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Calcium-channel blocker verapamil administration in prolonged and refractory status epilepticus
Paola Iannetti1, Alberto Spalice, Pasquale Parisi
1Division of Child Neurology, Department of Paediatrics, University La Sapienza 2, Rome, Italy. paola.iannetti@uniroma1.it
Insights
Intravenous verapamil successfully treated refractory status epilepticus (SE) in a child unresponsive to standard drugs. Verapamil
Area of Science:
- Neurology
- Pharmacology
Background:
- Refractory status epilepticus (SE) poses a significant treatment challenge, often unresponsive to conventional antiepileptic drugs (AEDs).
- Verapamil, a calcium channel blocker, has demonstrated anticonvulsant properties in preclinical animal models.
Observation:
- An 11-year-old boy with refractory SE, unresponsive to standard AEDs, presented with supraventricular tachycardia.
- Intravenous verapamil was administered due to its potential anticonvulsant activity and the patient's cardiac condition.
Findings:
- A dramatic resolution of electrical SE and clinical improvement, including regained consciousness and spontaneous respiration, was observed after verapamil administration.
- The patient received a cumulative dose of 3.125 mg of verapamil over 1.5 hours.
Implications:
- Verapamil may represent a novel therapeutic option for refractory SE, potentially acting via direct anticonvulsant mechanisms involving calcium channels.
- Verapamil's P-glycoprotein inhibitory effect could enhance the brain penetration of concurrently administered AEDs, improving their efficacy in SE treatment.
Abstract:
We report on an 11-year healthy boy who presented refractory status epilepticus (SE), which was unresponsive to conventional antiepileptic drugs used in the algorithm of the treatment of SE. Based on evidence that verapamil has anticonvulsant activity in animal models and the fact that the boy had a supraventricular tachycardia (140-160 b/min), i.v. verapamil (0.034 mg/min) was administered on day 37, and after a 3.125 mg cumulative verapamil dose (1.5 hour after initiation of the infusion), the patient regained consciousness was able to breathe spontaneously and the electrical SE promptly disappeared. The apparent dramatic response to i.v. verapamil may be explained by its direct anticonvulsant action on the basis of the potential involvement of calcium channels in epileptic activity and that verapamil, a known Pgp inhibitor in the cerebrovascular endothelium in the epilepticus focus, acted by facilitating the brain penetration of the antiepileptic drugs that our patient was receiving simultaneously.
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