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Published on: July 8, 2025
The influence of levetiracetam on psychosocial and behavioral functioning in children: A case-control and follow-up
Gonca Bektaş1, Uğur Tekin2, Melis Ulak Özkan1
1Department of Pediatric Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Insights
Levetiracetam (an antiepileptic drug) did not show frequent psychosocial or behavioral side effects in children compared to valproic acid over 3 months. Most children experienced no significant issues, indicating a favorable safety profile for levetiracetam in pediatric epilepsy treatment.
Area of Science:
- Pediatric Neurology
- Clinical Pharmacology
- Child Psychiatry
Background:
- Levetiracetam (LEV) is a common antiepileptic drug (AED) for pediatric epilepsy.
- Previous studies suggest LEV may be linked to psychosocial and behavioral problems in children.
- Epilepsy characteristics like seizure frequency and duration can also influence these issues.
Purpose of the Study:
- To assess the incidence and timing of treatment-emergent psychosocial and behavioral problems in children treated with LEV.
- To evaluate these problems independently of potential confounding epilepsy variables.
- To compare LEV with another AED, valproic acid (VPA), in terms of behavioral outcomes.
Main Methods:
- A prospective, 3-month case-control study included children aged 6-16 years with new-onset partial seizures.
- Participants were randomized to receive either LEV or VPA.
- Psychosocial and behavioral functioning were measured using the Strengths and Difficulties Questionnaire (SDQ) and Children's Depression Inventory (CDI) at baseline and at 1 and 3 months.
Main Results:
- 101 children were analyzed: 32 on LEV, 19 on VPA, and 50 healthy controls.
- No significant baseline differences in SDQ or CDI scores were found between patients and controls.
- No statistically significant differences in CDI or SDQ scores were observed between the LEV and VPA groups throughout the study.
- One patient on LEV experienced suicidal ideation and depression, which resolved upon switching to VPA; no other psychiatric side effects were noted.
Conclusions:
- Treatment-emergent psychosocial and behavioral side effects associated with levetiracetam are not frequent in children, especially at lower doses.
- After 3 months of treatment, standardized instruments did not reveal significant differences in behavioral outcomes between levetiracetam and valproic acid groups.
- Levetiracetam appears to have a generally favorable psychosocial and behavioral safety profile in pediatric epilepsy patients compared to valproic acid.
Background:
Levetiracetam, a widely used antiepileptic drug in children, has been associated with psychosocial and behavioral problems, which are also influenced by epilepsy variables, including duration or seizure frequency.
Purpose:
The objective of this study is to investigate the frequency and timing of treatment-emergent psychosocial and behavioral problems in children receiving levetiracetam, irrespective of seizure variables which are possible confounders.
Methods:
A prospective, case-control study with a 3-month follow-up was conducted. Consecutive children aged 6 to 16years with new-onset partial seizures were included in case of starting treatment with either levetiracetam or valproic acid. Psychosocial and behavioral functioning were assessed using a set of standardized questionnaires including Strengths and Difficulties Questionnaire (SDQ) and Children's Depression Inventory (CDI) at baseline, 1 and 3-month follow-up. Patients' baseline scores were compared to healthy subjects. The difference in the follow-up SDQ and CDI scores was evaluated in patients receiving levetiracetam and valproic acid.
Results:
A total of 101 participants were analyzed; 32 patients in levetiracetam group, 19 patients in valproic acid group and 50 healthy controls. Baseline SDQ and CDI scores were not statistically different between patients and healthy subjects (p>0.05). No statistically significant difference was observed in CDI, total and subscale SDQ scores between patients receiving levetiracetam or valproic acid during the study period (p>0.05). A girl aged 15years receiving levetiracetam had a CDI score of 18 without suicidal ideation at baseline. She developed suicidal ideation and depression, which resolved after switching of levetiracetam to valproic acid, at the 1-month follow-up. No other psychiatric or behavioral side-effects were observed in other patients.
Conclusion:
Psychosocial and behavioral side-effects of levetiracetam treatment are not frequent and they don't emerge in most of children at lower doses. At this dose, and after 3months, using these specific instruments, we did not observe any difference between the valproic acid and levetiracetam treatment groups.
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