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Journal of Child Neurology, Vol. 14, No. 5, 289-294 (1999)
DOI: 10.1177/088307389901400504

Characteristics and Prognosis of Epilepsy in Children With Cerebral Palsy

Dimitrios I. Zafeiriou, MD, PhD

First Pediatric Clinic, Aristotle University of Thessaloniki, Thessaloniki, Greece, jeff{at}med.auth.gr

Eleftherios E. Kontopoulos, MD, PhD

First Pediatric Clinic, Aristotle University of Thessaloniki, Thessaloniki, Greece

Ioannis Tsikoulas, MD, PhD

First Pediatric Clinic, Aristotle University of Thessaloniki, Thessaloniki, Greece

The aims of the study were to describe the prevalence and characteristics of epilepsy in a population of patients with cerebral palsy in a university referral center and to determine the rate of relapse caused by discontinuation of antiepileptic drugs after a 3-year seizure-free period. A total of 178 consecutive patients with cerebral palsy and epilepsy were prospectively followed for 9.2 ± 2.4 years after onset of seizures and compared to a control group of 150 epileptic patients without cerebral palsy (median follow-up period, 10.5 years). The overall prevalence of epilepsy was 36.1%. Patients with atonic-diplegic, dystonic, tetraplegic, and hemiplegic cerebral palsy had a higher incidence of epilepsy (87.5%, 87.1%, 56.5%, and 42%, respectively). In all, 134 (75.3%) patients were seizure free for more than 3 years and could discontinue therapy, whereas 44 patients (24.7%) were still on antiepileptic drugs. Eighteen of 134 patients relapsed after a 3-year seizure-free period and subsequent discontinuation of antiepileptic drugs, thus giving a relapse rate of 13.4%. First seizures occurred during the first year of life in 69.7% of the patients with epilepsy and cerebral palsy. Complete control of seizures could be achieved in 65.2% of the patients with cerebral palsy and epilepsy; however, regardless of the prognosis of seizures, epilepsy was a major prognostic factor regarding both the presence of mental retardation and the motor development of children with cerebral palsy. (J Child Neurol 1999;14:289-294).


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