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.

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