Related Experiment Video
Updated: Jul 25, 2026

Non-restraining EEG Radiotelemetry: Epidural and Deep Intracerebral Stereotaxic EEG Electrode Placement
Published on: June 25, 2016
Phenobarbital in the prophylaxis of late posttraumatic seizures
L Murri1, A Arrigo, U Bonuccelli
1Clinica Neurologica, Università di Pisa.
Insights
Phenobarbital (PB) effectively reduced the incidence of posttraumatic epilepsy (PTE) in severe head injury patients. This study shows PB
Area of Science:
- Neurology
- Clinical Pharmacology
- Traumatology
Background:
- Posttraumatic epilepsy (PTE) is a significant complication following severe head injuries.
- Effective prophylactic strategies for PTE are crucial for improving patient outcomes.
Purpose of the Study:
- To evaluate the efficacy of phenobarbital (PB) in reducing the incidence of posttraumatic epilepsy (PTE) in patients with severe head injuries.
- To determine optimal dosing and therapeutic plasma concentrations of PB for PTE prophylaxis.
Main Methods:
- A prospective study involving 390 patients with severe head injuries.
- Intramuscular and oral administration of phenobarbital (PB) for 12 months.
- Monitoring of serial plasma PB concentrations to maintain levels between 5 and 30 micrograms/ml.
Main Results:
- Out of 293 patients who completed the study, only 6 (2.04%) experienced seizures.
- Seizures occurred at plasma PB concentrations ranging from 20 to 28 micrograms/ml.
- PB administration demonstrated a prophylactic effect on PTE, even at relatively low doses.
Conclusions:
- Phenobarbital (PB) administered within the first 12 months post-trauma can significantly reduce the incidence of posttraumatic epilepsy (PTE).
- Therapeutic plasma concentrations of PB between 20-28 micrograms/ml appear effective in preventing seizures in this patient population.
Abstract:
390 patients with severe head injuries were treated with phenobarbital (PB) orally for a period of 12 months in order to determine whether this drug could reduce the incidence of posttraumatic epilepsy (PTE). An intramuscular PB dose of 2.5-3 mg/kg body weight per day was administered within 24 hours after the trauma; after 5 days, or longer if the coma persisted, the drug was administered orally. Maintenance dosage adjustments, when necessary, were based on serial plasma concentrations of the drug, sustained at between 5 and 30 micrograms/ml. 293 patients completed the study. 66% of these presented one risk factor, while 34% presented two or more. 6 patients (2.04%) had at least one seizure during the twelve months. Plasma drug levels at the time of the seizure, with one exception of 15 micrograms/ml, ranged from 20 to 28 micrograms/ml. The results of the study indicate that PB administered during the first twelve months after the trauma, even at relatively low doses, can have a prophylactic effect on PTE.
Related Concept Videos
CNS Depressants: Barbiturates and Benzodiazepines
Sedatives and Hypnotics Drugs: Barbiturates
Antiepileptic Drugs: Sodium Channel Blockers
Sodium channel blockers modulate ion channels, particularly voltage-gated sodium channels. They block only sodium ion movement.
Among the most commonly prescribed antiepileptic drugs are...
Antiepileptic Drugs: GABAergic Pathway Potentiators
The key GABA pathway potentiators used in epilepsy management are as follows.
Benzodiazepines are a well-known class of drugs used for their...
Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein
SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...
Antiepileptic Drugs: Potassium Channel Activators
Ezogabine has gained approval as an adjunctive treatment...

