Patterns in primary health care utilization among individuals with intellectual and developmental disabilities in Florida

Intellectual and Developmental Disabilities

Volumn 45, Issue 5, 2007, Pages 310-322

  Hall, Allyson ^a   Wood, David ^b   Hou, Tao ^c   Zhang, Jianyi ^a  

^a UNIVERSITY OF FLORIDA HEALTH   (United States)

^b UNIVERSITY OF FLORIDA   (United States)

^c UNIVERSITY OF NORTH FLORIDA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; DEVELOPMENTAL DISORDER; FEMALE; GEOGRAPHY; HUMAN; MALE; MEDICAID; MENTAL DEFICIENCY; MIDDLE AGED; PATIENT CARE; PRIMARY HEALTH CARE; UNITED STATES; UTILIZATION REVIEW;

ADOLESCENT; ADULT; CHILD; CONTINUITY OF PATIENT CARE; DEVELOPMENTAL DISABILITIES; FEMALE; FLORIDA; GEOGRAPHY; HUMANS; MALE; MEDICAID; MENTAL RETARDATION; MIDDLE AGED; PRIMARY HEALTH CARE;

EID: 35148839006     PISSN: 19349556     EISSN: None     Source Type: Journal    
DOI: 10.1352/0047-6765(2007)45[310:PIPHCU]2.0.CO;2     Document Type: Article

References (32)

