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Arthritis
Volume 2015, Article ID 607472, 6 pages
http://dx.doi.org/10.1155/2015/607472
Research Article

Role of Health Literacy in Self-Reported Musculoskeletal Disorders

1Rheumatology Unit, The Queen Elizabeth Hospital, 28 Woodville Road, Woodville South, SA 5011, Australia
2University of Adelaide, Adelaide, SA 5005, Australia
3Arthritis South Australia, 118 Richmond Road, Marleston, SA 5033, Australia
4Department of Social and Behavioral Sciences, Harvard School of Public Health, 677 Huntington Avenue, Kresge Building 7th Floor, Boston, MA 02115, USA
5Population Research & Outcomes Unit, University of Adelaide, Adelaide, SA 5005, Australia

Received 16 December 2014; Accepted 3 August 2015

Academic Editor: Anna Maria Iagnocco

Copyright © 2015 Catherine L. Hill et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. N. D. Berkman, S. L. Sheridan, K. E. Donahue, D. J. Halpern, and K. Crotty, “Low health literacy and health outcomes: an updated systematic review,” Annals of Internal Medicine, vol. 155, no. 2, pp. 97–107, 2011. View at Publisher · View at Google Scholar · View at Scopus
  2. L. P. A. Nielsen-Bohlman and D. A. Kindig, Eds., Committee on Health Literacy: A Prescription to End Confusion, National Academies Press, Washington, DC, USA, 2004.
  3. N. D. Berkman, D. DeWalt, M. P. Pignone et al., “Literacy and health outcomes,” in Book Literacy and Health Outcomes, Agency for Healthcare Research and Quality, Rockville, Md, USA, 2004. View at Google Scholar
  4. D. A. Dewalt, N. D. Berkman, S. Sheridan, K. N. Lohr, and M. P. Pignone, “Literacy and health outcomes: a systematic review of the literature,” Journal of General Internal Medicine, vol. 19, no. 12, pp. 1228–1239, 2004. View at Publisher · View at Google Scholar · View at Scopus
  5. R. J. Adams, S. L. Appleton, C. L. Hill, M. Dodd, C. Findlay, and D. H. Wilson, “Risks associated with low functional health literacy in an Australian population,” Medical Journal of Australia, vol. 191, no. 10, pp. 530–534, 2009. View at Google Scholar · View at Scopus
  6. Australian Bureau of Statistics, Adult Literacy and Life Skills Survey, Summary Results 2006 Reissue, Australian Bureau of Statistics, Canberra, Australia, 2008.
  7. M. Kutner, E. Greenberg, Y. Jin, and C. Paulsen, The Health Literacy of America's Adults: Results from the 2003 National Assessment of Adult Literacy, National Center for Education Statistics, Washington, DC, USA, 2006.
  8. T. K. Gill, C. L. Hill, R. J. Adams, D. Broderick, J. Black, and A. W. Taylor, “‘I know i have arthritis but i don't know what type’. Understanding and knowledge of this chronic condition,” BMC Musculoskeletal Disorders, vol. 11, article 174, 2010. View at Publisher · View at Google Scholar · View at Scopus
  9. B. T. Walitt, F. Constantinescu, J. D. Katz et al., “Validation of self-report of rheumatoid arthritis and systemic lupus erythematosus: the women's health initiative,” Journal of Rheumatology, vol. 35, no. 5, pp. 811–818, 2008. View at Google Scholar · View at Scopus
  10. T. K. Gill, A. W. Taylor, C. L. Hill, and P. J. Phillips, “Osteoporosis in the community: sensitivity of self-reported estimates and medication use of those diagnosed with the condition,” Bone & Joint Research, vol. 1, no. 5, pp. 93–98, 2012. View at Publisher · View at Google Scholar
  11. J. R. Curtis, A. O. Westfall, J. Allison, A. Freeman, S. H. Kovac, and K. G. Saag, “Agreement and validity of pharmacy data versus self-report for use of osteoporosis medications among chronic glucocorticoid users,” Pharmacoepidemiology and Drug Safety, vol. 15, no. 10, pp. 710–718, 2006. View at Publisher · View at Google Scholar · View at Scopus
  12. M. A. McAdams, J. W. Maynard, A. N. Baer et al., “Reliability and sensitivity of the self-report of physician-diagnosed gout in the Campaign Against Cancer and Heart Disease and the Atherosclerosis Risk in the Community cohorts,” Journal of Rheumatology, vol. 38, no. 1, pp. 135–141, 2011. View at Publisher · View at Google Scholar · View at Scopus
  13. D. H. Wilson, M. A. Wakefield, and A. W. Taylor, “The South Australian health omnibus survey,” Health Promotion Journal of Australia, vol. 2, pp. 47–49, 1992. View at Google Scholar
  14. B. D. Weiss, M. Z. Mays, W. Martz et al., “Quick assessment of literacy in primary care: the newest vital sign,” Annals of Family Medicine, vol. 3, no. 6, pp. 514–522, 2005. View at Publisher · View at Google Scholar · View at Scopus
  15. C. Y. Osborn, B. D. Weiss, T. C. Davis et al., “Measuring adult literacy in health care: performance of the newest vital sign,” American Journal of Health Behavior, vol. 31, supplement 1, pp. S36–S46, 2007. View at Publisher · View at Google Scholar · View at Scopus
