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National Disparities in the Quality of a Medical Home for Children

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Abstract

Objectives To examine socio-demographic disparities associated with a quality medical home. Methods A nationally representative sample of children ages 0–17 years (n = 102,353) from the 2003 National Survey of Children’s Health. Risk factors including non-white race/ethnicity, income <200% of the federal poverty level (FPL), uninsured, parent education lesser than high school, and non-English primary household language, were examined in relation to a quality medical home separately and together as a “profile” of risk. Fourteen questions were used to measure five medical home features: access, continuity, comprehensiveness, family-centered care, and coordination. Quality was defined as a value greater than median for each feature and for an overall score. Results Before and after adjustment for child demographics and health status, all studied risk factors were associated with poorer quality medical home features. Uninsured [odds ratio (OR) = 0.43, 95% confidence interval (CI): 0.40–0.47] and low-income children (OR = 0.65, CI: 0.62–0.69) had among the lowest odds of a quality medical home overall and across most features, except coordination that showed an opposite trend. Summarized through risk profiles, children experiencing all five risk factors had 93% lower odds of a quality medical home overall (OR = 0.07, CI: 0.04–0.25) compared to zero risk children. Conclusion This study demonstrates large national disparities in the quality of a medical home for children. That disparities were most prevalent for the uninsured and those in or near poverty, both modifiable risk factors, suggests that reforms to increase coverage and to lift families out of poverty are essential to assuring that children have access to the full complement of appropriate health care services including a quality medical home.

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References

  1. American Academy of Pediatrics. (2004). Policy statement: Organizational principles to guide and define the child health care system and/or improve the health of all children. Pediatrics, 113(5), 1545–1547.

    Google Scholar 

  2. Medical Home Initiatives for Children with Special Needs Project Advisory Committee. (2002). The medical home. Pediatrics, 110(1), 184–186. doi:10.1542/peds.110.1.184.

    Article  Google Scholar 

  3. Starfield, B. (1992). Primary care: Concept, evaluation, and policy. New York: Oxford University Press.

    Google Scholar 

  4. U.S. Department of Health and Human Services. (2000). Healthy people 2010. Understanding and improving health (2nd ed.). Washington, DC: US Government Printing Office.

    Google Scholar 

  5. Flores, G., Olson, L., & Tomany-Korman, S. C. (2005). Racial and ethnic disparities in early childhood health and health care. Pediatrics, 115(2), e183–e193. doi:10.1542/peds.2004-1474.

    Article  PubMed  Google Scholar 

  6. Flores, G., & Tomany-Korman, S. C. (2008). Racial and ethnic disparities in medical and dental health, access to care, and use of services in US children. Pediatrics, 121(2), e286–e298. doi:10.1542/peds.2007-1243.

    Article  PubMed  Google Scholar 

  7. Halfon, N., Inkelas, M., & Wood, D. (1995). Nonfinancial barriers to care for children and youth. Annual Review of Public Health, 16, 447–472.

    Article  CAS  PubMed  Google Scholar 

  8. Newacheck, P. W., Hughes, D. C., & Stoddard, J. (1996). Children’s access to primary care: differences by race, income and insurance status. Pediatrics, 97(1), 26–32.

    CAS  PubMed  Google Scholar 

  9. Shi, L., & Stevens, G. D. (2005). Disparities in access to care and satisfaction among U.S. children: The roles of race/ethnicity and poverty status. Public Health Reports, 120(4), 431–441.

    PubMed  Google Scholar 

  10. Seid, M., Stevens, G. D., & Varni, J. W. (2003). Parents’ perceptions of pediatric primary care quality: Effects of race/ethnicity, language, and access. Health Services Research, 38(4), 1009–1031. doi:10.1111/1475-6773.00160.

    Article  PubMed  Google Scholar 

  11. Stevens, G. D., & Shi, L. (2003). Racial and ethnic disparities in the primary care experiences of children: A review of the literature. Medical Care Research. Revista de Marina (Valparaiso, Chile), 60(1), 3–30.

    Google Scholar 

  12. Elster, A., Jarosik, J., VanGeest, J., & Fleming, M. (2003). Racial and ethnic disparities in health care for adolescents: A systematic review of the literature. Archives of Pediatrics and Adolescent Medicine, 157(9), 867–874.

    Article  PubMed  Google Scholar 

  13. Strickland, B., McPherson, M., Weissman, G., van Dyck, P., Huang, Z. J., & Newacheck, P. (2004). Access to the medical home: Results of the National Survey of Children with Special Health Care Needs. Pediatrics, 113(5, suppl), 1485–1492.

    PubMed  Google Scholar 

  14. Fulda, K.G., Lykens, K., Bae, S., & Singh, K. (2008). Factors for Accessing a Medical Home Vary Among CSHCN from Different Levels of Socioeconomic Status. Maternal and Child Health Journal, Jun 11 [Epub ahead of print].

  15. Mulvihill, B. A., Altarac, M., Swaminathan, S., Kirby, R. S., Kulczycki, A., & Ellis, D. E. (2007). Does access to a medical home differ according to child and family characteristics, including special-health-care-needs status, among children in Alabama? Pediatrics, 119(Suppl 1), S107–S113. doi:10.1542/peds.2006-2089P.

    Article  PubMed  Google Scholar 

  16. Nageswaran, S., Roth, M. S., Kluttz-Hile, C. E., & Farel, A. (2006). Medical homes for children with special healthcare needs in North Carolina. North Carolina Medical Journal, 67(2), 103–109.

    PubMed  Google Scholar 

  17. Blumberg, S., Olson, L., Frankel, M., Osborn, L., Srinath, K., & Giambo, P. (2005). Design and operation of the National Survey of Children’s Health, 2003. Hyattsville: National Center for Health Statistics.

