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Published on: May 16, 2019
Pharmacologic management of convulsive status epilepticus in childhood
Kai Eriksson1, Reetta Kälviäinen
1Pediatric Research Centre, Medical School, 33014 University of Tampere and Tampere University Hospital, Department of Pediatric Neurology, Tampere, Finland. kai.eriksson@uta.fi
Insights
Convulsive status epilepticus in children requires prompt treatment. Early intervention with benzodiazepines, like buccal midazolam, improves outcomes and reduces long-term neurological damage.
Area of Science:
- Pediatric Neurology
- Emergency Medicine
Background:
- Convulsive status epilepticus (CSE) affects 20-50/100,000 children annually, posing a significant medical emergency.
- Seizures lasting over 5 minutes require immediate intervention as they rarely resolve spontaneously.
- Delayed treatment of CSE drastically increases mortality and morbidity, particularly after 60 minutes.
Purpose of the Study:
- To review current treatment strategies for pediatric convulsive status epilepticus.
- To highlight the importance of timely intervention and effective drug choices.
- To identify areas for future research and protocol development.
Main Methods:
- Literature review of current guidelines and studies on pediatric CSE management.
- Analysis of first-, second-, and third-line treatment options.
- Emphasis on the role of electroencephalogram (EEG) monitoring.
Main Results:
- Benzodiazepines are the first-line treatment, with buccal midazolam showing improved efficacy and ease of administration over rectal diazepam.
- Intravenous phenytoin/fosphenytoin and phenobarbital are recommended second-line treatments.
- Refractory cases may require barbiturates or midazolam as intravenous anesthetics, with EEG monitoring crucial for assessing response.
Conclusions:
- Optimizing treatment for pediatric CSE necessitates individualized protocols and pathways.
- Further randomized clinical trials are essential to evaluate novel treatment protocols for improved efficacy, safety, and neuroprotection.
- The goal is to minimize neuronal injury and reduce the risk of long-term neurological morbidity.
Abstract:
The incidence of convulsive status epilepticus in children is approximately 20-50/100,000/year, and is an emergency requiring prompt medical intervention. Prolonged seizures lasting over 5 min are unlikely to stop spontaneously, and time-to-treatment influences treatment response. Prolonged seizures should thus be treated as early status epilepticus. Mortality and morbidity increase significantly with the length of ongoing seizure activity, especially after 60 min. Benzodiazepines remain the first-line drug therapy due to their rapid onset of action. Recent studies imply that buccal midazolam is more effective and easier to administer than rectal diazepam. Phenytoin/fosphenytoin and phenobarbital administered intravenously remain the second-line treatments of choice, whilst barbiturates and midazolam as intravenous anesthetics are used for third-line treatment. Electroencephalogram monitoring is essential to evaluate the electrophysiologic treatment response and depth of anesthesia, especially in refractory status epilepticus. In the future, more individualized protocols and pathways are needed in order to optimize treatment responses. Randomized clinical trials are needed to evaluate new treatment protocols, which should not only stop the seizures more effectively but also be safer and include some neuroprotective elements to halt the cascade of neuronal injury and minimize the risk for neurologic morbidity caused by the convulsive status epilepticus.
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