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Does vigabatrin treatment for infantile spasms cause visual field defects? An international multicentre study
Raili Riikonen1, Zvonka Rener-Primec, Lionel Carmant
1Children's Hospital, Kuopio University Hospital, Kuopio, Finland.
Insights
Vigabatrin treatment in infancy was associated with visual field defects (VFDs) in 34% of school-aged children. The risk of VFDs increased significantly with longer treatment durations, highlighting the need for careful risk-benefit assessment.
Area of Science:
- Ophthalmology
- Pediatric Neurology
- Pharmacology
Background:
- Infantile spasms are a severe epilepsy syndrome in infants.
- Vigabatrin is an effective anti-seizure medication for infantile spasms.
- Potential long-term visual side effects of vigabatrin require investigation.
Purpose of the Study:
- To assess the prevalence and severity of visual field defects (VFDs) in school-aged children previously treated with vigabatrin for infantile spasms.
- To determine the relationship between vigabatrin treatment duration and the occurrence of VFDs.
Main Methods:
- A cohort of 35 children treated for infantile spasms in infancy underwent comprehensive visual field testing (static and kinetic perimetry).
- Etiologies of infantile spasms included tuberous sclerosis, other symptomatic causes, and cryptogenic cases.
- Children were stratified into groups based on vigabatrin treatment duration (<1 year, 1-2 years, >2 years).
Main Results:
- 34% of children (11/32) exhibited vigabatrin-attributed VFDs.
- VFD prevalence increased with treatment duration: 9% (<1 year), 30% (1-2 years), and 63% (>2 years).
- Six out of 10 children with tuberous sclerosis developed VFDs, indicating a higher risk in this subgroup.
Conclusions:
- Vigabatrin treatment for infantile spasms is associated with a significant risk of developing VFDs in school-aged children.
- The duration of vigabatrin therapy is a critical factor influencing the likelihood and severity of VFDs.
- A careful evaluation of the risk-benefit profile is essential when considering vigabatrin treatment, particularly for extended periods.
Aim:
The aim of this study was to examine whether vigabatrin treatment had caused visual field defects (VFDs) in children of school age who had received the drug in infancy.
Method:
In total, 35 children (14 males, 21 females; median age 11y, SD 3.4y, range 8-23y) were examined by static Humphrey perimetry, Goldmann kinetic perimetry, or Octopus perimetry. The aetiologies of infantile spasms identified were tuberous sclerosis (n=10), other symptomatic causes (n=3), or cryptogenic (n=22).
Results:
Typical vigabatrin-attributed VFDs were found in 11 out of 32 (34%) children: in one out of 11 children (9%) who received vigabatrin for <1 year (group 1), in three out of 10 children (30%) who received vigabatrin for 12 to 24 months (group 2), and in seven out of 11 children (63%) who received vigabatrin treatment for longer than 2 years (group 3). VFDs were mild in five and severe in six children. Patients with tuberous sclerosis were at higher risk of VFDs (six out of 10 children). The mean cumulative doses of vigabatrin were 140.5, 758.8, and 2712g in group 1, 2, and 3, respectively.
Interpretation:
VFDs were found in 34% of the cohort of children in this study. The rate of VFD increased from 9% to 63% as duration of treatment increased. The results of this study showed that the risk-benefit ratio should always be considered when using vigabatrin.
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