Pain, coping and health care utilization in younger and older adults with sickle cell disease

Journal of Health Psychology

Volumn 15, Issue 1, 2010, Pages 131-137

  Sanders, Kathryn A ^a   Labott, Susan M ^b   Molokie, Robert ^b   Shelby, Sarah R ^b   Desimone, Joseph ^b  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

Author keywords

Coping; Health care utilization; Pain; Sickle cell disease

Indexed keywords

ADAPTIVE BEHAVIOR; ADOLESCENT; ADULT; AGED; ARTICLE; FEMALE; HEALTH SERVICE; HUMAN; MALE; MIDDLE AGED; PAIN; PSYCHOLOGICAL ASPECT; SICKLE CELL ANEMIA; UTILIZATION REVIEW;

ADAPTATION, PSYCHOLOGICAL; ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; ANEMIA, SICKLE CELL; FEMALE; HEALTH SERVICES; HUMANS; MALE; MIDDLE AGED; PAIN; YOUNG ADULT;

EID: 75149198597     PISSN: 13591053     EISSN: 14617277     Source Type: Journal    
DOI: 10.1177/1359105309345554     Document Type: Article

References (28)

1. Andersen, R., & Newman, J.F. (1973). Societal and individual determinants of medical care utilization in the United States. The Millbank Memorial Fund Quaterly, Health and Society, 51, 95-124.
2. Anie, K.A., Steptoe, A., & Bevan, D.H. (2002). Sickle cell disease: Pain, coping, and quality of life in a study of adults in the UK. British Journal of Health Psychology, 7, 331-334.
3. Barrett, D.H., Wisotzek, I.E., Abel, G.G., Rouleau, J.L., Platt, A.F., Pollard, W.E., & Eckman, J.R. (1988). Assessment of psychosocial functioning of patients with sickle cell disease. Southern Medical Journal, 81, 745-750.
4. Barry, L.C., Kerns, R.D., Guo, Z., Duong, B.D., Iannone, L.P., & Reid, M.C. (2004). Identification of strategies used to cope with chronic pain in older persons receiving primary care from a Veterans Affairs medical center. Journal of American Geriatrics Society, 52, 950-956.
5. Derogatis, L.R. (1993). Brief symptom inventory: Administration, scoring, and procedures manual. Minnesota National Computer Systems.
6. Derogatis, L.R., & Melisaratos, N. (1983). The Brief Symptom Inventory: An introductory report. Psychological Medicine, 13, 595-605.
7. Folkman, S., Lazarus, R.S., Pimley, S., & Novacek, J. (1987). Age differences in stress and coping processes. Psychology and Aging, 2, 171-184.
8. Gil, K.M., Abrams, M.R., Phillips, G., & Keefe, F.J. (1989). Sickle cell disease pain: Relation of coping strategies to adjustment. Journal of Consulting and Clinical Psychology, 57, 725-731.
9. Gil, K.M., Carson, J.W., Porter, L.S., Scipio, C., Bediako, S.M., & Orringer, E. (2004). Daily mood and stress predict pain, health care use, and work activity in African American adults with sickle-cell disease. Health Psychology, 23, 267-274.
10. Gil, K.M., Williams, D.A., Thompson, R.J., Jr, & Kinney, T.R. (1991). Sickle cell disease in children and adolescents: The relation of child and parent pain coping strategies to adjustment. Journal of Pediatric Psychology, 16, 643-663.
11. Harris, A., Parker, N., & Barker, C. (1998). Adults with sickle cell disease: Psychological impact and experience of hospital services. Psychology, Health & Medicine, 3, 171-179.
12. Howard, J., & Davies, S.C. (2007). Sickle cell disease in North Europe. Scandinavian Journal of Clinical and Laboratory Investigation, 67, 27-38.
13. McCrae, J.D., & Lumley, M.A. (1998). Health status in sickle cell disease: Examining the roles of pain coping strategies, somatic awareness, and negative affectivity. Journal of Behavioral Medicine, 21, 35-55.
14. Midence, K., & Elander, J. (1996). Adjustment and coping in adults with sickle cell disease: An assessment of research evidence. British Journal of Health Psychology, 1, 95-111.
15. Platt, A.F., & Sacerdote, A. (2002). Hope and destiny: The patient"s and parent"s guide to sickle cell disease and sickle cell trait. Roscoe, IL: Hilton Publishing Company.
16. Platt, O.S., Brambilla, D.J., Rosse, W.F., Miler, P.F., Castro, O., Steinberg, M.H., & Klug, P.P. (1994). Mortality in sickle cell disease. New England Journal of Medicine, 330, 1639-1644.
17. Porter, L.S., Gil, K.M., Carson, J.W., Anthony, K.K., & Ready, J. (2000). The role of stress and mood in sickle cell disease pain: An analysis of daily diary data. Journal of Health Psychology, 5, 53-63.
18. Porter, L.S., Gil, K.M., Sedway, J.A., Ready, J., Workman, E., & Thompson, R.J. (1998). Pain and stress in sickle cell disease: An analysis of daily pain records. International Journal of Behavioral Medicine, 5, 185-203.
19. Powars, D.R., Chan, L.S., Hiti, A., Ramicone, E., & Johnson, C. (2005). Outcome of sickle cell anemia: A 4-decade observational study of 1056 patients. Medicine, 84, 363-376.
20. Reese, F.L., & Smith, W.R. (1997). Psychosocial determinants of health care utilization in sickle cell disease patients. Annals of Behavioral Medicine, 19, 171-178.
21. Reid, M.C., Crone, K.T., Otis, J., & Kerns, R.D. (2002 a). Differences in pain-related characteristics among younger and older veterans receiving primary care. Pain Medicine, 3, 102-107.
22. Reid, M.C., Guo, Z., Towle, V.R., Kerns, R.D., & Concato, J. (2002 b). Pain-related disability among older male veterans receiving primary care. Journal of Gerontology, 57A, M727 - M732.
23. Rosenstiel, A.K., & Keefe, F.J. (1983). The use of coping strategies in low back pain patients: Relationship to patient characteristics and current adjustment. Pain, 17, 33-40.
24. Serjeant, G.R. (1997). Sickle-cell disease. Lancet, 350, 725-730.
25. Sherbourne, C.D., & Stewart, A.L. (1991). The MOS social support survey. Social Science and Medicine, 32, 705-714.
26. Sickle Cell Disease Guideline Panel. (1993). Sickle cell disease: Screening, diagnosis, management, and counseling in newborns and infants. Clinical Practice Guideline no. 6. Rockville, MD: Agency for Health Care Policy and Research, US Public Health Service.
27. Smith, W.R., Penberthy, L.T., Bovbjerg, V.E., McClish, D.K., Roberts, J.D., Dahman, B. et al. (2008). Daily assessment of pain in adults with sickle cell disease. Annals of Internal Medicine, 148, 94-101.
28. Wierenga, K.J.J., Hambleton, I.R., & Lewis, N.A. (2001). Survival estimates for patients with homozygous sickle-cell disease in Jamaica. The Lancet, 9257, 680-683.