4), 349363.
  • Centers for Medicare and Medicaid Services. (2008). 42 CFR§418, Medicare and Medicaid Programs: Hospice Conditions of Participation o. Document Number)
  • Chilcoat, Y., & DeWine, S. (1985). Teleconferencing and interpersonal communication perception. Journal of Applied Communication Research, 13(1), 1432.
  • Demiris, G., Speedie, S., & Finkelstein, S. (2001). Change of patients' perceptions of TeleHomeCare. Telemedicine Journal & E-Health., 7(3), 241248.
  • Demiris, G., Speedie, S., Finkelstein, S., & Harris, I. (2003). Communication patterns and technical quality of virtual visits in home care. Journal of Telemedicine & Telecare, 9(4), 210215.
  • Egbert, N., & Parrott, R. (2003). Empathy and social support for the terminally ill: Implications for recruiting and retaining hospice and hospital volunteers. Communication Studies, 54, 1834.
  • Evans, W. G., Cutson, T. M., Steinhauser, K. E., & Tulsky, J. A. (2006). Is there no place like home? Caregivers recall reasons for and experience upon transfer from home hospice to inpatient facilities. Journal of Palliative Medicine, 9(1), 100110.
  • Griffith, J. C., Brosnan, M., Lacey, K., Keeling, S., & Wilkinson, T. J. (2004). Family meetings–a qualitative exploration of improving care planning with older people and their families. Age Ageing, 33(6), 577581.
  • Hebert, R. S., Schulz, R., Copeland, V., & Arnold, R. M. (2008). What questions do family caregivers want to discuss with health care providers in order to prepare for the death of a loved one? An ethnographic study of caregivers of patients at end of life. Journal of Palliative Medicine, 11(3), 476483.
  • Hensel, B. K., Parker-Oliver, D., & Demiris, G. (2007). Videophone communication between residents and family: a case study. Journal of the American Medical Directors Association, 8(2), 123127.
  • Hwang, S. S., Chang, V. T., Alejandro, Y., Osenenko, P., Davis, C., Cogswell, J., 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(4), 319329.
  • Kazanowski, M. (2005). Family caregivers' medication management of sypmtoms in patients with cancer near death. Journal of Hospice and Palliative Nursing, 7(3), 174181.
  • Keefe, F. J., Ahles, T. A., Porter, L. S., Sutton, L. M., McBride, C. M., Pope, M. S., et al. (2003). The self-efficacy of family caregivers for helping cancer patients manage pain at end-of-life. Pain., 103(1-2), 157162.
  • Lowey, S. E. (2008). Communication between the nurse and family caregiver in end-of-life care: A review of the literature. Journal of Hospice & Palliative Nursing, 10(1), 3548.
  • Mangan, P. A., Taylor, K. L., Yabroff, K. R., Fleming, D. A., & Ingham, J. M. (2003). Caregiving near the end of life: unmet needs and potential solutions. Palliative & Supportive Care, 1(3), 247259.
  • National Hospice and Palliative Care Organization. (2008, December). NHPCO Facts and Figures: Hospice Care in America. from www.nhpco.org
  • Parker Oliver, D. R., Demiris, G., Day, M., Courtney, K. L., & Porock, D. (2006). Telehospice support for elder caregivers of hospice patients: two case studies. Journal of Palliative Medicine, 9(2), 264267.
  • Query, J. L. J., Wright, K. B., & Gilchrist, E. (2007). Communication and cancer hospice care: Toward negotiating attitudinal and research obstacles. In D.O’Hair, G. J.Kreps & L.Sparks (Eds.), Handbook of Communication and Cancer Care (pp. 293311). Cresskill, NJ: Hampton Press.
  • Rabow, M. W., Hauser, J. M., & Adams, J. (2004). Supporting family caregivers at the end of life: “they don't know what they don't know”. Journal of the American Medical Association, 291(4), 483491.
  • Razani, J., Kakos, B., Orieta-Barbalace, C., Wong, J. T., Casas, R., Lu, P., et al. (2007). Predicting caregiver burden from daily functional abilities of patients with mild dementia. Journal of the American Geriatrics Society, 55(9), 14151420.
  • Saltz, C. C., & Schaefer, T. (1996). Interdisciplinary teams in health care: integration of family caregivers. Social Work in Health Care, 22(3), 5969.
  • Street, R. L., Jr. (2007). Aiding medical decision making: a communication perspective. Medical Decision Making, 27(5), 550553.
  • Street, R. L., Jr. & Gordon, H. S. (2006). The clinical context and patient participation in post-diagnostic consultations. Patient Education & Counseling, 64(1-3), 217224.
  • Street, R. L., Jr., Gordon, H. S., Ward, M. M., Krupat, E., & Kravitz, R. L. (2005). Patient participation in medical consultations: why some patients are more involved than others. Medical Care, 43(10), 960969.
  • Street, R. L., Jr., Krupat, E., Bell, R. A., Kravitz, R. L., & Haidet, P. (2003). Beliefs about control in the physician-patient relationship: effect on communication in medical encounters. Journal of General Internal Medicine, 18(8), 609616.
  • Street, R. L., Jr., & Millay, B. (2001). Analyzing patient participation in medical encounters. Health Communication, 13(1), 6173.
  • Von Friederichs-Fitzwater, M. M., & Gilgun, J. (2001). Relational control in physician-patient encounters. Health Commun, 13(1), 7587.
  • Zimmerman, S., & Applegate, J. L. (1992). Person-centered comforting in the hospice interdisciplinary team. Communication Research, 19, 240263.