You are here: Home Search Researchers

ResearchCrossroads

RCID: 755118
Link to this profile: http://www.researchcrossroads.org/Researchers/755118

SUSAN C MILLER
BROWN UNIVERSITY


Department
Center For Gerontology And Health Care Research

Degrees
Ph.D.
MBA (Health Services Management)

Interests
End-of-life care
Long-term care
Access and utilization
Health care policy

All Funding
$ 310,096


Biography


Dr. Susan Miller is Associate Professor of Community Health (Research) at The Warren Alpert Medical School of Brown University. She is a gerontologist and epidemiologist whose research focuses on nursing home end-of-life care, hospice care, and long-term care access and utilization (especially at the end of life). Dr. Miller’s recent research includes an applied policy study aimed at understanding how state policies and practices influence access to and quality of palliative care/hospice for persons receiving long-term care services
a RWJ-funded study to identify and disseminate nursing home/hospice “collaborative solutions
” and research funded by the National Institute on Aging to develop a model for predicting mortality for persons with advanced dementia (so to identify earlier the need for palliative care/hospice).


Grants (Principal Investigator)

Grants for which SUSAN C MILLER acted as the principal investigator
Title/Granting Organization
Fiscal Years
Total Funding
Hospice Enrollment And Ltc Policy (help)
    Agency for Health Care Research and Quality(AHRQ)2007
Factors Associated With Hospice Utilization
    Agency for Health Care Research and Quality(AHRQ)2000
Nursing Home Care At The End-of-life: Cost & Quality
    Agency for Health Care Research and Quality(AHRQ)2000$ 310,096
Allied Health Project Grants
    Unknown1993


Publications


1.Miller, SC. 1983. Documentation in the hospice medical record - survey results.
Journal of the American Medical Record Association, November:17-24.

2.Miller, SC. 1983. Medical record-related practices in hospices - survey results. Journal of the American Medical Record Association, December:18-29.

3. Miller, SC. 1985. Hospice medical record documentation and management: opportunity for improvement. Topics in Health Record Management, March:13-23.

4. Miller, SC. 1985. Home care project survey data - part I. Journal of the American Medical Record Association, November:21-8.

5. Miller, SC. (1985). Home care project survey data - Part II. Journal of the American Medical Record Association, December, 21-26.

6. Benjamin, CD & Miller, SC. 1988. Model approach for a community clinic information system. Topics in Health Record Management, 8 (3):65-71.

7. Miller, S.C. 1992. Multiple transfers between care settings: is there an alternative for the frail elderly? The Journal of Health Information Management Research, 1(2):32-43.

8. Brody, JA, Grant, MD, Frateschi, LJ, Miller, SC, Zhang, H. 1998. Epidemiology and
aging: Maximum reproductive age unaffected by increased life expectancy in the twentieth century. Aging Clinical and Experimental Research, 10 (2):170-1.

9. Miller SC, Prohaska TR. Furner SE, Freels S, Brody, JA, Levy PS. 1998. Time to
nursing home admission for persons with Alzheimer’s disease: The effect of health care
system characteristics. Journal of Gerontology: Social Sciences, 53B (6): S341-S353.

10. Miller SC, Mor V, Coppola K, Teno J, Laliberte L, Petrisek AC. 1998. The Medicare Hospice Benefit's influence on Dying in nursing homes, Journal of Palliative Medicine, 1 (4):367-376.

11. Miller SC, Prohaska TR, Furner SE. 1999. Nursing home admission for African
Americans with Alzheimer’s Disease, the Journals of Gerontology: Medical Sciences, 54A(7): M365-369.
12. Brody JA, Grant MA, Frateschi LJ, Miller SC, Zhang H. 2000. Reproductive longevity
and increased life expectancy. Age and Aging, 29: 75-78.

13. Fennell, M, Miller SC, Mor V. 2000. Facility effects on racial differences in nursing home quality, American Journal of Medical Quality, 15(4): 174-181.

14. Miller SC, Gozalo P, Mor V. 2001. Hospice enrollment and hospitalization of dying
nursing home patients. American Journal of Medicine, 111:38-44.

15. Miller SC, Mor V. 2001. The emergence of Medicare hospice care in U.S. Nursing Homes, Palliative Medicine, 15: 471-480.

16. Miller SC, Mor V, Wu N, Gozola P, Lapane K. 2002. Does receipt of hospice care in nursing homes improve the management of pain at the end-of-life? The Journal of the American Geriatrics Society, 50:507-515.

17. Miller SC, Mor V. 2002. The role of hospice care in the nursing home setting, The Journal of Palliative Medicine, 5:271-277.

18. Miller, SC, Kinzbrunner B, Pettit P, Williams JR. 2003. How does the timing of hospice referral influence hospice care in the last days of life? The Journal of the American Geriatrics Society, 51:798-806.

19. Miller SC, Mor V, Teno J. 2003. Hospice Enrollment and Pain Assessment and Management in Nursing Homes. Journal of Pain and Symptom Management, 26 (3): 791--799.

20. Miller SC, Weitzen S, Kinzbrunner B. 2003. Factors Associated with the high prevalence of short hospice stays. Journal of Palliative Medicine, 6 (5): 725--736.

