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Modified Atkins diet versus levetiracetam for non-surgical drug-resistant epilepsy in children: A randomized
Archna1, Divyani Garg2, Shaiphali Goel1
1Department of Pediatrics (Neurology division), Kalawati Saran Children's Hospital and Lady Hardinge Medical College, New Delhi, India.
Insights
The modified Atkins diet (MAD) significantly reduced seizures in children with drug-resistant epilepsy (DRE) more effectively than levetiracetam. Both treatments were well-tolerated, with MAD showing superior efficacy in this pediatric population.
Area of Science:
- Pediatric Neurology
- Clinical Nutrition
- Epileptology
Background:
- Drug-resistant epilepsy (DRE) poses a significant challenge in pediatric populations.
- The modified Atkins diet (MAD) is an emerging therapeutic option for DRE.
- Levetiracetam is a commonly used anti-seizure medication in children.
Purpose of the Study:
- To compare the efficacy of add-on modified Atkins diet (MAD) versus levetiracetam in children with non-surgical drug-resistant epilepsy (DRE).
- To evaluate seizure reduction and tolerability of MAD and levetiracetam as adjunctive therapies.
Main Methods:
- An open-label, randomized controlled trial involving 101 children (aged 2-12 years) with non-surgical DRE.
- Participants were randomized to receive either add-on MAD or levetiracetam for 12 weeks.
- Primary outcome was the proportion of responders achieving >50% seizure reduction, assessed via parental seizure logs.
Main Results:
- A significantly higher proportion of children in the MAD group (52.9%) responded compared to the levetiracetam group (22%) (p < 0.001).
- Mean seizure frequency reduction was greater with MAD (-47.33%) than levetiracetam (-31.15%) (p = 0.03).
- Constipation was the most common adverse event in the MAD group (41.1%), while sedation/lethargy (18%) and irritability (14%) were most frequent with levetiracetam.
Conclusions:
- Add-on modified Atkins diet (MAD) is superior to levetiracetam in achieving seizure reduction in children with non-surgical DRE, particularly those with generalized seizures.
- Both MAD and levetiracetam were well-tolerated in the study population.
- Adverse effects were manageable and consistent with known side effect profiles for each intervention.
Background:
This study was undertaken to compare the efficacy of modified Atkins diet (MAD) among children with non-surgical drug-resistant epilepsy (DRE) to levetiracetam, when added to on-going anti-seizure medications.
Methods:
An open-label, randomized controlled trial among children aged 2-12 years with non-surgical DRE was conducted. Eligible children were randomized in a 1:1 ratio to receive add-on MAD or levetiracetam. Baseline and post-intervention seizure frequency at 12 weeks was determined from seizure logs maintained by parents. The primary outcome was the proportion of responders, i.e., patients who achieved > 50% seizure reduction from baseline. Adverse events were compared. Analysis was intention-to-treat. (NCT04172311) RESULTS: One hundred and one children were enrolled (MAD-51, levetiracetam-50). The majority of the enrolled children had generalized seizures of mixed types secondary to structural brain lesions and Lennox-Gastaut syndrome was the most common electroclinical syndrome (46%). The proportion of children with >50% seizure reduction at 12 weeks was significantly higher in the MAD arm compared to the levetiracetam arm (27/51(52.9%) vs 11/50(22%); p < 0.001). At 12-weeks post-intervention, the change in mean seizure frequency compared to baseline was -47.33 ± 39.57% in the MAD arm and -31.15 ± 32.18% in the levetiracetam arm (p = 0.03). Constipation (41.1%) was the most frequent adverse effect with MAD. Sedation/lethargy (18%) and anxiety and irritability (14%) were the most frequent adverse effects in the levetiracetam group.
Conclusion:
Addition of MAD was found to be superior to levetiracetam among children with non-surgical DRE with predominant generalized seizures in achieving seizure reduction at 12 weeks. Both treatments were well tolerated. Adverse effects, although higher with MAD, were expected side effects.
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