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Clinical Use and Efficacy of Levetiracetam for Absence Epilepsies
Danielle Nolan1, Shannon G Lester2, Stephanie M Rau2
11 Division of Epilepsy, Department of Neurology, University of Michigan, Ann Arbor, MI, USA.
Insights
Levetiracetam is frequently used for absence epilepsy, but efficacy is limited, with most children not achieving seizure freedom. Early consideration of alternative treatments is recommended if levetiracetam is ineffective.
Area of Science:
- Pediatric Neurology
- Epileptology
- Clinical Pharmacology
Background:
- Levetiracetam is a broad-spectrum anti-seizure medication.
- It lacks a specific indication for absence epilepsy.
- Common clinical practice involves its use in pediatric absence epilepsy cases.
Purpose of the Study:
- To evaluate the efficacy of levetiracetam in treating absence epilepsy in children.
- To determine if electroencephalographic (EEG) findings can predict treatment response.
- To assess the real-world effectiveness of levetiracetam for absence seizures.
Main Methods:
- Retrospective chart review of 158 children diagnosed with new-onset absence epilepsies.
- Analysis of 72 children treated with levetiracetam between 2011 and 2016.
- Evaluation of seizure control, side effects, EEG findings, and dosage.
Main Results:
- Levetiracetam was discontinued in 74% of patients due to inadequate seizure control or side effects.
- Only about one-quarter of treated children achieved seizure freedom.
- Lower maximal doses were associated with treatment effectiveness (29 mg/kg/d vs. 42 mg/kg/d).
Conclusions:
- Levetiracetam has limited efficacy for absence epilepsy in routine pediatric practice.
- Approximately 25% of children experienced seizure freedom with levetiracetam.
- Early transition to alternative medications is advised if levetiracetam fails to control seizures.
Background:
Levetiracetam is prescribed for a broad spectrum of seizure types but does not have a specific indication for absence epilepsy. We hypothesized that levetiracetam is commonly prescribed for children with absence epilepsies and evaluated the efficacy of this medication for absence epilepsy treatment in clinical practice. We also hypothesized that electroencephalographic (EEG) findings could help predict levetiracetam efficacy.
Methods:
We reviewed the charts of all patients treated for new-onset absence epilepsies at our pediatric neurology clinic between January 2011 and January 2016. Among 158 children diagnosed with absence epilepsies, 72 were treated with levetiracetam.
Results:
Levetiracetam was discontinued in 74% (n = 53/72) because of incomplete seizure control (59%, n = 35/72) and/or intolerable side effects (41%, n = 24/72) after a median 8.5 months (interquartile range 2, 17 months). Among patients for whom levetiracetam was effective, 44% (n = 8/18) had polyspikes on their initial EEG, versus 27% (n = 14/52) of patients for whom levetiracetam was discontinued ( P = .17). The maximal prescribed dose was lower for children in whom levetiracetam was effective (29 ± 13 mg/kg/d) than those for whom levetiracetam failed (42 ± 20 mg/kg/d; P = .005).
Conclusion:
In routine clinical practice, levetiracetam is often chosen for patients with absence seizures. However, only about one-quarter of children with absence epilepsy in this study became seizure free with levetiracetam. When effective, levetiracetam can control absence epilepsy at a relatively low dose. Lack of seizure control requiring continued dose escalation should prompt early consideration of a therapeutic medication transition.
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