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The ketogenic diet in infants--Advantages of early use
Anastasia Dressler1, Petra Trimmel-Schwahofer1, Eva Reithofer1
1Department of Pediatrics and Adolescent Medicine, Medical University Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria.
Insights
The ketogenic diet (KD) is effective for infant epilepsy, with more infants achieving long-term seizure freedom compared to older children. This epilepsy treatment is well-tolerated and recommended for early use.
Area of Science:
- Neurology
- Pediatric Epilepsy
- Ketogenic Diet Therapy
Background:
- The ketogenic diet (KD) is a well-established therapy for drug-resistant epilepsy.
- Its efficacy and safety in infants (<1.5 years) compared to older children are not well-defined.
Purpose of the Study:
- To compare the efficacy and safety of the ketogenic diet (KD) in infants versus older children with epilepsy.
- To evaluate long-term seizure control and diet acceptance in different age groups.
Main Methods:
- Retrospective analysis of 115 patients with epilepsy on KD for ≥3 months.
- Comparison of two groups: infants (<1.5 years) and children (>1.5 years) at KD initiation.
Main Results:
- No significant difference in responder rates at 3 months (63.8% vs. 57.9%).
- Infants showed higher seizure freedom rates at 3, 6, and 12 months (34.5% vs. 19%; 32.7% vs. 17.5%) and long-term (30.6% vs. 3.9%).
- Similar safety profiles and side effects; better initial acceptance in infants, though challenging with solid food introduction.
Conclusions:
- The ketogenic diet (KD) is highly effective and well-tolerated in infants with epilepsy.
- Early initiation of KD in infants leads to superior and sustained seizure freedom.
- The KD is recommended as an early therapeutic option for pediatric epilepsy.
Objective:
To evaluate the efficacy and safety of the ketogenic diet (KD) in infants (< 1.5 years of age) compared with older children.
Methods:
Patients with complete follow-up data of ≥ 3 months after initiation of the KD were analyzed retrospectively. Infants < 1.5 years at initiation of the KD (Group A) were compared with children > 1.5 years (Group B).
Results:
127 children were screened, 115 (Group A: 58/Group B: 57) were included. There were no significant differences between groups with respect to responder rates (63.8% vs. 57.9% at 3 months), but more infants became seizure free (34.5% vs. 19% at 3 months; 32.7% vs. 17.5% at 6 and 12 months). This result remained stable also after termination of the KD (30.6% vs. 3.9% at last follow-up) (p = 0.000). Looking at infants < 9 months of age separately (n = 42), this result was even stronger with significantly more infants being seizure free at 6 and at 12 months (p = 0.005, p = 0.014, respectively). In addition, a significantly higher number of infants remained seizure free in the long-term (p = 0.001). No group differences between infants and children with respect to safety were observed. Overall 52/115 patients (45.21%) reported side effects, but withdrawal of the KD was only necessary in one infant. Acceptance of the KD was better in infants compared with children at 3 months (0 vs. 14, p = 0.000), but became difficult when solid food was introduced (16 vs. 14; n.s.).
Significance:
According to our results, the KD is highly effective and well tolerated in infants with epilepsy. Seizure freedom is more often achieved and maintained in infants. Acceptance of the diet is better before the introduction of solid food. Therefore, we recommend the early use of the KD during the course of epilepsy.
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