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Efficacy and safety of ketogenic dietary theraphies in infancy. A single-center experience in 42 infants less than two years of age.
Ruiz-Herrero, Jana; Cañedo-Villarroya, Elvira; Pérez-Sebastián, Isabel; Bernardino-Cuesta, Beatriz; Pedrón-Giner, Consuelo.
Afiliación
  • Ruiz-Herrero J; Department of Pediatric Gastroenterology, Pediatric Service, San Rafael Hospital, Madrid, Spain. Electronic address: jana.ruizherrero@hotmail.com.
  • Cañedo-Villarroya E; Department of Gastroenterology and Nutrition, University Children´s Hospital Niño Jesús, Madrid, Spain.
  • Pérez-Sebastián I; Department of Pediatric Neurology, Pediatric Service, University Hospital La Moraleja, Madrid, Spain.
  • Bernardino-Cuesta B; Department of Neurology, University Children´s Hospital Niño Jesús, Madrid, Spain.
  • Pedrón-Giner C; Department of Gastroenterology and Nutrition, University Children´s Hospital Niño Jesús, Madrid, Spain. Electronic address: consuelocarmen.pedron@salud.madrid.org.
Seizure ; 92: 106-111, 2021 Nov.
Article en En | MEDLINE | ID: mdl-34500220
ABSTRACT

PURPOSE:

Ketogenic dietary therapies (KDT) are high-fat and low-carbohydrate diets that may achieve seizure control and improve cognitive state. We describe our KDT experience in infants (children less than two years of age). RESEARCH METHODS & PROCEDURES We conducted a retrospective, descriptive and observational study of 42 infants treated with KDT between 2000-2018.

RESULTS:

The types of KDT started were classic ketogenic diet ratio 31 (40), ratio 41 (1) and modified ketogenic diet with medium-chain triglycerides (1). Four patients switched to a modified Atkins diet. During follow-up, 79%, 57%, 38% and 17% of infants remained on KDT at 3, 6, 12 and 24 months, respectively. Seizure reduction ≥50% compared to baseline was achieved in 50%, 45%, 38% and 17% at 3, 6, 12 and 24 months, respectively. Seizure control was excellent (reduction >90%) in 33%, 31%, 26% and 12%, and seizure-free infants were 9, 9, 10 and 4, at different follow-up intervals, respectively. Sixty-three percent of infants with West syndrome were responders to KDT. Mean length of KDT was 390 days (16 days-4.9 years). Ineffectiveness was the reason for withdrawal in 50% of patients. Early adverse effects (during first month) occurred in 40% of infants. The most frequent early side effects were asymptomatic hypoglycemia and gastrointestinal disturbances. Late-onset side effects occurred in 55-14% of infants during therapy, and most frequent were hypercalciuria and dyslipidaemia.

CONCLUSION:

KDT are useful and effective treatments in infancy. Side effects are frequent but mild and easy to manage.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dieta Cetogénica / Epilepsia Refractaria Tipo de estudio: Observational_studies Límite: Child / Humans / Infant Idioma: En Revista: Seizure Asunto de la revista: NEUROLOGIA Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dieta Cetogénica / Epilepsia Refractaria Tipo de estudio: Observational_studies Límite: Child / Humans / Infant Idioma: En Revista: Seizure Asunto de la revista: NEUROLOGIA Año: 2021 Tipo del documento: Article