High dose phenobarbitone coma in pediatric refractory status epilepticus; a retrospective case record analysis, a

Sheffali Gulati1, Vishal Sondhi1, Biswaroop Chakrabarty1

  • 1Child Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.

Brain & Development
|January 8, 2018
PubMed

Insights

High-dose phenobarbitone coma effectively treated pediatric refractory status epilepticus when other treatments failed. This study outlines a protocol for its use in children, showing promising results with a high response rate.

Area of Science:

  • Neurology
  • Pediatric Epilepsy
  • Critical Care Medicine

Background:

  • Refractory status epilepticus (RSE) carries high morbidity and mortality.
  • Therapeutic coma is induced with agents like midazolam, thiopentone, phenobarbitone, or propofol for RSE.
  • Phenobarbitone has a favorable profile but is understudied in pediatric RSE.

Purpose of the Study:

  • To describe the use of phenobarbitone coma in pediatric refractory status epilepticus.
  • To evaluate the efficacy of high-dose phenobarbitone in this patient population.

Main Methods:

  • Retrospective analysis of pediatric patients with status epilepticus from 2014-2016.
  • Inclusion criteria: RSE unresponsive to midazolam infusion.
  • Phenobarbitone coma was initiated following a standardized protocol.

Main Results:

  • 34 children had RSE; 13 received high-dose phenobarbitone coma.
  • 12 out of 13 children responded to phenobarbitone.
  • Median time to seizure resolution was 16 hours; EEG changes occurred within 72 hours.

Conclusions:

  • High-dose phenobarbitone is an effective treatment for pediatric RSE.
  • The study provides a protocol for phenobarbitone coma in children.
  • Further validation with larger sample sizes is recommended.
Abstract

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