×

Message

EU e-Privacy Directive

This website uses cookies to manage authentication, navigation, and other functions. By using our website, you agree that we can place these types of cookies on your device.

View e-Privacy Directive Documents

You have declined cookies. This decision can be reversed.

Anticonvulsants

Ketogenic Diet for the Management of Epilepsy Associated with Tuberous Sclerosis Complex in Children📎

Written by CYBERMED LIFE NEWS
Attachments:
Download this file (Ketogenic Diet for the Management of Epilepsy Associated with Tuberous Sclerosis Complex in Children..pdf)Ketogenic Diet for the Management of Epilepsy Associated with Tuberous Sclerosis Complex in Children..pdf[Ketogenic Diet for the Management of Epilepsy Associated with Tuberous Sclerosis Complex in Children.]357 kB
Abstract Title:

Ketogenic Diet for the Management of Epilepsy Associated with Tuberous Sclerosis Complex in Children.

Abstract Source:

J Epilepsy Res. 2017 Jun ;7(1):45-49. Epub 2017 Jun 30. PMID: 28775955

Abstract Author(s):

Soyoung Park, Eun Joo Lee, Soyong Eom, Hoon-Chul Kang, Joon Soo Lee, Heung Dong Kim

Article Affiliation:

Soyoung Park

Abstract:

BACKGROUND AND PURPOSE: In the present study, we reviewed the outcome of ketogenic diet (KD) use for the management of epilepsy in children with tuberous sclerosis complex (TSC).

METHODS: A total of 12 children with intractable epilepsy associated with TSC who were treated with KD at our hospital between March 1, 2008 and February 28, 2015 were retrospectively enrolled.

RESULTS: The mean age at the time of KD initiation was 73.1± 38.0 months. Patients were medically refractory to a mean of 4.8 ± 1.7 antiepileptic drugs. Nine patients (75.0%) had a history of infantile spasms. At 3 months after KD initiation, 10 patients (83.3%) had>50% seizure reduction. Moreover, 7 patients (58.3%) exhibited qualitative improvements in cognition and behavior after KD initiation, as reported by caregivers/parents. The mean duration of dietary therapy was 14.8± 12.8 months. Half of the patients in this study eventually underwent epilepsy surgery due to persistent seizures or seizure relapse.

CONCLUSION: KD is an important non-pharmacological treatment option for patients with intractable epilepsy associated with TSC. KD may improve cognition and behavior in addition to reducing seizure frequency.