Neuropsychological assessment, neuroimaging, and neuropsychiatric evaluation in pediatric and adult patients with sickle cell disease (SCD)

Neuropsychiatric Disease and Treatment

Volumn 3, Issue 6, 2007, Pages 705-709

  Edwards, Christopher L ^a   Raynor, Renee Dunn ^a   Feliu, Miriam ^a   McDougald, Camela ^a   Johnson, Stephanie ^b   Schmechel, Donald ^a   Wood, Mary ^a   Bennett, Gary G ^c   Saurona, Patrick ^d   Bonner, Melanie ^a   Wellington, Chante' ^a   DeCastro, Laura M ^a   Whitworth, Elaine ^a   Abrams, Mary ^a   Logue, Patrick ^a   Edwards, Lekisha ^a   Martinez, Salutario ^a   Whitfield, Keith E ^e  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b AMERICAN PSYCHOLOGICAL ASSOCIATION   (United States)

^c HARVARD SCHOOL OF PUBLIC HEALTH   (United States)

^d NewYork Presbyterian Hospital   (United States)

^e DUKE UNIVERSITY   (United States)

Author keywords

Cerebral vascular event; Neuroimaging; Neuropsychological assessment; Sickle cell disease

Indexed keywords

ADULT; BRAIN INFARCTION; CEREBROVASCULAR DISEASE; CHILD; COGNITIVE DEFECT; EARLY DIAGNOSIS; HUMAN; MENTAL DISEASE; MORBIDITY; NEUROIMAGING; NEUROLOGIC DISEASE; NEUROLOGIC EXAMINATION; NEUROPSYCHIATRY; NEUROPSYCHOLOGICAL TEST; NUCLEAR MAGNETIC RESONANCE IMAGING; PEDIATRICS; REVIEW; SICKLE CELL ANEMIA; SYMPTOM; TRANSIENT ISCHEMIC ATTACK;

EID: 38149019128     PISSN: 11766328     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (46)

