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Published on: May 29, 2017
Treatment of neonatal seizures with carbamazepine
1Department of Neurology, University of Texas Southwestern Medical Center, Dallas 75235-9129, USA.
Insights
Carbamazepine shows promise as a safe and effective anticonvulsant for neonatal seizures, achieving therapeutic levels quickly with excellent seizure control and no significant side effects in this preliminary study.
Area of Science:
- Neonatal Neurology
- Pharmacology
- Clinical Pediatrics
Background:
- Carbamazepine is a well-established anticonvulsant in adults and older children.
- Its use as a primary anticonvulsant in neonates has been limited.
- Neonatal seizures, particularly those due to hypoxic-ischemic encephalopathy, require effective treatment options.
Purpose of the Study:
- To evaluate the long-term safety and efficacy of carbamazepine in neonates.
- To assess carbamazepine absorption, therapeutic levels, and elimination half-life in this population.
- To determine the anticonvulsant effect and side effect profile of carbamazepine in neonates.
Main Methods:
- Ten full-term neonates with hypoxic-ischemic encephalopathy-related seizures received carbamazepine via nasogastric tube.
- Loading doses were followed by two different maintenance regimens (21 mg/kg/day or 15 mg/kg/day).
- Therapy duration ranged from 3 to 9 months, with intensive drug level monitoring.
Main Results:
- Excellent carbamazepine absorption was observed in neonates, with therapeutic levels reached within 2-4 hours.
- Seizure control was excellent, with only two patients experiencing a single seizure post-treatment initiation.
- No significant gastrointestinal, hepatic, hematologic, renal, or dermatologic side effects were reported.
Conclusions:
- Carbamazepine demonstrates potential as an effective anticonvulsant for neonatal seizures.
- The drug is well-absorbed and tolerated in neonates, even those who are critically ill.
- This preliminary study supports further investigation into carbamazepine for neonatal seizure management.
Abstract:
Carbamazepine has been used in adults and children for over 30 years. In spite of an excellent therapeutic and side-effect profile in older children, it has never been used as a primary anticonvulsant in neonates. This is the first report of the long-term use of carbamazepine in neonates. Ten full-term neonates with two or more seizures due to hypoxic-ischemic encephalopathy were given 10 mg/kg of carbamazepine as a loading dose via nasogastric tube. Twenty-four hours later, the first five patients began a maintenance regimen of 21 mg/kg/daily, and the remaining five patients began a maintenance regimen of 15 mg/kg/daily, all via nasogastric tube. Therapy was continued for 3 to 9 months. Drug levels were monitored every 2 to 4 hours during the first 24 hours, and on days 2, 4, 8, 15, 30, 45, and 60, and monthly thereafter. Absorption of carbamazepine was excellent even in sick neonates. Therapeutic levels were reached in 2 to 4 hours in all patients. Peak levels were achieved in 4 to 16 hours (mean, 9.2 +/- 4.2). Elimination half-life was 24.5 hours. Levels dropped precipitously around 8 to 15 days and thereafter declined slowly over the next 3 months. Seizure control was excellent; only two patients had one seizure each during the first 10 hours. There were no gastrointestinal, hepatic, hematologic, renal, or dermatologic side effects. This preliminary study shows that carbamazepine may be an effective anticonvulsant for neonatal seizures.
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