Generalized convulsive status epilepticus (GCSE) is a common neurological emergency in children. Benzodiazepines are the recommended first line antiseizure medication (ASMs), but they fail to control seizures in a third of cases. Combination of benzodiazepines with another ASM that has a different mechanism of action may be a promising option for faster control of GCSE. In this study, the investigators aim to evaluate the efficacy and safety of ketamine plus midazolam versus midazolam alone as first-line therapy of pediatric GCSE.
Generalized convulsive status epilepticus (GCSE) is a common neurological emergency in children, which is associated with significant morbidity and mortality. This condition is defined as \> 5 minutes of continuous or recurrent generalized tonic-clonic seizure activity without regaining consciousness. GCSE requires immediate evaluation and management in order to control ongoing seizures. According to most guidelines, benzodiazepines are the recommended first line antiseizure medication (ASMs). Second-line ASMs for benzodiazepines-refractory GCSE include multiple options, such as fosphenytoin/phenytoin, valproic acid, or levetiracetam. Last, refractory GCSE requires treatment with third-line ASMs, such as another second-line ASMs or infusion with thiopental, midazolam, pentobarbital, propofol, or ketamine. However, about 35% of cases with GCSE are not controlled by benzodiazepines, and up to 40% of benzodiazepines-refractory GCSE don't respond to second-line ASMs. As GCSE persists for a longer time, it becomes more difficult to control with worse prognosis. Indeed, the effectiveness of benzodiazepines to control seizures decreases by 50% when given after 10-15 minutes of continuous seizures. Therefore, new ASMs or combinations are required for earlier control of seizures, which will contribute to better outcome. Combination of benzodiazepines with another ASM that has a different mechanism of action may be a promising option for faster control of GCSE. One of the potential drugs for such combination is ketamine. Several adult and pediatric studies have shown effectiveness of ketamine in refractory and super-refractory GCSE. Unlike benzodiazepines that act through inhibitory Gamma-aminobutyric acid (GABA), ketamine is a non-competitive antagonist for N- methyl- d- aspartate (NMDA) receptors, which mediates excitatory glutamate action. Continuous seizure activity is associated with internalization of GABA receptors and upregulation of NMDA receptors. A number of animal studies have demonstrated synergistic action of combined ketamine and benzodiazepines for status epilepticus. While combined ketamine and benzodiazepines have been used in pediatric sedation/analgesia, there are limited studies on such combination for children with GCSE. In this study, the investigators aim to evaluate the efficacy and safety of ketamine plus midazolam versus midazolam alone as first-line therapy of pediatric GCSE.
Sohag University Hospital
Sohag, Egypt
Cessation of seizures at 5 minutes
Cessation of clinical seizures at 5 minutes study timepoint
Time frame: 5 minutes
Need for repeating midazolam
Need for repeating midazolam during the first therapy phase
Time frame: 15 minutes
Cessation of seizures at 15 minutes
Cessation of clinical seizures at 15 minutes study timepoint
Time frame: 15 minutes
Cessation of seizures at 35 minutes
Cessation of clinical seizures at 35 minutes study timepoint
Time frame: 35 minutes
Cessation of seizures at 55 minutes
Cessation of clinical seizures at 55 minutes study timepoint
Time frame: 55 minutes
Seizure recurrence
Recurrence of clinical seizures after initial cessation in the first 24 hours
Time frame: 24 hours
Hypotension
Occurrence of hypotension
Time frame: 24 hours
Hypertension
Occurrence of hypertension
Time frame: 24 hours
Intubation
Need for endotracheal intubation
Time frame: 24 hours
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Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
144
Arrhythmia
Occurrence of Arrhythmia
Time frame: 24 hours
Emergence phenomenon
Occurrence of emergence phenomenon, as one or more of the following: hallucination, delirium, vivid dreams, blurred/double vision, nausea/vomiting, hypersalivation.
Time frame: 24 hours
Skin rash
Occurrence of skin rash
Time frame: 24 hours
Mortality
Occurrence of death
Time frame: 24 hours