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Low Glycemic Index Treatment in pediatric refractory epilepsy: the first Middle East report
Parvaneh Karimzadeh1, Mostafa Sedighi2, Maryam Beheshti3
1Paediatric Neurology Research Center, Mofid Children's Hospital, Tehran, Iran; Department of Paediatric Neurology, Mofid Children's Hospital, Tehran, Iran.
Insights
Low Glycemic Index Treatment (LGIT) effectively reduced seizures in pediatric patients with intractable epilepsy. This safe dietary therapy offers an alternative when ketogenic diets are not feasible.
Area of Science:
- Pediatric Neurology
- Dietary Therapy
- Epilepsy Management
Background:
- Intractable epilepsy presents significant challenges in pediatric care.
- Effective treatment options are crucial for improving quality of life in affected children.
Purpose of the Study:
- To evaluate the efficacy and tolerability of Low Glycemic Index Treatment (LGIT) in pediatric patients with intractable epilepsy.
- To assess LGIT as a potential alternative antiepileptic therapy.
Main Methods:
- A study involving 42 children (1.5-17 years) with refractory epilepsy.
- LGIT involved a diet of 65% fat, 25% protein, 10% carbohydrate (40-60g) with a glycemic index below 50.
- Data collected included clinical status, seizure frequency, biochemistry, neuro-imaging, and EEG.
Main Results:
- Significant seizure reduction (>50%) observed in 71.4% by week 2, 73.8% by month 1, and 77.8% by month 2.
- Mild increase in blood urea nitrogen (BUN) noted in 30% of patients.
- Dietary restrictiveness and lack of satiation were primary reasons for discontinuation; no significant complications occurred.
Conclusions:
- LGIT demonstrates safety and efficacy as an adjunctive antiepileptic treatment.
- LGIT can serve as a viable alternative to the ketogenic diet for pediatric epilepsy when the latter is not suitable.
Purpose:
Intractable epilepsy is a challenging aspects of pediatric epilepsy. This study was conducted to determine the efficacy and tolerability of Low Glycemic Index Treatment (LGIT) in pediatric patients referred to a Children's Hospital in Iran with intractable epilepsy.
Methods:
We studied 42 children with refractory epilepsy aged between 1.5 and 17 years of age, from October 2009 to April 2011 in the pediatric neurology department of Mofid Children's Hospital. Patient information on clinical status, seizure type, and baseline frequency, blood and urine biochemistry, neuro-imaging and the EEG were collected. LGIT was initiated on an outpatient basis and the diet was composed of 65% fat, 25% protein and 10% carbohydrate (40-60 g), and the glycemic index of foods was limited to below 50.
Results:
84% of patients were categorized as having more than one seizure per day at study entry, with the remaining children as experiencing over one seizure per week. A greater than 50% seizure reduction was observed in 71.4% of the patients after the second week, in 73.8% at the end of the first month and in 77.8% at the end of the second month. In 30% of the patients a mild increase in blood urea nitrogen (BUN) was detected. The most important reasons for discontinuation of LGIT were restrictiveness, lack of satiation and excessive meat in this diet. No significant complications were observed during the administration of the diet.
Conclusion:
LGIT is a safe and effective adjuvant antiepileptic therapy and may be used as an alternative to the ketogenic diet in conditions when this diet cannot be used.
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