21. Wu N, Miller SC. 2003. Lapane K, Gozalo P. The problem of assessment bias when measuring the hospice effect on nursing home residents’ pain, Journal of Pain and Symptom Management, 26 (5): 998-1009.

22. Miller SC. 2004. Hospice care in nursing homes: How does site of care influence visit
volume? Journal of American Geriatrics Society, 52: 1331-1336.

23. Miller SC, Intrator O, Gozalo P, Roy J, Barber J, Mor V. 2004. Government
expenditures at the end-of-life for short and long-stay nursing home residents:
Differences by hospice enrollment, Journal of American Geriatrics Society, 52: 1284-92.

24. Mor V, Zinn J, Angelleli J, Teno J, Miller S. 2004. Driven to tiers: Socioeconomic and
racial disparities in the quality of nursing home care. The Milbank Quarterly, 82(2):227-
56.

25. Miller SC, Mor V, Teno J. 2004. Hospice and palliative care in long-term care
facilities. In: Emanuel, L. Clinics in Geriatric Medicine: End-of-Life Care, 20: 717-34.

26. Miller SC, Mor V. 2004. The opportunity for collaborative care provision: Nursing
homes contracting with hospices in U.S. states, Journal of Pain and Symptom Management, 28: 537-47.

27. Mitchell SL, Teno JM, Miller SC, Mor V. 2005. A national study of the location of death for older persons with dementia. Journal of American Geriatrics Society, 53: 299-305.

28. Mor, V, Papandonatos G, Miller SC. 2005. End-of-life hospitalization for African-
American and non-Latino White nursing home residents: Variation by race and a facility’s racial composition. Journal of Palliative Medicine, 8: 58-68.

29. Wu N, Miller SC, Lapane K, Roy J, Mor V. 2005. The quality of the quality indicator
of unmanaged pain derived from the Minimum Data Set (MDS). Journal of Health Services Research, 4: 1197-1216.

30. Wu N, Miller SC, Lapane K, Roy J, Mor V. 2005. Impact of cognitive function on
assessments of nursing home residents’ pain. Medical Care, 43: 934-39.

31. Miller SC and Ryndes T. 2005. Quality of life at the end of life: The public health
perspective. Generations. 29: 41-47.

32. Shield RS, Wetle T, Teno J, Miller SC, Welch L. 2005. Physicians “missing in action:”
Family Perspectives on physician and staffing problems in end-of-life care in the nursing
home. Journal of American Geriatric Society. J Am Geriatr Soc. 53: 1651-7.

33. Wetle T, Shield RS, Teno J. Miller SC, Welch L. 2005. Family perspectives on end-of-
life care experiences in nursing homes, Gerontologist. 45: 642-50.

34. Schockett ER, Teno JM, Miller SC, Stuart B. 2005. Late Referral to Hospice and Bereaved Family Member Perception of Quality of End of Life Care. Journal of Pain and Symptom Management. 30: 400-07.

36. Gruneir A, Miller SC. 2006. Hospice care in the nursing home: Changes in visit volume from enrollment to discharge among longer-stay residents. Journal of Pain and Symptom Management, 32(5):478-87.

37. Miller SC. Papandonatos G, Fennell M, Mor V. 2006. Facility and county effects on
racial differences in nursing home quality indicators, Social Science and Medicine,63(12):3046-59.

38. Gozalo P, Miller SC. 2007. Hospice Enrollment and Evaluation of its Causal Effect on Hospitalization of Dying Nursing Home Patients. Health Serv Res., 42(2): 587-610.

39. Intrator O, Grabowski D, Zinn J, Schleinitz M, Feng Z, Miller S, Mor V. 2007.
Hospitalizations of Nursing Home Residents: The Effects of States’ Medicaid Payment
and Bedhold Policies. Health Serv Res, 42: 1651-1671.

40. Mitchell SL, Kiely D, Miller SC, Connor S, Spence C, Teno J. 2007. Hospice Care for
Patients with Dementia. Journal of Pain and Symptom Management, 34: 7 – 16.

41. Gruneir A, Miller SC, Intrator O, Mor V. 2007. Hospitalization of Nursing Home Residents with Cognitive Impairments: The Influence of Organizational Features and State Policies. The Gerontologist, 47: 447-456.

42. Gruneir A, Lapane KL, Miller SC, Mor V. Long-Term Care Market Competition and
Nursing Home Dementia Special Care Units. Medical Care, IN PRESS.

43. Gozalo P, Miller SC, Intrator O, Roy J, Barber J, Mor V. Hospice Effect on Government Expenditures among Nursing Home Residents. Health Services Research, IN PRESS.

43. Gruneir A, Miller SC, Feng Z, Intrator, O, Mor V. The Effect of State Medicaid
Policies and Nursing Home Racial Composition on the Risk of Hospitalization for Black and White Residents. Health Services Research, IN PRESS.

44. Gruneir A, Lapane K, Miller SC, Mor V. Is dementia care really special? A new way
of looking at an old question. Journal of American Geriatrics Society, IN PRESS.



Patents

Search USPTO for SUSAN C MILLER Patents