Literature DB >> 22789633

Routine developmental and autism screening in an epilepsy care setting.

Breanne Fisher1, Catherine Dezort, Douglas R Nordli, Anne T Berg.   

Abstract

Developmental delay (delay) and co-morbidities like autism are common in children with epilepsy. We assessed the yield of routine screening for delay and autism in a hospital-based program. Parents completed developmental and autism screeners for 65 children (average age=2.5y; 38(58%) boys). Forty-nine (75%) were established epilepsy patients, and 16 (25%) were new patients. For development, 47 (72%) children screened positive and 8 (12%) had borderline results. Twenty-four (37%) scored positive for autism, all of whom also screened positive for developmental delay. Delays and neurologic deficits accounted for the positive autism results in 20 of the 24. Developmental findings were confirmatory (already receiving services) in 32/55 (58%) children and actionable in 17 (31%) (requiring further evaluation). Referrals for further evaluations were made for most with actionable findings. The yield of routine screening of children in a tertiary center is sufficiently high to support its use and to consider screening of all children seen with epilepsy.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22789633     DOI: 10.1016/j.yebeh.2012.06.006

Source DB:  PubMed          Journal:  Epilepsy Behav        ISSN: 1525-5050            Impact factor:   2.937


  4 in total

Review 1.  Autism Spectrum Disorder and Epilepsy: Two Sides of the Same Coin?

Authors:  Shafali Spurling Jeste; Roberto Tuchman
Journal:  J Child Neurol       Date:  2015-09-14       Impact factor: 1.987

2.  Defining incident cases of epilepsy in administrative data.

Authors:  Paul M Bakaki; Siran M Koroukian; Leila W Jackson; Jeffrey M Albert; Kitti Kaiboriboon
Journal:  Epilepsy Res       Date:  2013-06-20       Impact factor: 3.045

3.  Incidence and prevalence of treated epilepsy among poor health and low-income Americans.

Authors:  Kitti Kaiboriboon; Paul M Bakaki; Samden D Lhatoo; Siran Koroukian
Journal:  Neurology       Date:  2013-04-24       Impact factor: 9.910

4.  Kv1.1 deficiency alters repetitive and social behaviors in mice and rescues autistic-like behaviors due to Scn2a haploinsufficiency.

Authors:  Jagadeeswaran Indumathy; April Pruitt; Nicole M Gautier; Kaitlin Crane; Edward Glasscock
Journal:  Brain Behav       Date:  2021-01-23       Impact factor: 2.708

  4 in total

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