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Volumn 7, Issue 2-3, 2011, Pages 195-215

Providing support at time of death from cancer: Results of a 5-year post-bereavement group study

Author keywords

Bereavement; Consentient care; End of life; Family support; Secondary cancer survivors

Indexed keywords

ARTICLE; BEREAVEMENT; CAREGIVER; DEATH; FAMILY; FEMALE; FRIEND; HUMAN; MALE; MORTALITY; NEOPLASM; PSYCHOLOGICAL ASPECT; SELF HELP; TERMINAL CARE;

EID: 80052452915     PISSN: 15524256     EISSN: 15524264     Source Type: Journal    
DOI: 10.1080/15524256.2011.593156     Document Type: Article
Times cited : (21)

References (58)
  • 2
    • 64549139382 scopus 로고    scopus 로고
    • A systematic review of informal caregivers' needs in providing home-based end-of-life care to people with cancer
    • Bee, P. E., Barnes, P., & Luker, K. A. (2009). A systematic review of informal caregivers' needs in providing home-based end-of-life care to people with cancer. Journal of Clinical Nursing, 18, 1379-1393.
    • (2009) Journal of Clinical Nursing , vol.18 , pp. 1379-1393
    • Bee, P.E.1    Barnes, P.2    Luker, K.A.3
  • 4
    • 0038013620 scopus 로고    scopus 로고
    • The impact on the family of terminal restlessness and its managemet
    • Brajtman, S. (2003). The impact on the family of terminal restlessness and its managemet. Palliative Medicine, 17, 454-460.
    • (2003) Palliative Medicine , vol.17 , pp. 454-460
    • Brajtman, S.1
  • 6
    • 26444585999 scopus 로고    scopus 로고
    • Preferences for place of care and place of death among informal caregivers of the terminally ill
    • Brazil, K., Howell, D., Bedard, M., Krueger, P., & Heidebrecht, C. (2005). Preferences for place of care and place of death among informal caregivers of the terminally ill. Palliative Medicine, 19, 492-499.
    • (2005) Palliative Medicine , vol.19 , pp. 492-499
    • Brazil, K.1    Howell, D.2    Bedard, M.3    Krueger, P.4    Heidebrecht, C.5
  • 7
    • 0030078339 scopus 로고    scopus 로고
    • The role of the nurse in patient-focused care: Models of competence and implications for education and training
    • Burchell, H., & Jenner, E. A. (1996). The role of the nurse in patient-focused care: Models of competence and implications for education and training. International Journal of Nursing Studies, 33(1), 67-75.
    • (1996) International Journal of Nursing Studies , vol.33 , Issue.1 , pp. 67-75
    • Burchell, H.1    Jenner, E.A.2
  • 8
    • 0037080137 scopus 로고    scopus 로고
    • Lifestyle interference and emotional distress in family caregivers of advanced cancer patients
    • Cameron, J. I., Franche, R., Cheung, A. M., & Stewart, D. (2001). Lifestyle interference and emotional distress in family caregivers of advanced cancer patients. Cancer, 94(2), 521-527.
    • (2001) Cancer , vol.94 , Issue.2 , pp. 521-527
    • Cameron, J.I.1    Franche, R.2    Cheung, A.M.3    Stewart, D.4
  • 9
    • 3042827889 scopus 로고    scopus 로고
    • Grounded theory: Objectivist and constructivist methods
    • N. K Denzin, & Y. S. Lincoln (Eds.), Thousand Oaks, CA: Sage
    • Charmaz, K. (2003). Grounded theory: Objectivist and constructivist methods. In N. K Denzin, & Y. S. Lincoln (Eds.), Strategies of qualitative inquiry (pp. 249-291). Thousand Oaks, CA: Sage.
    • (2003) Strategies of Qualitative Inquiry , pp. 249-291
    • Charmaz, K.1
  • 11
    • 22544461071 scopus 로고    scopus 로고
    • Family evaluation of hospice care: Results from voluntary submission of data via website
    • Connor, S. R., Teno, J., Spence, C., & Smith, N. (2005). Family evaluation of hospice care: Results from voluntary submission of data via website. Journal of Pain and Symptom Management, 30, 9-17.
