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Published on: April 5, 2011
[Management of convulsive status epilepticus in infants and children]
1Unité de réanimation pédiatrique polyvalente, hôpital Necker-Enfants-Malades, AP-HP, 149, rue de Sèvres, 75743 Paris cedex 15, France. philippe.hubert@nck.aphp.fr
Insights
Childhood convulsive status epilepticus is a medical emergency requiring prompt treatment to prevent neurological damage. Benzodiazepines are first-line, with clonazepam suggested in France, followed by phenytoin or phenobarbital.
Area of Science:
- Pediatric Neurology
- Emergency Medicine
- Pharmacology
Context:
- Childhood convulsive status epilepticus (CSE) is a life-threatening neurological emergency.
- Prolonged seizures pose significant risks for immediate and long-term adverse outcomes in developing brains.
- Prompt treatment is crucial for children experiencing generalized convulsive seizures exceeding five minutes.
Purpose:
- To review current evidence-based management strategies for pediatric convulsive status epilepticus.
- To highlight first-line and second-line pharmacological interventions.
- To discuss treatment options for refractory cases and specific regional considerations (e.g., France).
Summary:
- CSE in children carries a 3-5% mortality rate and higher morbidity, often linked to central nervous system infections.
- Immediate goals include airway, breathing, and circulation stabilization, followed by seizure termination.
- Benzodiazepines (e.g., clonazepam, rectal diazepam, buccal midazolam) are first-line; intravenous phenytoin/fosphenytoin and phenobarbital are second-line.
- Refractory CSE management may involve high-dose midazolam infusion, with propofol lacking a favorable risk-benefit ratio in children.
Impact:
- Provides guidance for managing a critical pediatric condition with limited evidence-based data.
- Informs clinical decision-making regarding drug selection and sequencing.
- Emphasizes the importance of timely intervention to mitigate neurological sequelae in affected children.
Abstract:
Convulsive status epilepticus in childhood is a life threatening condition with serious risk of neurological sequelae which constitutes a medical emergency. Clinical and experimental data suggest that prolonged seizures can have immediate and long-term adverse consequences on the immature and developing brain. So the child who presents with a continuous generalized convulsive seizure lasting greater than five minutes should be promptly treated. The outcome is mainly determined by the underlying etiology, age and duration of status epilepticus. In children the mortality from status epilepticus ranges from 3 to 5% and the morbidity is two-fold higher. Mortality and morbidity are highest with status epilepticus associated with central nervous system infections, which is the most important cause of status epilepticus. There are few evidence-based data to guide management decisions for the child with status epilepticus. Immediate goals are stabilization of airways, breathing and circulation and termination of seizures. Benzodiazepines remain the first-line drugs recommended for prompt termination of seizures. As intravenous lorazepam is not available in France, we suggest clonazepam as the best choice for initial therapy. Rectal diazepam or buccal midazolam remain important options. Intravenous phenytoin/fosphenytoin and phenobarbital are the second-line drugs. Phenytoin is being increasingly substituted by fosphenytoin, but pediatric data are scarce and fosphenytoin is not authorized for use in France below five years old. In children, phenytoin is often preferred to phenobarbital, even though no comparative studies have demonstrated a better efficacy. To manage status epilepticus refractory to a benzodiazepine and administration of phenytoin and/or phenobarbital, many pediatricians today prefer high-dose midazolam infusion rather than thiopental to minimize serious side effects from barbiturate anesthesia. There is no benefit/risk ratio to support the use of propofol for children with refractory status epilepticus.
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