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N. Allcock , J. McGarry , & R. Elkan (2002). Management of pain in older people within the nursing home: A preliminary study. Health & Social Care in the Community, 10, 464–471.
K.O. Anderson , T.R. Mendoza , V. Valero , (2000). Minority cancer patients and their providers: Pain management attitudes and practice. Cancer, 88, 1929–1938.
R.R. Baier , D.R Gifford ., G. Patry , (2004). Ameliorating pain in nursing homes: A collaborative quality-improvement project. Journal of the American Geriatrics Society, 52, 1988–1995.
J.T. Berger (1998). Culture and ethnicity in clinical care. Archives of Internal Medicine, 158, 2085–2090.
L. Crawley , R. Payne , J. Bolden , (2000). Palliative and end-of-life care in the African American community. JAMA, 284, 2518–2521.
H.B. Degenholtz , R.A. Arnold , A. Meisel , & J.R. Lave (2002). Persistence of racial disparities in advance care plan documents among nursing home residents. Journal of the American Geriatrics Society, 50, 378–381.
V.F. Engle , E. Fox-Hill , & M.J. Graney (1998). The experience of living-dying in a nursing home: Self-reports of black and white older adults. Journal of the American Geriatrics Society, 46, 1091–1096.
B.A. Ferrell (1993). The assessment and control of pain in the nursing home. In Improving Care in the Nursing Home: Comprehensive Reviews of Clinical Research, L.Z. Rubenstein (ed.), pp. 241–250. Thousand Oaks, CA: Sage Publications.
B.A. Ferrell (1995). Pain evaluation and management in the nursing home. Annals of Internal Medicine, 123, 681–687.
L.C. Hanson , K.S. Reynolds , M. Henderson , (2005). A quality improvement intervention to increase palliative care in nursing homes. Journal of Palliative Medicine, 8, 576–584.
M.B. Happ , E. Capezuti , N.E. Strumpf , (2002). Advance care planning and end-of-life care for hospitalized nursing home residents. Journal of the American Geriatrics Society, 50, 829–835.
F.P. Hopp (2000). Preferences for surrogate decision makers, informal communication, and advance directives among community-dwelling elders: Results from a national study. Gerontologist, 40, 449–457.
F.P. Hopp & S.A. Duffy (2000). Racial variations in end-of-life care. Journal of the American Geriatrics Society, 48, 658–663.
M. Kagawa Singer & L.J. Blackhall (2001). Negotiating cross-cultural issues at the end of life: “You got to go where he lives”. JAMA, 286, 2993–3001.
D.K. Kiely , S.L. Mitchell , A. Marlow , K.M. Murphy , & J.N. Morris (2001). Racial and state differences in the designation of advance directives in nursing home residents. Journal of the American Geriatrics Society, 49, 1346–1352.
C.R. Kovach , D.E. Weissman , J. Griffie , (1999). Assessment and treatment of discomfort for people with late-stage dementia. Journal of Pain & Symptom Management, 18, 412–419.
N. Lurie , A.M. Pheley , S.H. Miles , (1992). Attitudes toward discussing life-sustaining treatments in extended care facility patients. Journal of the American Geriatrics Society, 40, 1205–1208.
D.H. Mark , J. Bahr , E.H. Duthie , (1995). Characteristics of residents with do-not-resuscitate orders in nursing homes. Archives of Family Medicine, 4, 463–467.
S.C. Miller & V. Mor (2004). The opportunity for collaborative care provision: The presence of nursing home/hospice collaborations in the U.S. Journal of Pain and Symptom Management, 28, 537–547.
S.L. Mitchell , D.K. Kiely , & M.B. Hamel (2004). Dying with advanced dementia in the nursing home. Archives of Internal Medicine, 164, 321–326.
R.S. Morrison , L.H. Zayas , M. Mulvihill , (1998). Barriers to completion of health care proxies: An examination of ethnic differences. Archives of Internal Medicine, 158, 2493–2497.
L.A. O'Brien , J.A. Grisso , G. Maislin , (1995). Nursing home residents' preferences for life-sustaining treatments. JAMA, 274, 1775–1779.
D.P. Oliver , D. Porock , & S. Zweig (2005). End-of-life care in US nursing homes: A review of the evidence. Journal of the American Medical Directors Association, 6(Suppl.), S20–S30.
E. Phipps , G. True , D. Harris , (2003). Approaching the end of life: Attitudes, preferences, and behaviors of African-American and white patients and their family caregivers. Journal of Clinical Oncology, 21, 549–554.
K.S. Reynolds , M. Henderson , A. Schulman , & L.C. Hanson (2002). Needs of the dying in nursing homes. Journal of Palliative Medicine, 5, 895–901.
P.A. Singer , D.K. Martin , & M. Kelner (1999). Quality end-of-life care: Patients' perspectives. JAMA, 281, 163–168.
W.M. Stein (2001). Pain in the nursing home. Clinics in Geriatric Medicine, 17, 575–594.
K.E. Steinhauser , N.A. Christakis , E.C. Clipp , (2000). Factors considered important at the end of life by patients, family, physicians, and other care providers. JAMA, 284, 2476–2482.
J.M. Teno (2004). Do-not-resuscitate orders and hospitalization of nursing home residents: Trumping, neglect, or shared decision-making at the eleventh hour. Journal of the American Geriatrics Society, 52, 159–160.
J.M. Teno , S. Weitzen , T. Wetle , (2001). Persistent pain in nursing home residents. JAMA, 285, 2081.
M. Terry & S. Zweig (1994). Prevalence of advance directives and do-not-resuscitate orders in community nursing facilities. Archives of Family Medicine, 3, 141–145.
A. Won , K. Lapane , G. Gambassi , (1999). Correlates and management of nonmalignant pain in the nursing home. Journal of the American Geriatrics Society, 47, 936–942.