The impact of sickle cell disease on cognitive functioning and learning

School Psychology Review

Volumn 28, Issue 2, 1999, Pages 182-193

  Bonner, Melanie J ^a   Schumacher, Elizabeth ^b   Gustafson, Kathryn E ^b   Thompson Jr , Robert J ^b  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0039254534     PISSN: 02796015     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (50)

1. Adams, R. J., McKie, V. C., Brambilla, D., Carl, E., Gallagher, D., Nichols, F. T., Roach, S., Abbound, M., Berman, B., Driscoll, C., Files, B., Hsu, L., Hurlet, A., Miller, S., Olivieri, N., Pegelow, C., Scher, C., Vichinsky, E., Wang, W., Woods, G., Kutlar, A., Wright, E., Hagner, S., Tighe, F., Lewin, J., Cure, J., Zimmerman, R. A., & Waclawiw, M. A. (1998). Stroke prevention trial in sickle cell anemia. Controlled Clinical Trials, 19, 110-129.
2. Armstrong, F. D., Thompson, R. J., Jr., Wang, W., Zimmerman, R. A., Pegelow, C. H., Miller, S., Moser, F., Bello, J., Hurtig, A., & Vass, K. (1996). Cognitive functioning and brain magnetic resonance imaging in children with sickle cell disease. Pediatrics, 97, 864-870.
3. Bayley, N. (1993). Bayley scales of infant development: Second edition. New York: The Psychological Corporation.
4. Brown, R. T., Armstrong, F. D., & Eckman, J. R. (1993). Neurocognitive aspects of pediatric sickle cell disease. Journal of Learning Disabilities, 26, 33-45.
5. Brown, R. T., Buchanan, I., Doepke, K., Eckman, J. R., Baldwin, K., Goonan, B., & Schoenherr, S. (1993). Cognitive and academic functioning in children with sickle-cell disease. Journal of Clinical Child Psychology, 22, 207-218.
6. Charache, S., Lubin, B., & Reid, C. D. (1989). Management and therapy of sickle cell disease (NIH Publication No. 89-2117). Washington, DC: National Institutes of Health.
7. Charache, S., Terrin, M. L., Moore, R. D., Dover, G. J., Barton, F. B., Eckert, S. V., McMahon, R. P., Bonds, D. R., and the Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. (1995). Effects of hydroxyurea on the frequency of painful crises in sickle cell anemia. The New England Journal of Medicine, 332, 1317-1322.
8. Chua-Lim, C., Moore, R. B., McCleary, G., Shah, A., & Mankad, V. N. (1993). Deficiencies in school readiness skills of children with sickle cell anemia. Southern Medical Journal, 86, 397-402.
9. Cohen, M. J., Branch, W. B., McKie, V. C., & Adams, R. J. (1994). Neuropsychological impairment in children with sickle cell anemia and cerebrovascular accidents. Clinical Pediatrics, 33, 517-524.
10. Eaton, M. L., Haye, J. S., Armstrong, F, D., Pegelow, C. H., & Thomas, M. (1995). Hospitalizations for painful episodes: Association with school absenteeism and academic performance in children and adolescents with sickle cell anemia. Comprehensive Pediatric Nursing, 18, 1-9.
11. Fowler, M. G., Johnson, M. P., & Atkinson, S. S. (1985). School achievement and absence in children with chronic health conditions. Journal of Pediatrics, 106, 683-687.
12. Fowler, M. G., Whitt, J. K., Lallinger, R. R., Nash, K. B., Atkinson, S. S., Wells, R. J., & McMillan, C. (1988). Neuropsychologic and academic functioning of children with sickle cell anemia. Developmental and Behavioral Pediatrics, 9, 213-220.
13. Frankenburg, W. K., & Dodds, J. B. (1967). The Denver Developmental Screening Test. Journal of Pediatrics, 71, 181-191.
14. Gil, K. M., Thompson, R. J., Jr., Keith, B. R., Tota-Faucette, M., Noll, S., & Kinney, T. R. (1993). Sickle cell disease pain in children and adolescents: Change in pain frequency and coping strategies over time. Journal of Pediatric Psychology, 18, 621-637.
