Psychosocial Issues in HIV/AIDS Palliative Care
Articles
Coleman, C. (1999). Spirituality, psychological well-being, and HIV symptoms for African Americans living with HIV disease
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. J Assoc Nurs AIDS Care 10(1): 42-50.
PubMed Abstract.
Nannis, E., Patterson, T. & Semple, S. (1997). Coping with HIV disease among seropositive women: Psychosocial correlates
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. Women Health 25(1): 1-22.
PubMed Abstract.
Patrick, D., Engelberg, R. & Curtis, J. (2001). Evaluating the quality of dying and death
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. Journal of Pain and Symptom Management 22(3): 717-726.
PubMed Abstract.
Pierson, C.. Curtis, J. & Patrick, D. (2002). A good death: A qualitative study of patients with advanced AIDS
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. AIDS Care 14(5): 587-98.
PubMed Abstract.
Sarna, L., van Servellen, G., Padilla, G. & Brecht, M. (1999). Quality of life in women with symptomatic HIV/AIDS
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. J Adv Nurs 30: 597-605.
PubMed Abstract.
Schietinger, H. (1998). Psychosocial support for people living with HIV/AIDS
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. Discussion Papers on HIV/AIDS Care and Support (5): This is a 1998 discussion paper, prepared by the Health Technical Services Project of TvT. www.synergyaids.com/documents/408_care5.pdf.
Serovich, J., Bruckner, P. & Kimberly, J. (2000). Barriers to social support for persons living with HIV/AIDS
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. AIDS Care 12(5): 651-662.
PubMed Abstract.
Singer, P., Martin, D. & Kelner, M. (1999). Quality end-of-life care: Patient’s perspectives
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. JAMA 281(2): 163-168.
PubMed Abstract.
Steinhauser, K., Christakis, N., Clipp, E., McNeilly, M., Grambow, S., et al. (2001). Preparing for the end of life: Preferences of patients, families, physicians, and other care providers
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. J Pain Symptom Manage 22(3): 727-37.
PubMed Abstract.
Steinhauser, K., Christakis, N., Clipp, E., McNeilly, M., McIntyre, L. & Tulsky, J. (2000). Factors considered important at the end of life by patients, family, physicians, and other care providers
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. JAMA 284(19): 2476-82.
PubMed Abstract.
Steinhauser, K., Clipp, E., McNeilly, M., Christakis, N., McIntyre, L. & Tulsky, J. (2000). In search of a good death: Observations of patients, families, and providers
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. Ann Intern Med 132: 825-32.
PubMed Abstract.
Teno, J., Casey, V., Welch, L. & Edgman-Levitan, S. (2001). Patient-focused, family-centered end-of-life medical care: Views of the guidelines and bereaved family members
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. Journal of Pain and Symptom Management 22(3): 738-51.
PubMed Abstract.
Trillin, A. (1981). Of dragons and garden peas: A cancer patient talks to doctors
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. NEJM 304(12): 699-701.
PubMed Abstract.
Wenrich, M., Curtis, J., Ambrozy, D., Carline, J., Shannon, S. & Ramsey, P. (2003). Dying patients' need for emotional support and personalized care from physicians: perspectives of patients with terminal illness, families, and health care providers
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. Journal of Pain and Symptom Management 25(3): 236-246.
PubMed Abstract.
Books
Aronstein, D. & Thompson, B. (1998). HIV and social work: A practitioner's guide (psychosocial issues of HIV/AIDS). New York, NY: Haworth Press.
Catalaan, J., Sherr, L. & Hedge, B. (1997). The impact of AIDS: Psychological and social aspects of HIV infection. Newark, NJ: Harwood Academic Publishers.
Dean, L. (1995). The epidemiology and impact of AIDS-related death and dying in New York's gay community, pp. 29-42. In: Sherr, L., (Eds.). Grief and AIDS. New York, NY: John Wiley & Sons.
Ferris, F., Flannery, J., McNeal, H., Morissette, M., Cameron, R. & Bally, G. (1995). A comprehensive guide for the care of persons with HIV disease. Toronto, Ont: Mount Sinai Hospital and Casey House Hospice.
Lloyd, G. & Fimbres, M. (1993). The changing face of AIDS: Implications for social work practice. Westport, CT: Auburn House.
Meyer, C. (2000). A good death: Challenges, choices, and care options. Mystic, CT: Twenty-Third Publications.
O'Leary, A. & Jermmott, L. (1996). Women and AIDS: Coping and care. New York, NY: Plenum Press.
Stein, T. (1998). The social welfare of women and children with HIV and AIDS. New York, NY: Oxford University Press.
Last Updated 7/22/03 at 1:31 PM
