Three and Six Months of Ketogenic Diet for Intractable Childhood Epilepsy: A Systematic Review and Meta-Analysis
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Xian Yu Liu1, Jing Chen1, Min Zhu1
1Department of Pediatric Neurology, Children's Hospital of Nanjing Medical University, Nanjing, China.
Insights
The ketogenic diet (KD) effectively treats childhood epilepsy. Spasm remission at 3 months on KD can predict treatment success at 6 months, allowing for timely, personalized support.
Area of Science:
- Neurology
- Dietary Therapies
Background:
- The ketogenic diet (KD) is a recognized treatment for intractable childhood epilepsy.
- The optimal duration for assessing KD efficacy, specifically 3 months, lacks statistical definition.
- This study evaluates if early spasm remission predicts longer-term (6-month) therapeutic outcomes.
Approach:
- A systematic literature search was conducted across major databases up to May 2018.
- Included studies focused on intractable childhood epilepsy with specific 3- and 6-month follow-ups and spasm remission data.
- Data on seizure reduction, diet types, and study design were extracted from 18 eligible articles involving 1,062 patients.
Key Points:
- Meta-analysis of 18 studies with 1,062 patients confirmed the ketogenic diet's role in childhood epilepsy.
- No statistically significant differences were found in 50% seizure reduction (-0.01), 90% seizure reduction (-0.036), or seizure freedom (-0.031) between 3- and 6-month treatment periods.
- Early spasm remission at 3 months shows potential as a predictive index for 6-month outcomes.
Conclusions:
- Three months of the ketogenic diet can serve as a reliable predictor for 6-month spasm remission in childhood epilepsy.
- This finding supports using the 3-month mark for timely seizure remission evaluation.
- Early assessment enables personalized support and intervention adjustments for pediatric epilepsy patients on the ketogenic diet.
Abstract:
Objective: The ketogenic diet (KD) has been an effective antiepileptic treatment for intractable childhood epilepsy. The appropriate timing to evaluate the effect of KD is 3 months which is still not defined statistically. Therefore, we aim to realistically assess whether spasm remission during the period of 3 months KD can be a prediction index for the therapeutic effect of 6 months treatment. Methods: To investigate the duration and effect of the KD therapy for intractable childhood epilepsy, we searched the relevant articles up to May 20, 2018 from PubMed, Cochrane, Embase, Ovid, Web of Science, Google Scholar, and Conference literature. The inclusion criteria were: (i) confirmed cases of intractable childhood epilepsy, (ii) specific 3 and 6 months follow-up time, (iii) classified spasm remission evaluation. The exclusion criteria were: (i) including other therapy, (ii) unspecific follow-up time, (iii) no specific index for seizure reduction. The data extracted by two researchers independently included proportion of KD duration, seizure remission, year of publication, author, study design, and diet varieties. Results: The search strategy included a total of 542 citations, 18 articles were met the criteria with a total of 1,062 patients included in the final analysis. Compared with 3 and 6 months KD treatment, the rate difference of 50% seizure reduction was -0.01(95% CI: -0.09 to 0.06). And 90% seizure reduction was -0.036(95% CI: -0.090 to 0.017) and seizure free was -0.031(95% CI: -0.081 to 0.020). Conclusion: This meta-analysis provides statistical support that a period of 3 months KD can be a prediction index of 6 months duration in term of spasm remission. The 3 months KD can be implemented to evaluate seizure remission timely and provide personalized early support.
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