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Delivering palliative care to patients and caregivers in inner-city communities: Challenges and opportunities

Published online by Cambridge University Press:  24 October 2013

Karen Kayser*
Affiliation:
Graduate School of Social Work, Boston College, Boston, Massachusetts
Rosanna F. DeMarco
Affiliation:
Connell School of Nursing, Boston College, Boston, Massachusetts
Charu Stokes
Affiliation:
Graduate School of Social Work, Boston College, Boston, Massachusetts
Susan DeSanto-Madeya
Affiliation:
Connell School of Nursing, Boston College, Boston, Massachusetts
Philip C. Higgins
Affiliation:
Graduate School of Social Work, Boston College, Boston, Massachusetts
*
Address correspondence and reprint requests to: Karen Kayser, Kent School of Social Work, University of Louisville, Oppenheimer Hall, Louisville, Kentucky 40292. E-mail: [email protected]

Abstract

Objective:

Social and economic barriers can hinder access to quality palliative and end-of-life care for patients living in inner-city communities. Using a community-based participatory research (CBPR) approach, we investigated the stresses associated with living with a chronic disease and barriers to access and utilization of palliative care resources experienced by low-income patients and caregivers in five inner-city communities.

Methods:

Four focus groups (N = 33) were conducted with community stakeholders, including healthcare professionals (social workers and nurses), persons living with chronic illnesses (e.g., HIV/AIDS, cardiovascular disease, and cancer), and caregivers. Focus group responses were analyzed using thematic analyses.

Results:

Patients' and caregivers' stresses centered around five themes: lack of family support, communication barriers with healthcare professionals, minority stress, caregiver burden, and lack of spiritual support. The community stakeholders identified resources and services to improve access to care and the quality of life of underserved, low-income populations living with chronic illnesses.

Significance of Results:

A CBPR approach enabled us to develop an interdisciplinary and culturally sensitive intervention to begin addressing the palliative and end-of-life needs of the patients and caregivers of the inner-city community.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 2013 

