Developmental Function in Toddlers With Sickle Cell Anemia

作者: F. D. Armstrong , T. D. Elkin , R. C. Brown , P. Glass , S. Rana

DOI: 10.1542/PEDS.2012-0283

关键词:

摘要: BACKGROUND: Neurocognitive impairment occurs in children and adults with sickle cell anemia, but little is known about neurodevelopment very young children. We examined the neurodevelopmental status of infants participating Pediatric Hydroxyurea Phase III Clinical Trial (Baby Hug) to determine relationships age, cerebral blood flow velocity, hemoglobin concentration. METHODS: Standardized measures infant were administered 193 SS or S-β 0 thalassemia between 7 18 months age at time their baseline evaluation. Associations scores family income, parent education, concentration, transcranial Doppler velocity examined. RESULTS: Mean functioning on scales was average range. There no mental development CONCLUSIONS: Whereas overall normal range, behavioral adaptive function poorer older even this group Explanatory mechanisms for association developmental need be identified.

参考文章(23)
Pegelow Ch, Moser F, Miller S, Bello J, Wang W, Thompson Rj, Zimmerman R, Hurtig A, Armstrong Fd, Vass K, Cognitive functioning and brain magnetic resonance imaging in children with sickle cell disease Pediatrics. ,vol. 97, pp. 864- 870 ,(1996)
Lynn A. Sleeper, Charles H. Pegelow, Kwaku Ohene-Frempong, Frances M. Gill, Scott T. Miller, Stephen Embury, John W. Moohr, Doris L. Wethers, Steven J. Weiner, Cerebrovascular Accidents in Sickle Cell Disease: Rates and Risk Factors Blood. ,vol. 91, pp. 288- 294 ,(1998) , 10.1182/BLOOD.V91.1.288
Mark T. Gladwin, Role of the red blood cell in nitric oxide homeostasis and hypoxic vasodilation. Advances in Experimental Medicine and Biology. ,vol. 588, pp. 189- 205 ,(2006) , 10.1007/978-0-387-34817-9_17
Winfred C Wang, Knashawn H Morales, Charles D Scher, Lori Styles, Nancy Olivieri, Robert Adams, Don Brambilla, STOP Investigators, None, Effect of Long-term Transfusion on Growth in Children with Sickle Cell Anemia: Results of the Stop Trial The Journal of Pediatrics. ,vol. 147, pp. 244- 247 ,(2005) , 10.1016/J.JPEDS.2005.02.030
Steven G. Pavlakis, Renée C. Rees, Xiangke Huang, R. Clark Brown, James F. Casella, Rathi V. Iyer, Ram Kalpatthi, Judy Luden, Scott T. Miller, Zora R. Rogers, Courtney D. Thornburg, Winfred C. Wang, Robert J. Adams, , Transcranial doppler ultrasonography (TCD) in infants with sickle cell anemia: Baseline data from the BABY HUG trial Pediatric Blood & Cancer. ,vol. 54, pp. 256- 259 ,(2009) , 10.1002/PBC.22282
Gregory J. Kato, Mark T. Gladwin, Martin H. Steinberg, Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes Blood Reviews. ,vol. 21, pp. 37- 47 ,(2007) , 10.1016/J.BLRE.2006.07.001
Mark T. Gladwin, James H. Shelhamer, Frederick P. Ognibene, Margaret E. Pease-Fye, James S. Nichols, Beth Link, Daksesh B. Patel, Marcin A. Jankowski, Lewis K. Pannell, Alan N. Schechter, Griffin P. Rodgers, Nitric oxide donor properties of hydroxyurea in patients with sickle cell disease. British Journal of Haematology. ,vol. 116, pp. 436- 444 ,(2002) , 10.1046/J.1365-2141.2002.03274.X
Winfred C. Wang, Steven G. Pavlakis, Kathleen J. Helton, Robert C. McKinstry, James F. Casella, Robert J. Adams, Renee C. Rees, , MRI abnormalities of the brain in one-year-old children with sickle cell anemia. Pediatric Blood & Cancer. ,vol. 51, pp. 643- 646 ,(2008) , 10.1002/PBC.21612
Winfred C. Wang, Ranjeet Grover, Dianne Gallagher, Mark Espeland, Alma Fandal, Developmental screening in young children with sickle cell disease. Results of a cooperative study. Journal of Pediatric Hematology Oncology. ,vol. 15, pp. 87- 91 ,(1993) , 10.1097/00043426-199302000-00011
Janet L. Kwiatkowski, Robert A. Zimmerman, Avrum N. Pollock, Wendy Seto, Kim Smith-Whitley, Justine Shults, Anne Blackwood-Chirchir, Kwaku Ohene-Frempong, Silent infarcts in young children with sickle cell disease. British Journal of Haematology. ,vol. 146, pp. 300- 305 ,(2009) , 10.1111/J.1365-2141.2009.07753.X