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Routine developmental, autism, behavioral, and psychological screening in epilepsy care settings
Author(s) -
Eom Soyong,
Fisher Breanne,
Dezort Catherine,
Berg Anne T
Publication year - 2014
Publication title -
developmental medicine and child neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.658
H-Index - 143
eISSN - 1469-8749
pISSN - 0012-1622
DOI - 10.1111/dmcn.12497
Subject(s) - epilepsy , autism , strengths and difficulties questionnaire , checklist , psychiatry , medical diagnosis , disease , psychology , medicine , clinical psychology , pediatric epilepsy , pediatrics , mental health , pathology , cognitive psychology
Aim Screening for cognitive impairment, developmental delay, and neuropsychiatric problems is not always performed in children with epilepsy. The aim of this study was to assess the value of this screening and its validity for determining previously unidentified (‘actionable’) problems in children with epilepsy. Method New and existing patients with epilepsy were recruited from a hospital‐based epilepsy center. The parent of the child completed screening evaluations for development (Ages and Stages Questionnaire [ASQ], 0–66mo), autism (Modified Checklist for Autism in Toddlers [mCHAT], 16–30mo), social communication (Social Communication Questionnaire [SCQ], ≥4y), and psychiatric concerns (Strengths and Difficulties Questionnaire [SDQ], 4–17y). Results We screened 236 children overall (136 males [58%], 100 females [42%]; mean age [SD] 6y 7mo [4y 6mo]). Of these, 176 children (75%) had established epilepsy diagnoses and 60 (25%) were patients with new‐onset epilepsy. Of those with new‐onset disease, 22 (37%) were determined not to have epilepsy. Positive findings by test were 82% (ASQ), 54% (mCHAT), 15%, (SCQ), and 58% (SDQ). Findings were actionable in 46 children (20%): 18% of findings in children with established epilepsy and 23% of findings in patients with new‐onset epilepsy. Of the 46 children for whom further referrals were made, the parents of 28 (61%) have pursued further evaluations. Interpretation In this study, children with existing and new‐onset diagnoses of epilepsy had actionable screening findings. These findings support the development of systematic screening of comorbidities for children with epilepsy.

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