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Updated: Jun 21, 2026

Cerebral Ischemic Coma Model Induced by Modified Four-Vessel Occlusion
Published on: July 5, 2024
Reversible coma associated with prolonged high-dose phenobarbital therapy in bilateral Sturge-Weber syndrome
Hiroyuki Wakamoto1, Yasuko Nakamura, Tomohiro Ebihara
1Department of Pediatrics, Ehime Prefecture Central Hospital, Matsuyama City, Ehime Prefecture, Japan. hirwaka@hotmail.com
Insights
High-dose phenobarbital effectively treats refractory status epilepticus. However, prolonged use in infants with severe cerebrovascular disease may cause neurological complications, necessitating careful monitoring.
Area of Science:
- Neurology
- Pediatrics
- Pharmacology
Background:
- High-dose phenobarbital is a recognized treatment for refractory status epilepticus in children.
- Limited data exists on the safety of long-term phenobarbital administration.
Observation:
- An infant with intractable epilepsy and bilateral Sturge-Weber syndrome developed coma after 1 2/3 months of high-dose phenobarbital.
- Recovery of consciousness correlated with decreased serum phenobarbital levels (<40 microg/mL).
- Electroencephalogram and brainstem auditory evoked potentials documented the neurological changes.
Findings:
- Prolonged high-dose phenobarbital therapy can lead to cerebral and brainstem dysfunction.
- Patients with severe cerebrovascular disease may be at higher risk for these complications.
Implications:
- This case highlights the potential neurotoxicity of long-term high-dose phenobarbital in vulnerable pediatric populations.
- Careful monitoring of neurological function is crucial during extended phenobarbital treatment, especially in patients with underlying cerebrovascular conditions.
Abstract:
High-dose phenobarbital therapy is an effective treatment for refractory status epilepticus in children. The advantages of this therapy include milder adverse effects without limits for maximal phenobarbital levels or doses during the initial phase of treatment. However, little is known about the safety of continuing the treatment. We describe an infant with intractable epilepsy associated with bilateral Sturge-Weber syndrome who became comatose after 1(2/3) months of high-dose phenobarbital treatment. The patient regained consciousness as serum phenobarbital concentration decreased to below 40 microg/mL. The progression and recovery were also documented by electroencephalogram and brainstem auditory evoked potentials. The present case suggests that prolonged high-dose phenobarbital therapy may cause cerebral and brainstem dysfunction in patients with severe cerebrovascular diseases. The underlying baseline metabolic and perfusion deficit related to the disease can precipitate the neurological complication during long-term high-dose phenobarbital therapy.
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