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Ketogenic diet in Indian children with uncontrolled epilepsy
J K Nathan1, A S Purandare, Z B Parekh
1Department of Neurology, Shushrusha Hospital, Mumbai, India. jsvpnat@hotmail.com
Insights
The ketogenic diet is effective for controlling difficult epilepsy in Indian children. Epileptic encephalopathies showed better response to this diet compared to localization-related epilepsies.
Area of Science:
- Pediatric Neurology
- Metabolic Therapies
- Epilepsy Management
Background:
- Epilepsy is a common neurological disorder in children, often requiring multiple anti-seizure medications.
- Uncontrolled epilepsy significantly impacts a child's quality of life and development.
- The ketogenic diet is a high-fat, low-carbohydrate diet that has shown promise in managing refractory epilepsy.
Purpose of the Study:
- To assess the efficacy of a ketogenic diet in Indian children with uncontrolled epilepsy.
- To compare the diet's effectiveness in different epilepsy types: epileptic encephalopathies and localization-related epilepsies.
Main Methods:
- A prospective observational study was conducted at a hospital.
- 105 children (4 months to 18 years) with uncontrolled epilepsy were enrolled in a ketogenic diet program.
- Seizure frequency reduction was the primary outcome measure, with follow-up for a median of 17 months.
Main Results:
- 68 out of 105 children (65%) remained on the ketogenic diet.
- 37% achieved 100% seizure control, and 22% achieved 90-99% control.
- Epileptic encephalopathies demonstrated a more favorable response to the ketogenic diet than localization-related epilepsies.
Conclusions:
- The Indian adaptation of the ketogenic diet is well-tolerated and effective for managing drug-resistant childhood epilepsy.
- The ketogenic diet offers a viable therapeutic option for pediatric epilepsy in India.
- Epileptic encephalopathies appear to benefit more significantly from ketogenic diet therapy.
Objective:
To evaluate the efficacy of the ketogenic diet in Indian children with uncontrolled epilepsy.
Study Design:
Prospective observational study.
Setting:
Hospital based.
Patients:
105 children (age 4 months to 18 years) with uncontrolled epilepsy enrolled in the ketogenic diet program over a period of 9 years and followed up for 25.7+/- 20.3 months (median:17 months) on the ketogenic diet.
Main Outcome Measures:
Reduction in seizure frequency and comparison of improvement in two main groups of epilepsies, namely epileptic encephalopathies and localization related epilepsies.
Results:
Thirty seven (35%) out of 105 children dropped out of the study and 68 remained on the diet. Thirty nine (37%) achieved 100% control, 23 (22%) achieved between 90 and 99% control, 7 (6.8%) achieved between 75 and 90% control, and 16 (15.2%) achieved between 50 and 75% control. Twenty (19%) achieved less than 50% control. Epileptic encephalopathies had a better response than localization related epilepsies.
Conclusion:
The Indian version of ketogenic diet used is well tolerated and efficacious in controlling difficult-to-control epilepsy in children. Epileptic encephalopathies respond better than localization related epilepsies.
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