Literature DB >> 18823325

Optimal clinical management of children receiving the ketogenic diet: recommendations of the International Ketogenic Diet Study Group.

Eric H Kossoff1, Beth A Zupec-Kania, Per E Amark, Karen R Ballaban-Gil, A G Christina Bergqvist, Robyn Blackford, Jeffrey R Buchhalter, Roberto H Caraballo, J Helen Cross, Maria G Dahlin, Elizabeth J Donner, Joerg Klepper, Rana S Jehle, Heung Dong Kim, Y M Christiana Liu, Judy Nation, Douglas R Nordli, Heidi H Pfeifer, Jong M Rho, Carl E Stafstrom, Elizabeth A Thiele, Zahava Turner, Elaine C Wirrell, James W Wheless, Pierangelo Veggiotti, Eileen P G Vining.   

Abstract

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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Year:  2008        PMID: 18823325     DOI: 10.1111/j.1528-1167.2008.01765.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  90 in total

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4.  The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients.

Authors:  Kavi P Patel; Thomas W O'Brien; Sankarasubramon H Subramony; Jonathan Shuster; Peter W Stacpoole
Journal:  Mol Genet Metab       Date:  2012-07       Impact factor: 4.797

5.  Dietary and medication adjustments to improve seizure control in patients treated with the ketogenic diet.

Authors:  Jessica H Selter; Zahava Turner; Sarah C Doerrer; Eric H Kossoff
Journal:  J Child Neurol       Date:  2014-05-22       Impact factor: 1.987

Review 6.  Epileptic encephalopathies: new genes and new pathways.

Authors:  Sahar Esmaeeli Nieh; Elliott H Sherr
Journal:  Neurotherapeutics       Date:  2014-10       Impact factor: 7.620

7.  The ketogenic diet is well tolerated and can be effective in patients with argininosuccinate lyase deficiency and refractory epilepsy.

Authors:  Rosanne Peuscher; Monique E Dijsselhof; Nico G Abeling; Margreet Van Rijn; Francjan J Van Spronsen; Annet M Bosch
Journal:  JIMD Rep       Date:  2011-12-25

8.  Pyruvate dehydrogenase-e1α deficiency presenting as recurrent demyelination: an unusual presentation and a novel mutation.

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9.  Ketogenic diet: rapid onset of selenium deficiency-induced cardiac decompensation.

Authors:  Naga S Sirikonda; William D Patten; John R Phillips; Charles J Mullett
Journal:  Pediatr Cardiol       Date:  2012-02-25       Impact factor: 1.655

10.  Ketogenic diets and thermal pain: dissociation of hypoalgesia, elevated ketones, and lowered glucose in rats.

Authors:  David N Ruskin; Tracey A C S Suter; Jessica L Ross; Susan A Masino
Journal:  J Pain       Date:  2013-03-15       Impact factor: 5.820

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