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Published on: January 7, 2019
Infantile spasms treated with the ketogenic diet: prospective single-center experience in 104 consecutive infants
Amanda M Hong1, Zahava Turner, Rana F Hamdy
1The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Insights
The ketogenic diet (KD) effectively treats intractable infantile spasms (IS) in about two-thirds of infants. Consider this diet after other treatments like corticosteroids and vigabatrin have failed.
Area of Science:
- Neurology
- Pediatrics
- Dietary Therapy
Background:
- Infantile spasms (IS) are a severe epilepsy syndrome in infants.
- Intractable IS often requires exploring alternative treatment options.
- The ketogenic diet (KD) has emerged as a potential therapy for refractory epilepsy.
Purpose of the Study:
- To evaluate the efficacy and safety of the KD for infantile spasms (IS).
- To assess the KD's impact on spasm frequency, development, and EEG findings.
- To identify factors associated with positive treatment response.
Main Methods:
- Prospective study of 104 infants with documented IS and hypsarrhythmia.
- Infants were initiated on a traditional KD between 1996 and 2009.
- Efficacy assessed via clinical evaluation, phone communication, and EEG monitoring.
Main Results:
- 64% of infants showed >50% spasm improvement at 6 months; 37% became spasm-free.
- 62% experienced developmental improvement, and 35% showed EEG improvement.
- Adverse effects occurred in 33%, with diminished linear growth in 6%.
Conclusions:
- The KD is an efficacious treatment for IS in approximately two-thirds of patients.
- The KD should be strongly considered after failure of first-line therapies like corticosteroids and vigabatrin.
- Older age at onset and fewer prior anticonvulsants predicted better spasm control.
Purpose:
In 2002, we reported our preliminary experience using the ketogenic diet (KD) for predominantly intractable infantile spasms (IS) in 23 infants. Since that time, we have increased our use of the KD for this condition including those with new-onset IS.
Methods:
Infants were referred and prospectively started on the traditional KD from 1996 to 2009 at our institution. Included subjects had documented clinical IS, hypsarrhythmia on electroencephalography (EEG), and parental consent to start the KD. Efficacy was assessed through phone communication, clinic visits, and EEG every 3 months.
Results:
One hundred four infants, mean age 1.2 years, were started on the KD for IS, of which 74 (71%) had a symptomatic etiology. Previous therapy for this patients included a mean of 3.6 anticonvulsants; 71% including corticosteroids or vigabatrin. Using an intent-to-treat analysis, > 50% spasm improvement occurred in 64% at 6 months and 77% after 1-2 years. Thirty-eight (37%) became spasm-free for at least a 6-month period within a median 2.4 months of starting the KD. In addition, 62% reported improvement in development, 35% had EEG improvement, and 29% were able to reduce concurrent anticonvulsants. Adverse effects were noted in 33%, of which 6% had diminished linear growth. Older age at onset of IS and fewer prior anticonvulsants were more likely to be associated with > 90% spasm improvement at 6 months.
Discussion:
The KD is an efficacious therapy for IS in approximately two-thirds of patients treated, and it should be considered strongly after failure of corticosteroids and vigabatrin.
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