15. 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.
16. Golden, C. J. (1987). Luria-Nebraska Neuropsychological Battery: Children's revision manual. Los Angeles: Western Psychological Services.
17. Hariman, L. M. F., Griffith, E. R., Hurtig, A. L., & Keehn, M. T. (1991). Functional outcomes of children with sickle cell disease affected by stroke. Archives of Physical Medicine and Rehabilitation, 72, 498-502.
18. Hindmarsh, P. C., Brozovic, M., Brook, C. G. D., & Davies, S. C. (1987). Incidence of overt and covert neurological damage in children with sickle cell disease. Postgraduate Medical Journal, 63, 751-753.
19. Katz, E. R., Rubenstein, C. L., Hubert, N. C., & Blew, A. (1988). School and social reintegration of children with cancer. Journal of Psychosocial Oncology, 6, 123-140.
20. Kaufiman, A. S., & Kaufman, N. L. (1983). Kaufman Assessment Battery for Children (K-ABC) administration and scoring manual. Circle Pines, MN: American Guidance Service.
21. Leiken, S. L., Gallagher, D., Kinney, T. R., Sloane, D., Klug, P., & Rida, W. (1989). Mortality in children and adolescents with sickle cell disease. Pediatrics, 84, 500-508.
22. Levine, M. D., & Schneider, E. A. (1985). The pediatric examination of educational readiness examiner's manual. Toronto: Educators Publishing Services.
23. McCarthy, D. (1972). Manual for the McCarthy Scales of Children's Abilities. New York: The Psychological Corporation.
24. Ohene-Frempong, K., & Smith-Whitley, K. (1997). Use of hydroxyurea in children with sickle cell disease: What comes next? Seminars in Hematology, 34(suppl. 3), 30-41.
25. Pavlakis, S. G., Bello, J., Prohovnik, I., Sutton, M., Ince, C., Mohr, J. P., Piomelli, S., Hilal, S., & DeVivo, D. C. (1988). Brain infarction in sickle cell anemia: Magnetic resonance imaging correlates. Annals of Neurology, 23, 125-130.
26. Platt, O. S., Brambilla, D. J., Rosse, W. F., Milner, P. F., Castro, O., Steinberg, M. H., & Klue, P. P. (1994). Mortality in sickle cell disease: Life expectancy and risk factors for early death. New England Journal of Medicine, 330, 1639-1644.
27. Portnoy, B. A., & Herion, J. C. (1972). Neurological manifestations in sickle cell disease. Annals of Internal Medicine, 76, 643-652.
28. Powars, D. R., Wilson, B., Imbus, C., Pegelow, C., & Allen, J. (1978). The natural history of stroke in sickle cell disease. American Journal of Medicine, 65, 461-471.
29. Ris, M. D., Kalinyak, K. A., Ball, W. S., Noll, R. B., Wells, R. J., & Rucknagel, D. (1996). Pre- and post-stroke MRI and neuropsychological studies in sickle cell disease: A case study. Archives of Clinical Neuropsychology, 11, 481-490.
30. Rodgers, G. P., Clark, C. M., & Kessler, R. M. (1984). Regional alterations in brain metabolism in neurologically normal sickle cell patients. Journal of the American Medical Association, 256, 1692-1700.
31. Serjeant, G. R. (1985). Sickle cell disease. New York: Oxford University Press.
32. Shapiro, B. S., Dinges, D. F., Orne, E. C., Bauer, N., Reilly, L. B., Whitehouse, W. G., Ohene-Frempong, K., & Orne, M. T. (1995). Home management of sickle cell-related pain in children and adolescents: Natural history and impact on school attendance. Pain, 61, 139-144.
33. Sickle Cell Disease Guideline Panel. (1993). Sickle cell disease: Screening, diagnosis, management, and counseling in newborns and infants. [Clinical Practice Guideline, No 6, AHCPR Pub. No. 93-0562]. Rockville, MD: U.S. Department of Health and Human Services, Agency for Health Care Policy and Research Public Health Service.
