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Seizure control in glycine encephalopathy using the Ketamine-Dextromethorphan-Sodium benzoate triple therapy.

Laith Haddad, Samah Trad, Lama Charafeddine, Pascale E Karam

Epilepsy & behavior reports September 1, 2025 DOI: 10.1016/j.ebr.2025.100797 via PubMed

Summary

AI-generated from the abstract

Neonatal glycine encephalopathy, a rare genetic disorder causing severe seizures, was successfully treated with a combination of intravenous ketamine, oral dextromethorphan, and sodium benzoate in a newborn. The patient's status epilepticus resolved, and developmental improvement was observed on follow-up. Intravenous ketamine use in neonates is rare, with only two prior cases reported. This is the first report of efficacy using this triple therapy, suggesting a potential intervention for managing intractable seizures in glycine encephalopathy.

Study at a glance

Characteristics Case study Case report Peer reviewed
Sample size 1
Population Neonate with classical glycine encephalopathy
Interventions intravenous ketamine oral dextromethorphan sodium benzoate
Topics Ketamine
Keywords Dextrometorphan Glycine encephalopathy Non ketotic hyperglycinemia Sodium benzoate
Key finding A combination of intravenous ketamine, oral dextromethorphan, and sodium benzoate resolved status epilepticus and improved development in a neonate with glycine encephalopathy.

Abstract

Neonatal glycine encephalopathy is a rare genetic neurometabolic disorder secondary to glycine cleavage system deficiency. Patients typically present with early-onset intractable seizures, status epilepticus and encephalopathy. Seizures control remains challenging in view of their refractoriness to standard anti-seizure medications. Sodium benzoate is commonly used to control the elevated glycine level. Oral anti-NMDA receptor antagonists, ketamine and dextromethorphan, have been used in various combinations in the treatment of this complex disorder. In this report, we present a neonatal case of classical glycine encephalopathy with hypotonia and refractory myoclonic seizures. The status epilepticus was successfully treated using a combination of intravenous ketamine, oral dextromethorphan and sodium benzoate. Seizures resolved and the patient's development showed improvement on follow-up. The intravenous form of ketamine in the neonatal period is rarely used, and it has been reported in only two glycine encephalopathy patients in the literature. This is the first report in the literature of the efficacy of intravenous ketamine using the above triple therapy. This intervention might have implications on the management of neonatal intractable seizures in glycine encephalopathy, which might improve the outcome of this devastating disorder.

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