High-Dose Midazolam for Pediatric Refractory Status Epilepticus: A Single-Center Retrospective Study

Zachary S Daniels1, Nina Srdanovic2, Karen Rychlik1,3

  • 1Ann and Robert H. Lurie Children's Hospital, Chicago, IL.

Insights

Midazolam treatment failure is common in pediatric refractory status epilepticus (RSE). Doses above 525 µg/kg/hr are linked to decreased seizure cessation success, indicating a need for careful dose titration.

Area of Science:

  • Pediatric Critical Care Medicine
  • Neurology
  • Pharmacology

Background:

  • Refractory status epilepticus (RSE) in children often requires continuous infusions of sedatives like midazolam.
  • Treatment failure with midazolam necessitates escalation to other agents, impacting patient outcomes.

Purpose of the Study:

  • To determine the prevalence of midazolam treatment failure in pediatric RSE.
  • To identify a midazolam dose threshold associated with reduced seizure cessation rates.

Main Methods:

  • Retrospective cohort study of pediatric patients with RSE receiving continuous midazolam infusion.
  • Receiver operating characteristic (ROC) curve analysis and Youden's index to identify optimal dose thresholds.
  • Logistic regression to assess the association between midazolam dose and seizure cessation.

Main Results:

  • Of 45 patients, 60% achieved seizure cessation with midazolam; 40% required additional pentobarbital.
  • Higher maximum midazolam doses were associated with treatment failure.
  • A midazolam dose threshold of 525 µg/kg/hr was identified, above which seizure cessation frequency diminished.

Conclusions:

  • Pediatric RSE treatment with high-dose midazolam (above 525 µg/kg/hr) shows diminishing efficacy.
  • Significant time may be spent titrating midazolam in a range associated with decreased seizure cessation, suggesting potential for earlier intervention or alternative strategies.
Abstract