Effects of sodium valproate and levetiracetam on posterior segment parameters in children with epilepsy
Purpose To evaluate changes in posterior segment parameters in pediatric patients with epilepsy using sodium valproate or levetiracetam monotherapy for at least 12 months. Methods This study included 45 children with generalized epilepsy aged 6–17 years and 32 age- and gender-matched healthy subject...
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Veröffentlicht in: | International ophthalmology 2024-02, Vol.44 (1), p.28-28, Article 28 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Purpose
To evaluate changes in posterior segment parameters in pediatric patients with epilepsy using sodium valproate or levetiracetam monotherapy for at least 12 months.
Methods
This study included 45 children with generalized epilepsy aged 6–17 years and 32 age- and gender-matched healthy subjects. The patients were assigned to three groups: Group 1 included patients using valproate monotherapy at a dose of 20–40 mg/kg/day, group 2 included patients using levetiracetam monotherapy at a dose of 20–40 mg/kg/day, and group 3 consisted of healthy controls. Peripapillary retinal nerve fiber layer (RNFL) and macular ganglion cell layer-inner plexiform layer (mGCIPL) thicknesses were measured using spectral-domain optical coherence tomography (OCT).
Results
No significant differences were noted between the groups regarding age, gender distribution, visual acuity, spherical equivalent, and intraocular pressure (
p
> 0.05). The average and temporal, nasal, and superior quadrants RNFL values were significantly thinner in group 1 than in group 2 (
p
= 0.001,
p
= 0.023,
p
= 0.011, and
p
= 0.001, respectively) and group 3 (
p
0.05).
Conclusion
These findings support that there is an association between sodium valproate treatment and the reduction of RNFL thickness in epilepsy. Levetiracetam treatment appears to be a safe option, but care should be taken regarding ocular side effects that may occur with long-term and high-dose use of sodium valproate. |
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ISSN: | 1573-2630 0165-5701 1573-2630 |
DOI: | 10.1007/s10792-024-02987-0 |