    • (2005) Journal of Pain and Symptom Management , vol.30 , pp. 9-17
    • Connor, S.R.1    Teno, J.2    Spence, C.3    Smith, N.4
  • 12
    • 42649099652 scopus 로고    scopus 로고
    • Knowledge and information needs of informal caregivers in palliateive care: A qualitative systematic review
    • Docherty, A., Owens, A., Asadi-Lari, M., Petchey, R., Williams, J., & Carter, Y. H. (2008). Knowledge and information needs of informal caregivers in palliateive care: A qualitative systematic review. Palliative Medicine, 22(2), 153-171.
    • (2008) Palliative Medicine , vol.22 , Issue.2 , pp. 153-171
    • Docherty, A.1    Owens, A.2    Asadi-Lari, M.3    Petchey, R.4    Williams, J.5    Carter, Y.H.6
  • 14
    • 0346361453 scopus 로고    scopus 로고
    • Outline of a critical best practice perspective on social work and social care
    • Ferguson, H. (2003). Outline of a critical best practice perspective on social work and social care. British Journal of Social Work, 33(8), 1005-1024.
    • (2003) British Journal of Social Work , vol.33 , Issue.8 , pp. 1005-1024
    • Ferguson, H.1
  • 17
    • 3042553652 scopus 로고    scopus 로고
    • Family caregiver burden: Results of a longitudinal study of breast cancer patients and their principal caregivers
    • Grunfeld, E., Coyle, D., Whelan, T., Clinch, J., Reyno, L, Earle, C. C.,. . . Glossop, R. (2004). Family caregiver burden: Results of a longitudinal study of breast cancer patients and their principal caregivers. Canadian Medical Association Journal, 170(12), 1795-1801.
    • (2004) Canadian Medical Association Journal , vol.170 , Issue.12 , pp. 1795-1801
    • Grunfeld, E.1    Coyle, D.2    Whelan, T.3    Clinch, J.4    Reyno, L.5    Earle, C.C.6    Glossop, R.7
  • 18
    • 41149154299 scopus 로고    scopus 로고
    • 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
    • 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), 476-483.
    • (2008) Journal of Palliative Medicine , vol.11 , Issue.3 , pp. 476-483
    • Hebert, R.S.1    Schulz, R.2    Copeland, V.3    Arnold, R.M.4
  • 19
    • 58149402393 scopus 로고    scopus 로고
    • A dimensional analysis of patient-centered care
    • Hobbs, J. L. (2009). A dimensional analysis of patient-centered care. Nursing Research, 58(1), 52-62.
    • (2009) Nursing Research , vol.58 , Issue.1 , pp. 52-62
    • Hobbs, J.L.1
  • 20
  • 22
    • 15744400963 scopus 로고    scopus 로고
    • Screening for psychologic distress in ambulatory cancer patients: A multicenter evaluation of the distress thermometer
    • Jacobsen, P. B., Donovan, K. A., Trask, P. C., Fleishman, S. B., Zabora, J., Baker, F., & Holland, J. C. (2005). Screening for psychologic distress in ambulatory cancer patients: A multicenter evaluation of the distress thermometer. Cancer, 103(7), 1494-1502.
    • (2005) Cancer , vol.103 , Issue.7 , pp. 1494-1502
    • Jacobsen, P.B.1    Donovan, K.A.2    Trask, P.C.3    Fleishman, S.B.4    Zabora, J.5    Baker, F.6    Holland, J.C.7
  • 24
    • 0008038611 scopus 로고    scopus 로고
    • Preparation for oncology settings: What hospice social workers say they need
    • Kovacs, P. J., & Bronstein, L. R. (1999). Preparation for oncology settings: What hospice social workers say they need. Health & Social Work, 24(1), 57-64.
