Efficacy and tolerability of the modified Atkins diet in children with drug-resistant genetic generalized epilepsy (notice n° 612144)

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fixed length control field 02715cam a2200217 4500500
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control field 20250121162737.0
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Language code of text/sound track or separate title fre
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100 10 - MAIN ENTRY--PERSONAL NAME
Personal name Kacker, Shawn
Relator term author
245 00 - TITLE STATEMENT
Title Efficacy and tolerability of the modified Atkins diet in children with drug-resistant genetic generalized epilepsy
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Date of publication, distribution, etc. 2022.<br/>
500 ## - GENERAL NOTE
General note 37
520 ## - SUMMARY, ETC.
Summary, etc. Objective. The ketogenic diet therapy is a time-tested and potent non-pharmacologic treatment for epilepsy. However, the study of the ketogenic diet in patients with genetic generalized epilepsy (GGE) is not widely established. The aim of this study was to evaluate the efficacy and tolerability of the modified Atkins diet, a variation of the ketogenic diets, as a treatment for drug-resistant GGE.Methods. A retrospective chart review was performed in patients with epilepsy treated with the modified Atkins diet at the University of Chicago from 2017 to 2020. For three months following diet initiation, participants were monitored for diet tolerability and effect on seizures. Response to the treatment was recorded by self-reporting patients and guardians.Results. Thirteen patients with a diagnosis of drug-resistant GGE were identified. An average of 3.8 anti-seizure medications (ASMs) had been tried and 3.4 years had elapsed from seizure onset before dietary therapy was attempted. Patients were receiving a mean of 2.2 ASMs at the time of diet initiation. After undergoing dietary treatment for three months, 12/13 (92%) patients experienced a greater than 50% reduction in seizure frequency, 6/13 (46%) patients became seizure-free, and 7/13 (54%) were able to discontinue at least one ASM. All patients completed at least three months of dietary therapy with an average duration of 9.3 months at the time of report. One patient reported side effects of fatigue which may be attributed to the diet.Significance. The modified Atkins diet has shown to be an effective and well-tolerated treatment for children with drug-resistant GGE. The diet provides the additional benefit of aiding to discontinue ASMs and, therefore, minimize the side effects from polypharmacy. Given these results, it seems reasonable to consider the modified Atkins diet as an alternative and possibly earlier treatment option for patients with drug-resistant GGE.
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element pediatric epilepsy
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element non-pharmacological treatment
690 ## - LOCAL SUBJECT ADDED ENTRY--TOPICAL TERM (OCLC, RLIN)
Topical term or geographic name as entry element ketogenic diet
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Nordli Jr, Douglas R.
Relator term author
700 10 - ADDED ENTRY--PERSONAL NAME
Personal name Phitsanuwong, Chalongchai
Relator term author
786 0# - DATA SOURCE ENTRY
Note Epileptic Disorders | Vol 24 | 2 | 2022-02-01 | p. 295-301 | 1294-9361
856 41 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://shs.cairn.info/revue-epileptic-disorders-2022-2-page-295?lang=en&redirect-ssocas=7080">https://shs.cairn.info/revue-epileptic-disorders-2022-2-page-295?lang=en&redirect-ssocas=7080</a>

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