生酮饮食
中止
医学
神经学
不利影响
儿科
家庭医学
小儿神经病学
重症监护医学
癫痫
精神科
内科学
作者
Eric H. Kossoff,Beth Zupec‐Kania,Per Åmark,Karen Ballaban‐Gil,Anna Bergqvist,Robyn Blackford,Jeffrey Buchhalter,Roberto Caraballo,J. Helen Cross,Maria Dahlin,Elizabeth Donner,Joerg Klepper,Rana Jehle,Heung Dong Kim,Y. M. Christiana Liu,Judy Nation,Douglas R. Nordli,Heidi H. Pfeifer,Jong M. Rho,Carl E. Stafstrom
出处
期刊:Epilepsia
[Wiley]
日期:2008-09-24
卷期号:50 (2): 304-317
被引量:600
标识
DOI:10.1111/j.1528-1167.2008.01765.x
摘要
The ketogenic diet (KD) is an established, effective nonpharmacologic treatment for intractable childhood epilepsy. The KD is provided differently throughout the world, with occasionally significant variations in its administration. There exists a need for more standardized protocols and management recommendations for clinical and research use. In December 2006, The Charlie Foundation commissioned a panel comprised of 26 pediatric epileptologists and dietitians from nine countries with particular expertise using the KD. This group was created in order to create a consensus statement regarding the clinical management of the KD. Subsequently endorsed by the Practice Committee of the Child Neurology Society, this resultant manuscript addresses issues such as patient selection, pre-KD counseling and evaluation, specific dietary therapy selection, implementation, supplementation, follow-up management, adverse event monitoring, and eventual KD discontinuation. This paper highlights recommendations based on best evidence, including areas of agreement and controversy, unanswered questions, and future research.
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