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Clinical Impact and Safety Profile of Intravenous Lacosamide Administration as Adjunctive Therapy for Neonatal
C Cortes-Ledesma1, E Arias-Vivas2, G Ruiz-Ocaña de Las Cuevas2
1Division of Neonatology, Institute of Children and Adolescents, Hospital Clínico San Carlos, Madrid, Spain.
Insights
Lacosamide effectively treated refractory seizures in newborns, with 62.5% achieving remission. This study found lacosamide safe and well-tolerated in infants with neonatal seizures.
Area of Science:
- Neonatal Neurology
- Clinical Pharmacology
Background:
- Neonatal seizures, particularly refractory cases, present significant clinical challenges.
- Limited treatment options exist for symptomatic refractory seizures in newborns.
Purpose of the Study:
- To evaluate the clinical efficacy and safety of lacosamide in neonates with symptomatic refractory seizures.
- To assess the long-term outcomes and tolerance of lacosamide treatment up to 24 months of age.
Main Methods:
- Retrospective descriptive study of eight neonates with symptomatic refractory seizures.
- Lacosamide administered as third- or fourth-line therapy; data collected on dosage, duration, concurrent treatments, and adverse events.
Main Results:
- 62.5% of patients achieved complete seizure remission after lacosamide loading dose.
- Remaining patients experienced a reduction in seizure frequency.
- No adverse effects attributable to lacosamide were reported during the follow-up period.
Conclusions:
- Lacosamide demonstrates potential efficacy in achieving seizure remission in newborns with refractory seizures.
- Lacosamide exhibits excellent tolerance in the neonatal population.
- Further randomized controlled trials are warranted to confirm these preliminary findings.
Abstract:
The aim of this retrospective descriptive study was to evaluate the clinical impact and safety profile of lacosamide in neonates with symptomatic refractory seizures.Patients diagnosed with symptomatic refractory seizures who received lacosamide were included in the study. Follow-up assessments were conducted until 24 months of age, during which data on lacosamide dosage, duration of exposure, concurrent treatments, and potential side effects were collected. A total of eight patients were enrolled, with lacosamide administered as a third- or fourth-line treatment for symptomatic refractory seizures. Following loading dose, 62.5% of the patients achieved complete remission of seizure activity without recurrence. In the remaining cases, a reduction in seizure frequency was observed. No adverse effects attributable to lacosamide were reported.In conclusion, lacosamide may be effective in achieving seizure remission in newborns with symptomatic refractory seizures, and all patients demonstrate excellent tolerance. Brief exposure to lacosamide was sufficient, and no adverse effects were observed up to 24 months of age. However, randomized controlled trials are necessary to confirm these findings.
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