1. Armstrong FD, Thompson RJ Jr, Wang W, et al. 1996. Cognitive functioning and brain magnetic resonance imaging in children with sickle Cell disease. Neuropsychology Committee of the Cooperative Study of Sickle Cell Disease. Pediatrics, 97(6 Pt 1):864-70.
2. Baldeweg T, Hogan A, Saunders D, et al. 2005. Detecting white matter injury in sickle cell disease using voxel based morphometry. Annals of Neurology, 59:662-72.
3. Bernaudin F, Verihac S, Freard F, et al. 2000. Multicenter prospective study of children with sickle cell disease: radiographic and psychometric correlation. Journal of Child Neurology, 15:333-43.
4. Bonner M, Gustafson KE, Schumacher E, et al. 1999. The impact of sickle cell disease on cognitive functioning and learning. School Psychology Review, 28:182-93.
5. Briscoe G. 2001. The cognitive and neuropsychological impact of sickle cell anemia: a review and update. Journal of Psychological Practice, 7:88-102.
6. Broe G. 2001. The Cognitive and Neuropsychological impact of sickle cell anemia: a review and update. Journal of Psychological Practice, 7:88-102.
7. Brown RT, Armstrong FD, Eckman JR. 1993. Neurocognitive aspects of pediatric sickle cell disease. Journal of Learning Disabilities, 26:33-45.
8. Brown RT, Davis PC, Lambert R, et al. 2000. Neurocognitive functioning and magnetic resonance imaging in children with sickle cell disease. Journal of Pediatric Psychology, 25:503-13.
9. Burlew K, Telfair J, Colangelo L, et al. 2000. Factors that influence adolescent adaptation to sickle cell disease. Journal of Pediatric Psychology, 25:287-99.
10. Coelho MS, Max JE, Tranel DA. 2005. Matched lesion analysis of childhood versus adult-onset brain injury due to unilateral stroke: another perspective on neural plasticity and recovery of social functioning. Cognitive and Behavioral Neurology, 18:5-17.
11. Cohen AR, Galanello R, Pennell DJ, et al. 2004. Thalassemia. Hematology, 14-34.
12. DeBaun MR, Schatz J, Siegel MJ, et al. 1998. Cognitive screening examinations for silent cerebral infarcts in sickle cell disease. Neurology, 50:1678-82.
13. Edwards CL, Scales M, Loughlin C, et al. 2005. A brief review of the pathophysiology, associated pain, and psychosocial issues associated with sickle cell disease (SCD). International Journal of Behavioral Medicine, 12:171-9.
14. Edwards CL, Whitfield K, Sudhakar S, et al. 2006. Parental Substance Abuse, Reports of Chronic Pain, and Coping in Adult Patients with Sickle Cell Disease (SCD). J Natl Med Assoc, 98(3):420-28.
15. Fowler MG, Whitt JK, Lallinger RR, et al. 1988. Neuropsychologic and academic functioning of children with sickle cell anemia. Journal of Developmental and Behavioral Pediatrics, 9:213-20.
16. Grueneich R, Ris DM, Ball W, et al. 2004. Relationship of structural magnetic resonance imaging, magnetic resonance perfusion, and other disease factors to neuropsychological outcome in sickle cell disease. Journal of Pediatric Psychology, 29:83-92.
17. Hariman LM, Griffith ER, Hurtig AL, et al. 1991. Functional outcomes of children with sickle-cell disease affected by stroke. Archives of Physical Medicine and Rehabilitation, 72:498-502.
18. Hogan AM, Kirkham FJ, Prengler M, et al. 2006. An exploratory study of physiological correlates or neurodevelopmental delay in infants with sickle cell anaemia. British Journal of Haematology, 132:99-107.
19. Hogan AM, Pit-ten Cate IM, Vargha-Khadem F, et al. 2006. Physiological correlates of intellectual function in children with sickle cell disease: Hypoxaemia, hyperaemia and brain infarction. Dev Sci, 9:379-87.
20. Hogan AM, Vargha-Khadem F, Saunders DE, et al. 2006. Impact of frontal white matter lesions on performance monitoring: ERP evidence for cortical disconnection. Brain, 129:2177-88.
21. Izuora GI, Kaine WN, Emodi I. 1989. Neurological disorders in Nigerian children with homozygous sickle cell anaemia. East African Medical Journal, 66:653-7.
22. Kral MC, Brown RT, Hynd GW 2001. Neuropsychological aspects of pediatric sickle cell disease. Neuropsychology Review, 11: 179-96.
23. Ohene-Frempong K, Weiner SJ, Sleeper LA, et al. 1998. Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood, 91(1):288-94.
24. Pells J, Presnell K, Edwards CL, et al. 2005. Moderate Chronic Pain, Weight, and Dietary Intake in African American Adult Patients with Sickle Cell Disease (SCD). J Natl Med Assoc, 97:1622-9.
25. Powars DR, Wong WY, Vachon LA. 2001. Incomplete cerebral infarctions are not silent. Journal of Pediatric Hematology/Oncology, 23:79-83.
26. Schatz J. 2004. Brief report: Academic attainment in children with sickle cell disease. Journal of Pediatric Psychology, 29:627-3 3.
27. Schatz J, Craft S, Koby M, et al. 1999. Neuropsychologic deficits in children with sickle cell disease and cerebral infarction: role of lesion site and volume. Child Neuropsychology, 5:92-103.
28. Schatz J, Finke RL, Kellett JM, et al. 2002. Cognitive Functioning in Children with Sickle Cell Disease; A Meta-Analysis. Journal of Pediatric Psychology, 27:739-49.
29. Schatz J, Finke R, Roberts CW. 2004. Interactions of biomedical and environmental risk factors for cognitive development: a preliminary study of sickle cell disease. Journal of Developmental and Behavioral Pediatrics, 25:303-10.
30. Schatz J, McClellan C. 2006. Sickle cell disease as a neurodevelopmental disorder. Mental Retardation and Developmental Disabilities Research Reviews, 12:200-7.
31. Schatz J, White D, Moinuddin A, et al. 2002. Lesion burden and cognitive morbidity in children with sickle cell disease. Journal of Child Neurology, 17:891-5.
32. Steen G, Emudianughe T, Hankins G, et al. 2003. Brain imaging findings in pediatric patients with sickle cell disease. Radiology, 228:216-25.
33. Steen G, Emudianughe T, Hunte M, et al. 2005. Brain volume in pediatric patients with sickle cell disease: evidence of volumetric growth delay. American Journal of Neuroradiology, 26:455-62.
34. Steen G, Fineberg-Buchner C, Hankins G, et al. 2005. Cognitive deficits in children with sickle cell disease. Journal of Child Neurology, 20:102-7.
35. Steen G, Hankins G, Xiong X, et al. 2003. Prospective brain imaging evaluation of children with sickle cell trait: initial observation. Radiology, 228:208-15.
36. Steen G, Hu J, Elliot V, et al. 2002. Kindergarten readiness skills in children with sickle cell disease: evidence of early neurocognitive damage? Journal of Child Neurology, 17:111-16.
37. Steen G, Miles M, Helton K, et al. 2003. Cognitive impairment in children with hemoglobin ss sickle cell disease: relationship to MR imaging findings and hematocrit. American Journal of Neuroradiology, 24:382-9.
38. Steen G, Reddick W, Mulhern R, et al. 1998. Quantitative MRI of the brain in children with sickle cell disease reveals abnormalities unseen by conventional MRI. Journal of Magnetic Resonance Imaging, 8:535-43.
39. Steen G, Xiong X, Langston J, et al. 2003. Brain injury in children with sickle cell disease: prevalence and etiology. Annals of Neurology, 54:564-72.
40. Steen G, Xiong X, Mulbern R, et al. 1999. Subtle brain abnormalities in children with sickle cell disease: relationship to blood hematocrit. Annals of Neurology, 45:279-86.
41. Stringer A. 2003. Cognitive rehabilitation practice patterns. A survey of American Hospital Association Rehabilitation Programs. Clinical Neuropsychologist, 17:34-44.
42. Treadwell MJ, Law AW, Sung J, et al. 2005. Barriers to adherence of deferoxamine usage in sickle cell disease. Pediatric Blood and Cancer, 44:500-7.
43. Thompson RJ, Gustafson KE, Bonner MJ, et al. 2002. Neurocognitive development of young children with sickle cell disease through three years of age. Journal of Pediatric Psychology, 27:235-44.
44. Wasserman AL, Wilimas JA, Fairclougb DL, et al. 1991. Subtle neuropsychological deficits in children with sickle cell disease. American Journal of Pediatric Hematology/Oncology, 13:14-20.
45. Wang WC, Gallagher DM, Pegelow CH, et al. 2000. Multicenter comparison of magnetic resonance imaging and transcranial Doppler ultrasonography in the evaluation of the central nervous system in children with sickle cell disease. Journal of Pediatric Hematology/Oncology, 22:335-9.
46. Wang WC, Langston JW, Steen RG, et al. 1998. Abnormalities of the central nervous system in very young children with sickle cell anemia. Journal of Pediatrics, 132:994-8.