    • (1999) Health & Social Work , vol.24 , Issue.1 , pp. 57-64
    • Kovacs, P.J.1    Bronstein, L.R.2
  • 26
    • 0031957741 scopus 로고    scopus 로고
    • Selecting and implementing support groups for bereaved adults
    • Lorenz, L. (1998). Selecting and implementing support groups for bereaved adults. Cancer Practice, 6(3), 161-166.
    • (1998) Cancer Practice , vol.6 , Issue.3 , pp. 161-166
    • Lorenz, L.1
  • 27
    • 54449098611 scopus 로고    scopus 로고
    • Letting go before a death: A concept analysis
    • Lowey, S. E. (2008). Letting go before a death: A concept analysis. Journal of Advanced Nursing, 63(2), 208-215.
    • (2008) Journal of Advanced Nursing , vol.63 , Issue.2 , pp. 208-215
    • Lowey, S.E.1
  • 28
    • 33845797510 scopus 로고    scopus 로고
    • End-of-life care preferences of older adults and family memberswho care for them
    • Luptak, M. (2006). End-of-life care preferences of older adults and family memberswho care for them. Journal of SocialWork in End-of-Life & Palliative Care, 2(3), 23-44.
    • (2006) Journal of SocialWork In End-of-Life & Palliative Care , vol.2 , Issue.3 , pp. 23-44
    • Luptak, M.1
  • 30
    • 18044384993 scopus 로고    scopus 로고
    • Illness Trajectories and Palliative Care
    • Murray, S. A., Kendall, M., Boyd, K., & Sheikh, A. (2005). Illness trajectories and palliative care. BMJ, 330, 1007-1011.
    • (2005) BMJ , vol.330 , pp. 1007-1011
    • Murray, S.A.1    Kendall, M.2    Boyd, K.3    Sheikh, A.4
  • 33
    • 33749233814 scopus 로고    scopus 로고
    • Problems experienced by the informal caregivers of cancer patients and their needs for support
    • Osse, B. H. P., Vernooij-Dassen, M. J. F. J., Schade, E., & Grol, R. P. T. M. (2006). Problems experienced by the informal caregivers of cancer patients and their needs for support. Cancer Nursing, 29(5), 378-388.
    • (2006) Cancer Nursing , vol.29 , Issue.5 , pp. 378-388
    • Osse, B.H.P.1    Vernooij-Dassen, M.J.F.J.2    Schade, E.3    Grol, R.P.T.M.4
  • 34
    • 0038646713 scopus 로고    scopus 로고
    • The psychological impact of cancer on patients' partners and other key relatives: A review
    • Pitceathly, C., & Maguire, P. (2003). The psychological impact of cancer on patients' partners and other key relatives: A review. European Journal of Cancer, 39, 1517-1524.
    • (2003) European Journal of Cancer , vol.39 , pp. 1517-1524
    • Pitceathly, C.1    Maguire, P.2
  • 36
    • 1642458586 scopus 로고    scopus 로고
    • Supporting family caregivers at the end of life: They don't know what they don't know
    • 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. JAMA, 291, 483-491.
    • (2004) JAMA , vol.291 , pp. 483-491
    • Rabow, M.W.1    Hauser, J.M.2    Adams, J.3
  • 38
    • 23844437924 scopus 로고    scopus 로고
    • Family perceptions of prognosis, silence, and the "suddenness" of death
    • Russ, A. J., & Kaufman, S. R. (2005). Family perceptions of prognosis, silence, and the "suddenness" of death. Culture, Medicine and Psychiatry, 29, 103-123.
    • (2005) Culture, Medicine and Psychiatry , vol.29 , pp. 103-123
    • Russ, A.J.1    Kaufman, S.R.2
  • 39
    • 33748348663 scopus 로고    scopus 로고
    • Group bereavement support for spouses who are grieving the loss of a partner to cancer
    • Schneider, R. M. (2006). Group bereavement support for spouses who are grieving the loss of a partner to cancer. Social Work with Groups, 29(2), 259-278.