1. Alvarez, N. (2004). Epilepsy in children with mental retardation. Retrieved March 17, 2006, from http://www.emedicine.com/neuro/topic550.htm
2. American Academy of Pediatrics. Medical Home Initiatives for Children with Special Health Care Needs Project Advisory Committee. (2002). The medical home. Pediatrics, 110, 184-186.
3. American Academy of Pediatrics. Committee on Children with Disabilities. (1999). Care coordination: Integrating health and related systems of care for children with special health care needs. Pediatrics, 104, 978-981.
4. American College of Physicians. (2004). Patient-centered, guided care for the chronically ill. The American College of Physicians. Prescription for change (Public Policy Paper). Philadelphia: American College of Physicians.
5. Batshaw, M. L., & Perret, Y. M. (1992). Children with disabilities: A medical primer (3rd ed.). Baltimore: Brookes.
6. Betz, C. L., Baer, M. T., Poulsen, M., Vahanvaty, U., & Bare, M. (2004) Secondary analysis of primary and preventive services accessed and perceived service barriers by children with developmental disabilities and their families. Issues in Comprehensive Pediatric Nursing, 27, 83-106.
7. Bindman, A. B., Grumbach, K., Osmond, D., Vranizan, K., & Stewart, A. L. (1996). Primary care and the receipt of preventive services. Journal of General Internal Medicine, 11(5), 269-276.
8. Choi, K. H., & Wynne, M. E. (2000). Providing services to Asian Americans with developmental disabilities and their families: Mainstream service providers' perspective. Community Mental Health Journal, 36, 589-595.
9. Cooley, W. C., & McAllister, J. W. (2004). Building medical homes: Improvement strategies in primary care for children with special health care needs. Pediatrics, 113(Suppl), 1499-1506.
10. Coucouvanis, K., Prouty, R. W., Bruininks, R. H., & Lakin, K. C. (2006). Current populations and longitudinal trends of state residential settings (1950-2005). In R. W. Prouty, G. Smith, & K. C. Lakin (Eds.), Residential services for persons with developmental disabilities: Status and trends through 2005. Minneapolis: University of Minnesota, Research and Training Center on Community Living, Institute on Community Integration.
11. DeVoe, J. E., Fryer, G. E., Phillips, R., & Green, L. (2003). Receipt of preventive care among adults: Insurance status and usual source of care. American Journal of Public Health, 93, 786-791.
12. Ferrer, R. L., Hambidge, S. J., & Maly, R. C. (2005). The essential role of generalists in health care systems. Annals of Internal Medicine 142(8), 691-699.
13. Forrest, C. B., & Whelan, E. M. (2000). Primary care safety-net delivery sites in the United States: A comparison of community health centers, hospital outpatient departments, and physician offices. Journal of the American Medical Association, 286(16), 2077-2083.
14. Gill, J., & Mainous, A. G. (1998). The role of provider continuity in preventing hospitalizations. Archives of Family Medicine, 7, 352-357.
15. Gill, J., Mainous, A. G., & Nsereko, M. (2000). The effect of continuity of care on emergency department use. Archives of Family Medicine, 9, 333-338.
16. Grumbach, K., & Bodenheimer, T. (2002). A primary care home for Americans. Putting the house in order. Journal of the American Medical Association, 288(7), 889-893.
17. Harum, K. H. (2006). Mental retardation e-Medicine. Retrieved April 17, 2006, http://www.emedicine.com/neuro/topic605.htm
18. Havercamp, S. M., Scandlin, D., & Roth, M. (2004). Health disparities among adults with developmental disabilities, adults with other disabilities, and adults not reporting disability in North Carolina. Public Health Reports, 119, 418-426.
19. Horwitz, S. M., Kerker, B. D., Owens, P. L., & Zigler, E. (2000). The health status and needs of individuals with mental retardation (Rep. to Special Olympics). Washington, DC. Special Olympics.
20. Institute of Medicine. (1996). Primary care: America's health in a new era. Washington, DC: National Academy Press.
21. Janicki, M. P., Davidson, P. W., Henderson, C. M., McCallion, P., Taets, J. D., Force, L. T., Sulkes, S. B., Frangenberg, E., & Ladrigan, P. M. (2002). Health characteristics and health services utilization in older adults with intellectual disability living in community residences. Journal of Intellectual Disability Research, 46, 287-298.
22. Kastner, T. A., & Walsh, K. K. (2006). Medicaid managed care model of primary care and health care management for individuals with developmental disabilities. Mental Retardation, 44, 41-55.
23. Larson, A., Lakin, K. C., Anderson, L., Kwak, L., & Anderson, D. (2001). Prevalence of mental retardation and developmental disabilities: Estimates from the 1994/1995 National Health Interview Survey Disability Supplements. American Journal on Mental Retardation, 106, 231-252.
24. Lewis, M. A., Lewis, C. E., Leake, B., King, B. H., & Lindemann, R. (2002). The quality of health care for adults with developmental disabilities. Public Health Reports, 117, 174-184.
25. Liptak, G. S., Orlando, M., Yingling, J. T., Karin, M. S., Theurer-Kaufman, L., Malay, D. P., Tompkins, L. A., & Flynn, J. (2006). Satisfaction with primary health care received by families of children with developmental disabilities. Journal of Pediatric Health Care, 20(4), 245-252.
26. Long, S., Coughlin, T. A., & Kendall, S. J. (2002). Access to care among disabled adults on Medicaid. Health Care Financing Review, 23(4), 159-173.
27. Melville, C. A., Cooper, S-A., Morrison, J., Finlayson, J., Allan, L., Robinson, N., Burns, E., & Martin, G. (2006). The outcomes of an intervention study to reduce the barriers experienced by people with intellectual disabilities accessing primary health car services. Journal of Intellectual Disability Research, 50, 11-17.
28. Melville, C. A., Finlayson, J., Cooper, S-A., Allan, L., Robinson, N., Burns, E., Martin, G., & Morrison, J. (2005). Enhancing primary health care services for adults with intellectual disabilities. Journal of Intellectual Disability Research, 49, 190-198.
29. Reichard, A., Sacco, T. M., & Turnbull, H. R. (2004). Access to health care for individuals with developmental disabilities from minority backgrounds. Mental Retardation, 42, 459-470.
30. Reichard, A., & Turnbull, H. R. (2004). Perspectives of physicians, families, and case managers concerning access to health care by individuals with developmental disabilities. Mental Retardation, 42, 181-194.
31. Starfield, B. (1998). Primary care. Balancing health needs, services, and technology. New York: Oxford University Press.
32. U.S. Department of Health and Human Services. (2002). Closing the gap: A national blueprint to improve the health of persons with mental retardation. (Rep. of the Surgeon General's Conference on Health Disparities and Mental Retardation). Rockville, MD: U.S. Department of Health and Human Services, PHS, Office of the Surgeon General, Washington, DC. http://nichd.nih.gov/ publications/