34. Stein, R. E. K., & Jessop, D.J. (1984). Relationship between health status and psychological adjustment among children with chronic conditions. Pediatrics, 73, 169-174.
35. Swift, A. V., Cohen, M. J., Hynd, G. W., Wisenbaker, J. M., McKie, K. M., Makari, G., & McKie, V. C. (1989). Neuropsychologic impairment in children with sickle cell anemia. Pediatrics, 84, 1077-1085.
36. Thompson, R. J., Jr., Gil, K. M., Burbach, D. J., Keith, B. R., & Kinney, T. R. (1993). Role of child and maternal processes in the psychological adjustment of children with sickle cell disease. Journal of Consulting and Clinical Psychology, 61, 468-474.
37. Thompson, R. J., Jr., Gil, K. M., Keith, B. R., Gustafson, K. E., George, L. K., & Kinney, T. R. (1994). Psychological adjustment of children with sickle cell disease: Stability and change over a 10-month period. Journal of Consulting and Clinical Psychology, 62, 856-860.
38. Thompson, R. J., Jr., & Gustafson, K. E. (1996). Adaptation to chronic childhood illness. Washington, DC: American Psychological Association.
39. Thompson, R. J., Jr., Gustafson, K. E., Bonner, M. J., & Kinney, T. R. (1997, September). Cognitive functioning at twelve months of age of infants with sickle cell disease. Paper presented at the annual meeting of the National Sickle Cell Disease Program, Washington, DC.
40. Thompson, R. J., Jr., Gustafson, K. E., Bonner, M. J., & Schumacher, E. (1996, March). Cognitive functioning at six months of age of infants with sickle cell disease. Paper presented at the 21st annual meeting of the National Sickle Cell Disease Program, Mobile, AL.
41. Thompson, R. J., Jr., Gustafson, K. E., & Gil, K. M. (1995). Psychological adjustment of adolescents with cystic fibrosis or sickle cell disease and their mothers. In J. Wallander & L. Siegal (Eds.), Advances in pediatric psychology: II. Behavioral perspectives on adolescent health (pp. 232-247). New York: Guilford.
42. Thompson, R. J., Jr., Gustafson, K. E., & Ware, R. E. (1998). Hematologic disorders. In R. T. Ammerman & J. V. Campo (Eds.), Handbook of pediatric psychology and psychiatry; Disease, injury, and illness (vol. 2, pp. 298-312). Needham Heights, MA: Allyn and Bacon.
43. Thorndike, R. L., Hagen, E. P., & Sattler, J. M. (1986). Guide for administering and scoring the Stanford-Binet Intelligence Scale: Fourth edition. Chicago: Riverside.
44. Vinchinsky, E. P. (1997). Hydroxyurea in children: Present and future. Seminars in Hematology, 34, 22-29.
45. Walters, M. C., Patience, M., Leisenring, W., Eckman, J. R., Scott, J. P., Mentzer, W. C., Davies, S. C., Ohene-Frempong, K., Bernaudin, F., Matthews, D. C., Storb, R., & Sullivan, K. M. (1996). Bone marrow transplantation for sickle cell disease. The New England Journal of Medicine, 335, 369-376.
46. Wang, W. C., Grover, R., Gallagher, D., Espeland, M., & Fandal, A. (1993). Developmental screening in young children with sickle cell disease: Results of a cooperative study. American Journal of Pediatric Hematology/Oncology, 15, 87-91.
47. Wasserman, A. L., Wilimas, J. A., Fairclough, D. L., Mulhern, R. K., & Wang, W. (1991) Subtle neuropsychological deficits in children with sickle cell disease. American Journal of Pediatric Hematology/Oncology, 13, 14-20.
48. Weitzman, M. (1986). School absence rates as outcome measures in studies of children with chronic illness. Journal of Chronic Disease, 39, 799-808.
49. Weitzman, M., Walker, D. K., & Gortmaker, S. (1986). Chronic illness, psychosocial problems, and school absences. Clinical Pediatrics, 25, 137-141.
50. Wood, D. H. (1978). Cerebrovascular complications of sickle cell anemia. Stroke, 9, 73-75.