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References

REFERENCES

Aoun, S.M., Kristjanson, L.J., Currow, D.C., et al. (2005). Caregiving for the terminally ill: At what cost? Palliative Medicine, 19, 551555.Google Scholar
Baanders, A.N. & Heijmans, M. (2007). The impact of chronic diseases: The partner's perspective. Family and Community Health, 30, 305317.CrossRefGoogle ScholarPubMed
Bayliss, E.A., Edwards, A.E., Steiner, J.F., et al. (2008). Processes of care desired by elderly patients with multimorbidities. Family Practice, 25, 287293.Google Scholar
Biordi, D.L. (2002). Social isolation. In Chronic Illness: Impact and Interventions, 5th ed.Lubkin, I.M. & Larsen, P.D. (eds.), pp. 119145. Sudbury, MA: Jones and Bartlett.Google Scholar
Bookbinder, M., Glajchen, M., McHugh, M., et al. (2011). Nurse practitioner–based models of specialist palliative care at home: Sustainability and evaluation of feasibility. Journal of Pain and Symptom Management, 41, 2534.Google Scholar
Brown, M.A. & Powell-Cope, G. (1991). AIDS family caregiving: Transitions through uncertainty. Nursing Research, 40, 338345.CrossRefGoogle ScholarPubMed
Byock, I. & Twohig, J. (2006). Delivering palliative care in challenging settings and to hard-to-reach populations. In Textbook of Palliative Nursing, 2nd ed.Ferrell, B.R. & Coyle, N. (eds.), pp. 11091118. New York: Oxford University Press.Google Scholar
Centers for Disease Control and Prevention. (2011). Capacity building. http://www.cdc.gov/hiv/topics/cba/ (Accessed August 11, 2011).Google Scholar
Christopher, S., Watts, V., McCormick, A.K.H.G., et al. (2008). Building and maintaining trust in a community-based participatory research partnership. American Journal of Public Health, 98, 13981404.Google Scholar
Connor, S.R., Teno, J., Spence, C., et al. (2008). Family evaluation of hospice care: Results from voluntary submission of data. Journal of Pain & Symptom Management, 30, 917.Google Scholar
Davies, E. & Higginson, I.J. (eds.) (2004). Palliative Care. Copenhagen: World Health Organization.Google Scholar
DeMarco, R.F. & Segraves, M.M. (2012). Community assessment. In Community and Public Health Nursing: Evidence for Practice. Harkness, G. &. DeMarco, R. (eds.), pp. 175191. Philadelphia: Lippincott, Williams & Wilkins.Google Scholar
Dy, S.M., Reder, E.A., McHale, J.M., et al. (2003). Caring for patients in an inner-city home hospice: Challenges and rewards. Home Health Care Management & Practice, 15, 291299.Google Scholar
El Osta, B. & Bruera, B. (2006). Models of palliative care delivery. In Textbook of Palliative Medicine. Bruera, E., Higginson, I., von Gunten, C. & Ripamonti, C. (eds.), pp. 266276. New York: Oxford University Press.Google Scholar
Elsayem, A., Swint, K., Fisch, M.J., et al. (2004). Palliative care inpatient service in a comprehensive cancer center: Clinical and financial outcomes. Journal of Clinical Oncology, 22, 20082014.Google Scholar
Elsayem, A., Smith, M.L., Parmley, L., et al. (2006). Impact of a palliative care service on in-hospital mortality in a cancer center. Journal of Palliative Medicine, 9, 894902.Google Scholar
Fadul, N., Elsayem, A., Palmer, J.L., et al. (2007). Predictors of access to palliative care services among patients who died at a comprehensive cancer center. Journal of Palliative Medicine, 10, 11461152.Google Scholar
Faridi, Z., Grunbaum, J.A., Gray, B.S., et al. (2007). Community-based participatory research: Necessary next steps. Prevention in Chronic Disease, 4, A70.Google Scholar
Fatone, A.M., Moadel, A.B., Foley, F.W., et al. (2007). Urban voices: The quality-of-life experience among women of color with breast cancer. Palliative and Supportive Care, 5, 115125.Google Scholar
Ferrell, B.R., Virani, R. & Grant, M. (1998). Improving end-of-life care education in home care. Journal of Palliative Medicine, 1, 1119.Google Scholar
Ferrell, B.R., Virani, R. & Grant, M. (1999). Analysis of symptom assessment and management content in nursing textbooks. Journal of Palliative Medicine, 2, 161172.Google Scholar
Gaston, M.H., Barrett, S.E., Johnson, T.L., et al. (1998). Health care needs of medically underserved women of color: The role of the Bureau of Primary Health Care. Health and Social Work, 23, 8695.Google Scholar
Gaugler, J.E., Hanna, N., Linder, J., et al. (2005). Cancer caregiving and subjective stress: A multi-site, multi-dimensional analysis. Psycho-Oncology, 14, 771785.Google Scholar
Gysels, M. & Higginson, I. (2004). Improving Supportive and Palliative Care for Adults with Cancer: Research Evidence. London: National Institute for Clinical Excellence.Google Scholar
Harkness, G.A. & DeMarco, R.F. (eds.) (2012). Community and Public Health Nursing: Evidence for Practice. Philadelphia: Lippincott, Williams & Wilkins.Google Scholar
Hearn, J. & Higginson, I.J. (1998). Do specialist palliative care teams improve outcomes for cancer patients? A systematic literature review. Palliative Medicine, 12, 317332.Google Scholar
Higginson, I.J., Finlay, I., Goodwin, D.M., et al. (2002). Do hospital-based palliative care teams improve care for patients or families at end of life? Journal of Pain and Symptom Management, 23, 96106.Google Scholar
Hughes, A. (2005). Poverty and palliative care in the US: Issues facing the urban poor. International Journal of Palliative Nursing, 11, 613.Google Scholar