    • (2006) Social Work With Groups , vol.29 , Issue.2 , pp. 259-278
    • Schneider, R.M.1
  • 40
    • 33746135763 scopus 로고    scopus 로고
    • Would you like to talk about your future treatment options? Discussing the transition from curative cancer treatment to palliative care
    • Schofield, P., Carey, M., Love, A., Nehill, C., & Wein, S. (2006). Would you like to talk about your future treatment options? Discussing the transition from curative cancer treatment to palliative care. Palliative Medicine, 20, 397-406.
    • (2006) Palliative Medicine , vol.20 , pp. 397-406
    • Schofield, P.1    Carey, M.2    Love, A.3    Nehill, C.4    Wein, S.5
  • 41
    • 38549172172 scopus 로고    scopus 로고
    • Bereavement after caregiving
    • Schulz, R., Herbert, R., & Boerner, K. (2008). Bereavement after caregiving. Geriatrics, 63(1), 20-22.
    • (2008) Geriatrics , vol.63 , Issue.1 , pp. 20-22
    • Schulz, R.1    Herbert, R.2    Boerner, K.3
  • 42
    • 85016983516 scopus 로고    scopus 로고
    • Reciprocal suffering: The need to improve family caregivers' quality of life through palliative care
    • Sherman, D. W. (1998). Reciprocal suffering: The need to improve family caregivers' quality of life through palliative care. Journal of Palliative Medicine, 1, 357-366.
    • (1998) Journal of Palliative Medicine , vol.1 , pp. 357-366
    • Sherman, D.W.1
  • 43
    • 54049132508 scopus 로고    scopus 로고
    • Improving generalist end of life care: National consultation with practitioners, commissioners, academics, and service user groups
    • Shipman, C., Gysels, M., White, P., Worth, A., Murray, S. A., Barclay, S.,. . . Higginson, I. J. (2008). Improving generalist end of life care: National consultation with practitioners, commissioners, academics, and service user groups. BMJ, 337, 848-855.
    • (2008) BMJ , vol.337 , pp. 848-855
    • Shipman, C.1    Gysels, M.2    White, P.3    Worth, A.4    Murray, S.A.5    Barclay, S.6    Higginson, I.J.7
  • 45
    • 0035154932 scopus 로고    scopus 로고
    • How successful are oncologists in identifying patient distress, perceived social support, and need for psychosocial counseling?
    • Sollner, W., DeVries, A., Steixner, E., Lukas, P., Sprinzi, G., Rumpold, G., & Maislinger, S. (2001). How successful are oncologists in identifying patient distress, perceived social support, and need for psychosocial counseling? British Journal of Cancer, 84(2), 179-185.
    • (2001) British Journal of Cancer , vol.84 , Issue.2 , pp. 179-185
    • Sollner, W.1    Devries, A.2    Steixner, E.3    Lukas, P.4    Sprinzi, G.5    Rumpold, G.6    Maislinger, S.7
  • 46
    • 37849023146 scopus 로고    scopus 로고
    • Factors influencing family caregivers' ability to cope with providing end-of-life cancer care at home
    • Stajduhar, K. I., Martin, W. L., Barwich, D., & Fyles, G. (2008). Factors influencing family caregivers' ability to cope with providing end-of-life cancer care at home. Cancer Nursing, 31(1), 77-85.
    • (2008) Cancer Nursing , vol.31 , Issue.1 , pp. 77-85
    • Stajduhar, K.I.1    Martin, W.L.2    Barwich, D.3    Fyles, G.4
  • 48
    • 0034881825 scopus 로고    scopus 로고
    • Patient-focused, family-centered end-of-life medical care: Views of the guidelines and bereaved family members
    • Teno, J. M., Casey, V. A., Welch, L. C., & Edgman-Levitan, S. (2001). Patient-focused, family-centered end-of-life medical care: Views of the guidelines and bereaved family members. Journal of Pain and Symptom Management, 22(3), 738-751.
