DRAVET SYNDROME
The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: An Italian consensus
Article first published online: 4 APR 2011
DOI: 10.1111/j.1528-1167.2011.03010.x
Wiley Periodicals, Inc. © 2011 International League Against Epilepsy
Issue

Epilepsia
Special Issue: Severe Myoclonic Epilepsy – Dravet Syndrome: Thirty Years Later
Volume 52, Issue Supplement s2, pages 83–89, April 2011
Additional Information
How to Cite
Veggiotti, P., Burlina, A., Coppola, G., Cusmai, R., De Giorgis, V., Guerrini, R., Tagliabue, A. and Bernardina, B. D. (2011), The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: An Italian consensus. Epilepsia, 52: 83–89. doi: 10.1111/j.1528-1167.2011.03010.x
Publication History
- Issue published online: 4 APR 2011
- Article first published online: 4 APR 2011
- Abstract
- Article
- References
- Cited By
Keywords:
- Ketogenic diet;
- Clinical management;
- Drug-resistant epilepsy
Summary
Ketogenic diet is a nonpharmacologic treatment for childhood epilepsy not amenable to drugs. At the present time, two works based on national research, one in Germany and one in the United States provide international guidelines to ensure a correct management of the ketogenic diet. Our Italian collaborative study group was set up in order to formulate a consensus statement regarding the clinical management of the ketogenic diet, patient selection, pre–ketogenic diet, counseling, setting and enforcement of dietary induction of ketosis, follow-up management, and eventual discontinuation of the diet.

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