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[Continuous midazolam infusion for refractory nonconvulsive status epilepticus in children]
Tatsuro Nobutoki1, Kenji Sugai, Michio Fukumizu
1Department of Child Neurology, National Center Hospital for Mental, Nervous and Muscular Disorders, National Center of Neurology and Psychiatry, Kodaira, Tokyo. nobutokit@mie-m.hosp.go.jp
Insights
Continuous midazolam infusion effectively treated refractory nonconvulsive status epilepticus (NCSE) in children. This safe first-line therapy demonstrated efficacy in most cases without serious adverse events.
Area of Science:
- Pediatric Neurology
- Epileptology
- Clinical Pharmacology
Context:
- Refractory nonconvulsive status epilepticus (NCSE) presents a significant therapeutic challenge in pediatric populations.
- Existing treatment options for NCSE may have limited efficacy or significant side effects.
- Continuous intravenous infusion of midazolam (MDL) is an option for managing refractory NCSE.
Purpose:
- To evaluate the efficacy and safety of continuous midazolam infusion as a first-line therapy for pediatric refractory nonconvulsive status epilepticus (NCSE).
Summary:
- Seven episodes of refractory NCSE in five children were treated with continuous midazolam infusion.
- An initial bolus followed by a slow-titrated infusion (0.1-0.4 mg/kg/hr) was administered.
- Electroencephalogram (EEG) and vital signs were monitored throughout treatment.
- NCSE was abolished within hours in five of seven episodes.
- Two patients maintained normal functions during infusion.
- One patient experienced recurrence unresponsive to maximum dose.
- No serious complications like respiratory depression or hypotension were observed.
Impact:
- Continuous midazolam infusion demonstrates significant efficacy in controlling pediatric refractory NCSE.
- The treatment is well-tolerated, with a favorable safety profile, lacking serious adverse events.
- This approach offers a safe and effective first-line therapeutic option for pediatric NCSE, potentially improving patient outcomes.
Abstract:
We examined efficacy of continuous midazolam (MDL) infusion in seven episodes of refractory nonconvulsive status epilepticus (NCSE) in five children. Diagnosis included Lennox-Gastaut syndrome (two cases), and symptomatic generalized epilepsy, ring chromosome 20 syndrome, and epilepsy with continuous spike-waves during slow-wave sleep (one case each). One patient with Lennox-Gastaut syndrome and another with ring chromosome 20 syndrome had two episodes of NCSE. MDL was given as an initial bolus of 0.15 to 0.3 mg/kg, followed by continuous intravenous infusion at 0.1 to 0.2 mg/kg/hr. The infusion rate was increased slowly by 0.1 mg/kg/hr every 0.5 to 1.0 hr, up to 0.4 mg/kg/hr or until NCSE was controlled. The electroencephalogram, vital signs, blood pressure, and oxygen saturation were monitored during therapy. Electrical status epilepticus was abolished within a few hours in five of the seven episodes, and two patients could maintain wakefulness, oral intake, and bowel and bladder control throughout the continuous infusion. In one patient in whom NCSE recurred, it then remained uncontrolled even at a maximum dose. Serious complications such as respiratory depression or hypotension were not observed. Continuous intravenous infusion of MDL was effective and safe for NCSE in children, and can be used as firstline therapy for this condition.
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