    Google Scholar 

  18. Stevens, G. D. (2006). Gradients in the health status and developmental risks of young children: The combined influences of multiple social risk factors. Maternal and Child Health Journal, 10(2), 187–199. doi:10.1007/s10995-005-0062-y.

    Article  PubMed  Google Scholar 

  19. Stevens, G. D., Seid, M., & Halfon, N. (2006). Enrolling vulnerable, uninsured but eligible children in public health insurance: Association with health status and primary care access. Pediatrics, 117(4), e751–e759. doi:10.1542/peds.2005-1558.

    Article  PubMed  Google Scholar 

  20. Stevens, G. D., Seid, M., Mistry, R., & Halfon, N. (2006). Disparities in primary care for vulnerable children: The influence of multiple risk factors. Health Services Research, 41(2), 507–531. doi:10.1111/j.1475-6773.2005.00498.x.

    Article  PubMed  Google Scholar 

  21. Larson, K., Russ, S. A., Crall, J. J., & Halfon, N. (2008). Influence of multiple social risks on children’s health. Pediatrics, 121(2), 337–344. doi:10.1542/peds.2007-0447.

    Article  PubMed  Google Scholar 

  22. Bethell, C. D., Read, D., & Brockwood, K. (2004). Using existing population-based data sets to measure the American Academy of Pediatrics definition of medical home for all children and children with special health care needs. Pediatrics, 113(5), 1529–1537.

    PubMed  Google Scholar 

  23. Starfield, B., & Shi, L. (2004). The medical home, access to care, and insurance: A review of evidence. Pediatrics, 113(5), 1493–1498.

    PubMed  Google Scholar 

  24. Hoffman, C. B., & Paradise, J. (2008). Health insurance and access to health care in the United States. Annals of the New York Academy of Sciences, 1136, 149–160.

    Google Scholar 

  25. Lillie-Blanton, M., & Hoffman, C. (2005). The role of health insurance coverage in reducing racial/ethnic disparities in health care. Health Affairs (Project Hope), 24(2), 398–408. doi:10.1377/hlthaff.24.2.398.

    Article  Google Scholar 

  26. Warfield, M. E., & Gulley, S. (2006). Unmet need and problems accessing specialty medical and related services among children with special health care needs. Maternal and Child Health Journal, 10(2), 201–216. doi:10.1007/s10995-005-0041-3.

    Article  PubMed  Google Scholar 

  27. Mayer, M. L., Skinner, A. C., & Slifkin, R. T. (2004). Unmet need for routine and specialty care: Data from the National Survey of Children with Special Health Care Needs. Pediatrics, 113(2), e109–e115. doi:10.1542/peds.113.2.e109.

    Article  PubMed  Google Scholar 

  28. Christakis, D., Mell, L., Koepsell, T., Zimmerman, F., & Connell, F. (2001). Association of lower continuity of care with greater risk of emergency department use and hospitalization in children. Pediatrics, 107(3), 524–529. doi:10.1542/peds.107.3.524.

    Article  CAS  PubMed  Google Scholar 

  29. Christakis, D. A., Wright, J. A., Koepsell, T. D., Emerson, S., & Connell, F. A. (1999). Is greater continuity of care associated with less emergency department utilization? Pediatrics, 103(4 Pt. 1), 738–742. doi:10.1542/peds.103.4.738.

    Article  CAS  PubMed  Google Scholar 

  30. Benedict, R. E. (2008). Quality medical homes: Meeting children’s needs for therapeutic and supportive services. Pediatrics, 121(1), e127–e134. doi:10.1542/peds.2007-0066.

    Article  PubMed  Google Scholar 

  31. Martin, A. B., Crawford, S., Probst, J. C., et al. (2007). Medical homes for children with special health care needs: A program evaluation. Journal of Health Care for the Poor and Underserved, 18(4), 916–930.

    PubMed  Google Scholar 

  32. Turchi, R. M., Gatto, M., & Antonelli, R. (2007). Children and youth with special healthcare needs: there is no place like (a medical) home. Current Opinion in Pediatrics, 19(4), 503–508. doi:10.1097/MOP.0b013e32825a67b4.

    Article  PubMed  Google Scholar 

  33. Homer, C. J., Klatka, K., Romm, D., et al. (2008). A review of the evidence for the medical home for children with special health care needs. Pediatrics, 122(4), e922–e937. doi:10.1542/peds.2007-3762.

    Article  PubMed  Google Scholar 

  34. Federal Interagency Forum on Child and Family Statistics. (2007). America’s children: Key national indicators of well-being, 2007. Washington, DC: Government Printing Office, Federal Interagency Forum on Child and Family Statistics.

    Google Scholar 

Download references

Acknowledgments

Dr. Stevens and Dr. Seid conceptualized and designed the research study. Mr. Pickering and Ms. Tsai completed the statistical analyses and contributed to the methodology section of the manuscript. Dr. Stevens drafted the majority of the manuscript with revision and input from all of the co-authors. Dr. Stevens had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. The authors do not have any financial or other conflicts of interest regarding the results that are presented in this study. This project was funded by the Federal Maternal and Child Health Bureau (Grant #R40MC07844).

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Correspondence to Gregory D. Stevens.

Appendix

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See Table 4

Table 4 Sample sizes and weighted national percentages for the individual questions composing each medical home feature

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Stevens, G.D., Seid, M., Pickering, T.A. et al. National Disparities in the Quality of a Medical Home for Children. Matern Child Health J 14, 580–589 (2010). https://doi.org/10.1007/s10995-009-0454-5

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