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Published on: September 20, 2024
Retention rate of levetiracetam in children with intractable epilepsy at 1 year
D Peake1, S Mordekar, J Gosalakkal
1Department of Paediatric Neurology, Birmingham Children's Hospital, and Nottingham University Hospitals, UK. peagrew@doctors.org.uk
Insights
Levetiracetam (LEV) is an effective antiepileptic drug for children with refractory epilepsy. This study shows LEV is well-tolerated with good seizure reduction and retention rates at 12 months.
Area of Science:
- Pediatric Neurology
- Clinical Pharmacology
- Epileptology
Background:
- Levetiracetam (LEV) is a novel antiepileptic drug (AED) approved for pediatric use.
- Refractory epilepsies in children pose significant treatment challenges.
Purpose of the Study:
- To evaluate the efficacy, tolerability, and retention rate of LEV in pediatric patients with refractory epilepsies.
- To assess LEV's effectiveness in a large cohort of children with difficult-to-treat epilepsy.
Main Methods:
- Retrospective, multicenter observational study of 200 children (0.3-19 years) with refractory epilepsy.
- Analysis of LEV use over a 4-year period, including dosage (8-100 mg/kg/day) and co-medications.
- Assessment of seizure reduction, seizure freedom, adverse events, and retention rates at various time points up to 12 months.
Main Results:
- LEV demonstrated good tolerability with a 49% retention rate at 1 year.
- Significant seizure reduction (>50%) observed in 60% at 2 months, 40% at 6 months, and 32% at 12 months.
- Adverse events were infrequent (24%), primarily behavioral or emotional changes, with no serious events reported.
Conclusions:
- Levetiracetam is effective and well-tolerated in children with refractory epilepsies.
- The study confirms good response and retention rates for LEV in pediatric patients up to 12 months.
- This represents the largest published cohort of pediatric LEV use with a 1-year follow-up.
Unlabelled:
Levetiracetam (LEV) is a novel antiepileptic drug (AED) that has recently obtained marketing authorisation for use in children. The purpose of this study was to assess the efficacy, tolerability and retention rate of LEV in children with refractory epilepsies. It is a retrospective multicentre observational study reporting the use of LEV in 200 children, aged 0.3-19 years (median 9-years-old) over a 4-year period. All of the patients included in the study had refractory epilepsy with a median age of onset of epilepsy of 3 years (range 0-13 years). The 38% had failed and withdrawn 3 or more AEDs previously and 24% were taking at least 2 other AEDs in addition to LEV. The 47% had focal, and 58% had symptomatic epilepsies. The LEV dose ranged from 8 to 100 mg/kg/day (mean 39 mg/kg). The study comprised 215 person years of LEV exposure.
Results:
LEV was well tolerated with a retention rate of 49% at 1 year. No serious adverse events were reported with possibly related adverse events reported in only 24% of patients (mainly emotional or behavioural changes). At more than 2, 6 and 12 months, worthwhile improvement (>50% seizure reduction) was noted in 60, 40 and 32%, including seizure freedom in 14, 14 and 5%, respectively.
Conclusion:
Our results confirm the efficacy and tolerability of LEV in children with refractory epilepsies and demonstrate good response and retention rates at 12 months. It represents the largest cohort of paediatric patients published so far on LEV with a 1-year follow-up.
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