Israel, B.A., Schulz, A.J., Parker, E.A., et al. (1998). Review of community-based research: Assessing partnership approaches to improve public health. Annual Review of Public Health, 19, 173202.Google Scholar
Jablonski, A. & Wyatt, G.K. (2005). A model for identifying barriers to effective symptom management at end-of-life. Journal of Hospice and Palliative Nursing, 7, 2336.Google Scholar
Johnson, D.C., Kassner, C.T., Houser, J., et al. (2005). Barriers to effective symptom management in hospice. Journal of Pain & Symptom Management, 29, 6979.Google Scholar
Jones, L. & Wells, K. (2007). Strategies for academic and clinician engagement in community-participatory partnered research. The Journal of the American Medical Association, 297, 407410.Google Scholar
Kane, R.L., Wales, J., Berstein, L., et al. (1984). A randomized controlled trial of hospice care. The Lancet, 323, 890894.Google Scholar
Kane, R., Berstein, L., Wales, J., et al. (1985). Hospice effectives in controlling pain. The Journal of the American Medical Association, 253, 26832686.Google Scholar
Koffman, J., Burke, G., Dias, A., et al. (2007). Demographic factors and awareness of palliative care and related services. Palliative Medicine, 21, 145153.CrossRefGoogle ScholarPubMed
Krakauer, E.L., Crenner, C. & Fox, K. (2002). Barriers to optimum end-of-life care for minority patients. Journal of the American Geriatrics Society, 50, 182190.Google Scholar
Massachusetts Department of Public Health. (2007). Massachusetts deaths. http://www.mass.gov/dph/resep/resep.htm (Accessed October 26, 2009).Google Scholar
McCorkle, R., Hughes, L. & Levinson, B. (1998). Nursing interventions for newly diagnosed older cancer patients facing terminal illness. Journal of Palliative Care, 14, 3945.Google Scholar
Miller, J.F. (2000). Coping with Chronic Illness: Overcoming Powerlessness, 3rd ed.Philadelphia: F.A. Davis.Google Scholar
Minkler, M. & Wallerstein, N. (2003). Community-Based Participatory Research for Health. San Francisco: Jossey-Bass.Google Scholar
Morrison, R.S. & Meier, D.E. (2004). High rates of advance care planning in New York City's elderly population. Archives of Internal Medicine, 164, 24212426.Google Scholar
National Hospice and Palliative Care Organization. (2007). NHPCO facts and figures: Hospice care in America. http://www.caringinfo.org (Accessed September 10, 2009).Google Scholar
O'Hare, P.A., Malone, D., Lusk, E., et al. (1993). Unmet needs of black patients with cancer post-hospitalization: A descriptive study. Oncology Nursing Forum, 20, 659664.Google Scholar
O'Mahony, S., McHenry, J., Snow, D., et al. (2008). A review of barriers to utilization of the Medicare hospice benefits in urban populations and strategies for enhanced access. Journal of Urban Health, 85, 281–90.Google Scholar
Palattiyil, G. & Chakrabarti, M. (2008). Coping strategies of families in HIV/AIDS care: Some exploratory data from two developmental contexts. AIDS Care, 20, 881885.Google Scholar
Poochikian-Sarkissian, S., Sidani, S., Wenneberg, R.A., et al. (2008). Psychological impact of illness intrusiveness in epilepsy: Comparison of treatments. Psychology, Health Medicine, 13, 129145.Google Scholar
Reese, D.J., Aher, R.E., Nair, S., et al. (1999). Hospice access and use by African Americans: Addressing cultural and institutional barriers through participatory action research. Social Work, 44, 549559.Google Scholar
Reese, D.J., Melton, E. & Ciaravino, K. (2004). Programmatic barriers to providing culturally competent end-of-life care. American Journal of Hospice and Palliative Care, 21, 357364.Google Scholar
Smith, A.K., McCarthy, E.P., Paulk, E., et al. (2008). Racial and ethnic differences in advance care planning among patients with cancer: Impact of terminal illness acknowledgment, religiousness, and treatment preferences. Journal of Clinical Oncology, 26, 41314137.Google Scholar
Teno, J.M., Clarridge, B.R., Casey, V., et al. (2004). Family perspectives on end-of-life care at the last place of care. The Journal of the American Medical Association, 291, 8893.Google Scholar
Travis, S. & Piercy, K. (2002). Family caregivers. In Chronic Illness: Impact and Interventions, 5th ed.Lubkin, I.M. & Larsen, P.D. (eds.), pp. 233260. Sudbury: Jones and Bartlett.Google Scholar
Turner, H.A. & Catania, J.A. (1997). Informal caregiving to persons with AIDS in the United States: Caregiver burden among central cities residents eighteen to forty-nine years old. American Journal of Community Psychology, 25, 3559.Google Scholar
Wardlaw, L.A. (1994). Sustaining informal caregivers for persons with AIDS. Family in Society: The Journal of Contemporary Human Services, 75, 373384.Google Scholar
Watson, J., Hockley, J. & Dewar, B. (2006). Barriers to implementing an integrated care pathway for the last days of life in nursing homes. International Journal of Palliative Nursing, 12, 234240.Google Scholar
Winston, C.A., Leshner, P., Kramer, J., et al. (2005). Overcoming barriers to access and utilization of hospice and palliative care services in African-American communities. Omega, 50, 151163.Google Scholar
Zemzar, I.S. (1984). Adjustment to health loss: Implications for psychosocial treatment. In Community Health Care for Chronic Physical Illness: Issues and models. Milligan, S.M. (ed.), pp. 4448. Cleveland, OH: Case Western Reserve University Press.Google Scholar