Efficacy of a pre-specified timeline-based treatment protocol in children with acute repetitive seizures or seizure

Indar Kumar Sharawat1, Aparna Ramachandran2, Vinod Kumar1

  • 1Department of Pediatrics, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.

Insights

A new treatment protocol effectively managed acute repetitive seizures (ARSs) in children with epilepsy. The protocol demonstrated safety and efficacy, with successful outcomes in most patients, particularly when triggers like fever were addressed.

Area of Science:

  • Pediatric Neurology
  • Epilepsy Management
  • Clinical Protocol Development

Background:

  • Acute repetitive seizures (ARSs) are a common pediatric neurological emergency.
  • A standardized, evidence-based treatment protocol for ARSs in children is needed.
  • Current management lacks a defined timeline for intervention.

Purpose of the Study:

  • To evaluate the efficacy and safety of a pre-specified, timeline-based treatment protocol for pediatric ARSs.
  • To assess the protocol's effectiveness in children aged 1-18 with established epilepsy, excluding new-onset cases or critically ill patients.

Main Methods:

  • Retrospective chart review of 100 pediatric patients (1-18 years) with ARSs.
  • Application of a two-tier treatment protocol: intravenous lorazepam and ASM optimization (tier 1), followed by additional ASMs if needed (tier 2).
  • Analysis of treatment success, factors influencing efficacy, and adverse events.

Main Results:

  • The treatment protocol was successful in 89% of patients (58% required tier 1, 31% required tier 2).
  • Absence of pre-existing drug-resistant epilepsy and presence of acute febrile illness were associated with tier 1 success (P=0.02 and P=0.03, respectively).
  • Common adverse effects included excessive sedation (29%), incoordination (14%), gait instability (11%), and irritability (5%).

Conclusions:

  • The pre-specified treatment protocol is safe and efficacious for controlling ARSs in non-critically ill children with established epilepsy.
  • Further external validation in diverse epilepsy populations and international centers is recommended before widespread clinical adoption.
Abstract

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