Educational and Behavioral Problems in Children With
Epilepsy
Many children with epilepsy, a condition in which the electrical activity of
the central nervous system is disturbed and is often accompanied by seizures,
often receive mainstream education and are not restricted to day-to-day
activities. However, researchers from Utrecht in The Netherlands have studied
children diagnosed with epilepsy and found that they are more likely to require
special education services and have more behavioral
problems.
Fifty-one children recently diagnosed with epilepsy with no apparent
underlying cause underwent neurological and psychological testing three times
within the first year after their epilepsy diagnosis. The tests measured
learning, memory, academic skills, and mental and motor speed. The children's
parents and teachers also completed questionnaires about each child's behavior
in the classroom. The children with epilepsy were compared to a group of
classmates the same age who did not have epilepsy.
Fifty-one percent of children with epilepsy required special education
services, compared to only 27% of children without the diagnosis. Children with
epilepsy also had worse scores on cognitive and behavioral tests, and parents
and teachers rated children with epilepsy as having more behavioral problems.
Researchers also observed that children who were not able to adapt positively to
the epilepsy diagnosis (and who had parents who weren't able to adapt) were more
likely to have an increased risk of cognitive and behavioral problems.
What This Means to You: Children with epilepsy may be more likely to need
special education services. Children with epilepsy may also be at higher risk
for behavior problems. According to the results of this study, being unable to
adapt to the diagnosis - on the part of both parents and children - may increase
the risk of problems.
If your child has a chronic condition such as epilepsy, develop positive
working relationships with health care professionals, teachers, and others who
play important roles in your child's life. Ask questions and learn all you can
about your child's illness. It may also be helpful to join a support group or
meet regularly with other parents of children with your child's condition. Talk
to your child's doctor or specialist about local groups in your area that can
offer support and understanding to both you and your child.
Source: Kim J. Oostrom, PhD; Anneke Smeets-Schouten, PhD; Cas L.J.J.
Kruitwagen, MSc; A.C. Boudewyn Peters, MD, PhD; Aagje Jennekens-Schinkel, PhD
(for the Dutch Study group of Epilepsy in Childhood); Pediatrics,
December 2003
Reviewed by: Steven Dowshen, MD Date
reviewed: January 2004
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