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Ketogenic Diet Therapy in Infants: Efficacy and Tolerability
Elaine Wirrell1, Susan Eckert2, Lily Wong-Kisiel1
1Child and Adolescent Neurology and Epilepsy, Mayo Clinic, Rochester, Minnesota.
The ketogenic diet is an effective treatment for infants with intractable epilepsy, showing high responder rates and seizure freedom. In-hospital initiation is recommended to manage potential hypoglycemia risks.
Area of Science:
- Neurology
- Pediatric Neurology
- Metabolic Disorders
Background:
- Intractable epilepsy in infants presents significant management challenges.
- Limited treatment options exist for medically refractory epilepsy in neonates and infants.
- The ketogenic diet is a recognized therapeutic option for pediatric epilepsy.
Purpose of the Study:
- To evaluate the tolerability and efficacy of the ketogenic diet in infants under 12 months of age.
- To assess the safety profile and success rates of ketogenic diet initiation in this vulnerable population.
Main Methods:
- Retrospective review of 27 infants under 12 months initiated on the ketogenic diet between 2007 and 2016.
- Data collected included epilepsy details, diet initiation, efficacy (responder rates, seizure freedom), and tolerability (adverse events).
- Infants were initiated on a traditional ketogenic diet at full caloric intake, primarily in-hospital.
Main Results:
- The ketogenic diet was initiated in 27 infants (median age 7 months) with a high prevalence of daily seizures and various epilepsy syndromes.
- Responder rates were high (68% at 1 month, 91% at 12 months), with 20-27% achieving seizure freedom by 12 months.
- Hypoglycemia occurred in two infants during initiation; overall tolerability was good, with most discontinuations due to lack of efficacy or loss to follow-up.
Conclusions:
- The ketogenic diet is an effective and well-tolerated treatment for intractable epilepsy in infants.
- In-hospital initiation is crucial for monitoring and managing potential adverse events like hypoglycemia.
- The diet offers a viable therapeutic strategy for improving seizure control in young infants with difficult-to-treat epilepsy.
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