  16. M. N. Barber, M. Staples, R. H. Osborne, R. Clerehan, C. Elder, and R. Buchbinder, “Up to a quarter of the Australian population may have suboptimal health literacy depending upon the measurement tool: results from a population-based survey,” Health Promotion International, vol. 24, pp. 252–261, 2009. View at Publisher · View at Google Scholar
  17. Australian Bureau of Statistics, Estimated Residential Population by Age and Sex 2007, ABS, Canberra, Australia, 2008.
  18. E. Willis, “The making of expert patients: the role of online health communities in arthritis self-management,” Journal of Health Psychology, vol. 19, no. 12, pp. 1613–1625, 2013. View at Publisher · View at Google Scholar · View at Scopus
  19. R. E. Rudd, “Mismatch between skills of patients and tools in use: might literacy affect diagnoses and research?” Journal of Rheumatology, vol. 37, no. 5, pp. 885–886, 2010. View at Publisher · View at Google Scholar · View at Scopus
  20. Consumer Assessment of Healthcare Providers and Systems (CAPHS). About the CAHPS Item Set for Addressing Health Literacy, Agency for Healthcare Research and Quality, 2009.
  21. B. D. Weiss, Health Literacy and Patient Safety: Help Patients Understand. A Manual for Clinicians, American Medical Association Foundation and American Medical Association, Chicago, Ill, USA, 2nd edition, 2007.
  22. P. Ghosh, F. A. Borg, and B. Dasgupta, “Current understanding and management of giant cell arteritis and polymyalgia rheumatica,” Expert Review of Clinical Immunology, vol. 6, no. 6, pp. 913–928, 2010. View at Publisher · View at Google Scholar · View at Scopus
  23. D. Schillinger, J. Piette, K. Grumbach et al., “Closing the loop: physician communication with diabetic patients who have low health literacy,” Archives of Internal Medicine, vol. 163, no. 1, pp. 83–90, 2003. View at Publisher · View at Google Scholar · View at Scopus
  24. M. Pignone, D. A. DeWalt, S. Sheridan, N. Berkman, and K. N. Lohr, “Interventions to improve health outcomes for patients with low literacy: a systematic review,” Journal of General Internal Medicine, vol. 20, no. 2, pp. 185–192, 2005. View at Publisher · View at Google Scholar · View at Scopus
  25. RTI International, Literacy and Health Outcomes, Agency for Healthcare Research and Quality, Rockville, Md, USA, 2004.
  26. S. Clement, S. Ibrahim, N. Crichton, M. Wolf, and G. Rowlands, “Complex interventions to improve the health of people with limited literacy: a systematic review,” Patient Education and Counseling, vol. 75, no. 3, pp. 340–351, 2009. View at Publisher · View at Google Scholar · View at Scopus
  27. W. Lowe, C. Ballinger, J. Protheroe et al., “Effectiveness of musculoskeletal education interventions in people with low literacy levels: a systematic review,” Arthritis Care and Research, vol. 65, no. 12, pp. 1976–1985, 2013. View at Publisher · View at Google Scholar · View at Scopus
  28. R. E. Rudd, D. C. Blanch, V. Gall et al., “A randomized controlled trial of an intervention to reduce low literacy barriers in inflammatory arthritis management,” Patient Education and Counseling, vol. 75, no. 3, pp. 334–339, 2009. View at Publisher · View at Google Scholar · View at Scopus
  29. N. R. Sperber, H. B. Bosworth, C. J. Coffman et al., “Differences in osteoarthritis self-management support intervention outcomes according to race and health literacy,” Health Education Research, vol. 28, no. 3, pp. 502–511, 2013. View at Publisher · View at Google Scholar · View at Scopus
  30. D. A. DeWal, L. F. Callahan, V. H. Hawk, K. A. Brouksou, R. Rudd, and C. Brach, Eds., Health Literacy Universal Precautions Toolkit, Agency for Healthcare Research and Quality, Rockville, Md, USA, 2010.
  31. L. F. Callahan, V. Hawk, R. Rudd et al., “Adaptation of the health literacy universal precautions toolkit for rheumatology and cardiology—applications for pharmacy professionals to improve self-management and outcomes in patients with chronic disease,” Research in Social and Administrative Pharmacy, vol. 9, no. 5, pp. 597–608, 2013. View at Publisher · View at Google Scholar · View at Scopus
  32. N. B. Peterson, K. A. Dwyer, S. A. Mulvaney, M. S. Dietrich, and R. L. Rothman, “The influence of health literacy on colorectal cancer screening knowledge, beliefs and behavior,” Journal of the National Medical Association, vol. 99, no. 10, pp. 1105–1112, 2007. View at Google Scholar · View at Scopus
  33. J. Adams, J. Chapman, S. Bradley, and S. J. Ryan, “Literacy levels required to complete routinely used patient-reported outcome measures in rheumatology,” Rheumatology, vol. 52, no. 3, pp. 460–464, 2013. View at Publisher · View at Google Scholar · View at Scopus