AI Article Synopsis

  • Cerebral palsy (CP) is a motor disorder linked to brain damage, often accompanied by developmental challenges and epilepsy, requiring comprehensive management.
  • A notable number of CP patients show interictal epileptiform discharges (IEDs) in EEG tests without having clinical epilepsy, indicating underlying neuronal issues that could worsen their condition.
  • Research suggests that addressing IEDs could improve outcomes for CP patients, leading to a recommendation for integrating EEG assessments into their treatment plans to manage these discharges effectively.

Article Abstract

Cerebral palsy (CP) is a motor disorder due to cerebral damage. It is commonly associated with neuro-psychological retardation and also with epilepsy; hence, its management warrants a multi-dimensional approach. In a significant number of CP patients, interictal epileptiform discharges (IEDs) are obtained in their EEG even in absence of clinical epilepsy. Epileptiform discharge-firing cortical neurons are found to be associated with elevated intracellular Ca(2+) levels and exhibition of abnormal response on exposure to excitotoxic glutamate; both these features have been found to lead to subsequent death of these neurons. This further damage is likely to aggravate the already existing cortical damage in CP patients thereby worsening their prognosis. IEDs are also known to be associated with other neuro-psychological disorders like cognitive impairment and behavioral problems even in absence of clinical epilepsy. Thus, the IEDs cannot be viewed as benign events and their occurrence even in absence of clinical epilepsy cannot be ignored. A few trials aimed at treating IEDs in autistic patients without epilepsy and in children with behavior problems have yielded favorable results. Based on these studies, the author proposes inclusion of EEG investigation in the management protocol of CP patients and treatment of IEDs (when detected even in absence of clinical epilepsy) for a better outcome in their prognosis.

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http://dx.doi.org/10.1016/j.clineuro.2006.11.003DOI Listing

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