    • (2001) Journal of Pain and Symptom Management , vol.22 , Issue.3 , pp. 738-751
    • Teno, J.M.1    Casey, V.A.2    Welch, L.C.3    Edgman-Levitan, S.4
  • 50
    • 29244438140 scopus 로고    scopus 로고
    • Bereaved family member perceptions of quality of end-of-life care in U.S. regions with high and low usage of intensive care unit care
    • Teno, J. M., Mor, V., Ward, N., Roy, J., Clarridge, B., Wennberg, J. E., & Fisher, E. S. (2005). Bereaved family member perceptions of quality of end-of-life care in U.S. regions with high and low usage of intensive care unit care. Journal of the American Geriatrics Society, 53, 1905-1911.
    • (2005) Journal of the American Geriatrics Society , vol.53 , pp. 1905-1911
    • Teno, J.M.1    Mor, V.2    Ward, N.3    Roy, J.4    Clarridge, B.5    Wennberg, J.E.6    Fisher, E.S.7
  • 51
    • 6944243169 scopus 로고    scopus 로고
    • What's in a name: Who is a cancer survivor?
    • Twombly, R. (2004). What's in a name: Who is a cancer survivor? Journal of the National Cancer Institute, 96(19), 1414-1415.
    • (2004) Journal of the National Cancer Institute , vol.96 , Issue.19 , pp. 1414-1415
    • Twombly, R.1
  • 53
    • 3442901671 scopus 로고    scopus 로고
    • Individual telephone support for family caregivers of seriously ill cancer patients
    • Walsh, S.M., Estrada, G. B., & Hogan, N. (2004). Individual telephone support for family caregivers of seriously ill cancer patients. MEDSURG Nursing, 13(3), 181-189.
    • (2004) MEDSURG Nursing , vol.13 , Issue.3 , pp. 181-189
    • Walsh, S.M.1    Estrada, G.B.2    Hogan, N.3
  • 54
    • 0033032493 scopus 로고    scopus 로고
    • Family caregiver quality of life: Differences between curative and palliative cancer treatment settings
    • Weitzner, M. A., McMillan, S. C., & Jacobsen, P. B. (1999). Family caregiver quality of life: Differences between curative and palliative cancer treatment settings. Journal of Pain and Symptom Management, 17(6), 418-428.
    • (1999) Journal of Pain and Symptom Management , vol.17 , Issue.6 , pp. 418-428
    • Weitzner, M.A.1    McMillan, S.C.2    Jacobsen, P.B.3
  • 55
    • 0036041619 scopus 로고    scopus 로고
    • Advanced home care for cancer patients at the end of life: A qualitative study of hopes and expectations of family caregivers
    • Wennman-Larsen, A., & Tishelman, C. (2002). Advanced home care for cancer patients at the end of life: A qualitative study of hopes and expectations of family caregivers. Scandinavian Journal of Caring Sciences, 16, 240-247.
    • (2002) Scandinavian Journal of Caring Sciences , vol.16 , pp. 240-247
    • Wennman-Larsen, A.1    Tishelman, C.2
  • 56
    • 33846084176 scopus 로고    scopus 로고
    • End-of-life care: Findings from a national survey of informal caregivers
    • Wolff, J. L., Dy, S. M., Frick, K. D., & Kasper, J. D. (2007). End-of-life care: Findings from a national survey of informal caregivers. Archives of Internal Medicine, 167, 40-46.
    • (2007) Archives of Internal Medicine , vol.167 , pp. 40-46
    • Wolff, J.L.1    Dy, S.M.2    Frick, K.D.3    Kasper, J.D.4
  • 57
    • 53749094921 scopus 로고    scopus 로고
    • Associations between end-of-life discussions, patient mental health, medical care near death, and caregiver bereavement adjustment
    • Wright, A. A., Zhang, B., Ray, A., Mack, J. W., Trice, E., Balboni, T.,. . . Prigerson, H. G. (2008). Associations between end-of-life discussions, patient mental health, medical care near death, and caregiver bereavement adjustment. JAMA, 300(14), 1665-1673.
    • (2008) JAMA , vol.300 , Issue.14 , pp. 1665-1673
    • Wright, A.A.1    Zhang, B.2    Ray, A.3    Mack, J.W.4    Trice, E.5    Balboni, T.6    Prigerson, H.G.7


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