Dace Almane1, Jana E Jones2, Daren C Jackson2, Michael Seidenberg3, Monica Koehn4, David A Hsu2, Bruce P Hermann2. 1. Department of Neurology, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA. Electronic address: almane@neurology.wisc.edu. 2. Department of Neurology, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA. 3. Department of Psychology, Rosalind Franklin School of Medicine and Science, North Chicago, IL, USA. 4. Marshfield Clinic Neurosciences, Marshfield Clinic, Marshfield, WI, USA.
Abstract
OBJECTIVE: This study was conducted to determine the lifetime rate and distribution of supportive academic and educational services provided to children with new- or recent-onset epilepsy and typically developing controls, the relationship of this history to objective academic test performance, and the course of performance over serial evaluations (baseline and 2 and 5years later). METHODS: Research participants were 91 children aged 8-18 at study entry, including 50 youth with recent-onset epilepsy (28 focal [FE] and 22 generalized [GE] epilepsy) and healthy first-degree cousin controls (n=41). The sample with epilepsy included children with uncomplicated epilepsy and normal imaging and development. Lifetime history of a diversity of supportive educational services was determined via a structured interview with parents at the baseline study visit. Associations were examined between these support services and participants' academic performance in reading, spelling, and arithmetic (Wide Range Achievement Test-Revision 3 [WRAT3] [12]) during three serial study visits including baseline and 2 and 5years later. RESULTS: Children with epilepsy had a higher lifetime rate of provision of diverse academic supportive services compared to controls at the baseline visit (52% vs. 18%). These services antedated epilepsy diagnosis in the majority (80.8%) of the children with epilepsy. Among children with epilepsy, children who presented with academic services had significantly lower WRAT3 reading, spelling, and arithmetic performance at baseline and at 2- and 5-year follow-ups. CONCLUSION: A brief structured clinical interview conducted with parents identifies children with epilepsy who are at academic risk at the time of diagnosis, with that risk persisting up to 5years later.
OBJECTIVE: This study was conducted to determine the lifetime rate and distribution of supportive academic and educational services provided to children with new- or recent-onset epilepsy and typically developing controls, the relationship of this history to objective academic test performance, and the course of performance over serial evaluations (baseline and 2 and 5years later). METHODS: Research participants were 91 children aged 8-18 at study entry, including 50 youth with recent-onset epilepsy (28 focal [FE] and 22 generalized [GE] epilepsy) and healthy first-degree cousin controls (n=41). The sample with epilepsy included children with uncomplicated epilepsy and normal imaging and development. Lifetime history of a diversity of supportive educational services was determined via a structured interview with parents at the baseline study visit. Associations were examined between these support services and participants' academic performance in reading, spelling, and arithmetic (Wide Range Achievement Test-Revision 3 [WRAT3] [12]) during three serial study visits including baseline and 2 and 5years later. RESULTS:Children with epilepsy had a higher lifetime rate of provision of diverse academic supportive services compared to controls at the baseline visit (52% vs. 18%). These services antedated epilepsy diagnosis in the majority (80.8%) of the children with epilepsy. Among children with epilepsy, children who presented with academic services had significantly lower WRAT3 reading, spelling, and arithmetic performance at baseline and at 2- and 5-year follow-ups. CONCLUSION: A brief structured clinical interview conducted with parents identifies children with epilepsy who are at academic risk at the time of diagnosis, with that risk persisting up to 5years later.
Authors: David W Dunn; C S Johnson; S M Perkins; P S Fastenau; A W Byars; T J deGrauw; J K Austin Journal: Epilepsy Behav Date: 2010-11 Impact factor: 2.937
Authors: Angela M McNelis; David W Dunn; Cynthia S Johnson; Joan K Austin; Susan M Perkins Journal: Epilepsy Behav Date: 2007-02-12 Impact factor: 2.937
Authors: Jana E Jones; Ryann Watson; Raj Sheth; Rochelle Caplan; Monica Koehn; Michael Seidenberg; Bruce Hermann Journal: Dev Med Child Neurol Date: 2007-07 Impact factor: 5.449
Authors: Dace N Almane; Qianqian Zhao; Paul J Rathouz; Melissa Hanson; Daren C Jackson; David A Hsu; Carl E Stafstrom; Jana E Jones; Michael Seidenberg; Monica Koehn; Bruce P Hermann Journal: J Int Neuropsychol Soc Date: 2018-05-10 Impact factor: 2.892
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