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Nursing Research and Practice
Volume 2011, Article ID 270594, 5 pages
http://dx.doi.org/10.1155/2011/270594
Clinical Study

Self-Care Recommendations of Middle-Aged and Older Adults with Sickle Cell Disease

School of Nursing, The University of North Carolina at Chapel Hill, Campus Box 7460, Chapel Hill, NC 27599-7460, USA

Received 31 March 2011; Revised 2 July 2011; Accepted 4 July 2011

Academic Editor: Patrick Callaghan

Copyright © 2011 Coretta M. Jenerette 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. K. W. Watkins, C. M. Connell, J. T. Fitzgerald, L. Klem, T. Hickey, and B. Ingersoll-Dayton, “Effect of adults' self-regulation of diabetes on quality-of-life outcomes,” Diabetes Care, vol. 23, no. 10, pp. 1511–1515, 2000. View at Google Scholar · View at Scopus
  2. Curriculum in ethnogeriatrics, “core curriculum and ethnic specific modules,” Health and Health Care in African American Elders, 2001, http://www.stanford.edu/group/ethnoger/ebooks/african_american.pdf.
  3. S. S. Martin, J. Trask, T. Peterson, B. C. Martin, J. Baldwin, and M. Knapp, “Influence of culture and discrimination on care-seeking behavior of elderly African Americans: a qualitative study,” Social Work in Public Health, vol. 25, no. 3-4, pp. 311–326, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  4. J. N. Giger and R. Davidhizar, “Reflections on the elderly African American in health care,” Journal of Cultural Diversity, vol. 4, no. 3, pp. 88–96, 1997. View at Google Scholar · View at Scopus
  5. J. Shellman, “'Nobody ever asked me before': understanding life experiences of African American elders,” Journal of Transcultural Nursing, vol. 15, no. 4, pp. 308–316, 2004. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  6. B. Haight and J. Webster, Eds., The Art and Science of Reminiscing: Theory, Research, and Applications, Taylor & Francis, Washington, DC, USA, 1995.
  7. K. A. Sanders, S. M. Labott, R. Molokie, S. R. Shelby, and J. Desimone, “Pain, coping and health care utilization in younger and older adults with sickle cell disease,” Journal of Health Psychology, vol. 15, no. 1, pp. 131–137, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  8. D. L. Wethers, “Sickle cell disease in childhood: part I. Laboratory diagnosis, pathophysiology and health maintenance,” American Family Physician, vol. 62, no. 5, pp. 1013–1020, 1027–1028, 2000. View at Google Scholar · View at Scopus
  9. C. L. Edwards, M. T. Scales, C. Loughlin et al., “A brief review of the pathophysiology, associated pain, and psychosocial issues in sickle cell disease,” International Journal of Behavioral Medicine, vol. 12, no. 3, pp. 171–179, 2005. View at Publisher · View at Google Scholar · View at Scopus
  10. L. M. Diggs, “Anatomic lesions in sickle cell disease,” in Sickle Cell Disease: Diagnosis, Management, Education, and Research, H. Abramson, J. F. Bertles, and D. L. Wethers, Eds., pp. 189–229, C.V. Mosby, St. Louis, MO, USA, 1973. View at Google Scholar
  11. C. T. Quinn, Z. R. Rogers, T. L. McCavit, and G. R. Buchanan, “Improved survival of children and adolescents with sickle cell disease,” Blood, vol. 115, no. 17, pp. 3447–3452, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  12. O. S. Platt, B. D. Thorington, D. J. Brambilla et al., “Pain in sickle cell disease. Rates and risk factors,” New England Journal of Medicine, vol. 325, no. 1, pp. 11–16, 1991. View at Google Scholar · View at Scopus
  13. O. S. Platt, D. J. Brambilla, W. F. Rosse et al., “Mortality in sickle cell disease—life expectancy and risk factors for early death,” New England Journal of Medicine, vol. 330, no. 23, pp. 1639–1644, 1994. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  14. K. Maxwell, A. Streetly, and D. Bevan, “Experiences of hospital care and treatment seeking for pain from sickle cell disease: qualitative study,” British Medical Journal, vol. 318, no. 7198, pp. 1585–1590, 1999. View at Google Scholar · View at Scopus
  15. K. Maxwell, A. Streetly, and D. Bevan, “Experiences of hospital care and treatment seeking for pain from sickle cell disease: qualitative study,” British Medical Journal, vol. 318, no. 7198, pp. 1585–1590, 1999. View at Google Scholar · View at Scopus
  16. O. Strickland, G. Jackson, M. Gilead, D. B. McGuire, and S. Quarles, “Use of focus groups for pain and quality of life assessment in adults with sickle cell disease,” Journal of National Black Nurses Association, vol. 12, no. 2, pp. 36–43, 2001. View at Google Scholar · View at Scopus
  17. C. M. Jenerette and C. Brewer, “Health-related stigma in young adults with sickle cell disease,” Journal of the National Medical Association, vol. 102, no. 11, pp. 1050–1055, 2010. View at Google Scholar · View at Scopus
  18. C. Haywood, S. Lanzkron, N. Ratanawongsa et al., “The association of provider communication with trust among adults with sickle cell disease,” Journal of General Internal Medicine, vol. 25, no. 6, pp. 543–548, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  19. B. Ely, C. Dampier, M. Gilday, P. O'Neal, and D. Brodecki, “Caregiver report of pain in infants and toddlers with sickle cell disease: reliability and validity of a daily diary,” Journal of Pain, vol. 3, no. 1, pp. 50–57, 2002. View at Publisher · View at Google Scholar · View at Scopus
  20. K. Watkins, C. M. Connell, J. T. Fitzgerald, L. Klem, T. Hickey, and B. Ingersoll-Dayton, “Effect of adults' self-regulation of diabetes on quality-of-life outcomes,” Diabetes Care, vol. 23, no. 10, pp. 1511–1515, 2000. View at Google Scholar · View at Scopus
  21. K. Plummer, “The call of life stories in ethnographic research,” in Handbook of Ethnography, P. Atkinson, A. Coffey, S. Delamont, J. Lofland, and L. Lofland, Eds., pp. 395–406, Sage, London, UK, 2001. View at Google Scholar
  22. C. K. Riessman, Narrative Methods for the Human Sciences, Sage, Los Angeles, Calif, USA, 2008.
  23. S. F. Ofori-Acquah and K. Ohene-Frempong, “A global perspective on advances in sickle cell disease research and management, and new challenges in the genome era,” in Renaissance of Sickle Cell Disease Research in the Genome Era, B. Pace, Ed., pp. 333–345, London, UK, Imperial College Press, 2007. View at Google Scholar
  24. E. S. Puffer, J. C. Schatz, and C. W. Roberts, “Relationships between somatic growth and cognitive functioning in young children with sickle cell disease,” Journal of Pediatric Psychology, vol. 35, no. 8, pp. 892–904, 2010. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  25. G. Becker, Y. Beyene, E. M. Newsom, and D. V. Rodgers, “Knowledge and care of chronic illness in three ethnic minority groups,” Family Medicine, vol. 30, no. 3, pp. 173–178, 1998. View at Google Scholar · View at Scopus